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Synthesis of 1,2,3-Triazolyl Nucleoside Analogs as Potential Anti-Influenza A (H3N2 Subtype) Virus Agents.

Identifieur interne : 000635 ( Main/Exploration ); précédent : 000634; suivant : 000636

Synthesis of 1,2,3-Triazolyl Nucleoside Analogs as Potential Anti-Influenza A (H3N2 Subtype) Virus Agents.

Auteurs : Hanane Elayadi [Maroc] ; Michael Smietana [France] ; Jean-Jacques Vasseur [France] ; Jan Balzarini [Belgique] ; Hassan B. Lazrek [Maroc]

Source :

RBID : Hal:hal-01004380

Abstract

Montmorillonite K10 impregnated with copper dichloride and potassium iodide (CuCl2/KI/K10) was used as catalyst in the cycloaddition of azides and propargylnucleobases, to provide the corresponding 1,4-disubstituted 1,2,3-triazoles in good yield. All compounds 16-23 were evaluated for their antiviral activity in vitro. Compound 18 showed moderate inhibition against influenza virus A (H3N2).


Url:
DOI: 10.1002/ardp.201300260


Affiliations:


Links toward previous steps (curation, corpus...)


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