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来自球状小皮伞担子菌培养物的倍半萜及其11β-羟基类固醇脱氢酶抑制活性。

Sesquiterpenes from cultures of the basidiomycete Clitocybe conglobata and their 11 beta-hydroxysteroid dehydrogenase inhibitory activity.

作者信息

Xu Di, Sheng Yu, Zhou Zhong-Yu, Liu Rong, 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

Chem Pharm Bull (Tokyo). 2009 Apr;57(4):433-5. doi: 10.1248/cpb.57.433.

Abstract

A new drimane sesquiterpenoid, 3-keto-drimenol (1), were isolated from cultures of the basidiomycete Clitocybe conglobata together with 3beta-hydroxy-11-acetyldrimene (2), 3beta-hydroxydrimenol (3), 11,12-dihydroxydrimene (4), 3beta-hydroxy-11,12-O-isopropyldrimene (5), and 3beta,11,12-trihydroxydrimene (6). Their structures were established from MS and NMR experiments. Compounds 1, 3, and 6 showed inhibitory activities against two isozymes of 11 beta-hydroxysteroid dehydrogenases with IC(50) 1.7-8.0 microg/ml (human 11 beta-HSD1), 10.7-24.1 microg/ml (mouse 11 beta-HSD1); 177.0-220.0 microg/ml (human 11 beta-HSD2), 250.5-500.2 microg/ml (mouse 11 beta-HSD2), respectively, which catalyze the interconversion of active cortisol and inactive cortisone.

摘要

从担子菌团集离褶伞的培养物中分离出一种新的菖蒲烷倍半萜,3-酮基-菖蒲烯醇(1),以及3β-羟基-11-乙酰基菖蒲烯(2)、3β-羟基菖蒲烯醇(3)、11,12-二羟基菖蒲烯(4)、3β-羟基-11,12-O-异丙基菖蒲烯(5)和3β,11,12-三羟基菖蒲烯(6)。通过质谱和核磁共振实验确定了它们的结构。化合物1、3和6对11β-羟基类固醇脱氢酶的两种同工酶具有抑制活性,对人11β-HSD1的IC50为1.7 - 8.0微克/毫升,对小鼠11β-HSD1的IC50为10.7 - 24.1微克/毫升;对人11β-HSD2的IC50为177.0 - 220.0微克/毫升,对小鼠11β-HSD2的IC50为250.5 - 500.2微克/毫升,这两种同工酶催化活性皮质醇和无活性可的松的相互转化。

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