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台湾杉中的生物活性化合物。

Bioactive compounds from Taiwania cryptomerioides.

作者信息

He K, Zeng L, Shi G, Zhao G X, Kozlowski J F, McLaughlin J L

机构信息

Department of Medicinal Chemistry and Molecular Pharmacology, School of Pharmacy and Pharmacal Sciences, Purdue University, West Lafayette, Indiana 47907, USA.

出版信息

J Nat Prod. 1997 Jan;60(1):38-40. doi: 10.1021/np960513c.

DOI:10.1021/np960513c
PMID:9014350
Abstract

Two new sesquiterpenes, 10 alpha-hydroxyamorphan-4-en-3-one (1) and 4 alpha-methylcadinane-4 alpha-methyl-1 alpha,2 alpha,10 alpha-triol (2), together with four known compounds, sesquiterpenes 10 alpha-hydroxycadinan-4-en-3-one (3) and alpha-cadinol (4), diterpene ferruginol and lignan helioxanthin, were isolated from the whole plant of Taiwania cryptomerioides under bioassay-guided fractionations. The structures of 1 and 2 were elucidated mainly by the NMR spectroscopic analyses. Bioactivities of the isolated compounds against brine shrimp, yellow fever mosquito larvae, and human tumor cells are reported; compound 4 was the most bioactive, showing selectivity for the human colon tumor cell line (HT-29).

摘要

在生物活性导向分离的过程中,从台湾杉全株中分离出两种新的倍半萜,10α-羟基阿莫烷-4-烯-3-酮(1)和4α-甲基杜松烷-4α-甲基-1α,2α,10α-三醇(2),以及四种已知化合物,倍半萜10α-羟基杜松烷-4-烯-3-酮(3)和α-杜松醇(4)、二萜铁锈醇和木脂素日黄草素。化合物1和2的结构主要通过核磁共振光谱分析得以阐明。本文报道了分离得到的化合物对卤虫、黄热病蚊幼虫和人类肿瘤细胞的生物活性;化合物4的生物活性最强,对人结肠肿瘤细胞系(HT-29)具有选择性。

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