Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1361281 | Bioorganic & Medicinal Chemistry Letters | 2012 | 7 Pages |
Abstract
A new structural class of potent prolylcarboxypeptidase (PrCP) inhibitors was discovered by high-throughput screening. The series possesses a tractable SAR profile with sub-nanomolar in vitro IC50 values. Compared to prior inhibitors, the new series demonstrated minimal activity shifts in pure plasma and complete ex vivo plasma target engagement in mouse plasma at the 20 h post-dose time point (po). In addition, the in vivo level of CNS and non-CNS drug exposure was measured.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Thomas H. Graham, Wensheng Liu, Andreas Verras, Iyassu K. Sebhat, Yusheng Xiong, Kelly Bleasby, Urmi R. Bhatt, Qing Chen, Margarita Garcia-Calvo, Wayne M. Geissler, Judith N. Gorski, Huaibing He, Michael E. Lassman, JeanMarie Lisnock, Xiaohua Li,