Hu Baihua, Jetter James W, Wrobel Jay E, Antrilli Thomas M, Bauer Jean S, Di Li, Polakowski Sergiusz, Jain Uday, Crandall David L
Chemical and Screening Sciences, Wyeth Research, Collegeville, PA 19426, USA.
Bioorg Med Chem Lett. 2005 Aug 1;15(15):3514-8. doi: 10.1016/j.bmcl.2005.05.095.
We synthesized and evaluated a novel series of 2-carboxylic acid indole-based inhibitors of plasminogen activator inhibitor-1 (PAI-1). Systematic modification of the N-1 position and the 5-position of the indole scaffold resulted in the identification of several compounds that showed good potency against PAI-1 in the spectrophotometric assay. This potency did not always translate to the antibody assay. Solubility and serum protein binding studies on selected analogs revealed that protein binding might be a factor in the poor correlation between the two assays.
我们合成并评估了一系列新型的基于2-羧酸吲哚的纤溶酶原激活物抑制剂-1(PAI-1)抑制剂。对吲哚骨架的N-1位和5位进行系统修饰,从而鉴定出了几种在分光光度测定中对PAI-1显示出良好效力的化合物。但这种效力并不总能转化为抗体测定中的效力。对选定类似物的溶解度和血清蛋白结合研究表明,蛋白结合可能是两种测定之间相关性较差的一个因素。