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HMG-CoA 还原酶抑制剂:现状与未来展望。

Inhibitors of HMG-CoA Reductase: Current and Future Prospects.

机构信息

Torrey Pines Institute for Molecular Studies, Port St. Lucie, Florida 34987, USA.

出版信息

Mini Rev Med Chem. 2009 Oct;9(11):1272-83. doi: 10.2174/138955709789878105.

DOI:10.2174/138955709789878105
PMID:19929805
Abstract

High levels of cholesterol are a primary risk factor in the development of cardiovascular diseases. In this review, we have summarized the structural, chemical and computational aspects of hypocholesterolemic drugs, both statins and non-statins, that target enzyme 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA) to block cholesterol biosynthesis.

摘要

高胆固醇水平是心血管疾病发展的主要风险因素。在这篇综述中,我们总结了降低胆固醇药物(包括他汀类药物和非他汀类药物)的结构、化学和计算方面,这些药物靶向酶 3-羟基-3-甲基戊二酰基辅酶 A 还原酶(HMG-CoA)以阻断胆固醇生物合成。

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Inhibitors of HMG-CoA Reductase: Current and Future Prospects.HMG-CoA 还原酶抑制剂:现状与未来展望。
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Structural mechanism for statin inhibition of HMG-CoA reductase.他汀类药物抑制HMG-CoA还原酶的结构机制。
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Structural mechanism for statin inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase.他汀类药物抑制3-羟基-3-甲基戊二酰辅酶A还原酶的结构机制。
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The novel cholesterol-lowering drug SR-12813 inhibits cholesterol synthesis via an increased degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase.新型降胆固醇药物SR-12813通过增加3-羟基-3-甲基戊二酰辅酶A还原酶的降解来抑制胆固醇合成。
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The synergistic hypocholesterolemic activity of the potent cholesterol absorption inhibitor, ezetimibe, in combination with 3-hydroxy-3-methylglutaryl coenzyme a reductase inhibitors in dogs.强效胆固醇吸收抑制剂依折麦布与3-羟基-3-甲基戊二酰辅酶A还原酶抑制剂联合使用对犬的协同降胆固醇活性。
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