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Substituted chromones and quinolones as potent melanin-concentrating hormone receptor 1 antagonists
Authors:Dyck Brian  Zhao Liren  Tamiya Junko  Pontillo Joseph  Hudson Sarah  Ching Brett  Heise Christopher E  Wen Jenny  Norton Christi  Madan Ajay  Schwarz David  Wade Warren  Goodfellow Val S
Affiliation:Department of Medicinal Chemistry, Neurocrine Biosciences Inc., San Diego, CA 92130, USA. bdyck@neurocrine.com
Abstract:
A series of substituted chromones were designed, synthesized, and evaluated for their ability to bind melanin-concentrating hormone receptor 1. Compounds with subnanomolar binding affinity and 66% oral bioavailability in rats were discovered.
Keywords:
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