首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Design and synthesis of bisubstrate inhibitors of type 1 17beta-hydroxysteroid dehydrogenase: Overview and perspectives.
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Design and synthesis of bisubstrate inhibitors of type 1 17beta-hydroxysteroid dehydrogenase: Overview and perspectives.

机译:1型17β-羟基类固醇脱氢酶双底物抑制剂的设计和合成:概述和观点。

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摘要

Type 1 17beta-hydroxysteroid dehydrogenase (17beta-HSD1) is a key steroidogenic enzyme that catalyses the reduction of steroid estrone into the most potent endogenous estrogen estradiol using the cofactor NAD(P)H. Bisubstrate inhibition is a good way to enhance the potency of inhibitors of cofactor-assisted enzymes. The design of a bisubstrate inhibitor of 17beta-HSD1, the estradiol/adenosine hybrid EM-1745, is reviewed and strategies for future designs of inhibitors are proposed.
机译:1型17β-羟基类固醇脱氢酶(17beta-HSD1)是一种关键的类固醇生成酶,可使用辅因子NAD(P)H催化类固醇雌酮还原为最有效的内源性雌激素雌二醇。双底物抑制是增强辅因子辅助酶抑制剂效能的好方法。审查了17beta-HSD1的双底物抑制剂,雌二醇/腺苷杂化体EM-1745的设计,并提出了未来抑制剂设计的策略。

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