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抗代谢缓激肽拮抗剂:研发与应用

Metabolism-resistant bradykinin antagonists: development and applications.

作者信息

Stewart J M, Gera L, York E J, Chan D C, Whalley E J, Bunn P A, Vavrek R J

机构信息

Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Denver 80262, USA.

出版信息

Biol Chem. 2001 Jan;382(1):37-41. doi: 10.1515/BC.2001.006.

Abstract

Bradykinin plays many roles in normal and pathological physiology, but rapid enzymatic degradation made elucidation of its functions extremely difficult. Development of effective degradation-resistant antagonists made it possible to delineate these roles and to open the way for development of new drugs to control pathology due to excess production of bradykinin. Presently available peptide bradykinin antagonists are extremely potent, are completely resistant to enzymatic degradation, and are orally available. Non-peptide bradykinin antagonists have also been discovered. Development of bradykinin antagonists as drugs for cancer, inflammation and trauma is anticipated.

摘要

缓激肽在正常和病理生理学中发挥着多种作用,但由于其迅速被酶降解,使得阐明其功能极为困难。有效的抗降解拮抗剂的开发使得描绘这些作用以及为开发控制缓激肽过量产生所致病理状况的新药开辟了道路成为可能。目前可用的肽类缓激肽拮抗剂效力极强,对酶降解完全有抗性,并且可口服。非肽类缓激肽拮抗剂也已被发现。人们预期缓激肽拮抗剂会被开发成为用于癌症、炎症和创伤的药物。

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