Yip Yvonne, Victor Frantz, Lamar Jason, Johnson Robert, Wang Q May, Barket Donna, Glass John, Jin Ling, Liu Lifei, Venable Daryl, Wakulchik Mark, Xie Congping, Heinz Beverly, Villarreal Elcira, Colacino Joe, Yumibe Nathan, Tebbe Mark, Munroe John, Chen Shu-Hui
Lilly Research Laboratory, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285, USA.
Bioorg Med Chem Lett. 2004 Jan 5;14(1):251-6. doi: 10.1016/j.bmcl.2003.09.074.
We describe herein the design, syntheses and evaluation of a number of bicycloproline P2 bearing HCV protease inhibitors endowed with impressive enzyme potency, enzyme selectivity, cellular activity and favorable ADME profiles.
我们在此描述了一系列带有丙型肝炎病毒(HCV)蛋白酶抑制剂的双环脯氨酸P2的设计、合成及评估,这些抑制剂具有令人印象深刻的酶活性、酶选择性、细胞活性以及良好的药代动力学性质。