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pubmed-article:16039862pubmed:abstractTextHerpesviruses are a significant source of human disease; amongst these herpes simplex virus 1 (HSV-1) and HSV-2 are very prevalent and cause recurrent infections. We recently identified a pyrazolo[1,5-a]pyridine scaffold that showed promising activity against HSV-1 and HSV-2 in Vero cell antiviral assays. Here, we describe the synthesis and anti-herpetic activity of several 3-pyrimidinyl-2-phenylpyrazolo[1,5-a]pyridines with differing 2-phenyl substitution patterns. Approaches to rapidly access a number of analogs with different 2-phenyl substitution patterns are outlined. Several of the compounds described have comparable activity to acyclovir against HSV-1 and HSV-2.lld:pubmed
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pubmed-article:16039862pubmed:year2005lld:pubmed
pubmed-article:16039862pubmed:articleTitleSynthesis of novel substituted 2-phenylpyrazolopyridines with potent activity against herpesviruses.lld:pubmed
pubmed-article:16039862pubmed:affiliationDepartment of Medicinal Chemistry, GlaxoSmithKline Research and Development, Five Moore Drive, Research Triangle Park, NC 27709-3398, USA. Kristjan.gudmundsson@gsk.comlld:pubmed
pubmed-article:16039862pubmed:publicationTypeJournal Articlelld:pubmed