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Synthesis and anti-VZV activity of 6-heteroaryl derivatives of tricyclic acyclovir and 9-{[ cis-1′,2′-bis(hydroxymethyl)cycloprop-1′-yl]methyl}guanine analogues
Ist Teil von
European journal of medicinal chemistry, 2009-08, Vol.44 (8), p.3313-3317
Ort / Verlag
Kidlington: Elsevier Masson SAS
Erscheinungsjahr
2009
Quelle
MEDLINE
Beschreibungen/Notizen
A series of tricyclic analogues of acyclovir and 9-{[
cis-1′,2′-bis(hydroxymethyl)cycloprop-1′-yl]methyl}guanine substituted in the 6 position with thien-2-yl, 5-bromothien-2-yl or furan-2-yl group were synthesized. The new compounds
5a–
f were evaluated for their activity in vitro against varicella-zoster virus (VZV) and cytomegalovirus (CMV). The marked anti-VZV activities of
5a–
f remained comparable to those of their previously described 6-phenyl-substituted counterparts.
[Display omitted] A series of tricyclic analogues of acyclovir and 9-{[
cis-1′,2′-bis(hydroxymethyl)cycloprop-1′-yl]methyl}guanine substituted in the 6 position were synthesized and screened for their activity in vitro against varicella-zoster virus (VZV) and cytomegalovirus (CMV).