| Literature DB >> 25100568 |
Eric A Voight1, Arthur R Gomtsyan, Jerome F Daanen, Richard J Perner, Robert G Schmidt, Erol K Bayburt, Stanley DiDomenico, Heath A McDonald, Pamela S Puttfarcken, Jun Chen, Torben R Neelands, Bruce R Bianchi, Ping Han, Regina M Reilly, Pamela H Franklin, Jason A Segreti, Richard A Nelson, Zhi Su, Andrew J King, James S Polakowski, Scott J Baker, Donna M Gauvin, LaGeisha R Lewis, Joseph P Mikusa, Shailen K Joshi, Connie R Faltynek, Philip R Kym, Michael E Kort.
Abstract
The synthesis and characterization of a series of selective, orally bioavailable 1-(chroman-4-yl)urea TRPV1 antagonists is described. Whereas first-generation antagonists that inhibit all modes of TRPV1 activation can elicit hyperthermia, the compounds disclosed herein do not elevate core body temperature in preclinical models and only partially block acid activation of TRPV1. Advancing the SAR of this series led to the eventual identification of (R)-1-(7-chloro-2,2-bis(fluoromethyl)chroman-4-yl)-3-(3-methylisoquinolin-5-yl)urea (A-1165442, 52), an analogue that possesses excellent pharmacological selectivity, has a favorable pharmacokinetic profile, and demonstrates good efficacy against osteoarthritis pain in rodents.Entities:
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Year: 2014 PMID: 25100568 DOI: 10.1021/jm500916t
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446