Constituents from the stem wood of Euphorbia quinquecostata with phorbol dibutyrate receptor-binding inhibitory activity

被引:36
作者
Mbwambo, ZH
Lee, SK
Mshiu, EN
Pezzuto, JM
Kinghorn, AD
机构
[1] UNIV ILLINOIS, COLL PHARM, DEPT MED CHEM & PHARMACOGNOSY, PROGRAM COLLABORAT RES PHARMACEUT SCI, CHICAGO, IL 60612 USA
[2] UNIV DAR ES SALAAM, MUHIMBILI MED CTR, TRADIT MED RES INST, DAR ES SALAAM, TANZANIA
来源
JOURNAL OF NATURAL PRODUCTS | 1996年 / 59卷 / 11期
关键词
D O I
10.1021/np960412e
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Bioassay-guided fractionation of an EtOAc extract of the stem wood of Euphorbia quinquecostata using a phorbol dibutyrate receptor-binding assay system as a monitor yielded four inhibitory isolates (1-4), inclusive of one new compound, 17-hydroxyingenol 20-hexadecanoate (1), and three previously known compounds, ingenol 20-hexadecanoate (2), ent-16 alpha,17-dihydroxyatisan-3-one (3), and ent-3 beta,16 alpha,17-trihydroxyatisane (4). Also isolated from this extract were 10 constituents inactive in this bioassay, namely, 2,2'-dihydroxy-4,6-dimethoxy-3-methylacetophenone (5), a new structure, and nine known compounds identified as ent-13S-hydroxyatis-16-ene-3,14-dione; 2-hydroxy-4,6-dimethoxyacetophenone (xanthoxylin); 2-hydroxy-4,6-dimethoxy-3-methylacetophenone; 6-hydroxy-7-methoxycoumarin; lupeol acetate; beta-sitosterol; sitosterol beta-D-glucopyranoside; 6,7,8-trimethoxycoumarin; and 3,3',4'-tri-O-methyl-4-O-[alpha-L-rhamnopyranosyl (1 triple prime-->6 '')-beta-D-glucopyranosyl]ellagic acid. The structures of compounds 1 and 5 were established by chemical and spectroscopic methods.
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页码:1051 / 1055
页数:5
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