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Identification of novel azaindazole CCR1 antagonist clinical candidates
Authors:Christian Harcken  Daniel Kuzmich  Brain Cook  Can Mao  Darren Disalvo  Hossein Razavi  Alan Swinamer  Pingrong Liu  Qiang Zhang  Alison Kukulka  Donna Skow  Mita Patel  Monica Patel  Kimberly Fletcher  Tara Sherry  David Joseph  Dustin Smith  Melissa Canfield  Maryanne Brown
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;5. Non-Clinical Drug Safety Department, Boehringer Ingelheim Pharmaceuticals, Inc., 900 Ridgebury Road, PO Box 368, Ridgefield, CT 06877-0368, USA
Abstract:Exploring various cyclization strategies, using a submicromolar pyrazole HTS screening hit 6 as a starting point, a novel indazole based CCR1 antagonist core was discovered. This report presents the design and SAR of CCR1 indazole and azaindazole antagonists leading to the identification of three development compounds, including 19e that was advanced to early clinical trials.
Keywords:Chemokine receptors  CCR1  Indazole  Scaffold hopping  Clinical compound
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