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SAR of 3,4-dihydropyrido[3,2-d]pyrimidone p38 inhibitors
Authors:Liu Luping  Stelmach John E  Natarajan Swaminathan R  Chen Meng-Hsin  Singh Suresh B  Schwartz Cheryl D  Fitzgerald Catherine E  O'Keefe Stephen J  Zaller Dennis M  Schmatz Dennis M  Doherty James B
Institution:Department of Medicinal Chemistry, Merck Research Laboratories, PO Box 2000, Rahway, NJ 07065, USA. luping_liu@merck.com
Abstract:Development for a class of potent 3,4-dihydropyrido(3,2-d)pyrimidone inhibitors of p38a MAP kinase is described. Modification of N-1 aryl and C-6 arylsulfide in 3,4-dihydropyrido(3,2-d)pyrimidone analogues for the interaction with the hydrophobic pockets in p38 active site is also discussed.
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