NEW LIGNANS FROM ANOGEISSUS-ACUMINATA WITH HIV-1 REVERSE-TRANSCRIPTASE INHIBITORY ACTIVITY

被引:59
作者
RIMANDO, AM
PEZZUTO, JM
FARNSWORTH, NR
SANTISUK, T
REUTRAKUL, V
KAWANISHI, K
机构
[1] UNIV ILLINOIS,COLL PHARM,DEPT MED CHEM & PHARMACOGNOSY,PROGRAM COLLABORAT RES PHARMACEUT SCI,CHICAGO,IL 60612
[2] ROYAL FOREST DEPT,FOREST HERBARIUM,BANGKOK,THAILAND
[3] MAHIDOL UNIV,FAC SCI,DEPT CHEM,BANGKOK 10400,THAILAND
[4] KOBE WOMENS COLL PHARM,KOBE,JAPAN
来源
JOURNAL OF NATURAL PRODUCTS | 1994年 / 57卷 / 07期
关键词
D O I
10.1021/np50109a004
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Anolignan A [1] and anolignan B [3] are new dibenzylbutadiene lignans isolated from Anogeissus acuminata. Compounds 1 and 3 were identified as the active HIV-1 reverse transcriptase (RT) inhibitory constituents of this plant obtained by bioassay-guided fractionation. Compound 3, which was very weakly active when tested alone, showed high activity when combined with 1. The activity of 1 was likewise enhanced in the presence of 3. A concave isobole obtained from a plot of data derived from assays with 1 and 3 in combination indicated their synergistic effects. Another new lignan, anolignan C [5], and a known lignan, (-)secoisolariciresinol [10], were also isolated from this plant. Compounds 5 and 10 did not have activity against HIV-1 RT. Compounds 1, 3 and 5 were either weakly cytotoxic or noncytotoxic when rested in various cancer cell lines. The structures of 1-5 and 10 were established by spectroscopic methods, especially by 1D and 2D nmr experiments.
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收藏
页码:896 / 904
页数:9
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