Constituents of the Bark and Twigs of <i>Artocarpus </i><i>d</i><i>adah </i>with Cyclooxygenase Inhibitory Activity

Bao‐Ning Su(University of Illinois Chicago), Muriel Cuendet(Indonesian Institute of Sciences), Michael Hawthorne(Indonesian Institute of Sciences), Leonardus B.S. Kardono(Indonesian Institute of Sciences), Soedarsono Riswan(University of Illinois Chicago), Harry H. S. Fong(University of Illinois Chicago), Rajendra G. Mehta(University of Illinois Chicago), John M. Pezzuto(Indonesian Institute of Sciences), A. Douglas Kinghorn(University of Illinois Chicago)
Journal of Natural Products
January 25, 2002
Cited by 117Open Access
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Abstract

Fractionation of an ethyl acetate-soluble extract of the bark of Artocarpus dadah has led to the isolation of three new prenylated stilbenoid derivatives, 3-(gamma,gamma-dimethylallyl)resveratrol (1), 5-(gamma,gamma-dimethylallyl)oxyresveratrol (2), 3-(2,3-dihydroxy-3-methylbutyl)resveratrol (3), and a new benzofuran derivative, 3-(gamma,gamma-dimethylpropenyl)moracin M (4), along with six known compounds, oxyresveratrol, (+)-catechin, afzelechin-3-O-alpha-L-rhamnopyranoside, (-)-epiafzelechin, dihydromorin, and epiafzelechin-(4beta-->8)-epicatechin. From an ethyl acetate-soluble extract of the twigs of the same plant were isolated compound 4 and two new neolignan derivatives, dadahols A (5) and B (6), as well as 10 known compounds, oxyresveratrol, (+)-catechin, afzelechin-3-O-alpha-L-rhamnopyranoside, resveratrol, steppogenin, moracin M, isogemichalcone B, gemichalcone B, norartocarpetin, and engeletin. The structures of compounds 1-6 were determined using spectroscopic and chemical methods. Isolates were evaluated for their inhibitory effects against both cyclooxygenase-1 (COX-1) and -2 (COX-2) and in a mouse mammary organ culture assay.


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