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Discovery of N-benzyl-N′-(4-pipyridinyl) urea CCR5 antagonists as anti-HIV-1 agents (II): Modification of the acyl portion

M Duan, J Peckham, M Edelstein, R Ferris…

文献索引:Duan, Maosheng; Peckham, Jennifer; Edelstein, Mark; Ferris, Robert; Kazmierski, Wieslaw M.; Spaltenstein, Andrew; Wheelan, Pat; Xiong, Zhiping Bioorganic and Medicinal Chemistry Letters, 2010 , vol. 20, # 24 p. 7401 - 7404

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被引用次数: 4

摘要

Modification of the acyl moiety in the CCR5 lead molecule 2 led to identification of several new classes of CCR5 antagonists. Antiviral activity and pharmacokinetic properties of the synthesized compounds were evaluated. Structure–activity relationship (SAR) derived from these studies further guided the optimization efforts, ultimately leading to the discovery of 36 with an acceptable drug-like profile.