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南投秋海棠根茎的细胞毒性及抗HIV成分

Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis.

作者信息

Wu Pei-Lin, Lin Fu-Wen, Wu Tian-Shung, Kuoh Chang-Sheng, Lee Kuo-Hsiung, Lee Shiow-Ju

机构信息

Department of Chemistry, National Cheng Kung University, Taiwan.

出版信息

Chem Pharm Bull (Tokyo). 2004 Mar;52(3):345-9. doi: 10.1248/cpb.52.345.

DOI:10.1248/cpb.52.345
PMID:14993759
Abstract

Three new compounds: begonanline (1). nantoamide (2). and methyl (S)-glycerate (3). as well as forty-four known compounds have been isolated and characterized from the rhizomes of Begonia nantoensis. The structures of these compounds were determined by spectral analyses and/or X-ray crystallography. Among them, cucurbitacin B (4). dihydrocucurbitacin B (5). cucurbitacin E (6). dihydrocucurbitacin E (7). cucurbitacin I (8). and (-)-auranamide (9). showed cytotoxicity against four human cancer cell lines. 3beta,22alpha-Dihydroxyolean-12-en-29-oic acid (10), indole-3-carboxylic acid (11), 5,7-dihydroxychromone (12), and (-)-catechin (13) demonstrated significant activity against HIV replication in H9 lymphocyte cells.

摘要

从南投秋海棠的根茎中分离并鉴定出三种新化合物

南投秋海棠碱(1)、南投酰胺(2)和(S)-甘油酸甲酯(3),以及44种已知化合物。这些化合物的结构通过光谱分析和/或X射线晶体学确定。其中,葫芦素B(4)、二氢葫芦素B(5)、葫芦素E(6)、二氢葫芦素E(7)、葫芦素I(8)和(-)-金合欢酰胺(9)对四种人类癌细胞系显示出细胞毒性。3β,22α-二羟基齐墩果-12-烯-29-酸(10)、吲哚-3-羧酸(11)、5,7-二羟基色酮(12)和(-)-儿茶素(13)在H9淋巴细胞中对HIV复制表现出显著活性。

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