Development of CXCR3 antagonists. Part 4: discovery of 2-amino-(4-tropinyl)quinolines
Roland L Knight1, Daniel R Allen, Helen L Birch
1UCB Inflammation Discovery, Granta Park, Great Abington, Cambridge CB21 6GS, United Kingdom. roland.knight@ucb-group.com
Bioorganic & Medicinal Chemistry Letters
|December 11, 2007
Abstract:
The synthesis and biological evaluation of a novel series of 2-aminoquinoline substituted piperidines and tropanes incorporating a homotropene moiety is herein described. The series exhibits potent antagonism of the CXCR3 receptor and superior physicochemical properties. Compound 24d was found to be orally bioavailable, and PK/PD studies suggested it as a suitable tool for studying the role of CXCR3 in models of disease.
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