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来自担子菌帝王疣柄牛肝菌的戊醇衍生物及其11β-羟基类固醇脱氢酶抑制活性。

Pentanol derivatives from basidiomycete Catathelasma imperiale and their 11beta-hydroxysteroid dehydrogenases inhibitory activity.

作者信息

Zhang Ling, Shen Yu, Zhu Hua-Jie, Wang Fei, Leng Ying, Liu Ji-Kai

机构信息

State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, China.

出版信息

J Antibiot (Tokyo). 2009 May;62(5):239-42. doi: 10.1038/ja.2009.17. Epub 2009 Mar 27.

Abstract

Five new secondary metabolites derived from pentanol, namely catathelasmols A-E (1-5), were isolated from the fruiting bodies of the basidiomycete Catathelasma imperiale. Their structures were elucidated on the basis of spectroscopic analysis, and the absolute configurations were determined by computational chemistry. Compounds 3, 4 and 5 showed inhibitory activities against two isozymes of 11-hydroxysteroid dehydrogenases (11-HSD1 and 11-HSD2), with IC(50) values of 28.7-62.3 microg ml(-1) (human 11-HSD1), 30.4-149.2 microg ml(-1) (mouse 11-HSD1), 5.1-177 microg ml(-1) (human 11-HSD2) and 32.3-129.1 microg ml(-1) (mouse 11-HSD2), which catalyze the interconversion of cortisol and cortisone.

摘要

从担子菌大孔猫爪菌的子实体中分离出了五种源自戊醇的新次级代谢产物,即大孔猫爪菌素A - E(1 - 5)。基于光谱分析阐明了它们的结构,并通过计算化学确定了绝对构型。化合物3、4和5对11 - 羟基类固醇脱氢酶的两种同工酶(11 - HSD1和11 - HSD2)表现出抑制活性,其IC(50)值分别为28.7 - 62.3微克/毫升(人11 - HSD1)、30.4 - 149.2微克/毫升(小鼠11 - HSD1)、5.1 - 177微克/毫升(人11 - HSD2)和32.3 - 129.1微克/毫升(小鼠11 - HSD2),这两种同工酶催化皮质醇和可的松的相互转化。

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