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Sulfonamidolactam inhibitors of coagulation factor Xa
Authors:Smallheer Joanne M  Wang Shuaige  Laws Mia L  Nakajima Suanne  Hu Zilun  Han Wei  Jacobson Irina  Luettgen Joseph M  Rossi Karen A  Rendina Alan R  Knabb Robert M  Wexler Ruth R  Lam Patrick Y S  Quan Mimi L
Institution:Bristol-Myers Squibb Company, Cardiovascular Diseases Chemistry, PO Box 5400, Princeton, NJ 08543-5400, USA. joanne.smallheer@bms.com
Abstract:As part of an effort to identify novel backups for previously reported pyrazole-based coagulation Factor Xa inhibitors, the pyrazole 5-carboxamide moiety was replaced by 3-(sulfonylamino)-2-piperidone. This led to the identification of a structurally diverse chemotype that was further optimized to incorporate neutral or weakly basic aryl and heteroaryl P1 groups while maintaining good potency versus Factor Xa. Substitution at the sulfonamide nitrogen provided further improvements in potency and as did introduction of alternate P4 moieties.
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