Switching between agonists and antagonists at CRTh2 in a series of highly potent and selective biaryl phenoxyacetic acids.

T. Luker,R. Bonnert,Jerzy A. Schmidt,C. Sargent,S. Paine,S. Thom,G. Pairaudeau,Anil Patel,R. Mohammed,E. Akam,I. Dougall,A. Davis,Phillip A. Abbott,S. Brough,Ian Millichip,T. Mcinally

Published 2011 in Bioorganic & Medicinal Chemistry Letters

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