Ent-Abietanoids Isolated from Isodon serra

J. Wan, Hua-Yi Jiang, Jian-Wei Tang, Xing-Ren Li, Xue Du, Yan Li, Han-Dong Sun, J. Pu
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引用次数: 10

Abstract

Four new ent-abietane diterpenoids, along with four known ones were isolated from the aerial parts of Isodon serra, a traditional Chinese folk medicine. The new diterpenoids were named as serrin K (1), xerophilusin XVII (2), and enanderianins Q and R (3 and 4), while the known ones were identified as rubescansin J (5), (3α,14β)-3,18-[(1-methylethane-1,1-diyl)dioxy]-ent-abieta-7,15(17)-diene-14,16-diol (6), xerophilusin XIV (7), and enanderianin P (8), respectively. Their structures were elucidated by extensive spectroscopic analysis and comparison with the literature. Compound 1 showed remarkable inhibitory activity towards NO production in LPS-stimulated RAW264.7 cells (IC50 = 1.8 μM) and weak cytotoxicity towards five human tumor cell lines (HL-60, SMMC-7721, A-549, MCF-7, SW480).
从Isodon serra中分离的异戊二醇类化合物
从中国传统药材峨眉山中分离得到4个新的正戊二萜和4个已知的正戊二萜。新的二萜类化合物分别命名为serrin K(1)、xerophilusin XVII(2)和enanderianins Q和R(3和4),已知的二萜类化合物分别被鉴定为rubbescansin J(5)、(3α,14β)-3,18-[(1-甲基乙烷-1,1-二基)二氧基]- t-abieta-7,15(17)-二烯-14,16-二醇(6)、xerophilusin XIV(7)和enanderianin P(8)。它们的结构通过广泛的光谱分析和文献比较得以阐明。化合物1对lps刺激的RAW264.7细胞(IC50 = 1.8 μM)具有显著的NO生成抑制活性,对5种人肿瘤细胞系(HL-60、SMMC-7721、A-549、MCF-7、SW480)具有较弱的细胞毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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