Cinnamic acid esters as potent inhibitors of fungal 17β-hydroxysteroid dehydrogenase -: a model enzyme of the short-chain dehydrogenase/reductase superfamily

被引:32
作者
Gobec, S
Sova, M
Kristan, K
Rizner, TL
机构
[1] Univ Ljubljana, Fac Pharm, Ljubljana 1000, Slovenia
[2] Univ Ljubljana, Inst Biochem, Fac Med, Ljubljana 1000, Slovenia
关键词
D O I
10.1016/j.bmcl.2004.05.069
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We present the synthesis of a new family of nonsteroidal inhibitors of 17beta-hydroxysteroid dehydrogenase, designed from flavones and chalcones. Their inhibitory potential was screened on 17beta-hydroxysteroid dehydrogenase from the fungus Cochliobolus lunatus (17beta-HSDcl), a model enzyme of the short-chain dehydrogenase/reductase superfamily. In a series of cinnamates and related coumarin-3-carboxylates, a number of compounds proved to be potent inhibitors of both the oxidative and reductive reactions catalyzed by 17beta-HSDcl, with IC50 values in the low micromolar range. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3933 / 3936
页数:4
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