Author/Authors :
Hiroyuki Koshio، نويسنده , , Fukushi Hirayama، نويسنده , , Tsukasa Ishihara، نويسنده , , Yuta Taniuchi، نويسنده , , Kazuo Sato، نويسنده , , Yumiko Sakai-Moritani، نويسنده , , Seiji Kaku، نويسنده , , Tomihisa Kawasaki، نويسنده , , Yuzo Matsumoto، نويسنده , , Shuichi Sakamoto، نويسنده , , Shin-ichi Tsukamoto، نويسنده ,
Abstract :
Factor Xa (fXa) is a serine protease involved in the coagulation cascade, which has received great interest as a potential target for the development of new antithrombotic drugs. Herein we report a novel series of fXa inhibitors in which the 1,4-diazepane moiety was designed to interact with the S4 aryl-binding domain of the fXa active site. Compound 13 (YM-96765) showed potent fXa inhibitory activity (IC50 = 6.8 nM) and effective antithrombotic activity without prolonging bleeding time.
Keywords :
Anticoagulants , Antithrombotics , Enzyme inhibitors , Factor Xa