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用于治疗血栓栓塞性疾病的因子 Xa 抑制剂的研究进展。

Developments in factor Xa inhibitors for the treatment of thromboembolic disorders.

机构信息

Johnson & Johnson Pharmaceutical Research and Development, L.L.C., Welsh and McKean Roads, Spring House, Pennsylvania 19477-0776, USA.

出版信息

Med Res Rev. 2011 Mar;31(2):202-83. doi: 10.1002/med.20183.

Abstract

Thromboembolic diseases are the leading causes of morbidity and mortality in the developed world. Anticoagulants provide effective treatment for venous or arterial thromboembolism. Two coagulation factors, factor Xa (fXa) and thrombin, are the primary targets under active investigation for anticoagulant therapy. fXa, in contrast to the multifunctional roles of thrombin in the coagulation cascade, converts prothrombin to thrombin collectively at the junction of the intrinsic and extrinsic pathway of coagulation. The effectiveness of fXa inhibitors as antithrombotic agents and their potentially reduced bleeding risks may offer superior therapeutic profiles with respect to thrombin inhibitors. After decades of research, many fXa inhibitors are now in the advanced stages of clinical trials. Unlike most reviews, which only provide incremental updates, this review provides an overview of fXa and the medicinal chemistry of its inhibitors. Overviews on coagulation models, antithrombotic therapy, and fXa will be provided, followed by the evolution of the medicinal chemistry of fXa inhibitors over the past few decades.

摘要

血栓栓塞性疾病是发达国家发病率和死亡率的主要原因。抗凝剂为静脉或动脉血栓栓塞提供有效治疗。两个凝血因子,因子 Xa(fXa)和凝血酶,是抗凝治疗中积极研究的主要靶点。与凝血酶在凝血级联中的多功能作用相比,fXa 在凝血内源性和外源性途径的交界处共同将凝血酶原转化为凝血酶。fXa 抑制剂作为抗血栓药物的有效性及其潜在降低的出血风险可能在血栓酶抑制剂方面提供更好的治疗效果。经过几十年的研究,许多 fXa 抑制剂现在处于临床试验的后期阶段。与大多数仅提供增量更新的综述不同,这篇综述提供了 fXa 及其抑制剂的药物化学概述。将提供关于凝血模型、抗血栓治疗和 fXa 的概述,然后是过去几十年 fXa 抑制剂药物化学的演变。

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