Structure-activity relationships of (E)-5-(2-bromovinyl) uracil and related pyrimidine nucleosides as antiviral agents for herpes viruses

A series of (E)-5-(2-bromovinyl)uracil analogues and related nucleosides wa s synthesized, and their antiviral activities were evaluated. (E)-5-(2-Brom ovinyl)-2'-deoxy-L-uridine (L-BVDU, 2), 1-(beta-L-arabinofuranosyl)-(E)-5-( 2-bromovinyl)uracil (L-BVAU, 4), (E)-5-(2-bromovinyl)-1-(2-deoxy-2-fluoro-b eta-L-ribofuranosyl)uracil (L-FBVRU, 8) and (E)-5-(2-bromovinyl)-1-(2-deoxy -2-fluoro-beta-L-arabinofuranosyl)uracil (L-FBVAU, 10) were synthesized via appropriate 5-iodouracil analogues from L-arabinose. D- and L-Oxathiolane and -dioxolane derivatives 13, 16, 20, 21, and 29-34 were prepared by glyco sylation reaction of the oxathiolane and dioxolane intermediates with silyl ated uracil analogues using TMSI as the coupling agent. The synthesized com pounds were evaluated in cell cultures infected with the following viruses: varicella tester virus (VZV), Epstein Barr virus (EBV), and herpes simplex virus types 1 and 2 (HSV-1 and HSV-8). Among the tested compounds, beta-L- CV-OddU (29), beta-L-BV-OddU (31), and beta-L-IV-OddU (33) exhibited potent in vitro antiviral activity against VZV with EC50 values of 0.15, 0.07, an d 0.035 mu M, respectively, and against EBV with EC50 values of 0.49, 0.59, and 3.91 mu M, respectively.