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Discovery and optimization of pyrazole amides as antagonists of CCR1
Authors:Christian Harcken  Christopher Sarko  Can Mao  John Lord  Brian Raudenbush  Hossein Razavi  Pingrong Liu  Alan Swinamer  Darren Disalvo  Thomas Lee  Siqi Lin  Alison Kukulka  Heather Grbic  Mita Patel  Monica Patel  Kim Fletcher  David Joseph  Della White  David S. Thomson
Affiliation:1. Medicinal Chemistry Department, Boehringer Ingelheim Pharmaceuticals, Inc., 900 Ridgebury Road, PO Box 368, Ridgefield, CT 06877-0368, USA;2. Compound Profiling Department, Boehringer Ingelheim Pharmaceuticals, Inc., 900 Ridgebury Road, PO Box 368, Ridgefield, CT 06877-0368, USA;3. Drug Discovery Support Department, Boehringer Ingelheim Pharmaceuticals, Inc., 900 Ridgebury Road, PO Box 368, Ridgefield, CT 06877-0368, USA;4. Immunology & Respiratory Disease Research Department, Boehringer Ingelheim Pharmaceuticals, Inc., 900 Ridgebury Road, PO Box 368, Ridgefield, CT 06877-0368, USA
Abstract:A HTS screen for CCR1 antagonists afforded a novel sub-micromolar hit 5 containing a pyrazole core. In this report the design, optimization, and SAR of novel CCR1 antagonists based on a pyrazole core motif is presented. Optimization led to the advanced candidate compounds (S)-16q and (S)-16r with 250-fold improved CCR1 potency, excellent off-target selectivity and attractive drug-like properties.
Keywords:Chemokine receptors  CCR1  Pyrazole  HTS hit  Development candidate
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