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Por favor, use este identificador para citar o enlazar a este item: http://hdl.handle.net/10261/35847
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dc.contributor.authorÁlvarez, Rosa-
dc.contributor.authorJimeno, M. Luisa-
dc.contributor.authorDe Clercq, Erik-
dc.contributor.authorBalzarini, Jan-
dc.contributor.authorCamarasa Rius, María José-
dc.date.accessioned2011-05-19T09:47:47Z-
dc.date.available2011-05-19T09:47:47Z-
dc.date.issued1997-
dc.identifier.citationNucleosides, Nucleotides and Nucleic Acids16(7 & 9) : 1033 - 1036 (1997)es_ES
dc.identifier.issn0732-8311-
dc.identifier.urihttp://hdl.handle.net/10261/35847-
dc.description.abstractNovel TSAO-T analogues, in which the 3'-spiroaminooxatioledioxide moiety has been replaced by other 3'-spiro moieties bearing a NH group at the same position as the 4''-NH2 of TSAO-T have been prepared and evaluated for their inhibitory effect on HIV replication in cell culture. In contrast to the prototype compound TSAO-T, the novel TSAO derivatives were inactive at subtoxic concentrations.es_ES
dc.language.isoenges_ES
dc.publisherTaylor & Francises_ES
dc.rightsclosedAccesses_ES
dc.titleNovel analogues of the anti HIV-1 agent TSAO-T modified at the 3'-spiro moietyes_ES
dc.typeartículoes_ES
dc.identifier.doi10.1080/07328319708006126-
dc.description.peerreviewedPeer reviewedes_ES
dc.relation.publisherversionhttp://dx.doi.org/10.1080/07328319708006126es_ES
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.languageiso639-1en-
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