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Autor:
Carl P. Decicco, Nicole Stowell, George L. Trainor, Robert C. Newton, Nao Asakawa, Steven M. Friedman, Kimberly A. Solomon, Kim Harrison, Patricia K. Welch, Bin Jiang, Paul S. Watson, Maryanne B. Covington, Soo S. Ko, Eric A. Wadman, Paul Davies
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 16:5695-5699
Linear unselective CCR3 antagonist leads with IC(50) values in the 200 nM range were converted into low nM binding compounds selective at CCR3 by moving the piperidine nitrogen substituent to the carbon at the 2-position of the ring. Substitution of