作者:Thomas E. Barta、Michael A. Stealey、Paul W. Collins、Richard M. Weier
DOI:10.1016/s0960-894x(98)00627-1
日期:1998.12
The synthesis and activity of a series of 4,5-diarylimidazole analogs are described. One analog had an IC50 of 80 nM, was 6750-selective against COX-1, and demonstrated in vivo potency in the mouse air pouch model.
描述了一系列4,5-二芳基咪唑类似物的合成和活性。一种类似物的IC50为80 nM,对COX-1具有6750选择性,并在小鼠气袋模型中显示出体内效力。