Discovery and optimization of orally active cyclohexane-based prolylcarboxypeptidase (PrCP) inhibitors
作者:John S. Debenham、Thomas H. Graham、Andreas Verras、Yong Zhang、Matthew J. Clements、Jeffrey T. Kuethe、Christina Madsen-Duggan、Wensheng Liu、Urmi R. Bhatt、Dunlu Chen、Qing Chen、Margarita Garcia-Calvo、Wayne M. Geissler、Huaibing He、Xiaohua Li、JeanMarie Lisnock、Zhu Shen、Xinchun Tong、Elaine C. Tung、Judyann Wiltsie、Suoyu Xu、Jeffrey J. Hale、Shirly Pinto、Dong-Ming Shen
DOI:10.1016/j.bmcl.2013.09.094
日期:2013.12
The synthesis, SAR, binding affinities and pharmacokinetic profiles are described for a series of cyclohexane- based prolylcarboxypeptidase (PrCP) inhibitors discovered by high throughput screening. Compounds show high levels of ex vivo target engagement in mouse plasma 20 h post oral dose. (C) 2013 Elsevier Ltd. All rights reserved.