Structure–Activity relationships of substituted benzothiophene-anthranilamide factor Xa inhibitors
作者:Yuo-Ling Chou、David D Davey、Keith A Eagen、Brian D Griedel、Rushad Karanjawala、Gary B Phillips、Karna L Sacchi、Kenneth J Shaw、Shung C Wu、Dao Lentz、Amy M Liang、Lan Trinh、Michael M Morrissey、Monica J Kochanny
DOI:10.1016/s0960-894x(02)00938-1
日期:2003.2
non-amidine factor Xa inhibitor with good selectivity against thrombin and trypsin. A series of modifications of the three aromatic groups of 1 was investigated. Substitution of chlorine or bromine for fluorine on the aniline ring led to the discovery of subnanomolar factor Xa inhibitors. Positions on the anthranilic acid ring that can accommodate further substitution were also identified.
通过高通量筛选将化合物1鉴定为对凝血酶和胰
蛋白酶具有良好选择性的新型有效非non因子Xa
抑制剂。研究了1的三个芳族基团的一系列修饰。用
氯或
溴取代
苯胺环上的
氟导致发现亚纳摩尔因子Xa
抑制剂。还确定了可以适应进一步取代的
邻氨基苯甲酸环上的位置。