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新型因子 Xa 抑制剂的研发进展:专利述评。

Advances in the Development of Novel Factor Xa Inhibitors: A Patent Review.

机构信息

Faculty of Pharmacy, Kalabhavan Campus, The Maharaja Sayajirao University of Baroda, Vadodara, India.

出版信息

Mini Rev Med Chem. 2018;18(16):1332-1353. doi: 10.2174/1389557518666180424120726.

Abstract

Development of new anticoagulants has been in constant demand throughout the world due to increasing rate of morbidity and mortality caused by thrombotic diseases. Factor Xa (FXa), one of the enzymes and validated target for anticoagulation, regulates the production of thrombin in the coagulation cascade. The importance of oral FXa inhibitors like rivaroxaban, apixaban and edoxaban in thromboembolic conditions is well supported by increasing number of patents and research publications during the recent years. Direct FXa inhibitors as antithrombotic agents offer selective, efficacious and orally active therapy with respect to the other traditional anticoagulants. Newly developed patented molecules are mainly structural bioisosteres of existing drugs and have exhibited better efficacy and safety profile. Development of antidotes for oral direct FXa inhibitors is in pipeline and their expected approval for therapeutic purposes will be further beneficial to anticoagulation therapy. This review is mainly focused on industrial and academic patents on the discovery of direct FXa inhibitors. The review covers patented compounds from December 2011 till date, describing various structural modifications along with biological activity data and advances in the process and formulation technologies of the reported FXa inhibitors.

摘要

由于血栓性疾病导致的发病率和死亡率不断上升,全球对新型抗凝剂的开发需求一直居高不下。因子 Xa(FXa)是一种酶,也是抗凝的有效靶点,调节凝血级联反应中凝血酶的产生。近年来,越来越多的专利和研究出版物证实了口服 FXa 抑制剂(如利伐沙班、阿哌沙班和依度沙班)在血栓栓塞性疾病中的重要作用。与其他传统抗凝剂相比,直接 FXa 抑制剂作为抗血栓药物具有选择性、有效性和口服活性。新开发的专利分子主要是现有药物的结构生物等排体,表现出更好的疗效和安全性。口服直接 FXa 抑制剂的解毒剂正在研发中,预计将批准其用于治疗目的,这将对抗凝治疗更为有利。本文主要综述了直接 FXa 抑制剂发现方面的工业和学术专利。该综述涵盖了 2011 年 12 月至今的专利化合物,描述了各种结构修饰以及生物活性数据,并介绍了报道的 FXa 抑制剂在工艺和制剂技术方面的进展。

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