The present invention relates to compounds of Formula (I) and (Ia) useful in the treatment of CCR5-related diseases and disorders, for example, the prevention or treatment of an HIV infection, and in the treatment of the resulting acquired immune deficiency syndrome (AIDS).
The present invention relates to compounds of Formula (I) and (Ia)
useful in the treatment of CCR5-related diseases and disorders, for example, the prevention or treatment of an HIV infection, and in the treatment of the resulting acquired immune deficiency syndrome (AIDS).
Synthesis and evaluation of 2-phenyl-1,4-butanediamine-based CCR5 antagonists for the treatment of HIV-1
作者:Matthew D. Tallant、Maosheng Duan、George A. Freeman、Robert G. Ferris、Mark P. Edelstein、Wieslaw M. Kazmierski、Pat J. Wheelan
DOI:10.1016/j.bmcl.2011.01.030
日期:2011.3
We describe the synthesis and potency of a novel series of N-substituted 2-phenyl- and 2-methyl-2-phenyl-1,4-diaminobutane- based CCR5 antagonists. Compounds 7a and 12f were found to be potent in anti-HIV assays and bioavailable in the low-dose rat PK model. (C) 2011 Elsevier Ltd. All rights reserved.