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低分子量凝血酶抑制剂的设计进展

Progress in the design of low molecular weight thrombin inhibitors.

作者信息

Srivastava Stuti, Goswami Lalit N, Dikshit Dinesh K

机构信息

Medicinal Chemistry Division, Central Drug Research Institute, Lucknow, India.

出版信息

Med Res Rev. 2005 Jan;25(1):66-92. doi: 10.1002/med.20016.

Abstract

Intravascular thrombosis and its complication, embolism, is a leading cause of morbidity and mortality throughout the world. Past few decades have seen a great deal of progress in the development of antithrombotic agents, though the current treatment options are limited to heparin, LMW heparins, and warfarin. Detailed understanding of the biochemical and biophysical mechanisms of activation and regulation of blood coagulation have helped in developing specific inhibitors of enzymes, especially thrombin, within the coagulation cascade. Thrombin plays a central role in the coagulation cascade and so has become the primary target for the development of antithrombotic drugs. The review covers the main pharmacological aspects of haemostasis and thrombosis and provides an update on low molecular weight thrombin inhibitors along with the limitations of the prevalent antithrombotic agents. Recent developments in small molecule inhibitors of Protease Activated Receptor-1 (PAR-1) which can be helpful for the treatment of thrombotic and vascular proliferative disorders, have also been discussed.

摘要

血管内血栓形成及其并发症栓塞是全球发病和死亡的主要原因。过去几十年,抗血栓药物的研发取得了很大进展,不过目前的治疗选择仅限于肝素、低分子量肝素和华法林。对血液凝固激活和调节的生化及生物物理机制的深入了解有助于开发凝血级联中酶的特异性抑制剂,尤其是凝血酶。凝血酶在凝血级联中起核心作用,因此已成为抗血栓药物研发的主要靶点。本综述涵盖了止血和血栓形成的主要药理学方面,并提供了低分子量凝血酶抑制剂的最新情况以及现有抗血栓药物的局限性。还讨论了蛋白酶激活受体-1(PAR-1)小分子抑制剂的最新进展,其可能有助于治疗血栓形成和血管增殖性疾病。

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