1350711-78-2Relevant articles and documents
Discovery and optimization of orally active cyclohexane-based prolylcarboxypeptidase (PrCP) inhibitors
Debenham, John S.,Graham, Thomas H.,Verras, Andreas,Zhang, Yong,Clements, Matthew J.,Kuethe, Jeffrey T.,Madsen-Duggan, Christina,Liu, Wensheng,Bhatt, Urmi R.,Chen, Dunlu,Chen, Qing,Garcia-Calvo, Margarita,Geissler, Wayne M.,He, Huaibing,Li, Xiaohua,Lisnock, Jeanmarie,Shen, Zhu,Tong, Xinchun,Tung, Elaine C.,Wiltsie, Judyann,Xu, Suoyu,Hale, Jeffrey J.,Pinto, Shirly,Shen, Dong-Ming
, p. 6228 - 6233 (2013/11/19)
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.
NOVEL PROLYLCARBOXYPEPTIDASE INHIBITORS
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, (2011/12/04)
Compounds of structural formula I are inhibitors of prolylcarboxypeptidase (PrCP). The compounds of the present invention are useful for the prevention and treatment of conditions related to the enzymatic activity of PrCP such as abnormal metabolism, incl