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Bittermelon Tech
Bittermelon Tech
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BITTER MELON
(Momordica charantia)
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Bitter Melon
Preprinted from Herbal Secrets of the Rainforest, 2nd edition, by Leslie Taylor Published and copyrighted by Sage Press, Inc., 2002
Family: Cucurbitaceae Genus: Momordica Species: charantia Synonyms: Momordica chinensis, M. elegans, M. indica, M. operculata, M. sinensis, Sicyos fauriei Common names: Bitter melon, papailla, melao de sao caetano, bittergourd, sorosi, a'jayib al maasi, assorossie, balsam apple, balsam pear, chin li chih, ejinrin gule khandan, fu-kua, karela, k'u kua kurela, kor-kuey, ku gua, lai p'u t'ao, pava-aki, salsamino, sorci, sorossi, sorossie, sorossies, pare, peria laut, peria Part Used: Whole plant, Fruit, Seed Bitter melon grows in tropical areas, including parts of the Amazon, east Africa, Asia, and the Caribbean, and is cultivated throughout South America as a food and medicine. It's a slender, climbing annual vine with long-stalked leaves and yellow, solitary male and female flowers borne in the leaf axils. The fruit appears as a warty gourd, usually oblong and resembling a small cucumber. The young fruit is emerald green, turning to orange-yellow when ripe. At maturity the fruit splits into three irregular valves that curl backwards and release numerous brown or white seeds encased in scarlet arils. The Latin name Momordica means to bite (referring to the jagged edges of the leaf, which appear as if they have been bitten). All parts of the plant, including the fruit, taste very bitter. In the Amazon, local people and indigenous tribes grow bitter melon in their gardens for food and medicine. They add the fruit and/or leaves to beans and soup for a bitter or sour flavor; parboiling it first with a dash of salt may remove some of the bitter taste. Medicinally, the plant has a long history of use by the indigenous peoples of the Amazon. A leaf tea is employed for diabetes; as a carminative for colic; topically for sores, wounds, and infections; internally and externally for worms and parasites; as an emmenagogue; and as an antiviral for measles, hepatitis, and feverish conditions. In Brazilian herbal medicine, bitter melon is used for tumors, wounds, rheumatism, malaria, leucorrhea, inflammation, menstrual problems, diabetes, colic, fevers, worms, to induce abortions, and as an aphrodisiac. It is also employed topically for skin problems, vaginitis, hemorrhoids, scabies, itchy rashes, eczema, and leprosy. In Mexico the entire plant is used for diabetes and dysentery; the root is a reputed aphrodisiac. In Peruvian herbal medicine, the leaf or aerial parts of the plant are used to treat measles, malaria, and all types of inflammation. In Nicaragua the leaf commonly is used for stomach pain, diabetes, fevers, colds, coughs, headaches, malaria, skin complaints, menstrual disorders, aches and pains, hypertension, infections, and as an aid in childbirth. Many in vivo clinical studies have demonstrated the relatively low toxicity of all parts of the bitter melon plant when ingested orally. However, toxicity and even death in laboratory animals has been reported when extracts are injected intravenously or intraperitoneally (with the fruit and seed demonstrating greater toxicity than the leaf or aerial parts of the plant).1 Other studies have shown ethanol and water extracts of the fruit and leaf (ingested orally) to be safe during pregnancy. 2,3 The seeds, however, have demonstrated the ability to induce abortions in rats and mice, and the root has been documented with a uterine stimulant effect in animals.4-7 The fruit and leaf of bitter melon has demonstrated an in vivo antifertility effect in female animals; 8,9 in male animals, it was reported to affect the production of sperm negatively.10
1
Bitter melon contains an array of novel and biologically active phytochemicals including triterpenes, proteins and steroids. In numerous studies, at least three different groups of constituents found in all parts of bitter melon have clinically demonstrated hypoglycemic properties (blood sugar lowering) or other actions of potential benefit against diabetes mellitus.11-20 These hypoglycemic chemicals include a mixture of steroidal saponins known as charantins, insulin-like peptides, and alkaloids. The hypoglycemic effect is more pronounced in the fruit of bitter melon where these chemicals are in greater abundance. To date, close to 100 in vivo studies have demonstrated the blood glucose-lowering effect of this bitter fruit. The fruit has also shown the ability to enhance cells uptake of glucose,21 to promote insulin release, and potentiate the effect of insulin.22,23 In other in vivo studies, bitter melon fruit and/or seed has been shown to reduce total cholesterol and triglycerides in both the presence and absence of dietary cholesterol.24,25 In one study, elevated cholesterol and triglyceride levels in diabetic rats were returned to normal after 10 weeks of treatment.25 A novel phytochemical in bitter melon has clinically demonstrated the ability to inhibit an enzyme named guanylate cyclase. This enzyme is thought to be linked to the pathogenesis and replication of not only psoriasis, but leukemia and cancer as well.26-32 Other phytochemicals that have been documented with cytotoxic activity are a group of ribosome-inactivating proteins named alpha- and beta-momorcharin, momordin, and cucurbitacin B. A chemical analog of bitter melon proteins was developed and named MAP-30 and its inventors reported that it was able to inhibit prostate tumor growth.33 The phytochemical momordin has clinically demonstrated cytotoxic activity against Hodgkins lymphoma in vivo,34 and several other in vivo studies have demonstrated the cytostatic and antitumor activity of the entire plant of bitter melon. In one study, a water extract blocked the growth of rat prostate carcinoma;31 another study reported that a hot water extract of the entire plant inhibited the development of mammary tumors in mice.35 Numerous in vitro studies have also demonstrated the anti-cancerous and anti-leukemic activity of bitter melon against numerous cell lines including liver cancer, human leukemia, melanoma and solid sarcomas.28,36-38 Bitter melon (and several of its isolated phytochemicals) also has been documented with in vitro antiviral activity against numerous viruses including Epstein-Barr, herpes, and HIV viruses.39 In an in vivo study, a leaf extract demonstrated the ability to increase resistance to viral infections as well as to provide an immunostimulant effect in humans and animals (increasing interferon production and natural killer cell activity).40 Two proteins known as alpha- and beta-momorcharin (which are present in the seeds, fruit, and leaves) have been reported to inhibit the HIV virus in vitro.41-43 In one study, HIV-infected cells treated with alpha- and beta-momorcharin showed a nearly complete loss of viral antigen while healthy cells were largely unaffected.43 In 1996 the inventors of the chemical protein analog MAP-30 filed a U.S. patent, stating it was useful for treating tumors and HIV infections . . . In treating HIV infections, the protein is administered alone or in conjunction with conventional AIDS therapies.44 Another clinical study showed that MAP-30s antiviral activity was also relative to the herpes virus in vitro.45 In addition to these properties, leaf extracts of bitter melon have clinically demonstrated broad spectrum antimicrobial activity. Various water, ethanol, and methanol extracts of the leaves have demonstrated in vitro antibacterial activities against E. coli, Staphylococcus, Pseudomonas, Salmonella, Streptobacillus and Streptococcus;46-49 an extract of the entire plant was shown to have antiprotozoal activity against Entamoeba histolytica.50 The fruit and fruit juice has demonstrated the same type of antibacterial properties and, in another study, a fruit extract has demonstrated activity against the stomach ulcer-causing bacteria Helicobacter pylori.51 Over the years scientists have verified many of the traditional uses of this bitter plant that continues to be an important natural remedy in the natural health practitioners medicine chest. Bitter melon capsules and tinctures are becoming more widely available in the U.S. and are employed by natural health practitioners for diabetes, viruses, colds and flu, and psoriasis.
2
Concentrated fruit or seed extracts can be found in capsules and tablets, as well as whole herb/vine powders and extracts in capsules and tinctures. Documented Properties and Actions: Anthelmintic, antibacterial, antibiotic, antidiabetic, antiinflammatory, antileukemic, antimicrobial, antimutagenic, antimycobacterial, antioxidant, antitumor, antiulcer, antiviral, aperitive, aphrodisiac, astringent, carminative, cytostatic, cytotoxic, depurative, hormonal, hypocholesterolemic, hypotensive, hypotriglyceridemic, hypoglycemic, immunostimulant, insecticidal, lactagogue, laxative, purgative, refrigerant, stomachic, styptic, tonic, vermifuge Main Phytochemicals: Alkaloids, charantin, charine, cryptoxanthin, cucurbitins, cucurbitacins, cucurbitanes, cycloartenols, diosgenin, elaeostearic acids, erythrodiol, galacturonic acids, gentisic acid, goyaglycosides, goyasaponins, guanylate cyclase inhibitors, gypsogenin, hydroxytryptamines, karounidiols, lanosterol, lauric acid, linoleic acid, linolenic acid, momorcharasides, momorcharins, momordenol, momordicilin, momordicins, momordicinin, momordicosides, momordin, momordolo, multiflorenol, myristic acid, nerolidol, oleanolic acid, oleic
acid, oxalic acid, pentadecans, peptides, petroselinic acid, polypeptides, proteins, ribosome-inactivating proteins, rosmarinic acid, rubixanthin, spinasterol, steroidal glycosides, stigmasta-diols, stigmasterol, taraxerol, trehalose, trypsin inhibitors, uracil, vacine, v-insulin, verbascoside, vicine, zeatin, zeatin riboside, zeaxanthin, zeinoxanthin
Traditional Remedy: One-half to 1 cup of a standard leaf or whole herb decoction 12 times daily or 13 ml of a 4:1 tincture twice daily. One to 2 grams of powdered leaf in tablets or capsules daily can be substituted if desired. The traditional South American remedy for diabetes is to juice 12 fresh bitter melon fruits and drink twice daily. For seed or fruit extracts in capsules or tinctures, follow the labeled instructions. Contraindications: Bitter melon traditionally has been used as an abortive and has weak uterine stimulant activity; therefore, it is contraindicated during pregnancy. This plant has been documented to reduce fertility in both males and females and should therefore not be used by those undergoing fertility treatment or seeking pregnancy. The active chemicals in bitter melon can be transferred through breast milk; therefore, it is contraindicated in women who are breast feeding. All parts of bitter melon (especially the fruit and seed) have demonstrated in numerous in vivo studies that they lower blood glucose levels. As such, it is contraindicated in persons with hypoglycemia. Diabetics should check with their physicians before using this plant and use with caution while monitoring their blood sugar levels regularly. Although all parts of the plant have demonstrated active antibacterial activity, none have shown activity against fungi or yeast. Long-term use of this plant may result in the die-off of friendly bacteria with resulting yeast/candida opportunistic overgrowth. Cycling off the use of the plant (every 30 days for one week) may be warranted, and adding probiotics to the diet may be beneficial if this plant is used for longer than 30 days. The fruit and seed of bitter melon have demonstrated (in animal studies) to lower blood cholesterol levels. Persons on medications to lower blood cholesterol should monitor their cholesterol levels. Drug Interactions: May potentiate insulin and anti-diabetic drugs. May potentiate cholesterol-lowering drugs.
Bra zil
India
Mexico
M alaya
Nicaragua
Panama
Peru
Trinidad
Co untry
Uses Abdomen, abortifacient, allergy, amo eba, anemia, anthelmintic, app etite stim ulant, arthritis, as thm a, astringent, antibiotic, aphrodisiac, boil, burn, bilious, bladder, canc er, cancer (breast), carminative, cold, colic, colitis, cough, catarrh, cicatrizant, chilblain, childbirth, constipation, con trace ptive, depurative, diabetes, diarrhea, dyspepsia, dysentery, dysmenorrhea, earache, emetic, emm enagogue, eruption , eye (ve terinary), fever, flatulen ce, flu, food, gout, halitosis, headache, hea rt, hem orrh oids , hepatitis, hyperglycemia, hypertension, hypoglycemic, itch, indigestion, infection, inflamm ation, insecticide, jaundice, kidney (stones), lactagogue, laxative, leprosy, liver, m alignancy, night blindness, pain (intestine), phlegm, pile, poison, pruritus, psoriasis, purgative, pyrexia, malaria, menstrual abnormalities, m enstrual suppression, refrigerant, rheum atis m , ringworm , roun dwo rm s, sk in, skin (fun gal), snak ebite, s oap , sore, sore (m outh), spleen, splenitis, stomachache, stomachic, stone, styptic, throat (sore), thrush, tirednes s, tonic, ulcer (m alignant), ulcer (peptic) urethritis, vermifuge, wound
Elsew here
References:
1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. Sharma, V. N ., et al. Som e observa tions on hypoglycaem ic activity of Mo mordica charantia . Indian J. Med. Res. 1960; 48(4): 471-47. Dhawan, B. N., et al. Sc reen ing of Indian plants for biologica l activity. Part IX . Indian J. Ex p. B iol. 1980; 18: 594606. Prakash, A. O., et al. Screening of Indian plants for antifertility activity. Indian J. E xp. Bio l. 1976; 14: 623626. S hum , L. K . W ., et al. Effects of Mo mordica charantia seed extract on the rat mid-term placenta. Abstract 78. Abstract International Symposium on Chinese Medicinal Material Research. 1984; 1214. Dong, T. X., et al. Ribosome inactiva ting pro tein-like activity in seeds of dive rse Cucurbitace ae p lants. Indian J. E xp. Bio l. 1993; 25(3): 41519. Ng, T. B., et al. Investigation of ribosom e inac tivating protein-like activity in tissue s of C ucu rbitaceae plants . Ind ian J. E xp. Bio l. 1989; 21(12): 135358. Jam wa l, K. S., et al. Preliminary screening of so m e rep uted abo rtifacien t indigenou s plan ts. Indian J. Pharmacy 1962; 24: 21820. Stepka, W ., et al. Antifertility investigation on Momordica. Lloydia . 1974; 37(4): 645c. Ko entjoro-Soehadi, T., et al. P erspectives of m ale contraception with regards to Indo nes ian trad itional dru gs. Proc. Second National Congress of Indonesian Society of Andrology. 1982; Aug. 26: 12. Dixit, V. P., et al. Effects of Mo mordica charantia fruit extract on the testicular function of dog. Planta Med . 1978; 34: 28086. Raza, H., et al. Modu lation of xeno biotic metabolism and oxidative stress in chronic streptozotocin-induced diabetic rats fed with Momordica charantia fruit extract. J. B iochem. Mol. T oxicol. 2000; 14(3): 13139. Ahm ad, N., et al. Effect of Momordica charantia (Karolla) extracts on fasting and postprandial serum glucose levels in NIDD M patients. Ba ngladesh M ed. Res. Counc. Bu ll. 1999; 25(1): 1113. Akh tar, M. S. Trial of Mo mordica charantia Linn (K arela) pow der in patien ts with maturity-onset diabetes. J. Pak. Med. As soc . 1982; 32(4): 1067. Matsuda, H., et al. Inhibition of gastric emptying by triterpene saponin, mom ordin Ic, in mice: Roles of blood glucose, capsaicin-sensitive sensory nerve s, a nd central nervous system . J. Pharm acol. Exp. Ther. 1999; 289(2): 72934. Matsuda, H., et al. Antidiabetic principles of natural medicines. III. Structure-related inhibitory activity and action mode of oleanolic acid glycosides on hypoglycemic activity. Ch em . Pha rm. Bull. (Tokyo)1998; 46(9): 1399403. Ahm ed, I., et al. Effects of Momordica charantia fruit juice on islet morphology in the pancreas of the streptozotocin-diabetic rat. Diab etes Res. Clin. Prac t. 1998; 40(3): 14551. Matsuda, H., et al. Inhibitory mechanisms of oleanolic acid 3-O-monodesm osides on glucose abs orption in rats . Biol. Ph arm . Bull. 1997; 20(6): 71719. Pla tel, K., et al. Plant foods in the manageme nt of Diabetes mellitus: Vegetab les as poten tial hypoglycaem ic agents. Nahrung. 1997; 41(2): 6874. Zhang, Q. C. Preliminary report on the use of Momordica charantia extra ct by H IV pa tients. J. Naturopath. Med. 1992; 3: 659. Sarka r, S., et al. Dem onstration of the hypoglycemic action of Momordica charantia in a validated animal m odel 5
of diabetes. Pharmacol. Res. 1996; 33(1): 14. 21. Miura, T., et al. Hypoglycemic activity of the fruit of the Momordica charantia in type 2 d iabetic m ice. J. Nutr. Sc i. Vitam inol. 2001; 47(5): 34044. 22. Ali, L., et al. Studies on hypoglycemic effects of fruit pulp, seed and wh ole plant of Mo mordica charantia on norm al and diabetic mo del rats. Planta Med. 1993; 59(5): 40812. 23. Vikrant, V., et al. T reatm ent w ith extracts of Momordica charantia and Eugenia jambolana prev ents hyperglycem ia and hyperinsulinem ia in fruc tose fed ra ts. J. E thn opharm acol. 2001; 76(2): 13943. 24. Jayasooriya, A. P., et al. Effects of Mo mordica charantia powder on serum glucose levels and various lipid param eters in rats fed w ith cho lesterol-free and cho lesterol-enriched diets . J. Eth nopharmacol. 2000; 72 (12 ): 33136. 25. Ahm ed, I., et al. Hypotriglyceridemic and hypocholesterolemic effects of anti-diabetic Mo mordica charantia (Karela) fruit extract in streptozotocin-induced diabetic rats. Diabetes Res. Clin. Pract. 2001; 51(3):15561. 26. Takem oto, D. J., et al. Guanylate cyclase activity in human leukem ic and normal lymphocytes. Enzyme inhibition and cytotoxicity of plant extracts. Enzyme 1982; 27(3): 17988. 27. Takem oto, D. J. Purification and characterization of a cytostatic factor with anti-viral activity from the bitter m elon. Prep. Biochem. 1983; 13(4): 37193. 28. Ta kem oto D. J., et al. Purification and characterization of a cytostatic factor with anti-viral activity from the bitter m elon. Part 2. Prep Biochem . 1983; 13(5): 397-421. 29. Takem oto, D. J., et al. Purification and characterization of a cytostatic factor from the bitter melon Momordica charantia. Prep Biochem. 1982; 12(4): 355-75. 30. Takem oto, D. J., e t al. Pa rtial purificatio n and characterization of a guanylate cyclase inhibitor with cyto tox ic properties from the bitter melon ( Momordica charantia ). Biochem. Biophys. Res. Comm un . 1980; 94(1): 33239. 31. Claflin, A. J., et al. Inhibition of growth and guanylate cyclas e ac tivity of an un differentiate d pro state adenocarcinoma by an extract of the balsam pear ( Momordica charantia abbreviata). Proc. Natl. Aca d. Sci. 1978; 75(2): 98993. 32. Ve sely, D. L ., et al. Isolation of a guanylate cyclase inhibitor from the ba lsam pear ( Mo mordica charantia abbreviata). Biochem. Biophys. Res. Comm un. 197 7; 77(4): 12 94 99. 33. Lee-Huang, S., et al. Plant proteins useful for treating tumors and HIV infection. 1-28-1996 U.S. Patent #5484889. 34 Terenzi, A., et al. Anti-CD30 (BER=H2) immunotoxins containing the type-1 ribosome-inactivating proteins m om ordin and PAP-S (pokeweed antiviral protein from seeds) display powerful antitumor activity against CD30+ tumor cells in vitro and in SCID m ice. Br. J. Haem atol. 1996; 92(4): 87279. 35. Na gas awa , H., et al. Effects of bitter melon ( Mo mordica charantia ) or ginger rhizome ( Zin giber offifinale Rosc.) on spon taneous m am m ary tumorigenes is in SHN m ice. Am. J. Clin. Med. 2002; 30(23): 195205. 36. W est, M. E ., et al. The a nti-growth properties of extracts from Mo mordica charantia . W est Indian Med. J. 1971; 20(1): 2534. 37. Takem oto, D. J., et al. The cytotoxic and cytostatic effects of the bitter melon ( Mo mordica charantia ) on human lymphoc ytes. Toxicon. 1982; 20: 59399. 38. Zhu, Z. J., et al. Studies on the active constituents of Mo mordica charantia l. Yao. Hsueh. Hsueh. Pao . 1990; 25(12): 898903. 39. Frame, A. D ., et al. P lants from Puerto R ico with anti- My cobacte rium tuberculosis prop erties. P. R . Health S ci. J . 1998; 17(3): 24352. 40. Hu ang , T. M ., et al. Studies on antiviral activity of the extract of Momordica charantia and its active principle. Virologica. 1990; 5(4): 36773. 41. Lee-Huang, S., et al. Inhibition of the integrase of human imm unodeficiency virus (HIV) type 1 by anti-HIV plant proteins MA P30 an d GA P31. Proc. Natl. A cad. S ci. 1995; 92(19): 881822. 42. Lee-Huang, S., et al. Anti-HIV and anti-tumor activities of recombinant MAP 30 from bitter m elon. Ge ne. 1995; 161(2): 15156. 43. Lee-Huang, S., MAP 30: A new inhibitor of HIV-1 infection and replication. FE BS Lett . 1990; 272(12): 1218. 44. Lifson, J. D., et al. Method of inhibiting HIV. 1-28-1989 U.S. Patent #4795739. 45. Bourinbaiar, A. S., et al. The activity of plant-derived antiretroviral proteins MAP30 and GAP31 against Herpes simplex virus in vitro . Biochem. Biophys. Res. Comm un. 199 6; 219(3): 92329 . 46. George, M., et al. Investigations on plant antibiotics. Part IV. Further search for antibiotic substances in Indian m edicinal plants. Indian J. Med. Res. 1949; (37): 16981. 47. Khan, M. R., et al. Momordica charantia and Allium sativum : Broad spec trum a ntibacterial activity. Korean J. Pharm aco g. 1998; 29(3): 15558. 48 Om oregbe, R. E., et al. Antimicrobial activity of some m edicinal plants extracts on Es cherichia coli , Sa lmonella paratyphi and Shigella dysenteriae . Afr. J. M ed. M ed. S ci. 1996; 25(4): 37375. 49. Hussain, H. S. N., et al. Plan ts in Ka no e thom edicine: Screening for antim icrobial activity and alka loids. Int. J. Pharmacog . 1991; 29(1): 516.
50. Bh ak uni, D. S., et al. Screening of Indian plants for biological activity: Part XIII. Indian J. Ex p. Biol. 1988; 26(11 ): 883RY904. 51. Yesilada, E., et al. Screening of Turkish anti-ulcerogenic folk remedies for anti- Helicobacter pylori activity. J. Ethnopharmacol . 1999; 66(3): 28993.
The inform ation c onta ined here in is intended for ed uca tion, res earc h, and inform ationa l purpose s on ly. This information is not intended to be used to diagnose, prescribe or replace proper m edical care. The statem ents contained herein have not been evaluated by the Food and Drug Administration. The plant described herein is not intended to diagnose, treat, cure, mitigate, or prevent any disease.
Used By
Hu man Adult Hu man Female Hu man Adult
Ref #
ZZ1049 T05032 ZZ1019
ZZ1019 ZZ1019
Lea f Belize Lea f Belize Vine Bimini Meristem B razil En tire P lant Brazil En tire P lant Brazil En tire P lant Brazil
Raw / Oral Hot H2O Ext / Oral Hot H2O Ext / Oral Not Stated / External Tincture / Oral Decoction / Oral Not stated / External Tincture / Not stated Infusion / Not stated No t State d / O ral Juice / External Infusion / Oral H2O Ext / Oral Cataplasm / External Decoction / Oral
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult
ZZ1002
L15570 A00499
L04137
Used By
Hu man Adult Hu man Adult Hu man Adult Hu man Adult
Ref #
ZZ1096
ZZ1099
K07977 ZZ1093
ZZ1007
Ae rial P arts Colombia Leaf Costa R ica Entire Plant Cuba Leaf Cuba Vine Curacao Aerial Parts England Le af Juice Fiji Leaf Gu ate mala
Hu man Adult Hu man Female Hu man Female Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult
Infusion / Not stated H2O Ext / Rectal Juice / Oral Juice / Op hth almic Decoction / Oral Hot H2O Ext / Oral
T13846 T04647
Used By
Hu man Adult Hu man Adult Hu man Adult Hu man Female Hu man Child Hu man Adult Hu man Hu man Hu man Hu man Female Female Adult Adult
Ref #
T13846
Used regularly each month to avoid childbirth thro ugh early abortion. Used as an emmenagogue. Used as an aphro disiac. Leaves crushed and juice drun k with palm wine. Used as bush tea. Used for constipation, headache an d skin ailments. Used to treat diabetes. Used to tre at dysente ry. Used as an aphrodisiac. Used as a p urgative and an emetic. Used for belly pain, to build up the blood, for diabetes, fever, colds, cough, childbirth, headache, malaria, menstrual pain and as a purgative. Used for skin disease.
Hu man Female
A04902
A04179 A04941
Hot H2O Ext / Oral Not Stated / Oral Decoction / Oral Decoction / Oral Hot H2O Ext / Oral Juice / Oral Leaves / Oral
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Male Hu man Adult Hu man Adult
Hu man Adult
10
Used By
Hu man Adult Hu man Adult Hum an A dult
Ref #
K27070
L16047
Decoction / Oral Leaves / Oral Not Stated Plant / External H2O Ext / Oral
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult T06510 T07722 T07722 K08933
Aerial Parts Panama Leaf Panama Lea f Peru Lea f Peru Lea f Peru
Infusion / Oral Hot H2O Ext / Oral H2O Ext / Oral Not Stated / Oral Decoction / Oral Decoction / External Infusion / Oral Decoction / External Benzene Ext / Oral Leaves / Oral Decoction / Oral Hot H2O Ext / Oral Hot H2O Ext / Oral Hot H2O Ext / Oral
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Child Hu man Child Hu man Adult Hu man Adult Hu man Female Hu man Adult Hu man Adult
T10116
Leaf Philippines Leaf Philippines Vine Philippines Vine Puerto Rico Vine Puerto Rico
11
Used By
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult
Ref #
A06027 A14280 K26851 T09739 T12145
Hu man Adult
J12451
Entire Plant Thailand Leaf Thailand Leaf Thailand Leaf Thailand Leaf Togo Leaf Trinidad Fruit + Leaf + Stem Trinidad Leaf West Indies Leaf West Indies Leaf West Indies Vine West Indies
Hot H2O Ext / Oral Plant / Oral Leaves / Oral Hot H2O Ext / Oral Decoction / Oral Not Stated / Oral Decoction / Oral
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult
Used as an emmenagogue. Use d for diabetes, hypertension, worms an d ma larial fever. Used to make a bitter-tasting tea for its anti-diabetic properties. Used regularly each month by wo men to avoid childbirth b y early abortion. Used as a laxative. Infusion alone or with Bidens reptans for menstrual troubles. Use d as an abortifac ient. Fresh , dried or boiled vine with sa lt adde d given to women b efore or after childbirth.
Hot H2O Ext / Oral Hot H2O Ext / Oral Infusion / Oral Hot H2O Ext / Oral
Hot H2O Ext / Oral H2O Ext / Oral H2O Ext / Oral Hot H2O Ext / Oral
Hu man Adult Hu man Female Hum an (pregna nt) Hum an (pregna nt)
T00701
T00701
12
Used By
Hu man Adult
Ref #
M23109
Fruit Au stralia
Plant / Oral
Hu man Adult
A05524
Fruit / Oral Hot H2O Ext / External Juice / Oral Not Stated Not Stated Fruit / Oral Decoction / Oral Fruit / Oral Not Stated / Oral
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Male Hu man Adult Hu man Adult
T00359 A00499
Fruit Bra zil Fruit + Leaf Brazil Fruit Bra zil Fruit China Fruit China Fruit China
Infusion / External Hot H2O Ext / Oral Fruit / Oral Hot H2O Ext / Oral Fruit / Oral Fruit / Oral
Fruit Fiji
Hu man Adult
T10632
T07660 A14379
13
Used By
Hu man Adult Hu man Adult Hu man Adult Hu man Adult
Ref #
A14458 L15996 M22671 M27166
Fruit / Oral Hot H2O Ext / Oral Oil Ext / External or Juice / Not stated Decoction / Oral Not stated Not Stated / Oral Fruit / Oral Fruit / Oral Not Stated / Oral
Used for diabetes. Used as an antileprotic. Used as an anthelmintic. Used as an anthelmintic. Used as a common vegetable. Used for jaundice, piles, leprosy, rheumatism and gout. Used as a tonic and laxative, dysmenorrhea and as a emmenagogue. Commonly eaten as a vegetable. Used for diabetes mellitus. Used to treat diabetes. 5 ml of fruit juice mixed with 5 to 10 fruits of black pepper powder is given early in the morning 3-6 weeks. Used for malarial fevers. Used for leprosy. Used as an anthelmintic. Used for diabetes. Used for diabetes. Eaten as a pot herb. Used as a laxative and anthelmintic.
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult
L05654 W 00113
Fruit Ind ia
W 00678
K25290
Juice / Oral Not Stated / Not stated Not Stated / Oral Not Stated / Oral Hot H2O Ext / Oral Fruit / Oral Decoction / Oral
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult
M23219 W 00113
Used By
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Hu man Hu man Human Adult Adult Adult Female
Ref #
T07722 L03572 H19648 ZZ1049 T15323
Fruit Pe ru
L04137
Used for diarrhea and colic. Used for diabetes, rheumatism, gout, liver disorders, spleen disorders, pyrexia, colic, flatulence and menstrual suppression. Used for diabetes, rheumatism, gout, liver disorders, spleen disorders, pyrexia, colic and flatulence. Used for menstrual suppression. Use d as a hypo glycemic agent. Used as an anthelmintic. Used to treat diabetes mellitus. Used for diabetes. Said to be edible. Used as an anti-inflammatory. Used for diabetes. Used as a food. Used as a treatment for peptic ulcers. Used as an antiallergic, antihepatic and antipruritic. Used as an anti-inflammatory.
ZZ1008 M22673
T10348
Fruit Sri Lanka Fruit Sri Lanka Fruit Juice Sri Lanka Fruit Juice Sri Lanka Fruit Thailand Fruit Thailand Fruit Thailand Fruit Thailand Fruit Turkey Fruit Turkey
Hot H2O Ext / Oral Not Stated / Oral Juice / Oral Hot H2O Ext / Oral Plant / Oral Decoction / Oral Hot H2O Ext / Oral Fruit / Oral Not Stated / Oral Plant / Oral Plant / External
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult
T08396 W 00113 K17959 M17655 L12243 T16711 W 01792 J18457 K11898 K27792
15
Used By
Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hum an(pregna nt) Hu man Adult Hu man Adult
Ref #
K18219 A04179
Fruit USA
A04179
A04179
Hot H2O Ext / Oral Fruit / Oral Not Stated / Oral Fruit / Oral Juice / Oral Fruit / Not stated Fruit / Oral Not Stated / Oral Plant Juice / Oral Not Stated / Oral Not Stated / Oral Hot H2O Ext / Oral Hot H2O Ext / Oral Hot H2O Ext / Oral Hot H2O Ext / Oral Hot H2O Ext / Oral Tincture / Oral Hot H2O Ext / Oral Not Stated / Oral Hot H2O Ext / Oral
Hu man Adult Hu man Adult Hu man Adult Hum an (pregna nt) Hu man Adult Hu man Hu man Hu man Hu man Hum an Adult Adult Adult Adult (pregna nt) W 00903 T02106 W 00113 T00701 K19563
Fruit Virgin Islands Fruit West Africa Fruit West Africa Fruit West Indies Fruit Not Stated
Fruit Not Stated Root Africa Root East Africa Ro ot A ustralia Ro ot B razil
Used to treat diabetes. Used as an aphrodisiac. Use d as an abortifac ient. Claime d to be ab ortifacien t. Claimed Claimed Claime d Used as to be a purgative in small doses. to induce abortion. to have an aphrodisiac effect. an emetic or vomitive in large doses.
Hu man Adult Human Adult(male) Hum an (pregna nt) Hum an(pregna nt) Hu man Hum an Hu man Hu man Adult (pregna nt) Male Adult
Used for rheumatism and diarrhea. Used for fever, possibly malaria.
ZZ1099 T16158
16
Used By
Hum an(pregna nt) Hum an (pregna nt) Hum an (pregna nt)
Ref #
T04748 W 00002 W 04510 W 00384 A05825 A00115 A04179 T14891 A00136 A04179 A04179 A00115 ZZ1049 W 00408 W 00384 A14461 T05236 T02487
Ro ot In dia Root Mexico Root Philippines Ro ot V enezu ela Root W est Africa Seed A frica Se ed Bra zil Se ed India Se ed India Se ed India Se ed India
Use d as an abortifac ient. Used as an aphrodisiac. Used to produce abortions. Used as an antimalarial. Used as an abortifacient, together with the fruits or seeds. Used for roundworm. Used as an anthelmintic. Used as an anthelmintic. Used for diabetes. Used as an anthelmintic. The seeds are boiled and the extrem ely bitter effu sion is sa id to produce instantaneous vo miting. Used for diabetes, hepatic disorders, pain relief in gout and rheumatism. Used for diabetes. Used to treat pneumonia and leucorrhagia. Use d for diabetes, diabete s insipidu s, and lithontriptics. Use d to red uce fat. Used for suppu rations. Used for colic and as a vermifuge.
Decoction / Oral Not stated Hot H2O Ext / Oral Hot H2O Ext / Oral Not Stated / Oral Not Stated / Oral Seeds / Oral Seeds / Oral Hot H2O Ext / Oral Not Stated / Oral Hot H2O Ext / Oral
Hum an (pregna nt) Not Stated Hum an (pregna nt) Hu man Adult Hum an (pregna nt) Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult Hu man Adult
Se ed India
Hu man Adult
M25712
Seed P eru
T15323
17
Used By
Hu man Adult
Ref #
ZZ1008
Seed W est Indies Not Stated Bahamas No t State d Brazil No t State d Brazil No t State d Colombia Not Stated Co ngo-B razzaville Not Stated Cuba Not Stated Guam Not S tated Haiti Not Stated Honduras No t State d India Not Stated Jamaica No t State d Malaysia Not S tated Pue rto Rico Not S tated Pue rto Rico Not Stated Trinidad No t State d Venezu ela Not Stated W est Indies
Seeds / Oral Not Stated / Oral Not Stated / Oral Not Stated / Oral Not Stated / Oral Not Stated / Oral
Hu man Adult Hu man Adult Hu man Adult Hum an (pregna nt) Hu man Adult Hu man Female
Used for colitis, fever and hepatosis. Used as a litholytic. Used for malignant ulcers. Used as an insecticide. Used as a depurative. Used for scabies, psoriasis and other skin diseases. Used for colds, constipation, dysmenorrhea, fever and stomachache. Use d as an abortifac ient. Used as an antidiabetic.
Not Stated / Oral Not Stated / External Not Sstated Not Stated / Oral Not Stated / Oral Not Stated / Oral Hot H2O Ext / Oral Not Stated / Oral
Hu man Adult Hu man Adult Not Stated Hu man Adult Hu man Adult Hu man Adult Hum an (pregna nt) Hu man Adult
Hu man Adult
A01947
Used for diabetes. Use d as a tonic for colds and fever. Used as an abortifacient and monthly as a metho d of birth control.
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
18
Type Extract
ETOH-H2O (1:1) Ext ETOH-H2O (1:1) Ext ETOH-H2O (1:1) Ext ETOH-H2O (1:1) Ext ETO H (95% ) Ext Not stated
Test Model
IP Mouse
Dosage
LD50= >1000 mg/kg
Result
Active
Notes/Organism tested
Ref #
T10126
IP Mouse
Active
T02678
IP Mouse
Active
K09153
Inactive Inactive Inactive Inactive No adverse influence on food intake, grow th and org an we ights seen. H em atologic param eters rem ained norm al.
R00001
L12432 AM1031
Abortifacient Effect
Oral Rat (pregna nt) IV Guinea Pig IG Rat Oral Mouse (Female) Oral Rat (pregna nt) IG Rat (pregna nt) Oral Ra t (Female) Oral Ra t (Fem ale)
100.0 mg/kg
Inactive
T02678
Leaf In dia
Abortifacient Effect
H2O Ext
200.0 mg/kg
Inactive
W 01362
Leaf In dia
Abortifacient Effect
ETO H (100 %) E xt
200.0 mg/kg
Inactive
L11141
Antiimplantation Effect
100.0 mg/kg
Inactive
T02678
Leaf In dia
Antiimplantation Effect
500.0 mg/kg
Inactive
A04902
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
19
Part -Origin
Leaf In dia
Type Extract
ETO H(100 %) E xt
Test Model
Intragastric Rat (Female) IP Rat (Female) Oral Ra t (Fem ale) Oral Ra t (Female) Rat
Dosage
200.0 mg/kg
Result
Inactive
Notes/Organism tested
vs. e arly pregn anc y.
Ref #
L11141
Leaf In dia
Antiimplantation Effect
Not stated
Not stated
Inactive
T14891
Leaf In dia
Em bryotoxic Effect
H2O Ext
200.0 mg/kg
Inactive
W 01362
Leaf In dia
Em bryotoxic Effect
Hot H2 O E xt
500.0 mg/kg
Inactive
A04902
Hot H2 O E xt
2 .0 m g
Active
A00706
Antileukem ic Activity
In ration Cats
2 mg
Active
Feline infectious leukemia. 60% impro vem ent in symp tom s in cats treated w ith extract for 3-6 months. Feline infectious leukemia. 80% impro vem ent in symp tom s in cats treated w ith extract for 3-6 months. Ad m inistered to one lym phatic leukemia patient. Caused a m ark ed incr ease in he m oglobin conte nt o f blood and decrea se in W BC. Dosing 3 times daily for 62 days. Mam mary tumors. Sarcoma 180 (asc). Slight increase in lifespan. P388 tumor cells.
AM1074
Entire Plant
Antileukem ic Activity
IM Ca ts
0 .5 m l
Active
AM1074
Hot H2 O E xt
1 5.0 m l
Active
A00706
Leaf Japan Entire Plant W est Indies Entire Plant USA Entire Plant
Hot H2 O E xt Hot H2 O E xt
0.5% 0 .4 m g
AM1001 A00706
H2O Ext Fraction: Alpham om orc harin Fraction: Alpham om orc harin
T09137 AM1042
Entire Plant
Antitum or Activity
Not stated
Not stated
Active
AM1053
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
20
Part -Origin
Entire Plant
Type Extract
Fraction: Betam om orc harin Fraction: Betam om orc harin Fraction: Mo m ord in
Test Model
Cell Culture
Dosage
Not stated
Result
Active
Notes/Organism tested
Human squamous carcinoma of the tongu e and larynx.
Ref #
AM1055
Entire Plant
Antitum or Activity
Not stated
Not stated
Active
AM1042
Entire Plant
Antitum or Activity
Cell Culture
Active
Inh ibite d protein synthe sis in Ho dgkin s dis ease and anaplastic large-cell lymphoma-derived CD30+ cell lines. vs. mice xenografted with CD30+ human ALCL. 3 day treatment with extract started 24 hours after transplantation, prevented tumor development in 40% of cases and delayed tu m or g row th rate in others. Uterine adenomyosis. Blo ck ed the gro wth of rat prostatic adenocarcinoma and (3H) thymidine incorporation into DNA. Hep2 cells.
AM1065
Entire Plant
Antitum or Activity
Fraction: Mo m ord in
Mouse
LD50=7mg/kg
Active
AM1065
Active Active
AM1001 AM1041
Cytotoxic Activity
Hot H2 O E xt
Cell Culture
4 .0 m g/m l
Active
A00706
Cytotoxic Activity
Protein Fractuibs
Not stated
Prostate adenocarcinoma. Lymphoma. Melanoma. Hepatoma. Thy 1.1-expressing mouse lympho m a cell line AK R-A Mouse lymphoma EL4 cells which lacked Thy 1.1 antigen Cells-BHK-21.
Entire Plant
Cytotoxic Activity
Fraction: Alpham om orc harin Fraction: Mo m ord in Fraction: Mo m ord in Ch rom ato gra phic Fraction Fraction: Cucurbitacin B
Not stated
Entire Plant
Cytotoxic Activity
Cell Culture
Entire Plant
Cytotoxic Activity
Cell Culture
Inactive
Entire Plant
Cytotoxic Activity
Cell Culture
Not stated
Active
Entire Plant
Cytotoxic Activity
Not stated
Not stated
Active
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
21
Part -Origin
Entire Plant
Type Extract
Fractions: Protein ext
Test Model
IP Mice
Dosage
8 mcg twice a week for 0-4 weeks
Result
Active
Notes/Organism tested
Activated peritoneal exudate cells; dem onstrated cytotoxicity to L1210, P388 and MOLT-4 tumor cells. Virus - vesicular sto ma titis
Ref # AM1033
Entire Plant
Metastasis Inhibition
Cell Culture
Not stated
Active
T08985
Mouse
Not stated
Active
vs. cyclophosphamide induced m uta genesis vs. m ethylnitros am ine, m ethyl methane sulfonate and tetra cycline -indu ced gen otoxicity. Artemia salina Assa y system is intende d to pre dict fo r antitum or activity. vs. 12-o-tetradecanoylphorbol-13acetate(tp a)-induced epstein-barr virus early antigen activation. vs. EBV activation induced by HPA (40 ng/m l).
AM1043
Entire Plant
ME OH in soluable Fraction
Not stated
Not stated
Active
K17876
Anticrustace an Activity
Not stated
L D5 0= 33 .0 m cg /m l
Active
L12432
Leaf Thailand
Antitumor-promoting Activity
ME OH Ext
2 00 .0 m cg /m l
Strong Activity
L12243
Leaf Thailand
ME OH Ext
2 00 .0 m g/m l
K25144
Leaf China
ME OH Ext
1 00 .0 m cg /m l
L13363
Leaf Turkey
H2O Ext
Not stated
Eq uiv
Enhanced intracellular killing of neutrophils. Increased interferon production. Type 1 interferon inducer. En hanced natural killer cell activity.
J14375
AM1068 AM1068
J14375 K27017
Leaf N igeria
ATP-ase Inhibition
ETO H (100 %) E xt
IG Ra t
385.0 mg/kg
Active
L14997
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
22
Part -Origin
Entire Plant W est Indies Leaf N igeria
Type Extract
Hot H2 O E xt
Test Model
Se a U rch in (Ova) IG Rat (Brain) IG R at (Liver) IG Rat
Dosage
0 .1 m g/m l
Result
Active
Notes/Organism tested
Antim itotic effect.
Ref #
A00706
ETO H (100 %) E xt
385.0 mg/kg
Active
L14997
Leaf N igeria
ETO H (100 %) E xt
385.0 mg/kg
Active Inactive
Increase in muscle and liver protein levels. Re ductio n in the leve ls of bra in protein. Induces resistance to viral infection. HIV-1 reverse transcriptase and HIV-1 protease. InhibitedHIV-1 integrase 26.19 6.3 % . vs. Japanese B encephalitis virus. Administered 18 hr, 12 hr and 4 hr before subcutaneous challenge with the virus protected the tr ea te d g ro up by 6 6% . Retrovirus such as HIV.
L14997
Antiviral Activity
Not stated
in vitro
Not stated
Active
AM1068
Entire Plant
Antiviral Activity
100 nM
AM1052
Leaf China
Antiviral Activity
H2O Ext
IP Mice
0 .4 m g
AM1068
Entire Plant
Antiviral Activity
Not stated
Not stated
Active
AM1074
Entire Plant
Antiviral Activity
Cell Culture MDCK cells MA 104 cells Cell Culture MT-4 cells Oral Kitten
0 .1 m g/m l 1 m u g/m l
Active Active
vs. influenza virus. Vs. herpes virus. Virus inhibited b y m o re th an 90 % . vs. HIV. 50% protection against HIV -indu ced cytop athoge nicity. Kittns were injected several times with feline HIV. 100% of control group developed feline HIV vs. 20% of the group treated with the extract. Cats with feline HIV were treated with the extract for 3-6 months. 60% im pro vem ent in sym pto m s in treated group.
AM1074
Entire Plant
Anti-HIV A ctivity
E C5 0= 15 m u g/m l
Active
AM1074
Entire Plant
Anti-HIV A ctivity
2 mg
Active
AM1074
Entire Plant
Anti-HIV A ctivity
Oral Cat
2 mg
Active
AM1074
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
23
Part -Origin
Entire Plant
Type Extract
Fraction: Aljaline polysaccharides
Test Model
IM Ca ts
Dosage
0 .5 m l
Result
Active
Notes/Organism tested
Cats with feline HIV were treated for 3-6 months. 80% improvement in symptoms in treated group. HIV-1 reverse transcriptase. 82% reduction of viral core protein p24 expression in HIVinfected cells. Inhibited HIV-1 propagation.
Ref #
AM1074
Entire Plant
Anti-HIV A ctivity
Protein Ext
in vitro
IR 50 =1 8 m cg /m l 0 .1 75 m cg /m l
Active Active
H28024
Entire Plant
Anti-HIV A ctivity
Not stated
Not stated
Active
AM1042
Entire Plant
Anti-HIV A ctivity
100 nM
HIV-1 reverse transcriptase and HIV-1 protease. Inhibited HIV-1 integrase from 2 6.1 % to 96 .3 % . Related to its ribosome-inhibiting activity. Inhibition of viral replication and reverse tra nsc ripta se a ctivity. Los s of p 24 a ntige n after 4 days of exposure to momorcharin. T lymphocytes and monocyte/macrophages. HIV infec ted cells sh ow ed a ra pid and nearly complete loss of viral antigen; loss of HIV envelope protein or loss of HIV core pro tein . Un infe cte d cells larg ely unaffected. vs. streptozotocin-induced hyperglycemia. Decreased blood glucose levels by 25% 3 hrs after administration. Non-d iabetic rats. Resu lts were significant at 60 min.
AM1052
Entire Plant
Anti-HIV A ctivity
Not stated
Not stated
AM1053
Entire Plant
Anti-HIV A ctivity
Cell Culture
Not stated
Active
AM1076
Entire Plant
Anti-HIV A ctivity
0 .3 a nd 3 m u.g /m l
Active
AM1076
IG Rat
30.0 mg/kg
Active
J11388
Hyperglycem ic Activity
ME OH Ext
IG Rat
1 50 m g
Active
K13947
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
24
Part -Origin
En tire Plant In dia
Type Extract
ETO H (95% ) Ext
Test Model
IG Rat
Dosage
250.0 mg/kg 250.0 mg/kg
Result
Active Inactive Inactive Inactive Inactive
Notes/Organism tested
vs. rats fasted for 18 hrs. vs. overfed rats. vs. glucose-induced hyperglycemia. vs. streptozotocin-induced hyperglycemia. vs. glucose-induced hyperglycemia. vs. streptozotocin-induced hyperglycemia. Decreased blood glucose levels by 25% 3 hrs after administration. Non-d iabetic rats. Resu lts were significant at 60 min. vs. rats fasted for 18 hrs. vs. overfed rats. Vs. glucose-induced hyperglycemia. vs. streptozotocin-induced hyperglycemia. vs. glucose-induced hyperglycem ia.
Ref #
M22670
IG Rat
30.0 mg/kg
Active
J11388
Hyperglycem ic Activity
ME OH Ext
IG Rat
1 50 m g
Active
K13947
IG Rat
Inactive
M22670
Hypoglycem ic Activity An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity
A00637 M22670
IG Rat
30.0 mg/kg
Active
Vs. streptozotocin-induced hyperglycemia. Decreased blood glucose levels by 25% 3 hrs after administration. vs. streptozotocin-induced hyperglycemia. Single dose of the extract reduced plasma glucose concentration by about 50% after 5 hours. vs. normal and IDDM rats.
J11388
Decoction
IP Mouse
0 .5 m l
Active
M23565
Hypoglycem ic Activity
ME OH Ext
IG Rat
1 50 m g
Inactive
K13947
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
25
Part -Origin
Flower + Leaf Thailand En tire Plant In dia
Type Extract
MEOH-H2O (1:1) Ext ETOH-H2O (1:1) Ext ETO H(100 %) E xt ETO H(100 %) E xt ETOH-H2O (1:1) Ext ETOH-H2O (1:1) Ext ETOH-H2O (1:1) Ext ETO H(70% ) Ext
Test Model
IG Rat
Dosage
10.0 mg/kg 30.0 mg/kg 250.0 mg/kg
Result
Active Active Inactive
Notes/Organism tested
Intraperitoneal glucose. Oral glucose.
Ref #
J11388
Hypoglycem ic Activity
IG Rat
K09153
Analges ic Activity
IG Mouse
Not stated
Inactive
vs. hot plate method. vs. tail clip method. vs. supramaximal electroshockinduced convulsions. vs. metrazole-induced convulsions. vs. strychnine-induced convulsions. Man ages va rious grade s of acne: comedos, papules, pustules and nodules. Also active against furuncles. Did not inhibited radioligand binding to serotonin, dopamine, beta-2-adrenergic or muscarinic receptors nor to adenosine NMDR recepto r chann el com plex. Inhibited radioligand binding to adrenergic-receptor in human frontal cortex. (Hippocampus) Inhibited the binding of 3h-rau wolscine to serotonin receptors.
K09153
IP Mouse
Not stated
Inactive
K09153
Leaf N igeria
IP Mouse
Variable
Inactive
T06510
Antiacne Activity
Acidic Ext
External Hu m an Ad ult
Not stated
Active
AM1073
Binding Effect
Hu m an Ad ult
1 0.0 m cg /m l
Inactive
J12451
Binding Effect
Hu m an Ad ult
1 00 .0 m cg /m l
Active
J12451
CHC L3 Ext
Ca lf
1 00 .0 m cg /m l
Inactive
J10986
Leaf In dia
Estrogenic Effect
Hot H2 O E xt
SC R at (Female)
2 0.0 m g
Inactive
A04902
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
26
Part -Origin
Entire Plant Thailand
Type Extract
ETOH-H2O (1:1) Ext ETO H (70% ) Ext ETOH-H2O (1:1) Ext ETOH-H2O (1:1) Ext ETOH-H2O (1:1) Ext ETOH-H2O (1:1) Ext ETOH-H2O (1:1) Ext ETO H(100 %) E xt
Test Model
Guinea Pig (Ile um ) IP Mouse Guinea Pig (Ile um ) GI Ra bbit
Dosage
0 .0 1 gm /m l
Result
W eak Activity Active W eak Activity Inactive
Notes/Organism tested
Ref #
W 3022A
Va riab le 0 .0 1 gm /m l
Antipyretic Activity
Variable
W 3022A
IV Dog
Variable
Inactive
W 3022A
Hypothe rm ic Activity
IG Rat
Not stated
Inactive
K09153
Diuretic Activity
IG Rat
510.7 mg/kg
Inactive
K09153
Leaf N igeria
Alanine Transaminase Level Decrease Alanine Transaminase Level Decrease Aspartate Transaminase Level Decrease Aspartate Transaminase Level Decrease
385.0 mg/kg
Active
L14997
Leaf N igeria
ETO H(100 %) E xt
385.0 mg/kg
Active
L14997
Leaf N igeria
ETO H(100 %) E xt
385.0 mg/kg
Inactive
L14997
Leaf N igeria
ETO H(100 %) E xt
IG Rat
385.0 mg/kg
W eak Activity
L-aspartate transaminase and adeno sine triphospha tase activity slightly elevated. L-aspa rtate transam inase activity unaffected. Adenosine triphosphatase activity reduced. Re duced cyclic GMP leve ls in tum or.
L14997
ETO H(100 %) E xt
IG Rat
385.0 mg/kg
W eak Activity
L14997
Not stated
Active
AM1041
Leaf USA
H2O Ext
Not stated
M00425
Leaf N igeria
ETO H(100 %) E xt
IG Rat (Plasma)
385.0 mg/kg
L14997
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
27
Part -Origin
Leaf N igeria
Type Extract
ETO H(100 %) E xt
Test Model
IG Rat (Plasma) Not Not Not Not Not Not stated stated stated stated stated stated
Dosage
385.0 mg/kg
Result
Active
Notes/Organism tested
Ref #
L14997
CHCL3 Sol Fract ETOAC Sol Fract H2O Ext H2O -insol Ext Hexan e Ext MEOH-CH2CL2 MEOH-H2O(1:1) Ext H2O Ext Hexan e Ext MEOH-CH2CL2 1:1 ME OH Ext
m cg /m l m cg /m l m cg /m l m cg /m l m cg /m l m cg /m l
L18181
Not stated
1 00 m cg /m l
L18181
L18181
Leaf Philippines
Gluco se Tran sport Inhibition Gluco se Tran sport Stimulation Antihepa totoxic Activity
Cell Culture
5 .0 m cg /m l
Active
Cells-ehrlich.
J17272
Leaf Philippines
ME OH Ext
Cell Culture
1 .0 m cg /m l
Ca-ehrlich-ascites.
J16266
Hot H2 O E xt
Cell Culture
1 .0 m g
Hepatocytes measured by leakage of LDH and ASAT. Hepatocytes monitered by production of malonaldehyde. Measured by decoloration of diphenylpicryl hydroxyl radical solution. Decoloration 6%. Entamoeba histolytica
K23019
Hot H2 O E xt
Cell Culture
1 .0 m g
Inactive
K23019
Hot H2 O E xt
Not stated
250.0 mg/liter
Inactive
K23019
Antiprotozoa n Activity
ETOH-H2O (1:1) Ext CHC L3 Ext CCH L3 Ext H2O Ext H2O Ext H2O Ext H2O Ext
Broth C ulture
1 25 .0 m g/m l
Active
K09153
42.0 mg/kg 496.0 mg/kg 3.44 gm/kg 2.37 gm/kg 2.37 gm/kg 1.0 gm/kg
A00785
Flowe rs B razil
Plasmodium berghei
K07998
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
28
Part -Origin
Ae rial P arts Bolivia
Type Extract
Not stated
Test Model
Rodent
Dosage
Not stated
Result
W eak Activity Inactive Active Active Inactive
Notes/Organism tested
P. vinckei petteri 279BY (rodent m alaria). Plasmodium berghei Plasmodium berghei Plasmodium berghei Plasmodium berghei
Ref #
AM1016
J11857 J13276
J13276
ETO H(100 %) E xt
Not stated
IC 50 =1 25 .0 m cg /m l
Plasmodium falciparum
L11358
Leaf Togo
Not stated
IC 50 6 8.4 m cg /m l
Plasmodium falciparum
M23556
Antimycobacterial Activity
Agar P late
500.0 mcg
L12432
Leaf In dia
Antibacterial Activity
ETO H(95% ) Ext ETO H(95% ) Ext Hot H2 O E xt Hot H2 O E xt ETOH-H2O(1:1) Ext ME OH Ext MEOH-H2O(1:1) Ext
Es cheric hia coli Staphylococcus aureus Es cheric hia coli Staphylococcus aureus Pseudomonas aeruginosa
W 03693
Antibacterial Activity
Broth C ulture
K09153
Active Active Inactive Inactive Inactive Inactive Inactive Active Active Active
Sarcina lutea Staphylococcus aureus Ba cillus subtilis Es cheric hia coli Proteus species Pseudomonas aeruginosa Staphylococcus albus Es cheric hia coli Salmonella paratyphi Shigella dysenteriae
T09739 J00209
Leaf N igeria
Antibacterial Activity
Agar P late
L07663
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
29
Part -Origin
Leaf N igeria
Type Extract
ME OH Ext
Test Model
Agar P late
Dosage
2 .0 m g/m l
Result
Active Active Active Active Active Active Inactive Inactive Active
Notes/Organism tested
Corynebacterium diphtheriae Neisseria species Pseudomonas aeruginosa Salmonella species Streptobacillus species Streptococcus species Staphylococcus aureus Es cheric hia coli Staphylococcus aureus Es cheric hia coli Staphylococcus aureus Candida albicans Cryptococcus neoformans Sp oro trichum schenckii Epidermophyton floccosum Mic ros porum canis Trichoph yton me ntagrop hytes va r. Algodonosa Trichoph yton me ntagrop hytes va r. Gran ulare Aspergillus fumigatus Trichophyton mentagrophytes
Ref #
M27767
Leaf In dia
Antibacterial Activity
Undiluted Undiluted
W 03693
Antiyeast Activity
Broth C ulture
1 .0 m g/m l
Inactive
K09153
Antifungal Ac tivity
Hot H2 O E xt
Broth C ulture
1 .0 m l
Inactive
M27151
Antifungal Ac tivity
ETOH-H2O(1:1) Ext
Broth C ulture
1 .0 m g/m l
Inactive
K09153
Molluscicidal Activity
Not stated
Inactive
Lymn aea colume lla Lymn aea cubensis Blatella germanica Periplaneta americana Oncopeltus fasciatus
T04621
Leaf Origin Not Specified Leaf Origin Not Specified Entire Plant W est Indies Aerial Parts Co lom bia
Insecticide Activity
H2O Ext
Not stated
40.0 ml/kg
W 03405
Insecticide Activity
H2O Ext
Not stated
Va riab le
W 03405
Hot H2 O E xt
Not stated
20.0 ppm
Active
A00706
ETO H(100 %) E xt
Not stated
Not stated
Inactive
vs. bo th ro ps atro x ve no m.
L15991
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
30
Type Extract
ETOH-H2O (1:1) Ext H2O Ext
Test Model
IP Mouse
Dosage
LD50= 681.0 mg/kg
Result
Active
Notes/Organism tested
Ref #
K09153
Fruit USA
IP Mouse
L D5 0= 1 6.0 m cg /m l
Active
T09137
Fruit USA
H2O Ext
SC Mouse
L D5 0= 2 7.0 m cg /m l
Active
T09137
H2O Ext
IP Rat
Active
T01769
Fruit In dia
Daily dosing for 30 days. Daily dosing for 30 days. 20-30% of animals died within 30 days. Died within 18 hours. Died within 18 hours.
M01152
Fruit In dia
J11478
Fruit In dia
L10702
Fruit In dia
Decoction
5 00 .0 m g
Inactive
A14458
Inactive Active Active Death occurred within 23 days. Two pregnant animals suffered from uterine hemorrhage and then died. Death occurred within 18 hours.
Active Inactive
A14328 T02678
Abortifacient Effect
8.0 mg/kg
Active
T00398
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
31
Part -Origin
Seed China
Type Extract
Aceton e Ext
Test Model
IP Mouse (pregna nt) IP Mouse (pregna nt) IP Mouse (pregna nt) Oral Ra t (Female) Rat (Female)
Dosage
4.0 mcg/gm
Result
Active
Notes/Organism tested
Do sing on d ay 12 of pregn anc y.
Ref #
T10072
Seed China
Abortifacient Effect
H2O Ext
0 .0 4 m g/m l
Active
Midterm abortion.
K21690
Seed China
Abortifacient Effect
H2O Ext
80.0 mg/kg
Active
J12388
Fruit In dia
Antiimplantation Effect
100.0 mg/kg
Inactive
T02678
Fruit In dia
Not stated
Inactive
Uterus(n on-preg ).
T02678
Antifertility Effect(unspecified)
Gastric Intubation R at (Male) IG Mouse (Female) Rat (Male) (S pe rm ) IG Dog (Female) IG Rat and IP Rat
5.0 ml/kg
Active
T05027
Fruit In dia
Not stated
Not stated
Active
J11478
Juice
Not stated
Active
T05027
An tisp erm ato genic Effect An tisp erm ato genic Effect
Not stated
1.75 gm
Active
J11478
Se ed Ind ia
Active Active
Num ber of spermatocytes, spermatids and spermatozoa decre ased. Stero idogenesis inhibited. Daily dosing for 20 days. Seminiferous tubules lacked primary spermatocytes:38.7% of tubule contained normal spermatids. Tubule diameter decreased to 167 microns (220 = control). Testes exhibited variable degrees of spermatogenic arrest, mainly at spermatid stage.
J19694
Fruit In dia
1.75 gm
Active
M01152
Fruit In dia
Active
M01152
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
32
Part -Origin
Fruit In dia
Type Extract
ETO H (95% ) Ext
Test Model
Oral Dog (Male)
Dosage
1.75 gm Daily dosing for 60 days.
Result
Active
Notes/Organism tested
Se m inife rou s tu bules com pletely devoid of spermatozoa: 75% com pletely lacke d step 1-8 spermatid. Resulted in reduction in testicular weight and disruption of spermatogenesis without affecting seminal vesicle or prostrate. Increased hepatic levels of GST and acid soluble su lfhyd ryl in lactating dams (p<0.01) after 14 or 21 days of treatment, and translactationally exposed neona tes (p<0.0 5).
Ref #
M01152
Fruit In dia
200.0 mg/kg 200.0 mg/kg Daily dosing for 14 days. 100 microl
Active
M01152
Pe el + Se ed + Fruit Ind ia
Translactational Effect
Not stated
Mice
Active
AM1022
Juice Juice
Inactive Inactive
J11478 T12703
Fruit Thailand
Lyophilized Ext
6.25 % of diet
W eak Activity Active Protected against the development of skin tum or and increa sed life exp ectanc y. Re duced carc inogen-in duced lipid peroxidation in the liver and DNA damage in lymphocytes. Activated liver enzymes glutathione-S-transferase, glutathione peroxidase and catalase which were depressed after carcinogen exposure. Cells-CBA/D1.
L04084
Fruit In dia
Antitum or Activity
Not stated
AM1010
Fruit In dia
Antitum or Activity
Oral Mice
Not stated
Active
AM1010
Fruit In dia
Antitum or Activity
Oral Mice
Not stated
Active
AM1010
Fruit USA
Antitum or Activity
H2O Ext
IP Mouse
1 00 .0 m cg /m l
T09137
Fruit USA
Antitum or Activity
H2O Ext
IP Mouse
Not stated
T09137
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
33
Part -Origin
Fruit USA
Type Extract
H2O Ext
Test Model
IP Mouse
Dosage
Not stated
Result
W eak Activity
Notes/Organism tested
LEUK-P388. Drug was preincubate d w ith tu m or c ell line in vitro. Lymphocytes. Salmonella typhimurium ta100 Salmonella typhimurium ta98 Ca-755. LEU K-CM L (hum an). DD-lymphocytes-human-leukemic. Lymphocytes-human. Lymphoblasts-human
Ref #
T09137
Saline Ext Saline Ext Saline Ext Not stated Not stated H2O Ext H2O Ext H2O Ext
Agar P late Agar P late Agar P late Cell Culture Cell Culture Cell Culture Cell Culture Cell Culture
40.0 mcg 40.0 mcg 40.0 mcg Not stated Not stated Not stated Not stated Not stated
K27792 K27792
Fruit China Fruit China Fruit USA Fruit USA Fruit Origin Not Specified Fruit Not Stated Seed Not Stated Fruit USA-CA Fruit USA
Cytotoxic Activity Cytotoxic Activity Cytotoxic Activity Cytotoxic Activity Cytotoxic Activity
Lymphocytes-human. Sarco m a (yoshida asc ). Cells-CBA/D1. Me lanom a-b eta cell-m 9 viable ce lls decreased from 100% to 5% between 18 and 26 hrs. Lymphocytes-human-leukemic. Lymphocytes-human.
Fruit USA Fruit USA Fruit + Seed Not Stated Fruit Thailand
E D5 0= 0 .1 6 m g E D5 0= 0 .3 5 m g Not stated
1.0 gm/kg
Active
L14935
Fruit Philippines
CCL4 ME OH Ext Pet Ethe r Ext CHC L3 Ext Hexan e Ext ME OH Ext
Active Inactive Active Inactive Salmonella typhimurium ta100 vs.direct acting mutagens in the am es m utagen icity test.
M24272
Fruit Thailand
Agar P late
L04084
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
34
Part -Origin
Fruit Thailand
Type Extract
CHC L3 Ext Hexan e Ext ME OH Ext ETO H(80% ) Ext
Test Model
Agar P late Agar P late Agar P late Agar P late
Dosage
> 1.0 m g < 1.0 m g < 5.0 m g Va riab le
Result
Active
Notes/Organism tested
Salmonella typhimurium ta100 vs. indirect acting mutagens in the am es m utagen icity test. Salmonella typhimurium ta100 vs. mutagenicity of b(alpha)p. Salmonella typhimurium ta98. Inhibited the mutagenicity of IQ, MEIQ, MEIQX, PHIP, GLU-P-2 and AFB1. vs. DM BA -initiate d, c roton oil promoted skin tumors. vs. DM BA -initiate d, c roton oil promoted skin tumors. vs. DM BA -initiate d, c roton oil promoted skin tumors. vs. DM BA -initia ted , cro ton oil promoted skin tumors. Virus-Epstein-ba rr vs. 12-o-hexadecanoylphorbol-13acetate-induced epstein-barr virus activation. Hep2 cells. Sea urchin ova.
Ref #
L04084
Fruit Thailand
Active
L14935
Fruit Thailand
Agar P late
Va riab le
Active
L14935
Fruit In dia
Ca rcin ogenesis Inhibition Ca rcin ogenesis Inhibition Ca rcin ogenesis Inhibition Ca rcin ogenesis Inhibition Tumor Promotion Inhibition
H2O Ext
External Mouse External Mouse External Mouse External Mouse Cell Culture
100.0 mcl
Active
J14866
H2O Ext
100.0 mcl
Active
J14866
H2O Ext
100.0 mcg
Active
J14866
Se ed Ind ia
H2O Ext
100.0 mcl
Active
J14866
Fruit Japan
ME OH Ext
200.0 mcg
Inactive
T15279
Fruit In dia
J11478
Fruit Thailand
DNA Adduct Formation Inhibition DN A S ynth esis Inhibition RN A S ynth esis Inhibition Prote in Synth esis Inhibition
L14935
Seed China
ETO H(100 %) E xt
Cell Culture
Not stated
Active
M27078
Seed China
ETO H(100 %) E xt
Cell Culture
Not stated
Active
M27078
Seed China
H2O Ext
Not stated
1 0.0 m cg /m l
Active
J12388
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
35
Part -Origin
Fruit China
Type Extract
Not stated
Test Model
Cell Culture
Dosage
Not stated
Result
Active
Notes/Organism tested
Reticulocyte lysate(rabbit).
Ref #
T08662
Seed China
H2O Ext
Ra bbit
1 0.0 m cg /m l
Active
(reticulocytes)
J12388
Seed China
H2O Ext
Ra bbit
1 0.0 m cg /m l
K21690
Seed Origin Not Stated Fruit + Se ed Origin Not Stated Seed Bangladesh Seed China Seed Bangladesh
H2O Ext
Ra bbit
ID 50 =0 .0 1 m cg /m l
T01769
Not stated
Mouse
Not stated
Active
Activation of NK cells.
AM1033
Non-diabetic rats.
K13947 T08662
K13947
Infusion
Not stated
Inactive
J12034
Fruit In dia
90.0 mg/kg 250.0 mg/kg 3.0 ml/kg 3.0 ml/kg Not stated
vs. glucose tolerance tests. Vs. glucose tolerance tests. vs. alloxan-induced hyperglycemia. vs. alloxan-induced hyperglycemia. vs. alloxan-induced hyperglycemia.
L05654
Fruit In dia
A07281
Fruit In dia
J11478
Fruit In dia
Fruit
IG Mouse
Not stated
Active
J11478
Fruit In dia
Fruit
IG Rat
Not stated
Active
J11478
Fruit In dia
Juice
IG Rabbit
Not stated
Active
J11478
Fruit In dia
J11478
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
36
Part -Origin
Fruit In dia
Type Extract
ETO H(100 %) E xt H2O Ext
Test Model
IG Rat
Dosage
4 00 .0 m g 4 00 .0 m g
Result
Active Active
Notes/Organism tested
Ref #
L15207
Fruit In dia
H2O Ext
Mouse
200.0 mg/kg
Active
vs. streptozotocin-induced hyp erg lycem ia. M ean re ductio n in plasma glucose levels of 15.37% (day 40), 18.68% (day 50) and 22.86% (day 60). vs.alloxan-induced hyperglycemia. Mean reduction in plasma glucose levels of 64.33% (1 m onth), 66.96% (2 m onths), 69 .7% (3 m onths) an d 70.53% (4 m onths). vs. alloxan- and streptozotocin-induced hyperglycemia. A diabetic woman recovered from glycosuria after taking a kind of curry. Karela was believed to be an active ingredient. Fall in blood sugar of 49% in 30 days. Blood sugar was maintained within normal limits for 2 weeks after treatm ent ceas ed. vs. alloxan-induced hyperglycemia. vs.glucose-induced hyperglycemia.
L10702
Fruit In dia
H2O Ext
Rat
200.0 mg/kg
Active
L10702
Fruit China
Decoction
IG Rat IP Rat
Active Active
J17491
Fruit England
Fruit
Not stated
Active
M22031
Fruit In dia
Aceton e Ext
Oral Rat
250.0 mg/kg
Active
M22671
Fruit In dia
An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity
Benze ne Ext
IG Ra bbit
1.0 gm/kg
Active
M22131
Fruit In dia
CHC L3 Ext
250.0 mg/kg
Inactive
K19538
Fruit In dia
Decoction
5 00 .0 m g
Active
A14458
500.0 mg/kg
Active
Non-diabetic rat. Depressed plasma glucose level by 10-15% at 1 hr. Efficacy 25-30% of tolbutamide.
K27156
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
37
Part -Origin
Fruit In dia
Type Extract
ETO H(95% ) Ext
Test Model
IG Rat (Female) IP Rat
Dosage
250.0 mg/kg
Result
Active
Notes/Organism tested
vs. streptozotocin-induced hyperglycemia. vs. streptozotocin-induced hyperglycemia. vs. streptozotocin-induced hyperglycemia. Dosed for 2 months. Onset of retinopathy retarded. vs. alloxan-induced hyperglycemia. Urine volum e decre ased, urinary albumin level decreased, renal hypertrophy prevented. vs. streptozotocin-induced hyperglycemia. Reduced plasma glucose c on ce ntr atio ns by 2 4.4 % . vs. alloxan-induced hyperglycemia.
Ref #
K19538
Fruit In dia
7 5.0 m g
Inactive
T12220
Fruit In dia
H2O Ext
250.0 mg/kg
Active
K19538
Fruit In dia
H2O Ext
4.0 gm/day
Active
T14959
Fruit In dia
Lyophilized Ext
Oral Mouse
2 00 .0 m g
Active
L15573
Fruit In dia
An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity
Lyophilized Ext
Oral Mouse
2 00 .0 m g
Active
L15573
Fruit In dia
Powder
IG Rat
1.0 gm/kg
Active
J14657
Fruit In dia
Not stated
Not stated
Active
T13893
Fruit Pakistan
Fruit
1.0 gm/kg
Active
M22028
Fruit Pakistan
Not stated
IG Rabbit
Not stated
Active
L03572
Fruit Peru
H2O Ext
100.0 mg/kg
Active Inactive
vs. type 2 diabetic mice. Lowered serum insulin and blood glucose. Non-diabetic mice. Maximal change in blood sugar was 4 .33% . vs. alloxan-induced hyperglycemia. vs. alloxan-induced hyperglycemia.
L10622
IG Mouse
0 .5 m l
Inactive
M22673
0 .5 m l
Inactive
T10348
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
38
Part -Origin
Fruit Thailand
Type Extract
Hot H2 O E xt Hot H2 O E xt Lyophilized Ext Lyophilized Ext Juice
Test Model
Ra bbit Ra bbit Ra bbit Ra bbit IG Rat (Male)
Dosage
10.20 mg/kg Not stated 1.2 gm/kg 400 mg/kg 10.0 ml/kg
Result
Active Inactive Inactive Inactive Active
Notes/Organism tested
Diabetic rabbits used. Diabetic rabbits used. vs. alloxan-induced hyperglycemia. vs. alloxan-induced hyperglycemia. vs. streptozoto cin-induced type-1 diabetes. vs. streptozotocin-induced hyperglycemia. vs. alloxan-induced hyperglycemia. vs. alloxan-induced hyperglycemia. vs. streptozotocin-induced hyperglycemia. Assayed in NIDDM and IDDM patients. Blood sugar levels decreased 22%. vs. streptozotocin-induced hyperglycemia. vs. alloxan-induced hyperglycemia.
Ref #
P00050
Fruit Thailand
P00096
L18419
Powder
Oral Rat
0.5 % of diet
Inactive
K29851
Se ed Ind ia
H2O Ext
Oral R abbit
3.0 ml/kg
Inactive
A07281
Se ed Ind ia
Powder
IG Rabbit
Active Active
J11478
Se ed Ind ia
Powder
Not stated
Active
J11478
Fruit In dia
200.0 mg/kg
Active
K11849
Fruit In dia
An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity
Fruit
IG Rat
15.0 gm
Active
K12995
Fruit In dia
Fruit
Not stated
Active
J12465
Fruit In dia
H2O Ext
1.0 gm
Active
Reduction of initial blood sugar level after 3 week s from 220m g to 105mg. vs. alloxan-induced hyperglycemia. Streptozotocin-treated animals.
K12995
Se ed Ind ia
Not stated
GI Ra bbit
LC50 =0 gm
Active
T05236
Fruit In dia
Hot H2 O E xt
IG Rat
4.0 gm
Active
vs. alloxan-induced hyperglycemia. Inhibited cataract formation (depen dent on b lood suga r levels).
M23178
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
39
Part -Origin
Fruit In dia
Type Extract
Juice
Test Model
IG Rabbit
Dosage
6.0 ml/kg
Result
Active Active
Notes/Organism tested
vs. alloxan-induced hyperglycemia. vs. glucose-induced hyperglycemia. The su bjects included (433) sev ere to m ild (260) diabetics, aged 4 2 to 70 years. Blood sugar estimated 2,3,4 & 7 w eeks of treatm ent. Overall fall in blood sugar was 54%. vs.alloxan-induced hyperglycemia. Tested in 25 diabetics and 10 control subjec ts. Daily dosing for 2 weeks. vs. streptozotocin-induced hyperglycemia. Daily dosing for 30 days. vs. streptozotocin-induced hyperglycemia. Improved glucose tolerance in 73% of patients with maturity onset diabetes. Juice was given 30 m inutes before oral g lucose load in the glucose tolerance test. Significant decrease in nonfasting blood glucose levels of hyperglycemia induced mice. Results significant at p < 0.01 level. Im pro ved glucose to lera nce in diabetic patients. Trea tme nt for 8 to 11 weeks. Results significant at p < 0.0 5 level. Reduction (p<0.001) of fasting and post-pra ndial se rum glucose leve ls seen in 86 % of non-ins ulin dependent diabetic subjects after oral glucose intake.
Ref #
A14328
Fruit In dia
H2O Ext
1.0 gm
Active
K12995
Fruit In dia
Not stated
100.0 gm
Inactive
T06311
Fru it Ken ya
H2O Ext
IG Mouse
16.0 gm/kg
Active
M25031
Juice
IG Rat
10.0 ml/kg
Inactive
T16092
Juice
1 00 .0 m l
Not stated
T12706
Fruit Turkey
H2O Ext
IG Mouse (Male)
0.5 gm/kg
Active
K18219
Fruit England
Fruit
0.23 kg/day
Active
T12686
Pulp Barisal
Hu m an Ad ult
Not stated
Active
AM1013
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
40
Part -Origin
Seed Japan
Type Extract
H2O Ext
Test Model
IG Rat
Dosage
100.0 mg/kg
Result
Active
Notes/Organism tested
vs. streptozotocin-induced hyperglycemia.
Ref #
L12140
Se ed Ind ia
Decoction
Va riab le
Inactive
A14461
Seed Japan
H2O Ext
100.0 mg/kg
Active
vs. streptozotocin-induced hyperglycemia. vs. adrenaline induced hyperglycemia. vs. streptozotocin-induced hyperglycemia. vs. streptozotocin-induced hyperglycemia. vs. streptozotocin-induced hyperglycemia. vs. alloxan-induced hyperglycemia.
L12140
Se ed Ind ia
ME OH Ext
Oral Rat
10.0 mg/kg
Active
T14966
K13947
L12140
H2O Ext
IG Rat
100.0 mg/kg
Active
L12140
Benze ne Ext
IG Rabbit
1.0 gm/kg
Active
H24172
Fruit Egypt
Juice
IG Rat
Not stated
Active
J10963
Hot H2 O E xt
5.0 ml/kg
Eq uiv
vs. anterior pituitary extract-induced hyperglycemia. Im pro ved glucose to lera nce in diabetic patients. Trea tme nt for 8 to 11 weeks. Results significant at p < 0.0 1 level. vs. streptozotocin-induced hyperglycemia. A glucose tolerance test was used.
A07232
Juice
5 0.0 m l
Active
T12686
An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity
Juice
10.0 ml/kg
Active
L12020
Juice
5.0 ml/kg
Active
A14525
Hot H2 O E xt
IG
Not stated
Active
M17655
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
41
Part -Origin
Fruit Juice Sri Lanka
Type Extract
Hot H2 O E xt
Test Model
Oral Human Ad ult
Dosage
Not stated
Result
Active
Notes/Organism tested
Maturity onset diabetics. 73% improved glucose tolerance. vs. glucose-induced hyperglycemia. vs. alloxan-induced hyperglycemia.
Ref #
M17655
An tihyp erg lycem ic Activity An tihyp erg lycem ic Activity Hypoglycem ic Activity
IG Mouse
L19093
IG Rabbit
L06960
Juice
IG Rat
1 50 m g
Active
Lowered fasting blood glucose levels in non-diabetic rats; (p<0.05 at 120 m in). Lowered fasting blood glucose levels in non-diabetic rats; (p<0.05 at 60 m in / p<0.01 at 12 0 m in). Extract fed 45 minutes before oral glucose load in non-diabetic rats. IDDM model rats in fasting or postprandial states. Hypoglycemic effect in fasting and postprandial states in NIDDM rats. A saponin-free extract had no effect in normal and IDDM rats.
K13947
Hypoglycem ic Activity
IG Rat
1 50 m g
Active
K13947
Pulp Juice Bangladesh Pulp Juice Bangladesh Pulp Juice Bangladesh Seed Bangladesh
Hypoglycem ic Activity
IG Rat
1 50 m g
Active
K13947
Hypoglycem ic Activity
IG Rat
1 50 m g
Inactive
K13947
Hypoglycem ic Activity
IG Rat
1 50 m g
Active
K13947
Hypoglycem ic Activity
IG Rat
1 50 m g
Inactive
K13947
Fruit Juice In dia Se ed Ind ia Fruit Juice Sri Lanka Fruit Juice In dia Fruit Juice In dia
IG Rabbit IG Rat IG
IG Rabbit IG Ra bbit
5 00 .0 m g 2 00 .0 m g 5 00 .0 m g 10.0 ml/kg
A14310 W 00276
Hypoglycem ic Activity
Juice
T08396
Hypoglycem ic Activity
Juice
Not stated
Active
J10963
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
42
Part -Origin
Fruit P ulp Bangladesh Fruit Pulp Bangladesh Fruit P ulp Bangladesh Fruit P ulp Bangladesh Se ed + W hole Plant Bangladesh Se ed Ind ia
Type Extract
Juice
Test Model
IG Rat
Dosage
2.5 mg/kg
Result
Active
Notes/Organism tested
Extract fed 45 minutes before the oral glucose load. No n-d iabetic rats. R esult significant at 60-120 min. NIDDM rats. Hypoglycemic effect in fasting and postprandial states. IDDM rats.
Ref #
K13947
Hypoglycem ic Activity
IG Rat
2.5 gm/kg
Active
K13947
Hypoglycem ic Activity
IG Rat
2.5 mg/kg
Active
K13947
Hypoglycem ic Activity
IG Rat
2.5 mg/kg
Inactive
K13947
Hypoglycem ic Activity
IG Rat
2.5 mg/kg
K13947
Hypoglycem ic Activity
T14966
Hypoglycem ic Activity
IP Mouse (Male)
0 .3 m l
Active
1.0 m l of extract was equ ivalent to 10 gm of dried plant m aterial. Following a single dose of the extract, basal plasma glucose concentrations were reduced after 4 and 8 hours. Glucose tolerance was also improved 8 hr after dosing. Plasm a insulin levels were unaffecte d by the extract. Daily dosing of the extract for 13 days followed by IP glucose tolerance. Plasma glucose and plasma insulin were measured. There was no significant alteration of b ody we ight, food inta ke , fluid intake or plasma concentrations of glucose or insulin. Glucose tolerance, measured on day 13, was im proved by treatm ent.
M23565
Hypoglycem ic Activity
Mouse (Male)
0.2%
Inactive
M23565
Fruit Turkey
Hypoglycem ic Activity
IG Mouse (Male)
Inactive Inactive
K18219
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
43
Part -Origin
Fruit Pakistan Fruit Pakistan Fruit In dia Fruit In dia
Type Extract
Fruit Not stated Fruit Juice
Test Model
IG Ra bbit IG Rabbit IG Mouse IG Rat
Dosage
0.5 gm/kg Not stated Not stated Not stated
Result
Active Active Active Active
Notes/Organism tested
Ref #
M22028 L03572 J11478
J11478
Fruit China
Hypoglycem ic Activity
12.0 microcuries/ kg
Active Active
T08662
Fruit China
Hypoglycem ic Activity
Not stated
Not stated
Active
T08662
IG Rabbit IG Rat
Active Active In s trepto zotocin-in duced diabetic rats it improved oral glucose tolerance and reduced plasma glucose b y 26% at 3.5 hrs (metformin caused 45-50% reduction at 1, 2 a nd 3.5 hrs ). Poten tiation by using three plants in combination.
A14458 K27156
Fruit In dia
Hypoglycem ic Activity
250.0 mg/kg
Active
K19538
Fruit In dia
Hypoglycem ic Activity
250.0 mg/kg
Active
K09153
Fruit In dia
Hypoglycem ic Activity
Rat (Female)
250.0 mg/kg
Active
Potentiation effect if used with C. longa and E. o fficin alis . D ro p in b lo od su ga r of 15 m g rela tive to inert-tre ate d control. Dose = 20 gm of air-dried plant m ate rial.
K19538
Fruit In dia
Hypoglycem ic Activity
H2O Ext
Oral R abbit
10.0 mg/kg
Active
A14379
Fruit Jamaica
Hypoglycem ic Activity
Hot H2 O E xt
2 00 .0 m l
W eak Activity
T07170
Fruit Thailand
Hypoglycem ic Activity
P00096
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
44
Part -Origin
Fruit Thailand
Type Extract
Hot H2 O E xt
Test Model
Ra bbit
Dosage
5 mg/kg 10 mg/kg 20 mg/kg 1.0 % of diet 1.0 % of diet
Result
Inactive
Notes/Organism tested
Ref #
P00050
Fruit Japan
Hypoglycem ic Activity
Powder Powder
Oral Ra t (Male)
Active Inactive
Serum vs. fed cholesterol-free diets. Se rum vs. fed choleste rolenriched diets. The dose was given for 21 days. The fall in blood sugar was 25% of the initial level; however statistically is insignificant. The overall fall in blood sugar was 25%.
L11054
Fruit In dia
Hypoglycem ic Activity
Fruit
15.0 gm/day
Eq uiv
K12995
Juice Aqueous High Speed Supernatant Aqueous High Speed Supernatant H2O Ext
Active Active
A14328 T12135
Fruit B razil
Rat (Adipocytes)
50.0 mcl
Inactive
T12135
Fru it Ken ya
IG Mouse
16.0 gm
Inactive
vs. streptozotocin-induced hyperglycemia. (Intes tine , sm all) (Adipocytes) Muscle content of GLUT4 transporter was increased (p<0.01 ).
M25031
Fruit Israel
T12135
Fruit Peru
L10622
Fruit In dia
Juice
Diaphragm
Not stated
Active
J11478
Juice
10.0 ml/kg
Active
T12703
Not stated
Not stated
Active
K13947
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
45
Part -Origin
Fruit In dia
Type Extract
Not stated
Test Model
Hu m an Ad ult Mouse Pig IG Rat IG Rat IG Rat Not stated Intestine (sm all) Not stated
Dosage
Not stated Not stated Not stated 500.0 mg/kg 4 00 .0 m g 4 00 .0 m g Not stated Not stated Not stated Not stated
Result
Active Active Active Inactive Active Active Active Active Active Active
Notes/Organism tested
Ref #
J11478
Insulin Level Increase Insulin Potentiating Effect Hypoglycem ic Activity Glucose Absorption Inhibition Glucose Uptake Induction Glucose Utilization Inhibition Insulin Induction
ETO H(95% ) Ext ETO H(100 %)E xt H2O Ext Not stated ETO H(95% ) Ext H2O Ext Hot H2 O E xt
K27156 L15207
T11569 J11478
M17655
Not stated
Not stated
Active
J11478
H2O Ext
1 .0 m g/m l
Active
M21802
Fruit In dia
Insulin Release Stimulation Gluco se-6-ph ospha tase Inhibition Hexokinase Inhibition Gluconeogenesis Inhibition Gluconeogenesis Inhibition Liver Glycogen Increase
H2O Ext
Not stated
Active
J11478
Fruit In dia
Not stated
Active
J11478
Yeas t.
J11478 J11478
Fruit Juice Sri Lanka Fruit Juice Sri Lanka Fruit In dia
M17655
Hot H2 O E xt
Liver
Not stated
Active
M17655
IG Rat
200.0 mg/kg
Active
K11849
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
46
Part -Origin
Fruit In dia
Type Extract
H2O Ext
Test Model
Rat Mouse
Dosage
2 00 m g
Result
Active
Notes/Organism tested
In s trepto zotocin-in duced diabetic mice and alloxanized-induced diabetic rats, momordica restored hepatic and skeletal m uscle glycogen conte nt, hepatic glucokinase, hexokinase, glucose6-phosphate and phosphofructokinase. vs. streptozotocin-induced hyperglycemia. Activity decreased 23% . vs. streptozotocin-induced hyperglycemia.
Ref #
L10702
Fruit In dia
IG Rat
200.0 mg/kg
Active
K11849
Fruit In dia
Gluco se-6-ph osph-a te Dehydrogenase Stimulation Glucose Oxidase Inhibition Glucose Oxidase Inhibition Glucose Oxidase Inhibition Hexokinase Inhibition Hexokinase Inhibition Liver & Mu scle Glycogen Increase Glycogenic Effect
IG Rat
200.0 mg/kg
Active
K11849
Fruit Israel
1 25 .0 m g/m l
Active
Liver homogenates.
T12135
Fruit B razil
Supe rnatant
50.0 mcl
Active
T12135
Fruit B razil
Supernatant
50.0 mcl
Active
Liver homogenates.
T12135
Liver homogenates. Liver homogenates. Results significant at p < 0.01 level. 4-5-fold increase in the rate of glycogen synthesis. Study of the effect of fruit juice on the increase of alpha, beta, and gamm a cells in pancreas of streptozoto cin-ind uced diabetic rats. There was a significant increase in beta and delta cells.
IG Rat
500 mg/kg
Active
K27156
Miscellaneou s Effects
Fruit Juice
IG Rat (Male)
10.0 ml/kg
Active
L03902
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
47
Part -Origin
Fruit In dia
Type Extract
Powder
Test Model
IG Rat (Pancreas)
Dosage
1.0 gm/kg
Result
Active
Notes/Organism tested
Treatment significantly countered loss of islets and beta cells. Vs. streptozotocin-induced hyperglycemia.
Ref #
J14657
Active Inactive Active Eq uiv Dose given 30 m in before challenge to both rat and mouse. Naloxone did not inhibit effect. Vs. acetic acid-induced writhing. vs. hot plate method. vs. tail clip method. vs. metrazole-induced convulsions. vs. strychnine-induced convulsions. Uterus (u nspec .cond). Uterus (n on-preg ).
Fruit In dia
ETO H-H2 O E xt
IP Mouse
Not stated
Inactive
K09153
Fruit N igeria
IP Mouse
Va riab le
Inactive
T06510
Spas m olytic Activity Uterine Relaxation Effect Antiinflamm atory Activity Antiulcer Activity
Inactive Inactive
K09153 T02678
Fruit In dia
Not stated
Rat
Not stated
Active
J11478
Fruit Turkey
ETO H(95% ) Ext Hexan e Ext CHC L3 Ext Es sentia l Oil ETO H(100 %) E xt ETO H(100 %) E xt ETO H(100 %) E xt Hexan e Ext Olive O il Ext Olive O il Ext ETO H-H2 O E xt
IG Rat
500.0 500.0 500.0 500.0 310.0 310.0 620.0 290.0 330.0 660.0
mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg mg/kg
Inactive Inactive Inactive Inactive Active Active Active Active Active Inactive Inactive vs. vs. vs. vs. vs. vs. 80% ethanol-induced ulcers. DDC-induced ulcerogenesis. HCL/ethanol-induced ulcers. 80% ethanol-induc ed ulcers. 80% ethanol-induced ulcers. HCL/ethanol-induced ulcers.
K11898
Fruit Turkey
Antiulcer Activity
IG Rat (Stomach)
L09878
Fruit In dia
Diuretic Activity
IG Rat
510.7 mg/kg
K09153
Fruit In dia
Aceton e Ext
Oral Rat
250.0 mg/kg
Inactive
M22671
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
48
Part -Origin
Fruit In dia Se ed Ind ia
Type Extract
ETO H-H2 O E xt H2O Ext
Test Model
IG Rat IG Rat IP Rat IG Dog
Dosage
Not stated 250.0 mg/kg
Result
Inactive Active
Notes/Organism tested
Ref #
K09153 J19694
Fruit In dia
Not stated
1.75 gm
Active
J11478
Fruit In dia
Aceton e Ext
Oral Rat
250.0 mg/kg
Active
M22671
Fruit In dia
Fruit Powder
2.0 gm
Active
Ten mild diabetic patients (23-28 year s old) we re used in the stud y. 11 day treatm ent. Serum vs.fed cholesterol-free and-en riched diets. Elevated HDL levels. Reduced total cholesterol and triglyceride levels in both the presen ce and absen ce of dietary choleste rol.
M27532
Fruit Japan
Hypolipem ic Activity
Powder
Oral Ra t (Male)
1.0 % of diet
L11054
Fruit In dia
Fruit
IG Rat
Not stated
Active
J11478
Fruit Turkey
Juice
IG Ra t (Male)
10.0 ml/kg
Active
vs. streptozoto cin-induced type-1 diabetes. Over a 10 week period mom ordica returned to normal the increased cholesterol, triglycerides and phospholipids and LPO and malonedialdehyde as well as the reduced HDL. In the presence and absence of dietary choleste rol. Re duced free choleste rol. Increased HDL. No change in total cholesterol. Liver vs. fed cholesterol-free and-enriched diets. vs. streptozoto cin-induced type-1 diabetes.
L18419
Fruit Japan
Powder
1.0 % of diet
Active
L11054
Oil Japan
Oil
2%
Active Inactive
AM1005
Powder
1.0 % of diet
Active
L11054
Juice
10.0 ml/kg
Active
L18419
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
49
Part -Origin
Fruit Hong Kong
Type Extract
Aceton e Ext
Test Model
Rat (Adipocytes) Gastric Intubation Ra bbit Rat (Adipocytes)
Dosage
500.0 mcg
Result
Active
Notes/Organism tested
vs. Acta- Epinephrine bitartrateand Glucagon- induced lipolysis. In streptozotocin-treated animals.
Ref #
T11178
Se ed Ind ia
Lipolytic Effect
Seeds
3.0 gm
Active
T05236
Antilipolytic Activity
Aceton e Ext
500.0 mcg
Active
T11178
Fruit Japan
Not stated
1 00 .0 m g
Active
K27939
Fruit In dia
ETO H(100 %) E xt
400.0 mg/kg
Active
L10141
Fruit In dia
Juice
Not stated
Active
J11478
Juice
Cell Culture
0.1%
Active
L12020
Antilipolytic Activity
Acid-ET OH Ext
Adipocytes
Va riab le
Active
T13897
Hyperlipidem ic Activity
Hot H2 O E xt
Not stated
Active
M17655
Lipogenesis Stimulation
ETO H(95% ) Ext H2O Ext Saline Ext ETO H(95% ) Ext H2O Ext Saline Ext Juice
Not stated Not stated Not stated Not stated Not stated Not stated Not stated
J11478
Fruit In dia
Lipogenesis Stimulation
J11478
Fruit In dia
J11478
Fruit Japan
Not stated
Not stated
IC 50 =0 .8 3 m g/m l
Active
K27939
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
50
Part -Origin
Fruit Japan
Type Extract
Not stated
Test Model
Not stated
Dosage
IC 50 =4 .5 m cg /m l
Result
Active
Notes/Organism tested
Diphen yl picrylhyd ralaz ine a ssa y.
Ref #
K27939
Fruit Japan
Not stated
Not stated
IC 50 =0 .6 m g/m l
Active
Hypoxanthine/xanthine oxidase syste m. A h eat, ac id and alkali-s tab le component of extract acted as scavenger of both superoxide and hydroxy radicals. At the given concentration 90.16% scavenging of superoxide seen. A h eat, ac id and alkali-s tab le component of extract acted as scavenger of both superoxide and hydroxy radicals. At the given concentration 87.70% scavenging of hydroxy radical seen. vs. streptozotocin-induced hyperglycemia. Inc rea se in hyp ero xide s, p ossibly due to the occurrence of c9,t1118:2 in liver. vs. streptozotocin-induced hyperglycemia. Fe(2+)/ascorbate-induced oxidative damage. Re verse d th e effect o f ch ron ic diabetes on P450-dependent monooxygenase activities and glutathione-dependent oxidative stress related lipid peroxidation and glutathione-S-transferase activities.
K27939
Juice
Not stated
0 .1 m l
Active
T16453
Juice
Not stated
0 .3 3 m l
Active
T16453
Antioxidant Activity
Juice
Cell Culture
1.0% 5.0% 2%
L12020
Oil Japan
Oxidative Ac tivity
Oil
Oral Rat
AM1005
Antioxidant Activity
Juice
10.0 ml/kg
Active
L12020
Fruit Japan
Antioxidant Activity
Not stated
1 .0 m g/m l
Active
K27939
Antioxidant Activity
Juice
Not stated
Active
AM1015
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
51
Part -Origin
Fruit United Arab Emirates
Type Extract
Juice
Test Model
Rat
Dosage
Not stated
Result
Active
Notes/Organism tested
A 6 5% decre ase in hepatic glutathione (GSH) content and glutathione-S-transferase (GST) activity a nd an incr ease in br ain GSH and G ST activity o bserv ed in diabetic rats. Renal GST was reduced while GSH remained slightly higher than controls.
Ref #
AM1015
Fruit N igeria
IP Mouse
Va riab le
Active
T06510
Fruit In dia
ETO H(100 %) E xt
400.0 mg/kg
Active
L10141
Fruit In dia
ETO H(100 %) E xt
400.0 mg/kg
Active
L10141
Se ed Ind ia
Androgenic Effect
H2O Ext
250.0 mg/kg
Active
Mea sured b y changes in accesso ry reproductive organs. W eight of epididymis, prostate gland, seminal vesicle and levator ani increased. Re verse d 50-1 00% incr ease in aniline hydroxylase and ethoxyresorufin-O-deethylase activity. Reversed the 17-20% decreased activity of aminopyrene N-demethylase and ethoxycoumarin-O-deethylase. No rm alize d a red uced cyto solic glutathione concentration. Increa sed (20-30 % ) GST activ ity. Results significant at p <0.001 level. Results significant at p <0.001 level.
J19694
Juice
Active
AM1023
Fruit Juice Sri Lanka Fruit Juice Sri Lanka Fruit In dia
Gam m a-g lutam yl Transferase Induction Gam m a-g lutam yl Transferase Induction Cytochrom e B-5 Increase
Fruit Juice(unripe)
IG Rat (Male)
10.0 ml/kg
Active
K17959
Not stated
IG Rat (Male)
10.0 ml/kg
Active
K17959
H2O Ext
External Mouse
100.0 mcl
Active
J14866
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
52
Part -Origin
Fruit In dia
Type Extract
H2O Ext
Test Model
IG Mouse (Liver)
Dosage
100.0 mcl
Result
Active
Notes/Organism tested
Activity was passed translactationally to pups of dams treated with extract for 14 days.
Ref #
J16660
Se ed Ind ia
H2O Ext
External Mouse External Mouse IG Mouse (Female) (Liver) External Mouse IG Mouse (Female)
100.0 mcl
Active
J14866
H2O Ext
100.0 mcl
Inactive
J14866
H2O Ext
100.0 mcl
Inactive
J16660
H2O Ext
100.0 mcl
Active
J14866
H2O Ext
100.0 mcl
Active
Liver activity was passed translactationally to pups of dams treated w ith extract for 14 days.
J16660
Se ed Ind ia
H2O Ext
100.0 mcl
Active
J16660
H2O Ext
100.0 mcg
Active
Liver activity was passed translactationally to pups of dams treated with extract for 14 days.
J16660
Se ed Ind ia
H2O Ext
100.0 mcl
Active
J16660
H2O Ext
100.0 mcl
Inactive
J16660
Fruit In dia
H2O Ext
100.0 mcl
Active
Liver activity was passed translactationally to pups of dams treated w ith extract for 14 days. Microso m es-rat-liver.
J16660
Fruit China
Fruit
Oral Mouse
15.0 % of diet
Inactive
J18457
Fruit Thailand
Fruit
Oral Ra t (Male)
12.5 % of diet
Inactive
Microso m es-rat-liver.
J18457
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
53
Part -Origin
Fruit P eel Ind ia
Type Extract
H2O Ext
Test Model
IG Mouse (Female)
Dosage
100.0 mcl
Result
Active
Notes/Organism tested
Liver activity was passed translactationally to pups of dams treated with extract for 14 days. vs. DM BA initiated and croton oil: promoted sulfhydryl depletion.
Ref #
J16660
H2O Ext
External Mouse
100.0 mcl
Active
J14866
H2O Ext
100.0 mcl
Active
J16660
H2O Ext
100.0 mcl
Inactive
J16660
Fruit In dia
H2O Ext
100.0 mcl
Active
Liver activity was passed translactationally to pups of dams treated w ith extract for 14 days.
J16660
Se ed Ind ia
Glutathione-s-transferase Induction
H2O Ext
100.0 mcl
Active
J16660
H2O Ext
100.0 mcg
Active
J14866
H2O Ext
100.0 mcl
Active
Liver activity was passed translactationally to pups of dams treated w ith extract for 14 days.
J16660
H2O Ext
External Mouse IG Mouse (Female) (Liver) External Mouse External Mouse Oral Ra t (Male)
100.0 mcl
Inactive
J14866
H2O Ext
100.0 mcl
Inactive
J16660
Fruit In dia
10.0 mcl
Active
J14866
Se ed Ind ia
H2O Ext
100.0 mcl
Active
J14866
Fruit Thailand
Fruit
12.5 % of diet
Active
Microso m es-rat-liver.
J18457
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
54
Part -Origin
Fruit In dia
Type Extract
H2O Ext
Test Model
IG Mouse (Female)
Dosage
100.0 m cl
Result
Active
Notes/Organism tested
Liver activity was passed translactationally to pups of dams treated w ith extract for 14 days.
Ref #
J16660
Fruit USA-FL
H2O Ext
Not stated
Strong Activity
M00425
Seed USA-FL
H2O Ext
Rat (liver)
Not stated
Inactive
M00425
Fruit USA
Rat (prostate)
Not stated
Active
Guanylate cyclase activity was greater in tumor than normal prostate tissue and was reduced by the extract.
AM1041
Fruit In dia
Catalase Inhibition
ETO H(100 %) E xt
IG Mouse (Male) (He art) IG Mouse (Male) (He art) Oral Ra t (Male) Oral Ra t (Male) Oral Ra t (Male) Oral Ra t (Male) Ra t(sm all intestine) Oral Ra t (Male)
400.0 mg/kg
Active
L10141
Fruit In dia
Superoxide Dismutase Inhibition Am inopyrine- de-methylase Inhibition Am inopyrine- de-methylase Inhibition Aniline Hydroxylase Inhibition Aniline Hydroxylase Inhibition Alpha-glucosidase Inhibitory Activity Benzopyrene Metabolism Inhibition
ETO H(100 %) E xt
400.0 mg/kg
Active
L10141
Fruit China
Fruit
15.0 % of diet
Inactive
Microso m es-rat-liver.
J18457
Fruit Thailand
Fruit
12.5 % of diet
Inactive
Microso m es-rat-liver.
J18457
Fruit Thailand
Fruit
12.5 % of diet
Inactive
Microso m es-rat-liver.
J18457
Fruit China
Fruit
15.0 % of diet
Inactive
Microso m es-rat-liver.
J18457
Seed Japan
ME OH Ext
Not stated
Active
AM1002
Fruit China
Fruit
15.0 % of diet
Inactive
Microsomes-rat-liver s-9 fractions from animals fed fruit inhibited benzo[a]pyrene-induced mutagenicity towards salmo nella typhimurium .
J18457
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
55
Part -Origin
Fruit Thailand
Type Extract
Fruit
Test Model
Oral Ra t (Male)
Dosage
12.5 % of diet
Result
Active
Notes/Organism tested
Microsomes-rat-liver s-9 fractions from animals fed fruit inhibited benzo[a]pyrene-induced mutagenicity towards salmo nella typhimurium . Microsomes-rat-liver s-9 fractions from animals fed fruit inhibited aflatoxin-b-1-induced mu tagenicity towards salmonella typhimuriu. S-9 fraction s fro m anim als fed fruit inhibited aflatoxin-b-1- induced mutagenicity towards salmo nella typhimurium . Microso m es-rat-liver.
Ref #
J18457
Fruit China
Aflatoxin Inactivation
Fruit
Oral Ra t (Male)
15.0 % of diet
Inactive
J18457
Fruit Thailand
Aflatoxin Inactivation
Fruit
Oral Ra t (Male)
12.5 % of diet
Active
J18457
Fruit China
Fruit
15.0 % of diet
Inactive
J18457
Juice
50.0 ml/kg
Active
K17561
Androgenic Effect Adenyl Cyclase Inhibition Guanylate Cyclase Inhibition Guanylate Cyclase Inhibition Guanylate Cyclase Inhibition Hem agglutinin Activity Ch ondro genesis Inhibition
Active Inactive
M27078 T08662
H2O Ext
Cell Culture
E D5 0= 0.3 m g/m l
Active
Lymphoblasts-human.
T01575
Fruit USA
ETO H Ext
Not stated
E D5 0= 1 70 .0 m cg /m l
Active
Leukem ic lymphocytes.
T12861
Fruit China
Not stated
Cell Culture
Not stated
Active
T08662
Buffer ME OH Ext
Not stated 2 00 .0 m cg /m l
Active W eak Activity vs. 12-o-tetradecanoylphorbol-13ace-tate(tpa )-induced e pstein-barr virus early antigen activation.
M25317 L12243
Fruit Thailand
Hot H2 O E xt
Agar P late
Not stated
Active
P00050
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
56
Part -Origin
Fruit Japan
Type Extract
ME OH Ext
Test Model
Agar P late
Dosage
M IC =1 .0 g m/m l
Result
W eak Activity Inactive Active Active Active Active Active Active Inactive Inactive Active
Notes/Organism tested
Es cheric hia coli
Ref #
L07607
Not stated H2O Ext H2O Ext H2O Ext Pet Ethe r Ext Pet Ethe r Ext Pet Ethe r Ext H2O Ext Pet Ethe r Ext CHC Ll3 Ext ETO H(95% ) Ext H2O Ext
Agar P late Agar Agar Agar Agar Agar Agar P late P late P late P late P late P late
L19726 Bacillus subtilis Es cheric hia coli Pseudomonas aeruginosa Ba cillus subtilis Pseudomonas aeruginosa Staphylococcus aureus Staphylococcus aureus Es cheric hia coli Bacillus subtilis Es cheric hia coli Pseudomona s aeruginosa Staphylococcus aureus K19538
Fruit In dia
Antibacterial Activity
K19538
Fruit In dia
Antibacterial Activity
K19538
Fruit In dia
Antibacterial Activity
Broth C ulture
1 .0 m g/m l
Inactive
Pseudomona s aeruginosa
K19538
Fruit Turkey
Antibacterial Activity
Agar plate
Active
Helicobacte r pylori (one stan dard strain and 8 clinical isolates). Bacillus cereus Ba cillus subtilis Micrococcus luteus Micrococcus roseus Prote us mira bilis Pseudomonas aeruginosa Serratia marcescens Str eptoc occus faecalis Trichom onas vaginalis Prote us mira bilis Es cheric hia coli Micrococcus roseus Salmonella typhi Staphylococcus albus Staphylococcus aureus Sta phylococcus epidermidis
AM1018
Antibacterial Activity
H2O Ext
Agar P late
W eak Activity
J19353
Antibacterial Activity
H2O Ext
Agar P late
5.0 mcl
Active
J19353
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
57
Part -Origin
Fruit PapuaNew Guinea
Type Extract
H2O Ext
Test Model
Agar P late
Dosage
5.0 mcl
Result
Inactive
Notes/Organism tested
Bacillus cereus Es cheric hia coli Micrococcus luteus Pseudomonas aeruginosa Salmonella typhi Serratia marcescens Staphylococcus albus Staphylococcus aureus Sta phylococcus epidermidis Trichom onas vaginalis Salmonella typhimurium Ba cillus subtilis Staphylococcus aureus
Ref #
J19353
Fruit Thailand
Antibacterial Activity
ME OH Ext CHC L3 Ext Ether E xt H2O Ext Not stated CHC L3 Ext Ether E xt H2O Ext ME OH Ext Ether E xt Pet Ethe r Ext
Agar P late
M IC =< 50 .0 m g
Strong Activity
P00093
Eq uiv Actve Es cheric hia coli Pseudomonas aeruginosa Salmonella typhosa Sarcina lutea Shigella dysenteriae Ba cillus subtilis Es cheric hia coli Pseudomonas aeruginosa Salmonella typhosa Sarcina lutea Shigella dysenteriae Staphylococcus aureus Corynebacterium diphtheriae Diplococcus pneumoniae Staphylococcus aureus Streptococcus pyogenes Streptococcus viridans Ba cillus subtilis Es cheric hia coli Ps eudomo nas cic horii Salmonella typhimurium
L19726 P00093
Fruit Thailand
Antibacterial Activity
Agar P late
Not stated
Inactive
P00093
Se ed Ind ia
Antibacterial Activity
Agar P late
1 0.0 m g/m l
Inactive
M29966
Se ed Ind ia
Antibacterial Activity
Seeds
Agar P late
Not stated
Active
L07721
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
58
Part -Origin
Root Pakistan
Type Extract
ETO H(95% ) Ext
Test Model
Agar P late
Dosage
Not stated
Result
Active
Notes/Organism tested
Ba cillus subtilis Es cheric hia coli Staphylococcus aureus Vibrio cholera My cobacte rium My cobacte rium My cobacte rium My cobacte rium My cobacte rium smegma tis smegma tis smegma tis smegma tis smegma tis
Ref #
L11725
Fruit Thailand
Antimycobacterial Activity
P00093
Fruit In dia
Antifungal Ac tivity
Broth C ulture
1 .0 m g/m l
Aspergillus fumigatus Trichophyton mentagrophytes Mic ros porum canis Microsporum gypseum Phialophora jeanselmei Piedraia hortae Trichophyton mentagrophytes Candida Ca ndida Candida Ca ndida albicans tropicalis albicans tropicalis
K09153
Se ed Ind ia
Antifungal Ac tivity
Agar P late
1 0.0 m g/m l
Inactive
M29966
Se ed Ind ia
Antiyeast Activity
Agar P late
1 0.0 m g/m l
Inactive
M29966
Fruit In dia
Antiyeast Activity
ETO H-H2 O E xt
Broth C ulture
1 .0 m g/m l
Inactive
Candida albicans Cryptococcus neoformans Sp oro trichum schenckii Candida Candida Candida Candida Candida albicans albicans albicans albicans albicans
K09153
Fruit Thailand
Antiyeast Activity
P00093
Fruit In dia
Antiviral Activity
ETO H-H2 O E xt
Cell Culture
0 .0 5 m g/m l
K09153
Fruit In dia
Antiviral Activity
Not stated
Not stated
Not stated
Active
J11478
Antiviral Activity
Not stated
Not stated
Not stated
Active
AM1033
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
59
Part -Origin
Fruit In dia Fruit Juice In dia Se ed Ind ia Fruit In dia
Type Extract
ETO H(95% ) Ext ETO H(95% ) Ext Hot H2 O E xt ETOH-H2O (1:1) Ext ETO H(95% ) Ext H2O Ext ETO H(95% ) Ext ETO AC E xt ME OH Ext Pet Ethe r Ext Se ed Oil
Test Model
Not stated Not stated Not stated Broth C ulture
Dosage
1 00 .0 m g/m l 0 .1 m l 1-50 IC 10 0= 2 5.0 m cg /m l
Result
Active Active Active Active
Notes/Organism tested
As caridia galli As caridia galli Haemonchus contortus Entamoeba histolytica
Ref #
K03520 K03520 W 00384 K09153
Fruit B razil
Molluscicidal Activity
Not stated Not stated Not stated Not stated Not stated Not stated Not stated
1000 ppm 1000 ppm 50.0 mcg Not stated Not stated 1.0 ppm 0.5%
Biomph alaria glabrata Biomphalaria straminea Rhodnius neglectus Spodoptera litura larvae Spodoptera litura larvae Spodoptera litura larvae Athalia promina
W 02949
K18765 P00001
Se ed Oil India
T02572
Fruit In dia
Not stated
Not stated
Not stated
Active
J11478
Se ed Oil India
Se ed Oil
Oral Rat
20.0 % of diet
Active
J18799
GI = Gastric Intubation
IG = Intragastric
IP =Intraperitoneally
IV = Intravenously SC = Subcutaneous
IM = Intramuscular
60
Chemical type
Prote id
Plant Part
Seed Fruit Fruit Fruit Se ed oil Entire plant Seed Fruit Leaf Fruit Seed Seed Seed Seed Seed Fruit Aerial parts Fruit Leaf Se ed oil Entire plant Pericarp Pericarp
Plant Origin
Nepal Ind ia Ind ia Ind ia Japan Bangladesh Nepal Not stated Not stated Not stated Nepal Nepal Japan Japan Nepal Ind ia Peru Not stated Not stated Ind ia Bangladesh USA USA
Quantity
00.01577% Not stated Not stated Not stated Not stated Not stated 00.0323% 570-36,444 ppm 1,700-12,412 ppm Not stated Traces 00.009% Not Stated Not stated Traces Not stated Not stated 130-4,333 ppm 2,640-18,701 ppm Not stated Not stated Not stated Not stated
Ref #
T06653 A00487 A00487 A00487 M15045 L13425 T06653 ZZ1047 ZZ1047 ZZ1047 T06653 T06653 AM1028 H08562 T06653 A00487 M28611 ZZ1047 ZZ1047 M19217 L13425 K03650 K03650
Alanine, beta: Ala nine, p henyl: Amyrin, beta: Arachidic ac id Arginine As corbic acid
Ascorbigen Asparagine As partic acid BG IT Bitter gourd inhibitor bg-i-a Butyric acid, gamma-amino
Calceolarioside E Calcium
Ca pric acid
Lipid
Ca rotenoid Ca rotenoid
61
Compound
Ca rote ne, beta : 5-6 -ep oxy: Carotene, delta: Carotene, gamm a: Ch ara ntin
Chemical type
Ca rotenoid Ca rotenoid Ca rotenoid Ste roid
Plant Part
Pericarp Pericarp Pericarp Fruit Fruit Seed Fruit(unripe) Fruit Fruit Fruit(unripe) Seed
Plant Origin
USA USA USA Ind ia China China Ind ia Ind ia China Egypt China
Quantity
Not stated Not stated Not stated Not stated Not stated Not stated 00.035% 00.15% Not stated Not stated Not stated
Ref #
K03650 K03650 K03650 J11478 T08662 T08662 W 00678 A00485 L14446 H16247 M27078
Charine Cholesta-trans-7-trans-22-25(27)-trien-3-beta-ol, 5-alpha: 3-o -be ta-d -gluc osyl-2 4-b eta-eth yl Cholesterol Citrulline Copper Crypto xan thin Cu curbita- 5-2 4-d ien-1 9-a l,2-3 -dihyd roxy: Cucurbita-5-24-dien-3-beta-ol, 1o-alpha: Cucu rbita-5-24-diene , 3-beta-7-b eta- 23-trihydroxy: 7-o-beta-d-glucoside Cucurbitacin B Cucurbitacin K Cycloart-cis-23-ene-3-beta-25-diol Cycloartenol Cycloartenol, 24-methylene: Cymene, para:
Not stated Japan Not stated USA Bangladesh Japan Nig eria
Not stated 41.2 ppm 30 ppm Not stated Not stated Not stated 00.03238%
Not stated Not stated Not stated Not stated Not stated Not stated
62
Compound
Dio sgenin
Chemical type
Sa pogenin
Plant Part
Fruit(unripe) Suspension Kernel Cotyledons Fruit Plant Seed Fruit Fruit Fruit Leaf Seed Seed Fruit Seed Seed Endo sperm Fruit Fruit Fruit Fruit Fruit Fruit Fruit
Plant Origin
Ind ia Not stated Japan Not stated P.-New Guinea Not stated Japan USA Not stated Ind ia Trinidad Japan Japan Ind ia Nepal Nepal Thailand Japan Japan Japan Japan Japan Japan Japan
Quantity
01.69 mg/gm 13.66 mg/gm Not stated 65.89% Not stated Not stated Not stated Not stated Not stated 00.06% Not stated Not stated Not stated Not stated 00.0212% 00.00382% Not stated 00.00007% 00.00005% 00.00006% 00.00008% 00.0001% 00.00008% 00.00006%
Ref #
A00475 A00475 A00488 T06928 M27944 ZZ1047 H24527 T00436 ZZ1047 A00486 A06190 M16315 M16315 A00487 T06653 T06653 H28024 H27988 H27988 H27988 H27988 H27988 H27988 H27988
Lipid
Elasterol Erythrodiol Ethylene F la vo ch ro me Galacturonic acid, D: Gentisic acid Glucose, alpha: Glucose, beta: Gluta m ic ac id
Sterol Triterpene Alkene to c3 Unknown Carbo hydrate Be nze noid Carbo hydrate Carbo hydrate Prote id
Glycine Gourd protein mrk-29 Goyaglycoside A Goyaglycoside B Goyaglycoside C Goyaglycoside D Goyaglycoside E Goyaglycoside F Goyaglycoside G
63
Compound
Goyaglycoside H Goyasaponin I Go yasapon in II Go yasapon in III Guanylate cyclase inhibitor Gypsogenin Hexadecan-1-ol Histidine
Chemical type
Triterpene Triterpene Triterpene Triterpene Unknown Triterpene Alkano l c5 or mo re Prote id
Plant Part
Fruit Fruit Fruit Fruit Not stated Not stated Se ed essentia l oil Seed
Plant Origin
Japan Japan Japan Japan Not stated Egypt Japan Nepal
Quantity
00.00007% 00.0001% 00.00027% 00.00008% Not stated Not stated Not stated 00.00436%
Ref #
H27988 H27988 H27988 H27988 AM1041 J12384 M13369 T06653
Inu lin
Carbo hydrate
Callus tissue Fruit Fruit Callus tissue Fruit Fruit Leaf Fruit(unripe) Fruit(unripe) Fruit(unripe) Seed Seed Seed Seed Seed Fruit
Not stated Not stated Ind ia Not stated Not stated Not stated Not stated Ind ia Ind ia Ind ia Japan Japan Japan Japan Japan Not stated
Not stated Not stated 01.0 gm/100 gm 01.9 gm/100.0 g 0.41 ppm 2-560 ppm 50-357 ppm Not stated Not stated Not stated Not stated Not stated Not stated Not stated Not stated Not stated
Iodine Iron
Kak ara I-B Kak ara III-A Kak ara III-B Karounidiol Karounidiol, dihydro: 7-oxo: Karounidiol, iso: Karou nidiol,iso: 3-para-m ethoxy-benzo ate Karou nidiol-3-benzoate Lanosterol
Structure unknown Structure unknown Structure unknown Triterpene Triterpene Triterpene Triterpene Triterpene Sterol
64
Compound
Lauric acid
Chemical type
Lipid
Plant Part
Fruit Se ed oil Entire plant Seed Seed Seed Seed Seed Entire plant Se ed oil Fruit Cotyledons Cotyledons Se ed oil Fruit Cotyledons
Plant Origin
P.-New Guinea Ind ia Bangladesh Ind ia Ind ia China Nepal Nepal Bangladesh Ind ia P.-New Guinea Not stated Not stated Ind ia P.-New Guinea Not stated
Quantity
Not stated Not stated Not stated Not stated Not stated Not stated 00.00416% 00.00384% Not stated Not stated Not stated 07.22% 10.39% Not stated Not stated 09.96%
Ref #
M27944 M19217 L13425 N04644 N04644 T08662 T06653 T06653 L13425 M19217 M27944 T06928 T06928 M19217 M27944 T06928
Prote id Prote id
Linolenic acid
Lipid
Lutein Lycopene
Ca rotenoid Ca rotenoid
Pericarp Seed Fruit Pericarp Seed Fruit Fruit Seed Se ed essentia l oil Seed Seed
USA-RI Taiwan Taiwan USA Nepal Not stated Not stated China Japan China China
Not stated Not stated 00.02310% Not stated 00.0149% 195-3,800 ppm 10 ppm Not stated Not stated Not stated Not stated
K03650 M12169 T06649 K03650 T06653 ZZ1047 ZZ1047 M27144 M13369 M27078 M27078
Prote id Ino rga nic Ino rga nic Prote id Monoterpene Triterpene Triterpene
65
Compound
Momorcharin I Mom orcharin II Momorcharin, alpha:
Chemical type
Prote id Prote id Prote id
Plant Part
Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Seed Fruit Seed Fruit Seed Seed Seed Fruit Fruit Fruit
Plant Origin
China China Hong Kong Not stated Hong Kong Not stated China Hong Kong China Not stated Not stated Hong Kong Not stated Hong Kong Hong Kong Not stated China China Not stated China China China Pakistan Taiwan China Not stated USA USA USA
Quantity
Not stated Not stated Not stated Not stated Not stated Not stated 00.10000% Not stated Not stated Not stated Not stated Not stated Not stated Not stated Not stated Not stated 00.08000% Not stated Not stated Not stated Not stated Not stated 00.00003% Not stated Not stated Not stated Not stated Not stated Not stated
Ref #
K10925 K10925 K29357 T08079 T12146 T15210 T10072 T08376 T08662 T14056 T08064 T08376 T08079 K29357 T12146 T15210 T10072 T08662 T14056 H24792 H24792 K27541 H19648 M01395 K16937 T03229 T12489 T06213 T06213
Momorcharin, beta:
Prote id
Momorcharin, delta: Momorcharin, epsilon: Momorcharin, gamma: Momordenol Mo m ord ica agglutinin Momordica anti-HIV protein map-30 Mo m ord ica chara nth ia inh ibito r prote in Momordica charantia cytostatic factor Momordica charantia cytostatic factor 11000 daltons Momordica charantia cytostatic factor 40000 daltons
Prote id Prote id Prote id Ste roid Prote id Prote id Prote id Prote id Prote id Prote id
66
Compound
Mo m ord ica chara ntia lectin
Chemical type
Prote id
Plant Part
Seed Seed Seed Seed Seed Fruit Cotyledons Leaf Leaf Seed Seed Fruit Fruit Seed Seed Seed Seed Seed Seed Seed Fruit Fruit Leaf Leaf
Plant Origin
China Not stated Ind ia Not stated China Thailand Ind ia Nig eria Nig eria Japan China China Not stated Not stated Au stralia Au stralia Au stralia Au stralia Japan Japan Pakistan Pakistan Nig eria Ind ia
Quantity
Not stated Not stated 00.016% Not stated Not stated Not stated Not stated 00.02047% 00.02% Not stated Not stated Not stated Not stated Not stated Not stated Not stated Not stated Not stated Not stated Not stated 00.000015% 00.000018% 00.04404% 00.12%
Ref #
M22040 T03229 T03515 T01621 AM1020 C00037 T08932 M26112 M26112 H04816 H17847 J11634 K08504 K08504 K28076 K28076 K28076 K28076 H04816 H04816 H19648 H19648 M26112 L07241
Momordica charantia steroid glycoside Momordica charantia triterpene glycoside Momordica cucurbitane 3 Momordica cucurbitane 6 Mom ordica elastase inhibitor mcei-I Mo m ord ica lectin Momordica protein (mw-34,000) Momordica protein map-30
Mom ordica protein m s-1 Mom ordica protein m s-2 Mom ordica protein m s-3 Mom ordica protein m s-4 Mom ordica trypsin inhibitor mcti-I Mom ordica trypsin inhibitor mcti-II Mo m ord icilin Mo m ord icin Momordicin 8 Momordicin I
Prote id Prote id Prote id Prote id Prote id Prote id Triterpene Triterpene Triterpene Triterpene
67
Compound
Mom ordicin II
Chemical type
Triterpene
Plant Part
Leaf Leaf Leaf Part Not Specified Leaf + stem Fruit(unripe) Leaf Leaf + stem Leaf + stem Fruit Part Not Specified Seed Fruit Seed Seed Fruit Seed Seed Fruit(unripe) Fruit(unripe) Fruit(unripe) Fruit(unripe) Fruit(unripe) Fruit(unripe) Fruit
Plant Origin
Nig eria Ind ia Brazil Not stated Japan Not stated Ind ia Japan Japan Pakistan China Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan
Quantity
00.1919% 00.15% 00.008% Not stated 00.07% 00.05% Not stated 00.07% 00.12% 00.00002% Not stated 00.12874% 00.00128% 00.00898% 00.01141% 00.00016% 00.00228% 00.00365% 00.00104% 00.07560% 00.00126% 00.00720% 00.00060% 00.04340% 00.00012%
Ref #
M26112 L07241 A00499 A05062 T08353 J17890 M27271 T08353 T08353 H19648 L18292 T09095 H27988 T09095 T09094 H27988 T09094 T09094 T05957 T05957 T05957 T05957 T05957 T05957 H27988
Momordicine
Alkaloid-misc
Momordicine I
Triterpene
Mom ordicine II
Triterpene
Momordicoside B Momordicoside C
Triterpene Triterpene
Momordicoside D Momordicoside E Momordicoside E' Mom ordicoside E-1 Momordicoside Ex Momordicoside F Momordicoside F Mom ordicoside F-1
68
Compound
Mom ordicoside F-2
Chemical type
Triterpene
Plant Part
Fruit(unripe) Fruit(unripe) Fruit(unripe) Fruit(unripe) Fruit(unripe) Fruit(unripe) Fruit(unripe) Fruit Fruit(unripe) Fruit(unripe) Fruit(unripe) Fruit Fruit(unripe) Fruit(unripe) Fruit(unripe) Seed Seed Seed Seed Seed Seed Seed Fruit Se ed oil Pericarp Seed
Plant Origin
Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan Japan Taiwan China Japan Not stated Japan Japan Ind ia Pakistan Japan USA China
Quantity
Not stated 00.00400% Not stated 00.01236% 00.00740% Not stated 00.00818% 00.00006% 00.00080% Not stated Not stated 00.00002% Not stated Not stated 00.00360% Not stated Not stated Not stated Not stated Not stated Not stated Not stated 00.00004% Not stated Not stated Not stated
Ref #
T04513 T05957 T04513 T05957 T05957 T04513 T05957 H27988 T05957 T05887 T04513 H27988 T05887 T04513 T05957 M01395 H12613 K12780 M27569 H09788 H09788 H24720 H19648 M15045 K03650 M27078
Momordicoside G
Triterpene
Momordicoside H Momordicoside I
Triterpene Triterpene
Momordicoside J Momordicoside K
Triterpene Triterpene
Momordicoside L
Triterpene
69
Compound
Myristic ac id
Chemical type
Lipid
Plant Part
Fruit Se ed oil Entire plant Se ed essentia l oil Fruit Leaf Fruit Part Not Specified Entire plant Fruit Cotyledons Seed Fruit Fruit
Plant Origin
P.-New Guinea Ind ia Bangladesh Japan Not stated Not stated Not stated Egypt Bangladesh P.-New Guinea Not stated Nepal Not stated Not stated Ind ia Ind ia Bangladesh P.-New Guinea Ind ia Not stated Not stated P.-New Guinea Not stated Japan USA USA
Quantity
Not stated Not stated Not stated Not stated 3-50 ppm 15-103 ppm 33,800 ppm Not stated Not stated Not stated 15.58% 00.00632% 185-1,444 ppm 5 ppm Not stated Not stated Not stated Not stated Not stated 02.71% 51.95% Not stated Not stated Not stated Not stated Not stated
Ref #
M27944 M19217 L13425 M13369 ZZ1047
ZZ1047 J12384 L13425 M27944 T06928 T06653 ZZ1047 ZZ1047 M21799 M21799 L13425 M27944 M19217 T06928 T06928 M27944 ZZ1047 M13369 L18395 L18395
Prote id
Prote id
Fruit Seed Entire plant Fruit Se ed oil Cotyledons Cotyledons Fruit Fruit Se ed essentia l oil Fruit Fruit
Pa lm itic acid
Lipid
70
Compound
Peptide m c6.2 Peptide m c6.3 Peroxidase Pe troselinic a cid Phosphorus
Chemical type
Prote id Prote id
Plant Part
Fruit Fruit Fruit
Plant Origin
USA USA Not stated Ind ia Not stated Not stated USA Not stated Not stated Not stated Not stated Ind ia Not stated Not stated Not stated Not stated Japan Not stated Not stated Not stated Not stated Peru USA Nepal
Quantity
Not stated Not stated Not stated Not stated 320-8,333 ppm 540-33,467 ppm Not stated Not stated Not stated 2,700-45,000 ppm 5,100-33,117 ppm Not stated 9,000-181,000 ppm 51,000-371,000 ppm 0.4-9 ppm 4.6-31 ppm Not Stated Not stated Not stated Not stated Not stated Not stated Not stated 00.00399%
Ref #
L18395 L18395 ZZ1047 M19217 ZZ1047
Ca rotenoid
Proline Prote in
Prote id Prote in
A00487 ZZ1047
ZZ1047
Ribonuclease MC1 Ribosome-inactivating protein 1 Ribosome-inactivating protein 2 Ribosome-inactivating protein 3 Ribosome-inactivating protein 4 Ro sm arin ic ac id Ru bixa nth in Serine Prote id Prote id Prote id Prote id Ph enylpro panoid Ca rotenoid Prote id
71
Compound
Sitosterol, beta:
Chemical type
Ste roid
Plant Part
Fruit Fruit Fruit(unripe) Fruit Fruit Suspension Fruit Fruit Leaf Fruit Fruit Seed Entire plant Se ed oil Fruit Cotyledons Cotyledons Fruit Fruit Fruit Fruit(unripe) Fruit Fruit Fruit Fruit Fruit Fruit
Plant Origin
Thailand China Ind ia Not stated Not stated Not stated Not stated Not stated Not stated China Not stated Japan Bangladesh Ind ia P.-New Guinea Not stated Not stated Not stated Philippines Philippines Not stated Not stated Thailand Not stated Not stated Not stated Not stated
Quantity
Not Not Not Not Not Not stated stated stated stated stated stated
Ref #
P00001 L14446 A00475 A00670 A00671 A00475 ZZ1047 ZZ1047
Not stated 20-333 ppm 190-1,234 ppm Not stated Not stated Not stated Not stated Not stated Not stated 24.18% 12.12% Not stated Not stated Not stated 00.15% Not stated Not stated Not stated Not stated Not stated Not stated
L14446 A00631 M13369 L13425 M19217 M27944 T06928 T06928 A00671 M24272 M24272 J17890 A00671 P00001 A00670 A00671 A00631 A00631
Stigmasta-5-ene-3-beta-25-diol Stig m asta-5-2 5(2 7)- dien-3 -be ta-ol,3 -o- (6'-o-p alm itoylbeta-d-g lucosyl) Stigmasta-5-25-dien-3-beta-ol
Ste roid
Stigmasta-5-25-diene-3-beta-d-glucoside
Ste roid
Stigmasta-7-22-25-trien-3-beta-ol Stigmasta-7-22-dien-3-beta-ol
72
Compound
Stigmasterol
Chemical type
Ste roid
Plant Part
Fruit(unripe) Suspension Se ed oil Fruit Leaf Seed Seed Seed Seed Fruit Seed Fruit
Plant Origin
Ind ia Not stated Japan Not stated Not stated Nepal Nepal Japan China Ind ia Nepal China
Quantity
Not stated Not stated Not stated 0.2-12 ppm 1.3-8 ppm 00.00178% 00.39600% Not stated Not stated Not stated 00.0517% Not stated
Ref #
A00475 A00475 M15045 ZZ1047
Taraxerol Th iam in
Threonine Trehalose Trehalose, alpha-alpha: Trypsin inhibitor mci-3 Tryp tam ine, 5 -hyd roxy: Tyrosine Uracil
Prote id Carbo hydrate Carbo hydrate Prote id Ind ole alkaloid Prote id Non-alkaloid nitrogen heterocy
Ureas Vacine V-insulin Verbascoside Vicine Not Stated Prote id Ph enylpro panoid Non-alkaloid nitrogen heterocy
Seed Seed Fruit Aerial parts Seed Seed Seed Seed Seed Seed Seed Pericarp Pericarp
Not stated China Ind ia Peru Ind ia Nepal Egypt Ind ia China Ind ia Ind ia USA USA
Not stated Not stated Not stated Not stated 00.05000% 00.40000% Not stated Not stated Not stated Not stated Not stated Not stated Not stated
ZZ1047 AM1034 M27533 M28611 T05754 T06653 H16247 J11478 M27078 T05741 T05741 K03650 K03650
73
A00115
A00136
A00475
A00485
A00486
A00487
A00488
A00503
A00631
A00637
A00670
A00671
A01947
A04179
A04780
74
A04902
STUDY OF ANTIFERTILITY ACTIVITY OF THE LEAVES OF MOMOR DICA (KARELA). SAKSENA,SK: INDIAN J PHYSIOL PHARMACOL 15 : 79-80 (1971) (DEPT PHARMACOL POST GRAD INST MED ED RES CHANDIGARH UT INDIA) ALKALOID BEARING PLANTS AND THEIR CONTAINED ALKALOIDS. W ILLAMAN,JJ: SCHUBERT,BG: ARS, USDA, TECH BULL 1234, SUPT DOCUMENTS, GOVT PRINT OFF, W ASHINGTON DC, 1961 : - (1961) (NO ADDRESS GIVEN) FOLK-REMEDY PLANTS AND ESOPHAGEAL CANCER IN CORO, VENEZUELA. MORTON,JF: MORRIS ARBORETUM BULL 25 : 24-34 (1974) ( MORTON COLLECTANEA UNIV MIAMI CORAL GABLES FL USA) THE MEDICINAL AND POISONOUS PLANTS OF SOUTHERN AND EASTERN AFRICA. 2ND ED, E.+S. LIVINGSTONE,LTD.,LONDON. WATT,JM: BREYER-BRANDW IJK,MG: BOOK : - (1962) ( SOUTH AFRICAN INST MED RES JOHANNESBURG SOUTH AFRICA) ETHNOBOTANICAL NOTES FROM PUERTO RICO. STIMSON,W R: LLOYDIA 34 1: 165- (1971) (DEPT BIOL SCI COLUMBIA UNIV NEW YORK NY USA) ON THE DISTRIBUTION OF GENTISIC ACID IN GREEN PLANTS. GRIFFITHS,LA:J EXP BIOL 10 : 437- (1959)( REG RES CENT IMPERIAL COLL TROP AGR TRINIDAD/TOBAGO) PITUITARY DIABETES. III. EFFECT OF INDIGENOUS ANTIDIABETIC-DRUGS AGAINST THE ACUTE HYPERGLYCEMIC RESPONSE OF ANTERIOR PITUITARY EXTRACT IN GLUCOS E FED ALBINO RATS. GUPTA,SS: INDIAN J MED RES 51 : 716- (1963) (DEPT PHARMACO L GANDHI MED COLL BHOPAL MP INDIA) ON THE PRE SEN CE O F AN ANT IDIAB ETIC PRIN CIPL E IN M OM OR DICA CHA RAN TIA. CH ATT ERJ EE,K P: INDIA N J PH YSIO L PH ARM ACO L 7 : 240- (19 64) ( RES DIV EAST INDIA PHARM WORKS LTD CALCUTTA WEST BENGAL INDIA) PRELIMINARY CHEMICAL AND PHARMACOLOGICAL STUDIES ON "CUNDEAMOR," MOMORDICA CHARANTIA L. (PART I). RIVERA,G: AMER J PHARM 113 7: 281-297 (1941) ( USA PHILADELPHIA COLL PHARM SCI PHILADELPHIA PA USA) POTENTIATION OF TOLBUTAMIDE ACTION BY JASAD BHASMA AND KARELA (MOMORDICA CHARANTIA). KULKARNI,RD: GAITONDE,BB: INDIAN J MED RES 50 5: 715-719 (1962) (DEPT PHARMACOL GRANT MED COLL BOMBAY MAHARASTRA INDIA) SOME O BSERVATIONS ON HYPO GLYCAEMIC ACTIVITY OF MOMO RDICA CHARANTIA. SHARMA,VN: SOGAN I,RK: ARORA,RB: INDIAN J MED RES 48 4: 471-477 (1960) (DEPT PHARMACOL EXP THERAP SMS MED COLL JAIPUR RAJASTHAN INDIA) HYPOGLYCAEMIC DRUGS OF INDIAN INDIGENOUS ORIGIN. JAIN,SR: SHARMA,SN: PLANTA MED 15 4: 439-442 (1967) ( MP UNIV SAGAR SAGAR MP INDIA) A PR ELIM INAR Y ST UDY OF T HE H YPO GL YCA EM IC PR OP ERT IES O F IND IGE NO US P LAN TS. KH AN,A H: BU RNE Y,A: PA K J ME D RE S 2 : 100-1 16 (196 2) ( K E MED COLL LAHORE PAKISTAN) KARELA AND DIABETES. RAM,S: J INDIAN MED ASS 19 : 181-. (1956) ( NEW DELHI UT INDIA)
A05062
A05449
A05825
A06027 A06190
A07232
A07281
A14280
A14310
A14328
A14379
A14458
A14461 A14525
EFFECT OF MOM ORDICA CHIRANTIA LINN (KARELA) ON GLUCO SE TOLERANCE IN ALBINO RATS. GUPTA,SS: SETH,CB: J INDIAN MED ASS 39 : 581-584 (1962) (DEPT PHARMACOL GANDHI MED COLL BHOPAL MP INDIA) MOMO RDICA CHARANTIA L. THE ANTIDIABETIC SUBSTANCES. KORPSATEPO TH,C: WANG MEESRI,S: UNDERGR ADUATE SPECIAL PROJECT REPORT, FACULTY OF PHARMACY, MAHIDOL UNIVERSITY, BANGKOK, THAILAND : 32-, (1982) ( FAC PHARM MAHIDOL UNIV BANGKOK THAILAND) CHEMICAL STUDY IN MOMORDICA CHARANTIA L. ANANSAKUNW ATT,W: THANAKUNRUNGSANK,W : LARKRUNGSAP,S: UNDERGRADUATE SPECIAL PROJECT REPORT, FACULTY OF PHARMACY, MAHIDOL UNIVERSITY, BANGKOK, THAILAND : 29-. (1981) ( FAC PHARM MAHIDOL UNIV BANGKOK THAILAND)
C00034
C00037
75
H04816
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ISOLATION OF TOXIC AND NON-TOXIC LECTINS FROM THE BITTER PEAR MELON M OMO RDICA CHARANTIA. LIN,JY: HOU,MJ: CHEN,YC: TOXICON 16 : 653- (1978) (INST BIOCHEM COLL MED NATL TAIW AN UNIV TAIPEI TAIWAN) INSULIN-LIKE MOLECULES IN MOMOR DICA CHARANTIA SEEDS. NG,TB: W ONG,CM: LI,WW : YEUNG,HW : J ETHNOPHARMACOL 15 1: 107-117 (1986) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA) LYCOPENE FROM THE SEEDS OF RIPE BITTER MELON (MOMORDICA CHARANTIA) AS A POTENTIAL RED FOOD COLOR. II. STORAGE STABILITY, PREPARATION OF PO W DERED LYCOPENE AN D FOOD APPLICATIONS. YEN,GC: HW ANG,LS: CHUNG-KUO NUNG YEH HUA HSUEH HUI CHIH 23 1/2: 151-161 (1985) (DEP FOOD SCI NATL CHUNG HSING UNIV TAICHUNG TAIWAN) STEAM VOLATILE CONSTITUENTS FROM SEED OILS OF MOMO RDICA CHARANTIA L. ISHIKAW A,T: KIKUCHI,M: IIDA,T: SETO,S: TAMURA,T: MATSUMOTO,T: NIHON DAIGAKU KOGAKUBU KIYO BUNRUI 26 : 165-173 (1985) ( GRAD SCH ENG NIHON UNIV JAPAN) CHEMICAL STUDIES OF CRUDE VEGETABLE DRUGS. I. MOMORDICA CHARANTIA L. GARCIA,LL: CAPAL,TV: VILLANUEVA,BA: SALUDARES,EP: PHILIPPINE J SCI 114 3/4: 139-150 (1985) (NATL INST SCI TECHNOL MANILA PHILIPPINES) TRITERPENE ALCOHOLS IN THE SEED OILS OF MOMORDICA CHARANTIA L. KIKUCHI,M: ISHIKAWA,T: IIDA,T: SETO,S: TAMURA,T: MATSUMOTO,T: AGR BIOL CHEM 50 11: 2921-2922 (1986) (DEPT INDUST CHEM COLL ENGINEER NIHON UNIV FUKUSHIMA 963 11 JAPAN) CARBOHYDRATES IN THE SEEDS OF MOMORDICA CHARANTIA L. ISHIKAWA,T: KIKUCHI,M: IIDA,T: SETO,S: TAMURA,T: MATSUMOTO,T: NIHON DAIGAKU KOGAKUBU KIYO BUNRUI 28 : 165-170 (1987) ( COLL ENG NIHON UNIV KORIYAMA 693 11 JAPAN) THE AMINO ACID SEQUENCE OF A TRYPSIN INHIBITOR FROM THE SEEDS OF MOMORDICA CHARANTIA LINN. CUCURBITACEAE. ZENG,FY: QIAN,RQ: W ANG,Y: FEBS LETT 234 1: 35-38 (1988) ( INST ORG CHEM ACADEMIA SINICA SHANGHAI CHINA) ORAL HYPOGLYCAEMIC MEDICINAL PLANTS OF SRI LANKA. KARUNANAYAKE,EH: W ELIHINDA,J: ABSTR PRINCESS CONGRESS I BANGKOK THAILAND 10-13 DECEMBER 1987 : ABSTR-BP-37 (1987) (DEPT BIOCHEM UNIV COLOMBO COLOMBO SRI LANKA) CHARACTERISTICS AND COMPOSITION OF SEEDS AND OIL OF W ILD VARIETY OF MOMARDICA CHARANTIA L. FROM GUJARAT, INDIA. DAVE,GR: PATEL,RM: PATEL,RJ: FETTE SEIFEN ANSTRICHM 87 8: 326-327 (1985) m( SCI COLL ANAND GUJURAT 388001 INDIA) HYPOG LYCEMIC ACTIVITY OF POLYPEPTIDE-P FROM A PLANT SOUR CE. KHANNA,P: JAIN,SC: PANAGARIYA,A: DIXIT,VP: J NAT PROD 44 6: 648-655 (1981) (DEPT BOT LAB PLANT PHYSIOL & BIOCHEM UNIV RAJASTHAN JAIPUR RAJASTHAN 302 004 INDIA) THE INSULIN-RELEASING ACTIVITY OF THE TROPICAL PLANT MOMORDICA CHARANTIA. W ELIHINDA,J: ARVIDSON,G: GYLFE,E: HELLMAN,B: KARLSSON,E: ACTA BIOL MED GER 41 12: 1229-1240 (1982) (DEPT MED CELL BIOL MED CHEM BIOCHEM UNIV UPPSALA UPPSALA S-751 23 SW EDEN) INFLUENCE OF BALSAM PEAR (THE FRUIT OF MOMORDICA CHARANTIA) ON BLOOD SUGAR LEVEL. LEI,QJ: JIANG,XM: LUO,AC: LIU,ZF: HE,XC: W ANG,XD: CUI,FY: CHEN,PI: CHUNG I TSA CHIH(ENGL ED) 5 2: 99-106 (1985) ( GUANGZHOU MILITARY MED SCH GUANGZHOU CHINA) EFFECT OF MOMORDICA CHARANTIA ON BLOOD GLUCOSE LEVEL OF NORMAL AND ALLOXAN-DIABETIC RABBITS. AKHTAR,MS: ATHAR,MA: YAQUB,M: PLANTA MED 42 3: 205-212 (1981) (DEPT PHYSIOL PHARMACOL UNIV AGR FAISALABAD PAKISTAN) INTERACTION BETWEEN CURRY INGREDIENT (KARELA) AND DRUG (CHLORPROPAMIDE). ASLAM,M: STOCKLEY,IH: LANCET 1979 : 607-. (1979) (DEPT PHARM UNIV NOTTINGHAM NOTTINGHAM NG7 2RD ENGLAND) ISOLATION AND CHARACTERIZATION OF A GALACTOSE BINDING LECTIN W ITH INSULINOMIMETIC ACTIVITIES: FROM THE SEEDS OF THE BITTER GOUR D MOMO RDICA CHARANTIA (FAMILY CUCURBITACEAE). NG,TB: W ONG,CM: LI,WW : YEUNG,HW : INT J PEPTIDE PROTEIN RES 28 2: 163-172 (1986) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA)
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ALLOXAN RECOVERED RABBITS AS ANIMAL MODEL FOR SCREENING FOR HYPOGLYCAEMIC ACTIVITY OF COMPOUNDS. VENKANNA BABU,B: MO OR TI,R: PU GA ZHE NTH I,S: PRA BHU ,KM: S URY ANA RAY ANA MUR THY ,P: INDIA N J BIO CHE M BIO PHY S 25 6: 71 4-718 (1 988) (D EPT BIOC HEM UNIV COLL MED SCI DELHI UT 110 032 INDIA) BLOOD SUGAR LOW ERING POTENTIALITY OF SELECTED CUCURBITACEAE PLANTS OF INDIAN ORIGIN. CHANDRASEKAR,B: MUKHERJEE,B: MUKHERJEE,SK: INDIAN J MED RES 90 4: 300-305 (1989) ( CENT DRUG RES INST LUCKNOW UP INDIA) EFFECTS OF LONG TERM FEEDING OF ACETONE EXTRACT OF MOMORDICA CHARANTIA (WHO LE FRUIT POW DER) ON ALLOXAN DIABETIC ALBINO RATS. SINGH,N: TYAGI,SD: AGARWAL,SC: INDIAN J PHYSIOL PHARMACOL 33 2: 97-100 (1989) (DEPT ZOOL MEERUT COLL MEERUT UP 250 001 INDIA) A STUDY ON THE CRUDE ANTIDIABETIC DRUGS USED IN ARABIAN FOLK MEDICINE. MOSSA,JS: INT J CRUDE DRUG RES 23 3: 137-145 (1985) ( COLL PHARM KING SAUD UNIV RIYADH 11451 SAUDI ARABIA) TRADITIONAL PLANT REMEDIES FOR DIABETES. BAILEY,CJ: DAY,C: LEATHERDALE,BA: DIABETIC MED 3 2: 185-186 (1986) (DEPT MOL SCI ASTON UNIV BIRMINGHAM B4 7ET ENGLAND) EFFECT OF MOMORDICA CHARANTIA LINN. POMOUS AQUEOUS EXTRACT ON CATARACTOGENESIS IN MURRIN ALLOXAN DIABETICS. SRIVASTAVA,Y: VENKATAKRISHNA-BHATT,H: VERMA,Y: PHARMACOL RES COMMUN 20 3: 201-209 (1988) ( DEPT BIOCHEM AHMEDABAD GUJURAT 380016 INDIA) A SURVEY OF MEDICINAL PLANTS OF CHENCHU TRIBES OF ANDHRA PRADESH, INDIA. REDDY,MB: REDDY,KR: REDDY,MN: INT J CRUDE DRUG RES 26 4: 189-196 (1988) (DEPT BOT SRI VENKATESWARA UNIV TIRUPATI AP 517 502 INDIA) IN VITRO ANTIMALARIAL ACTIVITY OF SIX MEDICINAL PLANTS. GBEASSOR,M: KEDJAGNI,AY: KOUMAGLO,K: DE SOUZA,C: AGBO,K: AKLIKOKOU,K: AMEGBO,KA: PHYTOTHER RES 4 3: 115-117 (1990) (DEPT PHYSIOL FAC SCI UNIV BENIN LOME TOGO) CERASEE, A TRADITIONAL TREATMENT FOR DIABETES. STUDIES IN NORMAL AND STREPTOZOTOCIN DUABETIC MICE. BAILEY,CJ: DAY,C: TURNER,SL: LEATHERDALE,BA: DIABETES RES 2 : 81-84 (1985) (DEPT BIOL SCI UNIV ASTON BIRMINGHAM B4 7ET ENGLAND) ANTIMUTAGENS FROM MOMO RDICA CHARANTIA. GUEVARA,AP: LIM-SYLIANCO,C: DAYRIT,F: FINCH,P: MUTAT RES 230 2: 121-126 (1990) ( INST CHEM UNIV PHILIPPINES QUEZON CITY 1101 PHILIPPINES) HYPOG LYCAEMIC EFFECT OF MOM ORDICA CHARANTIA EXTRACTS. DAY,C: CARTWR IGHT,T: PROVO ST,J: BAILEY,CJ: PLANTA MED 56 5: 426-429 (1990) (DEPT PHARM SCI BIOL DIV ASTON UNIV BIRMINGHAM B47ET ENGLAND) NEW METHOD O F DETECTING THE LECTIN ACTIVITY OF MOM ORDICA CHARANTIA. KAMESAKI,T: OMI,T: KAJII,E: IKEMOTO,S: VOX SANG 58 4: 307-308 (1990) (DEPT LEGAL MED HUMAN GEN JICHI MED SCH TOCHIGI-KEN JAPAN) ANA LG ESIC EFFE CT O F MO MO RDIC A CH ARA NTIA SEE D EX TRA CT IN MICE AND RAT S. BISW AS,A R: RA MA SW AM Y,S: BA PNA ,JS: J ETHNOPHARMACOL 31 1: 115-118 (1991) (DEPT PHARMACOL JAWAHARAL INST POSTGRAD MED EDUC & RES PONDICHERRY UT 605 006 INDIA) NEW CUCURBITANE TRITERPENOIDS FROM MOMORDICA CHARANTIA. FATOPE,MO: TAKEDA,Y: YAMASHITA,H: OKABE,H: YAMAUCHI,T: J NAT PROD 53 6: 1491-1497 (1990) (DEPT CHEM BAYERO UNIV KANO NIGERIA) STUDIES ON THE ACTIVE CONSTITUENTS OF MO MORDICA CHARAN TIA L. ZHU,ZJ: ZHONG,ZC: LUO,ZY: XIAO,ZY: YAO HSUEH HSUEH PAO 25 12: 898-903 (1990) ( SICHUAN INST CHIN MAT MED CHONGQING 630065 CHINA) MA P-30: A NEW INHIBIT OR OF H IV-1 INF ECT ION AND REP LICA TION . LEE-H UAN G,S : HUA NG ,PL: NA RA,P L: CHE N,HC : KUN G,H F: HU ANG ,P: HUA NG ,HI: HUANG,PL: FEBS LETT 272 1/2: 12-18 (1990) (DEPT BIOCHEM SCH MED NEW YORK UNIV NEW YORK NY 10016 USA)
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PLANTS USED IN GUATEMALA FOR THE TREATMENT OF DERMATOPHYTIC INFECTIONS. 1. SCREENING FOR ANTIMYCOTIC ACTIVITY OF 44 PLANT EXTRACTS. CACERES,A: LOPEZ,BR: GIRON,MA: LOGEMANN,H: J ETHNOPHARMACOL 31 3: 263-276 (1991) (FAC CHEM SCI UNIV SAN CARLOS GUATEMALA 01012 GUATEMALA) A SURVEY OF PLANT CRUDE DRU GS OF RAYALASEEM A, ANDHRA PRADESH, INDIA. NAGARAJU,N: RAO,KN: J ETHNOPHARM ACOL 29 2: 137-158 (1990) (DEPT BOT MED PLANTS RES LAB SRI VENKATESW ARA UNIV TIRUPATI AP 517 502 INDIA) SUBCELLULAR DISTRIBUTION OF MOMORDICINE-II IN MOMORDICA CHARANTIA LEAVES. CHANDRAVADANA,MV: CHANDER,MS: INDIAN J EXP BIOL 28 2: 185-186 (1990)( IND INST HORTICUL RES BANGALORE KARNATAKA 560089 INDIA) EFFECT OF KARELA AS HYPOG LYCEMIC AND HYPOCHO LESTEROLEMIC AGENT. UPADHYAYA,GL: KUMAR,A: PANT,MC: J DIABET ASS INDIA 25 1: 12-15 (1983) (DEPT BIOCHEM SN MED COLL AGRA UP INDIA) CLINICAL TRIAL IN PATIENTS W ITH DIABETES MELLITUS OF AN INSULIN-LIKE COMPOUND OBTAINED FROM PLANT SOURCE. BALDWA,VS: BHANDARI,CM: PANGARIA,A: GOYAL,RK: UPSALA J MED SCI 82 1: 39-41 (1977) (DEPT MED SMS MED COLL HOSP JAIPUR RAJASTHAN INDIA) PRIM ARY STR UCT URE S O F N-LIN KED OLIG OS ACC HAR IDES OF M OM OR DIN-A , A RIBO SO ME -INAC TIVA TING PRO TEIN FRO M M OM OR DICA CHA RAN TIA SEEDS. KIMURA,Y: MINAMI,Y: TOKUDA,T: NAKAJIMA,S: TAKAGI,S: FUNATSU,G: AGR BIOL CHEM 55 8: 2031-2036 (1991) (DEPT AGR SCI FAC AGR OKAYAMA UNIV OKAYAMA 700 JAPAN) PLANTS IN KANO ETHOMEDICINE; SCREENING FOR ANTIMICROBIAL ACTIVITY AND ALKALOIDS. HUSSAIN,HSN: DEENI,YY: INT J PHARMACOG 29 1: 51-56 (1991) (DEPT BIOL SCI BAYERO UNIV KANO NIGERIA) CHEMICAL COMPO SITION OF MOMO RDICA CHARANTIA L. FRUITS. YUWAI,KE: RAO,KS: KALUWIN,C: JONES,GP: RIVETT,DE: J AGR FOO D CHEM 39 10: 1762-1763 (1991) (DEPT CHEM UNIV PAPUA NEW GUINEA PAPUA PAPUA-NEW G UINEA) PHENYLPROPANOID GLYCOSIDES AND ROSMARINIC ACID FROM MOMO RDICA BALSAMINA. DE TOMMASI,N: DE SIMONE,F: DE FEO,V: PIZZA,C: PLANTA MED 57 2: 201-. (1991) (DIPT CHIM SOST NAT UNIV STUDI NAPOLI NAPLES I-80131 ITALY) PHARMACEUTICAL COMPOSITION CONTANING EXTRACTS OF FRUITS AND VEGETABLES FOR TREATING AND PREVENTING DIABETES. LIU,Y: PATENT-US-4,985-248 : 6PP-. (1991) (NO ADDRESS GIVEN) ANTI-BACTERIAL, ANTI-FUNGAL AND ANTHELMINTIC INVESTIGATIONS ON INDIAN MEDICINAL PLANTS. NAOVI,SAH: KHAN,MSY: VOHORA,SB: FITOTERAPIA 62 3: 221-228 (1991) (DEPT MICROBIOL FAC SCI PHARM HAMDARD UNIV NEW DELHI UT 110 062 INDIA) ANTIFERTILITY STUDIES OF SOME INDIGENOUS PLANTS. DHAR,SK: GUPTA,S: CHANDHOKE,N: PROC XI ANN CONF INDIAN PHARMACOL SOC,NEW DELHI,1978 1978 : 1- (1978) (DEPT PHARMACOL REGIONAL RES LAB JAMMU TAWI J & K 180001 INDIA) INHIBITOR OF PRO TEIN SYNTHESIS IN VITRO BY PROTEINS FROM THE SEEDS O F MOMO RDICA CHARANTIA (BITTER PEAR MELON). BARBIERI,L: ZAMBONI,M: LORENZONI,E: MONTANARO,L: SPERTI,S: STIRPE,F: BIOCHEM J 186 : 443-452 (1980) ( INST PATHOL GENERALE UNIV BOLOGNA BOLOGNA I-40126 ITALY) STUDIES OF INSECTICIDAL ACTIVITY OF ORGANIC COMPOUNDS IN MOMORDICA CINARANTIA LINN. TUNTIVANICH,U: TIW AKORNPUNNARAI,S: DEJSUPA,C: SCI THAILAND 38 3: 750-754 (1981) (NO ADDRESS GIVEN) HYPOGLYCEMIC EFFECT OF MOMORDICA CHARANTIA IN RABBITS. PRAPHAPRADITCHOTE,K: NOOKHW AN,C: MEKMANEE,R: ABSTR 6TH CONGRESS OF THE PHARMACOLOGICAL AND THERAPEUTIC SOCIETY OF THAILAND BANGKOK THAILAND 1984 1984 : 75-. (1984) (DEPT PHARMACOL FAC PHARM MAHIDOL UNIV BANGKOK THAILAND) ANTIMICROBIAL ACTIVITY OF MOM ORDICA CHARANTIA. MANEELRT,S: SATTHAMPONGSA,A: UNDERGRADUATE SPEC IAL PROJECT REPORT 1978 : 18PP-. (1978)( FAC PHARM MAHIDOL UNIV BANGKOK THAILAND)
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HYPOGLYCEMIC EFFECT OF MOMORDICA CHARANTIA LINN. IN RABBITS. PRAPHADITCHOTE,K: THESIS-MASTER 1984 : 59PP-. (1984) (DEPT PHARMACOL FAC PHARM MAHIDOL UNIV BANGKOK THAILAND) STU DY O N TO XICITY OF T HAI M EDIC INAL PLAN TS. M OK KHA SM IT,M: SW ATD IMO NG KO L,K: SA TRA W AHA ,P: BUL L DE PT M ED S CI 12 2/4: 3 6-65 (19 71) ( THAILAND) TRADITIONAL MEDICAL PRACTICES AND MEDICINAL PLANT USAGE ON A BAHAMIAN ISLAND. HALBERSTEIN,RA: SAUNDERS,AB: CUL MED PSYCHIAT 2 : 177-203 (1978) ( USA) EFFECTS OF MOM ORDICA CHARANTIA SEED EXTRACT ON THE RAT M ID-TERM PLACENTA. SHUM,LKW: COI,VEC: YEUNG,HW : ABSTR INTERNATIONAL SYMPOSIUM ON CHINESE MEDICINAL MATERIALS RESEARCH HONG KONG JUNE 12-14 1984 : ABSTR-78 (1984) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA) INDUCTION OF RIPENING IN THE FRUITS OF MOMORDICA CHARAN TIA BY EHTYLENE. KAYS,SJ: HAYES,MJ: TROP AGR(TRINIDAD) 55 : 167- (1978) (DEPT HORT COASTAL PLAIN EXP STA TIFTON GA USA) MEDICINAL PLANTS OF THE W EST INDIES. AYENSU,ES: UNPUBLISHED MANUSCRIPT : 110 P- (1978) ( OFFICE OF BIOLOGICAL CONSERVAT SMITHSONIAN INSTITUTION W ASHINGTON DC 20560 USA) ETHNOPHARMACOGNOSITC OBSERVATIONS ON PANAMANIAN MEDICINAL PLANTS. PART I. GUPTA,MP: ARIAS,TD: CORREA,M: LAMBA,SS: Q J CRUDE DRUG RES 17 3/4: 115-130 (1979) (ORG AM ER ST PHARMACO G RES UNIT FAC CIENC NAT Y FARM UNIV PANAMA PANAMA CITY 10767 PANAMA) PARTIAL PURIFICATION AND CHARACTERIZATION OF A GUANYLATE CYCLASE INHIBITION W ITH CYTOTOXIC PROPERTIES FROM THE BITTER MELON (MOMORDICA CHARANTIA) . TAKEMOTO,DJ: KRESIE,R: VAUGHN,D: BIOCHEM BIOPHYS RES COMMUN 94 : 332-339 (1980) (DEPT BIOCHEM KANSAS STATE UNIV MANHATTAN KS 66506 USA) INHIBITION OF PROTEIN SYNTHESIS IN VITRO BY A LECTIN FROM MO MORDICA CHARAN TIA. BARBIERI,L: LORENZONI,E: STIRPE,F: BIOCHEM J 182 : 633-635 (1979) ( IST PATOL GEN UNIV BOLOGNA BOLOGNA I-40126 ITALY) SEED EXTRACTS INHIBITING PROTE IN SYNTHESIS IN VITRO. GASPERI-CAMPANI,A: BARBIERI,L: MORELLI,P: STIRPE,F: BIOCHEM J 186 : 439-441 (1980) ( INST PATOL GENERALE UNIV BOLOGNA BOLOGNA I-40126 ITALY) ORAL HYPOGLYCAEMIC PLANTS IN W EST AFRICA. OLIVER-BEVER,B: J ETHNOPHARMACOL 2 2: 119-127 (1980) ( 19 CREST DE VAULX GAILLARD I-74240 FRANCE) FATTY ACID CHANGES DURING MATURATION OF MOMORDICA CHARANTIA AND TRICHOSANTHES ANGUINA SEEDS. LAKSHMINARAYANA,G: KAIMAL,TNB: MANI,VVS: DEVI,KS: RAO,TC: PHYTOCHEMISTRY 21 : 301-303 (1982) ( REGIONAL RES LAB HYDERABAD AP 500 009 INDIA) NOTES ON THE ETHNOBOTANY OF LAHUL, A PROVINCE OF THE PUNJAB. KOELZ,WN: Q J CRUDE DRUG RES 17 : 1-56 (1979) ( MUSEUM OF ZOOLOGY UNIV MICHIGAN ANN ARBOR MI USA) STUDIES ON THE ANTIFEEDING AND INSECTICIDAL PROPERTIES OF BITTER GOUR D (MOMOR DICA CHARANTIA L.) AGAINST MUSTARD SAW FLY ATHALIA PROXIMA KLUG. KUMAR,A: TIW ARI,GD: PANDEY,ND: PESTOLOGY 3 5: 23-25 (1979) ( CHANDRA SHEKHAR AZAD UNIV KANPUR INDIA) SCREENING OF INDIAN PLANTS FOR BIOLOGICAL ACTIVITY. PART IX. DHAWAN,BN: DUBEY,MP: MEHROTRA,BN: RASTOGI,RP: TANDON,JS: INDIAN J EXP BIOL 18 : 594-606 (1980) ( CENTRAL DRUG RESEARCH INST LUCKNOW UP 226 001 INDIA) TOXICITY OF MOMORDICA CHARANTIA LECTIN AND INHIBITOR FOR HUMAN NORMAL AND LEUKEMIC LYMPHOCYTES. LICASTRO,F: FRANCESCHI,C: BARBIERI,L: STIRPE,F: VIRCHOWS ARCH B 33 : 257-265 (1980) ( IST PATOL GEN UNIV BOLOGNA BOLOGNA I-40126 ITALY)
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STUDIES ON LECTINS. XLVII. SOME PROPERTIES OF D-GALACTOSIDE BINDING LECTINS ISOLATED FROM THE SEEDS OF BUTEA FRONDOSA, ERY THR INA IND ICA A ND M OR MO RDIC A CH ARA NTIA . HO REJ SI,V: TIC HA,M : NO VO TNY ,J: KO CO URE K,J: BIO CHIM BIOP HYS ACT A 623 : 439-448 (1980) ( INST MO L GE NET CZE CH A CAD SCI VID ENS KA CZ ECH OS LO VAK IA BITTER PRINCIPLES AND THEIR RELATED COMPO UNDS IN THE FRUITS OF MOMO RDICA CHARANTIA L. OKABE,H: MIYAHARA,Y: YAMAUCHI,T: SYMPOSIUM O N THE CHEMISTRY OF NATURAL PRO DUCTS,OSAKA,1981 24 : 95-102 (1981) ( FAC PHARM SCI FUKUOKA UNIV FUKUOKA 814-01 JAPAN) TER RES TRIA L PLA NTS MO LLUS CICID AL TO LYM NAE ID HO STS OF F ASC ILIASIS HEP ATIC A IN PU ERT O R ICO . MED INA,FR : W OO DBU RY,R : J AG R UN IV PUERTO RICO 63 : 366-376 (1979) ( PUERTO RICO JUNIOR COLLEGE RIO PIEDRAS PUERTO RICO) PLANTS OF HAITI USED AS ANTIFERTILITY AGENTS. WENINGER,B: HAAG-BERRURIER,M: ANTON,R: J ETHNOPHARMACOL 6 1: 67-84 (1982) ( LAB CHIM FAC MED PO RT-A U-PR INCE HAITI) PLANTS IN AID OF FAMILY PLANNING PROGRAMME. OOMMACHAN,M: KHAN,SS: SCI LIFE 1 : 64-66 (1981) (DEPT BOTANY SAIFIA COLLEGE BHOPAL MP INDIA) EXTRACTS FROM MOMORDICA CHARANTIA L. VISARATA,N: UNGSURUNGSIE,M: Q J CRUDE DRUG RES 19 : 75-80 (1981) (DEPT MICROBIOL FAC PHARM MAHIDOL UNIV BANGKOK THAILAND) THE CYTO TOXIC AND CYTOS TATIC EFFECTS OF THE BITTER MELON (MOMO RDICA CHA RANTIA) ON H UMAN LYMPHO CYTES. TAKEM OTO ,DJ: DUNFORD,C: MC MURRAY,MM: TOXICON 20 : 593-599 (1982) (DEPT BIOCHEM KANSAS STATE UNIV MANHATTAN KS 66506 USA) MAYA MEDICINAL PLANTS OF SAN JOSE SUCCO TZ, BELIZE. ARNASON,T: UCK,F: LAMBERT,J: HEBDA,R: J ETHNOPHARM ACOL 2 4: 345-364 (1980) (BIOL DEPT UNIV OTTAW A OTTAW A CANADA) PERSPECTIVES OF MALE CONTRACEPTION WITH REGARDS TO INDONESIAN TRADITIONAL DRUGS. KOENTJORO-SOEHADI,T: SANTA,IGP: PROC SECOND NATIONAL CONGRESS OF INDONESIAN SOCIETY OF ANDROLOGY BALI INDONESIA AUGUST 2-6 1982 1982 : 12PP-. (1982) (DEPT BIOL MED FAC AIRLANGGA UNIV SURABAYA INDONESIA) CARIBBEAN AND LATIN AMERICAN FOLK MEDICINE AND ITS INFLUENCE IN THE UNITED STATES. MORTO N,JF: Q J CRUDE DRUG RES 18 2: 57-75 (1980) ( MORTON COLLECTANEA UNIV MIAMI CORAL GABLES FL USA) EFFECTS OF BITTERGOURD (MOMORDICA CHARANTIA) SEED & GLIBENCLAMIDE IN STREPTOZOTOCIN INDUCED DIABETES MELLITUS. KEDAR,P: CHAKRABARTI,CH: INDIAN J EXP BIOL 20 : 232-235 (1982) (DEPT BIOCHEM NAGPUR UNIV NAGPUR MAHARASTRA 440 010 INDIA) A CO NTR IBUT ION TO T HE T HAI P HYT OC HEM ICAL SUR VEY . CAN NO N,JR : DAM PAW AN,P : LOJA NAP IW ATN A,V: PH URIY AKO RN,B : SINCH AI,W : SIRIR UG SA,P : SUV ATA BHA NDH U,K: W IRIYA CHIT RA,P : J SCI SO C TH AILAN D 6 : 46-53 (1980) (D EPT CHE M FA C SC I PRINC E O F SO NG KLA UNIV HAT YAI THAILAND) ENDOG ENOUS CYTO KININS IN SEEDS OF BITTERGOU RD MOM ORDICA CHARANTIA L. IYER,RI: NAGAR,PK: SIRCAR,PK: INDIAN J EXP BIOL 19 : 766-767 (1981) (DEPT BOTANY PLANT PHYSIOL LAB UNIV CALCUTTA CALCUTTA WEST BENGAL 700 019 INDIA) STUDIES ON INDIAN MEDICINAL PLANTS. PART 64. VICINE, A FAVISM-INDUCING TOXIN FROM MOMORDICA CHARANTIA LINN. SEEDS. DUTTA,PK: CHAKRAVARTY,AK: CHOWDHURY,US: PAKRASHI,SC: INDIAN J CHEM 20B : 669-671 (1981) ( INDIAN INST OF CHEM BIOLOGY CALCUTTA W EST BENGAL 700 032 INDIA) STUDIES ON THE CONSTITUENTS OF MOMORDICA CHARANTIA L. 4. CHARACTERIZATION OF THE NEW CUCURBITACIN GLYCOSIDES OF THE IMMATURE FRUITS. (2). STRUCTURES OF THE BITTER GLYCOSIDES, MOMORDICOSIDES K AND L.mOKABE,H: MIYAHARA,Y: YAMAUCHI,T: CHEM PHARM BULL 30 : 4334-4340 (1982) ( FAC PHARM SCI FUKUOKA UNIV FUKUOKA 812 JAPAN)
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STUDIES ON THE CONSTITUENTS OF MOMORDICA CHARANTIA. 3. CHARACTERIZATION OF NEW CUCURBITACIN GLYCOSIDES OF THE IMMATURE FRU ITS. (1). ST RUC TUR ES O F MO MO RDIC OS IDES G, F1 , F2 AN D I. OK ABE ,H: MIY AHA RA,Y : YAM AUC HI,T: CH EM PHA RM BUL L 30 : 397 7-3986 (1982) ( FAC PHARM SCI FUKUOKA UNIV FUKUOKA 812 JAPAN) PURIFICATION AND CHARACTERIZATION OF A CYTOSTATIC FACTOR FROM THE BITTER MELON MOMORDICA CHARANTIA. TAKEMOTO,DJ: JILKA,C: KRESIE,R: PREP BIOCHEM 12 : 355-375 (1982) (DEPT BIOCHEM KANSAS STATE UNIV MANHATTAN KS 66506 USA) EFFECT OF MOMORDICA CHARANTIA (KARELA) EXTRACT ON BLOOD AND URINE SUGAR IN DIABETES MELLITUS. STUDY FROM A DIABETIC CLINIC. KIRTI,S: VINOD,K: NIGAM,P: SRIVASTAVA,P: CLINICIAN 46 1: 26-29 (1982) ( MLB MED COLL JHANSI UP H INDIA) STUDIES ON SOME PLANTS USED AS ANTICONVULSANTS IN AMERINDIAN AND AFRICAN TRADITIONAL MEDICINE. ADESINA,SK: FITOTERAPIA 53 : 147-162 (1982)(DRUG RES UNIT FAC PHARM UNIV IFE ILE-IFE NIGERIA) LYCOPENE FRO M THE SEEDS OF RIPE BITTER MELON (MOMO RDICA CHARANTIA) AS A POTENTIAL RED FOOD COLOR ANT. 1. IDENTIFICATION,SURVEY OF LYCOPENE CONTENT AND RIPENING TEST. YEN,GC: HW ANG,LS: LEE,TC: CHUNG-KUO NUNG YEH HUA HSUEH HUI CHIH 19 : 227-235 (1981) ( GRAD INST FOOD SCI NATL TAIW AN UNIV TAIPEI TAIWAN) COMPARATIVE STUDY OF TWO MEDICINAL CUCURBITACEAE. 1. SEEDS METABOLISM AND AMINO ACID COMPOSITION. BARRON,D: KAOUADJI,M: MARIOTTE,AM: PLANTA MED 46 : 184-186 (1982) (LAB PHARMACOGNOSY U.E.R.PHARMACIE DE GRENOBLE LA TRONCHE FRANCE) FATTY ACIDS OF CALLUS TISSUES OF SIX SPECIES OF CUCURBITACEAE. HALDER,T: GADGIL,VN: PHYTOCHEMISTRY 22 9: 1965-1967 (1983) (TISSUE CULTURE LABORATORY BOSE INSTITUTE CALCUTTA W EST BENGAL 700 009 INDIA) BACTERIAL GROW TH INHIBITION OF UNSAPONIFIABLE MATTER OF FIXED OIL FROM MOMORDICA CHARANTIA. SHARMA,AK: INDIAN DRUGS PHARM IND 16 : 29-30 (1981) (DEPT PHARM SCI UNIV SAUGER SAGAR MP INDIA) A PRELIMINARY STUDY OF THE EFFECTS OF SOME W EST INDIAN MEDICINAL PLANTS ON BLOOD SUGAR LEVELS IN THE DOG. MORRISON,EYSA: W EST ,M: W EST INDIAN MED J 31 : 194-1 97 (198 2) (DEP T BIO CHE M & P HAR MA CO LO GY UNIV W EST INDIES JAMA ICA PHYTOTHERAPY IN DOM ESTIC TRADITIONAL MEDICINE IN MATOUBA-PAPAYE(GUADELOUPE). VITALYOS,D: DISSERTATION-PH.D.-UNIV PARIS 1979 : 110PP-. (1979) ( UNIV PARIS PARIS FRANCE) W ILD AND CULTIVATED CUCURBITS IN NIGERIA. OKOLI,BE: ECON BOT 38 3: 350-357 (1984) ( SCHOOL OF BIOLOGICAL SCIENCES UNIV OF PORT HARCOURT PORT HARCOURT 5323 NIGERIA) BIOLOGICAL EFFECTS OF BETA-MOM ORCHARIN ON EAR LY MOUSE EMBR YOS AND ENDO METRIAL CELLS. CHAN,W Y: TAM,PPL: YEUNG,HW : ABSTR INTERNATIONAL SYMPOSIUM ON CHINESE MEDICINAL MATERIALS RESEARCH HONG KONG JUNE 12-14 1984 : ABSTR-59 (1984) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA) PURIFICATION AND CHARACTERIZATION OF MOMORCHARINS, ABORTIFACIENT PROTEINS FROM THE CRUDE DRUG KUGUAZI(MOMORDICA CHARANTIA SEEDS). YEUNG,HW: LI,W W : CHAN,W Y: ABSTR INTERNATIONAL SYMPOSIUM ON CHINESE MEDICINAL MATERIALS RESEARCH HONG KONG JUNE 12-14 1984 : ABSTR-17 (1984) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA) STRUCTURES OF MOMORDICINES I,II AND III,THE BITTER PRINCIPLES IN THE LEAVES AND VINES OF MOMORDICA CHARANTIA L. YASUDA,M: IWAMO TO,M: OKABE,H: YAMAUCHI,T: CHEM PHARM BULL 32 5: 2044-2047 (1984) ( FAC PHARM SCI FUKUOKA UNIV FUKUOKA 812 JAPAN) THE TERMINATION OF EARLY PREGNA NCY IN THE MOUSE BY BETA-MOM ORCHARIN. CHAN,W Y: TAM,PPL: YEUNG,HW : CONTRACEPTION 29 1: 91-100 (1984) (DEPT CHEM UNIV HONG KONG HONG KONG CHINA) ORAL HYPOGLYCAEMIC ACTIVITY OF SOME MEDICINAL PLANTS OF SRI LANKA. KARUNANAYAKE,EH: W ELIHINDA,J: SIRIMANNE,SR: SINNADORAI,G: J ETHNOPHARMACOL 11 2: 223-231 (1984) (DEPT BIOCHEM FAC MED UNIV COLOMBO COLOMBO SRI LANKA)
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BIO ACT IVE C ON STITU ENT S O F CU CUR BITA CEA E PLA NTS W ITH SP ECIA L EM PHA SIS O N MO MO RDIC A CH ARA NTIA AND TRIC HO SAN THE S KIR ILOW II. NG,TB: YEUNG,HW: PROC FIFTH ASIAN SYMPOSIUM ON MEDICINAL PLANTS AND SPICES SEOUL KOREA AUGUST 20-24 1984 BH HAN DS HAN YN HAN AND W S W OO(EDS) 5 : 183-196 (1984) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA) TRITERPENOID FEEDING DETERRENT OF RAPHIDOP ALPA FOVEICOLLIS L. (RED PUMPKIN BEETLES) FROM MOMO RDICA CHARANTIA L. CHANDRAVADANA,MV: PAL,AB: CURR SCI 52 2: 87-89 (1983) ( INDIAN INST HORTICUL RESER BANGALORE KARNATAKA 560 080 INDIA) PURIFICATION AND CHARACTERIZATION OF A CYTOSTATIC FACTOR W ITH ANTI-VIRAL ACTIVITY FROM THE BITTER MELON. TAKEMOTO,DJ: JILKA,C: ROCKENBAC H,S: HUGHES,JV: PREP BIOCHEM 13 5: 397-421 (1983) (DEPT BIOCHEM W ILLARD HALL KANSAS STATE UNIV MANHATTAN KS 66506 USA) STUDIES ON THE CONSTITUENTS OF MOMORDICA CHARANTIA L. II ISOLATION AND CHARACTERIZATION OF MINOR SEED GLYCOSIDES, MO MO RDIC OS IDES C, D AN D E. M IYAH ARA ,Y: OK ABE ,H: YAM AUC HI,T: CH EM PHA RM BUL L 29 : 156 1-1566 (1981) ( FA C PH ARM SCI FU KUO KA U NIV FUKUOKA 812 JAPAN) STUDIES ON THE CONSTITUENTS OF MOMORDICA CHARANTIA L. I. ISOLATION AND CHARACTERIZATION OF MOMORDICOSIDES A AND B, GLYCOSIDES OF A PENTAHYDROXY-CUCURBITANE TRITERPENE. OKABE,H: MIYAHARA,Y: YAMAUCHI,T: MIYAHARA,K: KAWASAKI,T: CHEM PHARM BULL 28 9: 2753-2762 (1980) ( FAC PHARM SCI FUKUOKA UNIV FUKUOKA 812 JAPAN) IN VIVO ANTITUMO R ACTIVITY OF TH E BITTER MELO N (MOM ORD ICA CHARAN TIA). JILKA,C: STRIFLER,B: FORTNE R,GW : HAYS,EF: TAKEMO TO,DJ: CANCER RES 43 11: 5151-5155 (1983) (DEPT BIOCHEM DIV BIOL KANSAS STATE UNIV MANHATTAN KS 66506 USA) ANT IMICR OB IAL AC TIVITY OF S OM E ME DICIN AL SP ECIE S O F DA KAR MAR KET S. LAU REN S,A: M BO UP,S : TIGN OK PA,M : SYLL A,O : MAS QU ELIER ,J PHARMAZIE 40 7: 482-485 (1985) (LAB CHIM SUB NATUR FAC MIX MED PHARM DAKAR SENEGAL) PURIFICATION AND PARTIAL CHARACTERIZATION OF MO MORCH ARINS, ABORTIFACIENT PROTEINS FROM THE CH INESE DRUG, KUGUAZI (MOMORDICA CHARANTIA SEEDS). YEUNG,HW : LI,WW : LAW ,LK: CHAN,WY: ADVANCES IN CHINESE MEDICINAL MATERIALS RESEARCH H M CHANG H W YEUNG W W TSO AND A KOO(EDS) W ORLD SCIENTIFIC PRESS PHILADELPHIA PA : 311-318 (1984) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA) HERBAL AND TRADITIONAL PRACTICES RELATED TO MATERNAL AND CHILD HEALTH CARE. VELAZCO,EA: RURAL RECONSTRUCTION REVIEW : 35-39 (1980) (NO ADDRESS GIVEN) SCREENING OF INDIAN PLANTS FOR BIOLOGICAL ACTIVITY: PART X. ASW AL,BS: BHAKUNI,DS: GOEL,AK: KAR,K: MEHROTRA,BN: MUKHERJEE,KC: INDIAN J EXP BIOL 22 6: 312-332 (1984) ( CENTRAL DRUG RESEARCH INST LUCKNOW UP 226 001 INDIA) A STUDY ON THE CRUDE ANTIDIABETIC DRUGS USED IN ARABIAN FOLK MEDICINE. MOSSA,JS: INT J CRUDE DRUG RES 23 3: 137-145 (1985) (DEPT PHARMACOG COLL PHARM KING SAUD UNIV RIYADH 11451 SAUDI ARABIA) TRADITIONAL MEDICINE IN FIJI: SOME HERBAL FOLK CURES USED BY FIJI INDIANS. SINGH,YN: J ETHNOPHARMACOL 15 1: 57-88 (1986) ( SCH NAT RES UNIV SO UTH PAC IFIC SU VA FIJI) SCREENING OF TRICHOSANTHES KIRILOWII, MOMORDICA CHARANTIA AND CUCURBITA MAXIMA (FAMILY CUCURBITACEAE) FOR COMPOUNDS W ITH ANTILIPOLYTIC ACTIVITY. WONG ,CM: NG,TB: YEUNG,HW: J ETHNOPHARMACOL 13 3: 313-321 (1985) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA) INDIAN PLANTS WITH ORAL HYPOGLYCAEMIC ACTIVITY. JAIN,HC: ABSTR INTERNAT RES CONG NAT PROD COLL PHARM UNIV N CAROLINA CHAPEL HILL NC JULY 7-12 1985 : ABSTR-152 (1985) (PUBLICATIONS & INFO DIRECT (CSIR) NEW DELHI UT 110012 INDIA) AN IN VITRO STUDY ON THE EFFECT OF MO MORDICA CHARAN TIA GLUCOSE UPTAKE AND G LUCOSE METABO LISM IN RATS. MEIR,P: YANIV,Z: PLANTA MED 51 1: 12-16 (1985) (DEPT MED & SPICE CROPS AGR RES ORG VO LCANI CENTER BET DAGAN 50250 ISRAEL)
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POPULAR MEDICINAL PLANTS OF THE MARKETS O F DAKAR (SENEGAL). TIGNOKP A,M: LAURENS,A: MBOUP,S: SYLLA,O: INT J CRUDE DRUG RES 24 2: 75-80 (1986) (LAB CHIM SUB NATUR FAC MED PHARM DAKAR SENEGAL) EFFECTS OF MOMORCHARINS ON THE MOUSE EMBRYO AT THE EARLY ORGANOGENESIS STAGE. CHAN,W Y: TAM,PPL: CHOI,HL: NG,TB: YEUNG,HW : CONTRACEPTION 34 5: 537-544 (1986) (DEPT ANATOMY CHINESE UNIV HONG KONG HONG KONG CHINA) HERBAL DRUGS IN DIABETES - PART I: HYPOGLYCAEMIC ACTIVITY OF INDIGENOUS PLANTS IN STREPTOZOTOCIN (STZ) INDUCED DIABETIC RATS. CHAKRABOR TY,T: PODDAR,G: J INST CHEM(INDIA) 56 1: 20-22 (1984) (DEPT CHEM CALCUTTA SCH TROP MED CALCUTTA W EST BENGAL 700 073 INDIA) PURIFICATION AND CHARACTERIZATION OF A CYTOSTATIC FACTOR W ITH ANTI-VIRAL ACTIVITY FROM THE BITTER MELON. TAKEMOTO,DJ: JILKA,C: ROCKENBACH,S: HUGHES,JV: PREP BIOCHEM 13 4: 371-393 (1983) (DEPT BIOCHEM W ILLARD HALL KANSAS STATE UNIV MANHATTAN KS 66506 USA) IMPROVEMENT IN GLUCO SE TOLERANCE DUE TO MOMO RDICA CHARANTIA (KARELA). LEATHERDALE,BA: PANESAR,RK: SINGH,G: ATKINS,TW : BAILEY,CJ: BIGNELL,AHC: BRIT MED J 282 6279: 1823-1824 (1981) (DEPT DIABETES & ENDOCRINOL CLIN INVEST UNIT DUDLEY ROAD HOSP BIRMINGHAM ENGLAND) EXTRA-PANCREATIC EFFECTS OF MOM ORDICA CHARANTIA IN RATS. WELIHINDA,J: KARUNANAYAKE,EH: J ETHNOPHARMACO L 17 3: 247-255 (1986) (DEPT BIOCHEM FAC MED UNIV COLOMBO COLOMBO 8 SRI LANKA) EFFECT OF MOMORDICA CHARANTIA ON THE GLUCOSE TOLERANCE IN MATURITY ONSET DIABETES. W ELIHINDA,J: KARUNANAYAKE,EH: SHERIFF,MHR: JAYASINGHE,KSA: J ETHNOPHARMACOL 17 3: 277-282 (1986) (DEPT BIOCHEM FAC MED UNIV COLOMBO COLOMBO 8 SRI LANKA) CHANYLATE CYCLASE ACTIVITY IN HUMAN LEUKEMIC AND NORMAL LYMPHOCYTES. TAKEMOTO,DJ: DUNFORD,C: VAUGHN,D: KRAMER,KJ: SMITH,A: POW ELL,RG: ENZYME 27 : 179-188 (1982) (DEPT BIOCHEM KANSAS STATE UNIV MANHATTAN KS USA) POPULAR MEDICINE OF THE CENTRAL PLATEAU OF HAITI. 2. ETHNOPHARMACOLOGICAL INVENTORY. WENIGER,B: ROUZIER,M: DAGUILH,R: HENRYS,D: HENRYS,JH: ANTON,R: J ETHNOPHARMACOL 17 1: 13-30 (1986) (LAB PHARMACOG FAC PHARM STRASBOURG 67048 FRANCE) A PRELIMINARY CLINICAL TRIAL OF VIJAYASARA COMPOUND IN CASES OF INSULIN-INDEPENDENT DIABETES. OJHA,JH: PRASAD,VV: SINGH,B: NAGARJUN 27 2: 37-39 (1983) (DEP DRAVYAGUNA IMS BANARAS HINDU UNIV VARANASI UP INDIA) ACID -ETH ANO L EXT RAC TAB LE C OM PO UND S FR OM FRU ITS AN D SE EDS OF T HE B ITTER GO URD MO MO RDIC A CH ARA NTIA : EFFE CTS ON LIPID METABOLISM IN ISOLATED RAT ADIPOCYTES. NG,TB: W ONG,CM: LI,WW : YEUNG,HW : AMER J CHINESE MED 15 1/2: 31-42 (1987) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA) TRICHOSANTHIN, ALPHA-MOMORCHARIN AND BETA-MOMORCHARIN: IDENTITY OF ABORTIFACIENT AND RIBOSOME-INACTIVATING PROTEINS. YEUNG,HW : LI,WW : FENG,Z: BARBIERI,L: STIRPE,F: INT J PEPTIDE PROTEIN RES 31 3: 265-268 (1988) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA) A REVIEW OF INDIAN MEDICINAL PLANTS W ITH INTERCEPTIVE ACTIVITY. KAMBOJ,VP: INDIAN J MED RES 1988 4: 336-355 (1988) ( CENTRAL DRUG RESEARCH INST LUCKNOW UP 226 001 INDIA) RETARDATION OF RETINOPATHY BY MOMORDICA CHARANTIA L. (BITTER GOURD) FRUIT EXTRACT IN ALLOXAN DIABETIC RATS. SRIVASTAVA,Y: VENKATAKRISHNA-BHATT,H: VERMA,Y: PERM,AS: INDIAN J EXP BIOL 25 8: 571-572 (1987) (DEPT BIOCHEM BJ MED CO LL AHMEDABAD GUJURAT 380 016 INDIA) HYPOGLYCAEMIC AND ANTIHYPERGLYCAEMIC EFFECTS OF MOMORDICA CHARANTIA SEED EXTRACTS IN ALBINO RATS. DUBEY,DK: BISW AS,AR: BAPNA,JS: PRADHAN,SC: FITOTERAPIA 58 6: 387-394 (1987) (DEPT PHARMACOL JAWAHARAL INST POSTGRAD MED EDUC + RES PONDICHERRY UT 605 006 INDIA)
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THE IMMUNOSUPPRESSIVE ACTIVITIES OF TW O ABORTIFACIENT PROTEINS ISOLATED FROM THE SEEDS OF BITTER MELON (MOMORDICA CHARANTIA). LEUNG,SO: YEUNG,HW: LEUNG,KN: IMMUNOPHARMACOLOGY 13 3: 159-171 (1987) (DEPT BIOCHEM CHINESE UNIV HONG KONG SHATIN N.T. CHINA) SCREENING OF EDIBLE PLANTS AGAINST POSSIBLE ANTI-TUMOR PROMOTING ACTIVITY. KOSHIMIZU,K: OHIGASHI,H: TOKUDA,H: KONDO,A: YAMAGUCHI,K: CANCER LETT 39 3: 247-257 (1988) (DEPT FOOD SCI TECHN FAC AGR KYOTO UNIV KYOTO 606 JAPAN) VEGETALES EMPLEADOS EN MEDICINA TRADICIONAL NORPERUANA. RAMIREZ,VR: MOSTACERO,LJ: GARCIA,AE: MEJIA,CF: PELAEZ,PF: MEDINA,CD: MIRANDA,CH: BANCO AGRARIO DEL PERU & NACL UNIV TRUJILLO, TRUJILLO, PERU, JUNE, 1988 : 54PP- (1988) ( UNIV TRUJILLO TRUJILLO PERU) A SURVEY OF MEDICINAL PLANTS OF MINAS GERAIS, BRAZIL. HIRSCHMANN,GS: ROJAS DE ARIAS,A: J ETHNOPHARMAC OL 29 2: 159-172 (1990) (INST INVEST CIENCIAS SALUD FAC CIENCIAS QUIM ASUNCION PARAGUAY) EFFECT OF MOMORDICA CHARANTIA FRUIT JUICE ON STREPTOZOTOCIN-INDUCED DIABETES IN RATS. KARUNANAYAKE,EH: JEEVATHAYAPARAN,S: TENNEKOON,KH: J ETHNOPHARMACOL 30 2: 199-204 (1990) (DEPT BIOCHEM FAC MED UNIV COLOMBO COLOMBO 8 SRI LANKA) STUDIES ON ANTIMALARIAL ACTION OF CRYPTOLEPIS SANGUINOLENTA EXTRACT. BOYE,GL: PROC INT SYMP ON EAST-WEST MED, SEOUL, KOREA, OCTOBER 10-11 1989 : 243-251 (1990) ( CENT SCI RES PLANT MED MAMPONG-AKWAPIM GHANA) OXYGEN FREE RADICAL SCAVENGING ACTIVITY OF THE JUICE OF MOMOR DICA CHARANTIA FRUITS. SREEJAYAN: RAO,MNA: FITOTERAPIA 62 4: 344-346 (1991) (DEPT PHARM CHEM COLL PHARM SCI MANIPAL KARNATAKA 576119 INDIA) ETH NO BO TAN ICAL REV IEW OF M EDIC INAL PLAN TS FR OM THA I TRAD ITION AL BO OK S, PAR T 1: PLA NTS W ITH AN TIINFL AM MA TO RY, A NTI-A STH MA TIC AND ANTIHYPERTENSIVE PROPERTIES. PANTHONG,A: KANJANAPOTHI,D: TAYLOR,WC: J ETHNOPHARMACOL 18 3: 213-228 (1986) (DEPT PHARMACOL FAC MED CHIANG MAI UNIV CHIANG MAI 50002 THAILAND) POISONOU S PLANTS OF INDIA. MANAGER O F PUBLICATIONS,GOVERNMENT O F INDIA PRESS,CALCUTT.VOLUME 1. CHOPRA,RN: BADHW AR,RL: GHOSH,S: BOOK : - (1949) ( DRUG RES LAB JAMMU TAWI J & K INDIA) MEDICINAL PLANTS OF W EST AFRICA. REFERENCE PUBLICATIONS,INC. ALGONAC,MICHIGAN,U.S.A. AYENSU,ES: BOOK : - (1978) (BOTANY DEPT SMITHSONIAN INSTITUTION W ASHINGTON DC USA) POTENTIATION OF TOLBUTAMIDE ACTION BY JASAD BHASMA AND KARELA (MOMORDICA CHARANTIA). KULKARNI,RD: GAITONDE,BB: INDIAN J MED RES 50 : 715-719 (1962) (DEPT PHARMACOL GRANT MED COLL BOMBAY MAHARASTRA INDIA) IN VITRO ANTHELMINTIC SCREENING OF INDIGENOU S MEDICINAL PLANTS AGAINST HAEMONCHUS CO NTORTUS (RUDO LPHI,1803) COBBOLD, 1898 OF SHEEP AND GOATS. SHARMA,LD: BAHGA,HS: SRIVASTAVA,PS: INDIAN J ANIM RES 5 1: 33-38 (1971) ( COLL VET MED U.P.AGR UNIV PANTNAGAR UP INDIA) CERTAIN LITTLE-KNOWN ANTHELMINTICS FROM BRAZIL. FRIESE,FW : APOTH ZTG 44 : 180- (1929) (NO ADDRESS GIVEN) PHARMACOLOGY OF A HYPOGLYCEMIC PRINCIPLE ISOLATED FROM THE FRUITS OF MOMORDICA CHARANTIA. LOTLIKAR,MM: RAJARAMA RAO,MR: INDIAN J PHARMACY 28 : 129- (1966) (DEPT CHEM TECHNOL UNIV BOMBAY BOMBAY MAHARASTRA 19 INDIA) THE W EST INDIAN WEEDW OMAN OF THE UNITED STATES VIRGIN ISLANDS. OAKES,AJ: MORRIS,MP: BULL HIST MED 32 : 164- (1958) (NO ADDRESS GIVEN) SCREENING OF INDIAN PLANTS FOR ANTIFERTILITY ACTIVITY. PRAKASH,AO: MATHUR,R: INDIAN J EXP BIOL 14 : 623-626 (1976) ( SCH STUDIES ZOOLOGY JIW AJI UNIV GWALIOR MP 474 002 INDIA)
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INVE STIG ATIO N INT O TH AI ME DICIN AL PL ANT S SA ID TO CUR E DIA BET ES. M UEL LER -OE RLIN GH AUS EN,B : NG AM W ATH ANA ,W : KAN CHA NAP EE,P : J MED ASS THAILAND 54 : 105-111 (1971) (DEPT MED SCI DIV MED RES MINISTRY PUBLIC HEALTH BANGKOK THAILAND) ANTIFERTILITY INVESTIGATION ON MOMO RDICA. STEPKA,W : WILSON,KE: MADGE,GE: LLOYDIA 37 4: 645C-. (1974) (DEPT PHARMACY & PHARMACEUTICS COLL PHARMACY MEDICAL COLL OF VIRGINIA RICHMOND VA USA) PLANTAS MEDICINALES, AROMATICAS O VENENOSAS DE CUBA. MINISTERIO DE AGRICULTURA, REPUBLICA DE CUBA, HAVANA. ROIG Y MESA,JT: BOOK 1945 : 872PP- (1945) ( CUBA) MOLLUSCICIDAL ACTIVITY OF PLANTS FROM NO RTHEAST BRAZIL. PINHEIRO DE SOUSA,M: ROUQ UAYROL,MZ: REV BRASIL PESQ MED BIOL 7 4: 389-394 (1974) (DEPT FARMACOL EXP CENT CIENC SAUDE UNIV FED CEARA CEARA BRAZIL) A SURVEY OF PLANTS FOR INSECTICIDAL ACTIVITY. HEAL,RE: ROGERS,EF: WALLACE,RT: STARNES,O: LLOYDIA 13 1: 89-162 (1950) ( RES LABS MERCK & CO. RAHWAY NJ USA) INVESTIGATIONS ON PLANT ANTIBIOTICS. PART IV. FURTHER SEARCH FOR ANTIBIOTIC SUBSTANCES IN INDIAN MEDICINAL PLANTS. GEORGE,M: PANDALAI,KM: INDIAN J MED RES 37 : 169-181 (1949) (DEPT BIOCHEM INDIAN INST SCI BANGALORE KARNATAKA INDIA) A LIST OF THAI MEDICINAL PLANTS, ASRCT, BANGKOK. REPORT NO.1 ON RES. PROJECT. 17. W ASUW AT,S: RESEARCH REPORT,A.S.R.C.T.,NO.1 ON RESEARCH PROJECT 17 1967 : 22PP-. (1967) ( A.S.R.C.T. BANGKOK THAILAND) PRELIMINARY SCREENING OF SOME REPUTED ABORTIFACIENT INDIGENOUS PLANTS. JAMW AL,KS: ANAND,KK: INDIAN J PHARMACY 24 : 218-220 (1962) (DEPT PHARMACOL REGIONAL RES LAB JAMMU J & K INDIA) THE CLINICAL PICTURE OF VENO-OCCLUSIVE DISEASE OF THE LIVER IN JAMAICAN CHILDREN. JELLIFFE,DB: BRAS,G: STUART,KL: ANN TROP MED PARASITOL 48 : 386-396 (1954) (DEPT MED & PATHOL UNIV COLL W EST INDIES KINGSTON JAMAICA) PHARMACOLOGICAL EVALUATION OF THAI MEDICINAL PLANTS. (CONTINUED). MOKKHASMIT,M: NGARMW ATHANA,W : SAWASDIMONGKOL,K: PERMPHIPHAT,U: J MED SS THAILAND 54 7: 490-504 (1971) (DEPT MED SCI DIV MED RES MINISTRY OF PUBLIC HEALTH BANGKOK THAILAND) PLANTAS MEDICINAIS BRAZILEIRAS, CONHECIMENTOS POPULARES E CIENTIFICOS. ALMEIDA,DE,ER: SAO PAULO: HEMUS EDITORA LTDA. 1993 PLANTAS MEDICINALES DE USO POPULAR EN LA AMAZO NIA PERUANA. MEJIA,KEMBER: RENGIFO,ELSA: LIMA: AECI AND IIAP, 1995 RAINFOREST REMEDIES, ONE HUNDRED HE ALING HERBS OF BELIZE. ARVIGO, ROSITA: BALICK, MICHAEL. TWIN LAKES, W I: LOTUS PRESS. 1993 AGROM IDIA SOFTW ARE. PLANTAS MEDICINAIS (CD-ROM) . SAO PAULO, BRAZIL, 2002. MA NUA L DE FITO TER APIA , 2 ND ED. COIMBRA, RAUL. SAO PAULO, BRAZIL: DADOS INTERNACIONAIS DE CATALOGACAO NA PU LICACAO. 1994 PLANTAS UTILES DE LA AMAZONIA PERUANA: CARACTERISTICAS, USOS, Y POSIBILIDADES. RUIZ, RODOLFO B. TRUJILLO, PERU: EDITORIAL LIBERDAD E.I.R.L, 1994 ETHNOBOTANICAL SURVEY OF THE MEDICINAL PLANTS IN THE DOMINION OF MEADOW S IN THE REGION OF TH ALTO RIO GRANDE - MINAS GERAIS. RODRIGUES, V.E.G., ET AL. CIENC. AGROTEC., LAVRAS V.25, N.1, 102-123 JAM/FEB. (2001)(BRAZIL) MEDICINAL PLANTS OF BRAZIL. MORS, W .B., C.T. RIZZINI, AND N.A. PEREIRA. ALGONAC, MICHIGAN, REFERENCE PUBLICATIONS, INC., 2000. THE PHYTOCHEM ICAL DATABASE. BECKSTROM-STERNBERG, STEPHEN M, AND JAMES A DUKE. ACEDB VERSION 4.3-DATA VERSION JULY 1994. NATIONAL GERMPLASM RESOURCES LABORATORY (NGRL), AGRICULTURAL RESEARCH SERVICE (ARS), U.S. DEPARTMENT OF AGRICULTURE.
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KINETICS OF IGE ANTIBODY RESPONSE TO TRICHOSANTH IN ALPHA-MOMORCHAR IN AND BETA-MOMORCH ARIN IN MICE. ZHENG,SS: WAI,W L: HIN,W Y: WU,AR: CHIN MED J (ENGL). 104 4: 292-9 (1991)(DEPT OF IMMUNOLOGY, CHINESE ACADEMY OF MEDICAL SCIENCES, W HO COLLABORATING CENTRE FOR IMMUNOLOGICAL RESEARCH, BEIJING) TOXICITIES OF TRICHOSANTHIN AND ALPHA-MOMORCHARIN, ABORTIFACIENT PROTEINS FROM CHINESE MEDICINAL PLANTS ON CULTURED TUMOR CELL LINES. TSAO,SW: NG,TB: YEUNG,HW: TOXICON. 28 10: 1183-92 (1990)(DEPT OF ANATOMY, CHINESE UNIVERSITY OF HONG KONG, SHATIN) EFFECTS OF ALPHA-MOMORCHARIN, BETA-MOMORCHARIN AND ALPHA-TRICHOSANTHIN ON LIPOGENESIS AND TESTICULAR AND ADRENAL STEROIDOG ENESIS IN VITRO AND PLASMA-GLUCO SE LEVELS IN VIVO. NG,TB: HON,W K: LO,LH: LI,W W : YEUNG,HW : J ETHNOPHARMACOL. 18 1: 4553 (1986) VIAB ILITY O F ALP HA-M OM OR CHA RIN-T REA TED MO USE BLAS TO CYT ES IN THE PSE UDO PRE GN ANT UTE RUS . TAM ,PP: CH AN,W Y: YEU NG ,HW : J REPROD FERTIL. 71 2: 567-72 (1984) EFFECTS OF ALPHA-MOMO RCHARIN ON PREIMPLANTATION DEVELOPM ENT IN THE MOUSE. TAM,PP: LAW ,LK: YEUNG,HW J REPROD FERTIL. 71 1: 33-8 (1984) EFFECTS OF ALPHA-TRICHOSANTHIN AND ALPHA-MOMORCHARIN ON THE DEVELOPMENT OF PERI-IMPLANTATION MOUSE EMBRYOS. LAW,LK: TAM,PP: YEUNG,HW : J REPROD FERTIL 69 2: 597-604 (1983) PRODUCTION O F ANTIVIRAL AND ANTITUMOR PRO TEINS MAP30 AND GAP31IN CUCURBITS USING THE PLANT VIRUS VECTOR ZYMV-AGII. ARAZI,T: LEE HUANG,: HUANG,PL: ZHANG,L: MOSHE SHIBOLETH,Y: GAL-ON A LEE-HUANG S: BIOCHEM BIOPHYS RES COM MUN. 292 2: 441-8 (2002) (VIROGENE LTD. HOD HASHARON , ISRAEL) ANTI-HIV AGENT MAP30 MODULATES THE EXPRESSION PROFILE OF VIRAL AND CELLULAR GENES FOR PROLIFERATION AND APOPTOSIS IN AIDSRELATED LYMPHOM A CELLS INFECTED W ITH KAPOSIS SARCOMA-ASSO CIATED VIRUS. SUN,Y: HUANG,PL: LI,JJ: HUANG,YQ: ZHANG,L: HUANG,PL: LEE-HUANG,S: BIOCHEM BIOPHYS RES COMMUN. 287 4: 983-94 (2001)(DEPT OF BIOCHEMISTRY, NEW YORK UNIVERSITY SCHOOL OF MEDICINE, NY) ANTI-CD30 (BER=H2) IMMUNOTOXINS CONTAINING THE TYPE-1 RIBOSOME-INACTIVATING PROTEINS MOMORDIN AND PAP-S (POKEWEED ANTIVIRAL PROTEIN FROM SEEDS) DISPLAY POW ERFUL ANTITUMOR ACTIVITY AGAINST CD30+ TUMOR CELLS IN VITRO AND IN SCID MICE. TERENZI,A: BOLOG NESI,A: PASQUALUCCI,L: FLENGHI,L: PILERI,S: STEIN,H: KADIN,M: BIGERNA,B: POLITO,L: TAZZARI,PL: MARTELLI,MF: STIRPE,F: FALINI,B: BR J HAEMATOL 92 4: 872-9 (1996)(INSTITUTE OF HAEMATOLOGY, UNIVERSITY OF PERUGIA, ITALY) SELECTIVE CYTOTOXIC ACTIVITY OF IMMUNOTOXINS COMPOSED OF A MONOCLO NAL ANTI-THY 1.1 ANTIBODY AND THE RIBOSOME-INACTIVATING PROTEINS BRYODIN AND MOMORDIN. STIRPE,F: W AW RZYNCZAK,EJ: BROW N, AN: KNYBA,RE: WATSON,GJ: BARBIERI,L: THORPE,PE: BR J CANCER. 58 5: 558-61 (1988)(DIPARTIMENTO DI PATOLOGIA SPERIMENTALE, UNIVERSITA DEGLI STUDI DI BOLOGNA, ITALY) TRADITIONAL PLANT MEDICINES AS TREATMENTS FOR DIABETES. REVIEW . BAILEY-CLIFFORD,J: DAY-CAROLINE. DIABETES CARE. 12 8: 553-564 (1989) (DIABETES RESEARCH UNIT, ASTON UNIVERSITY, BIRMINGHAM, UK) STUDIES ON ANTIVIRAL ACTIVITY OF THE EXTRACT OF MOM ORDICA CHARANTIA AND ITS ACTIVE PRINCIPLE. HUANG,TM: XU,ZX: W ANG,YD: QU,FZ: TONG,LL: VIROLOGICA 5 4: 367-373 (1990)(INST. VIROLOGY, CHINESE ACADEMY PREVENTIVE MEDICINE, BEIJING) EFFECTS OF MEDICINAL PLANTS ON INFECTION BY PLASMODIUM BERGH EI IN MICE. MENEZES-ORNELAS,H: STASI,LCD: CURI,PR: SALAT,E: REVISTA DE CIENCIAS FARMACEUTICAS. 12 0: 71-80 (1990)(DEPARTAMENTO DE PARASITOLOGICA-INSTITUTO DE BIOCIENCIAS-UNESP-18600-BOTUCATU,SP) BIOACTIVE POLYMERS FROM HIGHER PLANTS. W AGNER,H: GERHAUSER,C: SAMTLEBEN,R: PHYTOCHEMISTRY OF PLANTS USED IN TRADITIONAL MEDICINE. PROCEEDINGS OF THE PHYTOCH EMICAL SOCIETY OF EUROPE. CLARENDO N PRESS, OXFORD: 1995
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ORALLY ACTIVE FRACTION OF MOMO RDICA CHARANTIA, ACTIVE PEPTIDES THEREOF, AND THEIR USE IN THE TREATMENT OF DIABETES. NAG,BISHW AJIT: MEDICHERLA,SATYANARAYANA: SHARMA,SOMESH,D: US PATENT # 6391854, 1-14 (2002) (CALYX THERAPEUTICS, INC) ADULT-ONSET DIABETES TREATMENT METHO D. LAZARUS,DOUGLAS,D: US PATENT 6235,286: 1-15 (2001) USE OF PLANT EXTRACTS FOR TREA TMENT OF ACNE AND FUR UNCLE. REN,KAIJUN: US PATENT 6379718: 1-8 (2002) ANTI-VIRAL AGENT PREPARED BY BASIC AND ACIDIC EXTRACTION OF MANGROVES. NAKANO,MASATOSHI. US PATENT 5929047: 1-10 (1999) (MITSUI NORIN CO, LTD) PLANT PROTEINS USEFUL FOR TREATING TUMORS AND HIV INFECTION. LEE-HUANG,S: HUANG,PL: NARA,PL: CHEN,HC: KUNG,HF: HUANG,P: HUANG,HI: HUANG,PL: US PATENT 5484889: 1-28 (1996) (NEW YORK UNIVERSITY, AMERICAN BIOSCIENCES INC) METHOD OF INHIBITING HIV. LIFSON,JD: MCGRATH,MS: YEUNG,HW: HWANG,KM: US PATENT 4795739: 1-28 (1989)(GENE LABS INC; REGENTS OF UNIVERSITY OF CALIFORNIA)
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Clinical Abstracts
Clinical abstracts from PubMed on: Momordica charantia (235 studies) Momordin An active chemical in bitter melon (80 studies)
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