Novel Tsao Derivatives. Synthesis and Anti-HIV-1 Activity of Allofuranosyl-TSAO-T Analogues

Rosa Álvarez; Ana San‐Félix; De Clercq Erik; Jan Balzarini; Marı́a-José Camarasa

doi:10.1080/07328319608002389

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De Clercq Erik

KU Leuven

Novel Tsao Derivatives. Synthesis and Anti-HIV-1 Activity of Allofuranosyl-TSAO-T Analogues

Article 1996 en

Authors

RÁ
Rosa Álvarez
AS
Ana San‐Félix
De Clercq Erik
KU Leuven

Abstract

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Abstract Novel TSAO-T analogues, in which the ribofuranosyl moiety has been replaced by an hexofuranosyl sugar moiety, have been prepared and evaluated for their inhibitory effect on HIV-1 replication in cell culture. In contrast to the prototype compound TSAO-T, the hexofuranosyl derivatives proved not active at subtoxic concentrations.

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Novel Tsao Derivatives. Synthesis and Anti-HIV-1 Activity of Allofuranosyl-TSAO-T Analogues

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