New eudesmane derivatives from Melampodium camphoratum from the Suriname rainforest

被引:9
作者
Chaturvedula, VSP
Farooq, A
Schilling, JK
Malone, S
Derveld, I
Werkhoven, MCM
Wisse, JH
Ratsimbason, M
Kingston, DGI
机构
[1] Virginia Polytech Inst & State Univ, Dept Chem, Blacksburg, VA 24061 USA
[2] Natl Herbarium Suriname, Conservat Int Suriname, Paramaribo, Suriname
[3] Bedrijf Geneesmiddelen Voorziening Suriname, Geyersvlijt, Suriname
[4] Ctr Natl Applicat & Rech Pharmaceut, Antananarivo 101, Madagascar
来源
JOURNAL OF NATURAL PRODUCTS | 2004年 / 67卷 / 12期
关键词
D O I
10.1021/np049696q
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 leaves of Melampodium camphoratum using an assay for inhibitors of the degradation of hemin resulted in the isolation of six new eudesmane sesquiterpenes (1-6) and the known 6-epi-beta-verbesinol coumarate (7). The structures of compounds 1-6 were established as 6alpha-(4'-O-methyl-7'E-coumaryloxy)eudesm-4(14)-ene (1), 6alpha-({4'-O-stearyl}-7'E-coumaryloxy)eudesm-4(14)-ene (2),6alpha-({4'-O-palmityl}-7'E-coumaryloxy)eudesm-4(14)-ene (3),6alpha-({4'-O-[9"Z-hexadecenoyl]}- 7'E-coumaryloxy)eudesm-4(14)-ene (4), 6alpha(7'Z-coumaryloxy)eudesm-4(14)-ene (5), and 6alpha- ({4'-acetoxy}-7'Z-coumaryloxy)eudesm-4(14)-ene (6). Compounds 1-4 showed weak activity in the hemin degradation assay, while compounds 5-7 were inactive.
引用
收藏
页码:2053 / 2057
页数:5
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