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 : 000636Synthesis 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 :
- Archiv der Pharmazie / Chemistry in Life Sciences [ 0365-6233 ] ; 2014-02-03.
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...)
- to stream Hal, to step Corpus: 000281
- to stream Hal, to step Curation: 000281
- to stream Hal, to step Checkpoint: 000135
- to stream Main, to step Merge: 000636
- to stream Main, to step Curation: 000635
Le document en format XML
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<front><div type="abstract" xml:lang="en"> <p>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).</p>
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