Guay Daniel, Beaulieu Christian, Truchon Jean-Francois, Jagadeeswar Reddy T, Zamboni Robert, Bayly Christopher I, Methot Nathalie, Rubin Joel, Ethier Diane, David Percival M
Department of Medicinal Chemistry, Merck Frosst Canada & Co., 16711 Trans Canada Hwy, Kirkland, QC, Canada H9H 3L1.
Bioorg Med Chem Lett. 2009 Sep 15;19(18):5392-6. doi: 10.1016/j.bmcl.2009.07.114. Epub 2009 Jul 28.
A series of dipeptide nitriles with a thienyl alanine in P2 were identified as potent and selective cathepsin C inhibitors. Incorporation of a substituted cyclopropyl moiety in P1 effectively protects these derivatives against hydrolase activity in whole blood.
一系列在P2位含有噻吩基丙氨酸的二肽腈被鉴定为有效的选择性组织蛋白酶C抑制剂。在P1位引入一个取代环丙基部分可有效保护这些衍生物免受全血中的水解酶活性影响。