716358-34-8Relevant academic research and scientific papers
[2-(4-Phenyl-4-piperidinyl)ethyl]amine based CCR5 antagonists: derivatizations at the N-terminal of the piperidine ring
Duan, Maosheng,Aquino, Christopher,Ferris, Robert,Kazmierski, Wieslaw M.,Kenakin, Terry,Koble, Cecilia,Wheelan, Pat,Watson, Chris,Youngman, Michael
scheme or table, p. 1610 - 1613 (2009/11/30)
Several series of CCR5 antagonists have been discovered by derivatization at the N-terminal of the piperidine ring of the core template 2. Some derivatives exhibited potent inhibition against HIV-1infection. The pharmacokinetic properties of the lead comp
CCR5 ANTAGONISTS AS THERAPEUTIC AGENTS
-
Page 49, (2010/02/07)
The present invention relates to compounds of formula (I) or pharmaceutically acceptable derivatives thereof, useful in the treatment or prophylaxis of CCR5-related diseases and disorders, for example, in the inhibition of HIV replication, the prevention or treatment of an HIV infection, and in the treatment of the resulting acquired immune deficiency syndrome (AIDS).
