HIV-1 integrase inhibitory substances from Coleus parvifolius

被引:118
作者
Tewtrakul, S
Miyashiro, H
Nakamura, N
Hattori, M
Kawahata, T
Otake, T
Yoshinaga, T
Fujiwara, T
Supavita, T
Yuenyongsawad, S
Rattanasuwon, P
Dej-Adisai, S
机构
[1] Toyama Med & Pharmaceut Univ, Inst Nat Med, Toyama 9300194, Japan
[2] Osaka Prefectural Inst Publ Hlth, Higashinari Ku, Osaka 537, Japan
[3] Shionogi & Co Ltd, Discovery Res Labs, Osaka, Japan
[4] Prince Songkla Univ, Fac Pharmaceut Sci, Dept Pharmacognosy & Pharmaceut Bot, Hat Yai, Thailand
关键词
HIV-1; integrase; inhibition; anti-HIV activity; Thai plants; Coleus parvifolius; rosmarinic acid derivatives;
D O I
10.1002/ptr.1111
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
For the purpose of discovering anti-HIV-1 agents from natural sources, water and EtOH extracts of 50 Thai plants were screened for their inhibitory activity against HIV-1 integrase (IN), an enzyme essential for viral replication. Of these plants, an EtOH extract of Coleus parvifolius Benth. (aerial parts) showed potent activity against HIV-1 IN with an IC50 value of 9.2 mug/mL. From this extract, 11 compounds were isolated and identified as luteolin 5-O-beta-D-glucopyranoside (1), luteolin (2), luteolin 7-methyl ether (3), luteolin 5-O-beta-D-glucuronide (4), 5-O-beta-D-glueopyranosyl-luteolin 7-methyl ether (5), rosmarinic acid (6), rosmarinic acid methyl ester (7), daucosterol (8), a mixture of alpha- and beta-amyrin (9, 10) and phytol (11). Of these compounds, rosmarinic acid methyl ester (7), rosmarinic acid (6), luteolin (2) and luteolin 7-methyl ether (3) exhibited inhibitory activities against HIV-1 IN with IC50 values of 3.1, 5.0, 11.0 and 11.0 muM, respectively. Among rosmarinic acid derivatives, the HIV-1 IN inhibitory activity increased in turn for a dimer (IC50 = 5.0 muM), a trimer (IC50 = 1.4 muM), and a tetramer (IC50 = 1.0 muM). Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:232 / 239
页数:8
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