Structure–activity relationship studies of chloromethyl ketone derivatives for selective human chymase inhibitors

Structure–activity relationship studies of chloromethyl ketone derivatives for selective human chymase inhibitors Synthesis, Structure−Activity Relationships, and Pharmacokinetic Profiles of Nonpeptidic Difluoromethylene Ketones as Novel Inhibitors of Human Chymase Synthesis, Structure−Activity Relationships, and Pharmacokinetic Profiles of Nonpeptidic α-Keto Heterocycles as Novel Inhibitors of Human Chymase Identification of 6-substituted 4-arylsulfonyl-1,4-diazepane-2,5-diones as a novel scaffold for human chymase inhibitors SPF-32629 A and B, Novel Human Chymase Inhibitors Produced by Penicillium sp. Derivatives of oxoisoaporphine alkaloids: A novel class of selective acetylcholinesterase inhibitors Design, synthesis and structure–activity relationships of (±)-isochaihulactone derivatives SAR studies of differently functionalized chalcones based hydrazones and their cyclized derivatives as inhibitors of mammalian cathepsin B and cathepsin H Inhibitors of phenylethanolamine N-methyltransferase and epinephrine biosynthesis. 1. Chloro-Substituted 1,2,3,4-tetrahydroisoquinolines New 2-bromomethyl-8-substituted-benzo[c]chromen-6-ones. Synthesis and biological properties