Identification and optimization of a novel series of indoleamine 2,3-dioxygenase inhibitors
Jay A Markwalder1, Steven P Seitz1, Yuval Blat2
1Oncology Chemistry, Bristol-Myers Squibb Research and Development, Princeton, NJ 08543-5400, United States.
Bioorganic & Medicinal Chemistry Letters
|December 23, 2016
Abstract:
The discovery of a series of structurally-novel biaryl urea IDO inhibitors is described. Optimization of a micromolar hit through iterative cycles of synthesis and screening in an assay measuring IDO-mediated intracellular conversion of tryptophan to kynurenine led to potent inhibitors with favorable selectivity and metabolic stability profiles.
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