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从闭苞买麻藤中分离及仿生合成抗炎芪木脂素

Isolation and biomimetic synthesis of anti-inflammatory stilbenolignans from Gnetum cleistostachyum.

作者信息

Yao Chun-Suo, Lin Mao, Wang Lin

机构信息

Key Laboratory of Bioactive Substances and Resources Utilization of Chinese Herbal Medicine (Ministry of Education), Peking Union Medical College; Beijing 100050, PR China.

出版信息

Chem Pharm Bull (Tokyo). 2006 Jul;54(7):1053-7. doi: 10.1248/cpb.54.1053.

Abstract

One new stilbenolignan, gnetucleistol F (1), and four known stilbenolignans, gnetofuran A (2), lehmbachol D (3), gnetifolin F (4) and gnetumontanin C (5) were isolated from the lianas of Gnetum cleistostachyum C. Y. CHENG (Gnetaceae). Their structures and relative configurations were determined by means of spectroscopic evidence. Compounds 1, 2, 3 and 4 were synthesized for the first time on the basis of their biogenetic pathway, and their possible biomimetical synthetic mechanisms were discussed. The pharmacological activities of all stilbenolignans have been tested. Among them, 1, 2, 3, 4 and 5 showed moderate inhibitory activities on TNF-alpha and 1 also showed potent inhibitory activity on malondialdehyde.

摘要

从闭苞买麻藤(Gnetum cleistostachyum C. Y. CHENG,买麻藤科)的藤本植物中分离得到了一种新的芪木脂素——买麻藤醇F(1)以及四种已知的芪木脂素——买麻藤呋喃A(2)、雷姆巴赫醇D(3)、买麻藤黄素F(4)和买麻藤山奈酚C(5)。通过光谱证据确定了它们的结构和相对构型。化合物1、2、3和4基于其生源途径首次合成,并讨论了其可能的仿生合成机制。对所有芪木脂素的药理活性进行了测试。其中,1、2、3、4和5对肿瘤坏死因子-α显示出中等抑制活性,1对丙二醛也显示出较强的抑制活性。

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