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Discovery and optimization of RO-85, a novel drug-like, potent, and selective P2X3 receptor antagonist

Authors :
Brotherton-Pleiss, Christine E.
Dillon, Michael P.
Ford, Anthony P.D.W.
Gever, Joel R.
Carter, David S.
Gleason, Shelley K.
Lin, Clara J.
Moore, Amy G.
Thompson, Anthony W.
Villa, Marzia
Zhai, Yansheng
Source :
Bioorganic & Medicinal Chemistry Letters. Feb2010, Vol. 20 Issue 3, p1031-1036. 6p.
Publication Year :
2010

Abstract

Abstract: Despite the extensive literature describing the role of the ATP-gated P2X3 receptors in a variety of physiological processes the potential of antagonists as therapeutic agents has been limited by the lack of drug-like selective molecules. In this paper we report the discovery and optimization of RO-85, a novel drug-like, potent and selective P2X3 antagonist. High-throughput screening of the Roche compound collection identified a small hit series of heterocyclic amides from a large parallel synthesis library. Rapid optimization, facilitated by high-throughput synthesis, focusing on increasing potency and improving drug-likeness resulted in the discovery of RO-85. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
0960894X
Volume :
20
Issue :
3
Database :
Academic Search Index
Journal :
Bioorganic & Medicinal Chemistry Letters
Publication Type :
Academic Journal
Accession number :
47949879
Full Text :
https://doi.org/10.1016/j.bmcl.2009.12.044