Synthesis and pharmacological evaluation of aminopyrimidine series of 5-HT1A partial agonists
作者:Amy B. Dounay、Nancy S. Barta、Jack A. Bikker、Susan A. Borosky、Brian M. Campbell、Terry Crawford、Lynne Denny、Lori M. Evans、David L. Gray、Pil Lee、Edward A. Lenoir、Wenjian Xu
DOI:10.1016/j.bmcl.2008.12.087
日期:2009.2
the lipophilicity (c Log D) led to identification of methyl ether 31 (4-(1-(2-(1H-indol-3-yl)ethyl)piperidin-3-yl)-N-(2-methoxyethyl)pyrimidin-2-amine) as a substantially improved compound within the series.
氨基嘧啶2(4-(1-(2-(1 H-吲哚-3-基)乙基)哌啶-3-基)-N-环丙基嘧啶-2-胺作为一种新型5-HT从高通量筛选中出来。1A激动剂。该化合物在结合和功能测定中显示了对5-HT 1A中等的效力,以及中等的代谢稳定性。通过降低亲脂性(c Log D)来改善代谢稳定性的策略的实施导致鉴定了甲醚31(4-(1-(2-(1-(2-(1 H-吲哚-3-基)乙基))哌啶-3-基)-N-(2-甲氧基乙基)嘧啶-2-胺),是该系列中一种显着改进的化合物。