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1.
Chem Biodivers ; 9(8): 1500-7, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22899610

ABSTRACT

Four known sesquiterpene alcohols, i.e., 1-4, ten triterpene alcohols, i.e., 5-14, and four triterpene acids, i.e., 15-18, were isolated from the MeOH extract of Canarium ovatum resin (elemi resin). Upon evaluation of the previously described compounds 1-18 on the melanogenesis in B16 melanoma cells induced with α-melanocyte-stimulating hormone (α-MSH), three sesquiterpene alcohols, i.e., cryptomeridiol (1), 4-epicryptomeridiol (2), and cadin-1(14)-ene-7α,11-diol (4), exhibited inhibitory effects with 27.4-34.1 and 39.0-56.9% reduction of melanin content at 50 and 100 µM, respectively, with no or very low toxicity to the cells (80.9-103.9% of cell viability at 100 µM). Western-blot analysis revealed that compounds 1 and 2 reduced the protein levels of MITF (=microphtalmia-associated transcription factor), tyrosinase, and TRP-2 (=tyrosine-related protein 2), mostly in a concentration-dependent manner, suggesting that these compounds exhibit melanogenesis inhibitory activity on α-MSH-stimulated B16 melanoma cells by, at least in part, inhibiting the expression of MITF, followed by decreasing the expression of tyrosinase and TRP-2. Three sesquiterpene alcohols, i.e., 1, 2, and 4, are, therefore, considered to be valuable as potential skin-whitening agents.


Subject(s)
Burseraceae/chemistry , Melanins/antagonists & inhibitors , Melanoma, Experimental/metabolism , Resins, Plant/chemistry , Resins, Plant/pharmacology , Sesquiterpenes/chemistry , Sesquiterpenes/pharmacology , Animals , Cell Line, Tumor , Cell Survival/drug effects , Melanins/metabolism , Mice , Microphthalmia-Associated Transcription Factor/antagonists & inhibitors , Microphthalmia-Associated Transcription Factor/metabolism , Monophenol Monooxygenase/antagonists & inhibitors , Monophenol Monooxygenase/metabolism , Resins, Plant/isolation & purification , Sesquiterpenes/isolation & purification , alpha-MSH/antagonists & inhibitors , alpha-MSH/metabolism
2.
J Nat Prod ; 70(8): 1233-9, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17685651

ABSTRACT

Thirteen cucurbitane-type triterpene glycosides, including eight new compounds named charantosides I (6), II (7), III (10), IV (11), V (12), VI (13), VII (16), and VIII (17), and five known compounds, 8, 9, 14, 15, and 18, were isolated from a methanol extract of the fruits of Japanese Momordica charantia. The structures of the new compounds were determined on the basis of spectroscopic methods. On evaluation of these triterpene glycosides and five other cucurbitane-type triterpenes, 1-5, also isolated from the extract of M. charantia fruits, for their inhibitory effects on the induction of Epstein-Barr virus early antigen (EBV-EA) by 12-O-tetradecanoylphorbol-13-acetate (TPA) in Raji cells, these compounds showed inhibitory effects on EBV-EA induction with IC(50) values of 200-409 mol ratio/32 pmol TPA. In addition, upon evaluation of compounds 1-5 for inhibitory effects against activation of (+/-)-(E)-methyl-2[(E)-hydroxyimino]-5-nitro-6-methoxy-3-hexemide (NOR 1), a nitrogen oxide (NO) donor, compounds 1-3 showed moderate inhibitory effects. Compounds 1 and 2 exhibited marked inhibitory effects in both 7,12-dimethylbenz[a]anthracene (DMBA)- and peroxynitrite (ONOO-; PN)-induced mouse skin carcinogenesis tests.


Subject(s)
Anticarcinogenic Agents , Glycosides , Momordica charantia/chemistry , Plants, Medicinal/chemistry , Triterpenes , 9,10-Dimethyl-1,2-benzanthracene/pharmacology , Animals , Anticarcinogenic Agents/chemistry , Anticarcinogenic Agents/classification , Anticarcinogenic Agents/isolation & purification , Anticarcinogenic Agents/pharmacology , Antigens, Viral/drug effects , Fruit/chemistry , Glycosides/chemistry , Glycosides/classification , Glycosides/isolation & purification , Glycosides/pharmacology , Humans , Inhibitory Concentration 50 , Mice , Molecular Structure , Nitric Oxide Donors/pharmacology , Peroxynitrous Acid/pharmacology , Skin Neoplasms/chemically induced , Tetradecanoylphorbol Acetate/pharmacology , Triterpenes/chemistry , Triterpenes/classification , Triterpenes/isolation & purification , Triterpenes/pharmacology
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