Design, synthesis, and antiviral evaluations of 1-(substituted benzyl)-2-substituted-5, 6-dichlorobenzimidazoles as nonnucleoside analogues of 2, 5, 6-trichloro-1-(β-D …
…, LS Kucera, JC Drach, LB Townsend
文献索引:Porcari, Anthony R.; Devivar, Rodrigo V.; Kucera, Louis S.; Drach, John C.; Townsend, Leroy B. Journal of Medicinal Chemistry, 1998 , vol. 41, # 8 p. 1252 - 1262
We have recently reported that certain ribosylated polyhalogenated benzimidazoles are potent and selective inhibitors of HCMV replication at noncytotoxic concentrations. To extend the structure-activity relationship beyond these first-generation compounds, we alkylated 5, 6-dichloro-2-substituted-benzimidazoles with either a series of substituted benzyl halides or (2-bromoethyl) benzene to obtain five series of nonnucleoside ...
[Townsend, Leroy B.; Devivar, Rodrigo V.; Turk, Steven R.; Nassiri, M. Reza; Drach, John C. Journal of Medicinal Chemistry, 1995 , vol. 38, # 20 p. 4098 - 4105]