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胆固醇酯转运蛋白抑制剂作为升高高密度脂蛋白的药物。

Cholesteryl ester transfer protein inhibitors as high-density lipoprotein raising agents.

作者信息

Shinkai Hisashi

机构信息

Central Pharmaceutical Research Institute, JT, Inc., 1-1 Murasaki-cho, Takatsuki, Osaka 569-1125, Japan.

出版信息

Expert Opin Ther Pat. 2009 Sep;19(9):1229-37. doi: 10.1517/13543770903198451.

Abstract

BACKGROUND

Not only hypercholesterolemia, but also low levels of high-density lipoprotein cholesterol is a critical risk factor for atherosclerosis-related disease. Therefore, there has been great interest in identifying effective and selective cholesteryl ester transfer protein (CETP) inhibitors that can raise high-density lipoprotein. Recently, Phase III clinical studies of torcetrapib, one of the CETP inhibitors developed by researchers at Pfizer, were unexpectedly terminated because of an increase in cardiovascular events and mortality. Torcetrapib has some compound-specific and off-target effects, such as raising blood pressure and aldosterone, which could affect an increase in cardiovascular events and mortality.

OBJECTIVE

The aim of this review is to provide an update (from 2000 to early 2009) on the patenting activity in the field of CETP inhibitors and the status of the most advanced compounds.

CONCLUSION

Dalcetrapib (JTT-705) and anacetrapib, which have not been reported to have the off-target effects of torcetrapib, are currently in Phase III. They are expected to reveal whether CETP inhibition is beneficial for atherosclerosis-related diseases.

摘要

背景

不仅高胆固醇血症,而且高密度脂蛋白胆固醇水平低也是动脉粥样硬化相关疾病的关键危险因素。因此,人们对鉴定能够升高高密度脂蛋白的有效且选择性胆固醇酯转移蛋白(CETP)抑制剂有着浓厚兴趣。最近,辉瑞公司研究人员开发的CETP抑制剂之一托彻普(torcetrapib)的III期临床研究因心血管事件和死亡率增加而意外终止。托彻普有一些化合物特异性和脱靶效应,如升高血压和醛固酮,这可能会影响心血管事件和死亡率的增加。

目的

本综述的目的是提供关于CETP抑制剂领域专利活动以及最先进化合物状况的最新信息(从2000年至2009年初)。

结论

达塞曲匹(JTT - 705)和阿那曲匹尚未报道有托彻普的脱靶效应,目前处于III期。预计它们将揭示抑制CETP对动脉粥样硬化相关疾病是否有益。

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