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pubmed-article:11714616pubmed:abstractTextN-3-Benzyloxycarbonylmethyl- and N-3-carboxymethyl-TBDMS-substituted nucleosides were synthesized and evaluated for activity against HIV replication. It was found that the N-3-carboxymethyl-TBDMS-substituted nucleosides were specific inhibitors of HIV-1 replication. They should be considered as members of a novel and original class of NNRTIs.lld:pubmed
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pubmed-article:11714616pubmed:articleTitleIdentification of a novel family of nucleosides that specifically inhibit HIV-1 reverse transcriptase.lld:pubmed
pubmed-article:11714616pubmed:affiliationInstituto de Química Médica (C.S.I.C.), Juan de la Cierva 3, 28006-Madrid, Spain.lld:pubmed
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