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Synthesis and Antiviral Activity of Some C2-, C4-, and C6-Substituted Pyrazolo[3,4-D]Pyrimidine Acyclonucleosides with the Alkylating Chains of ACV,HBG, and ISO-DHPG
Authors:Omar Moukha-chafiq  Mohamed Labd Taha  Hassan Bihi Lazrek  Jean-Jacques Vasseur  Erik De Clercq
Affiliation:1. Laboratoire de Chimie Bio-Organique, Faculte des Sciences , Agadir, Maroc;2. Laboratoire de Chimie Bio-Organique, Faculte des Sciences I , Marrakech, Maroc;3. Lab. de Chimie Organique Biomoleculaire de synthèse , U.S.T. Montpellier II , Moukhao, Montpellier, France;4. Rega Institute for Medical Research, Katholieke Universiteit Leuven , Leuven, Belgium
Abstract:A useful route to obtain trisubstituted pyrazolo[3,4-d]pyrimidines 14–17 is described. Those later were coupled with the alkylating agents 18–20 as in ACV, HBG, and iso-DHPG to give, after deprotection, the desired acylonucleosides 33–44. Almost all of the new compounds were evaluated for their inhibitory effects against the replication of various DNA viruses in culture.
Keywords:C2-, C4-, and C6-substituted pyrazolo[3,4-d]pyrimidines  Acyclonucleoside  Analogues of ACV, HBG, and iso-DHPG
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