Data di Pubblicazione:
2019
Abstract:
The pyrimidine nucleus is a versatile core in the development of antiretroviral agents. On this basis, a series of pyrimidine-2,4-diones linked to an isoxazolidine nucleus have been synthesized and tested as nucleoside analogs, endowed with potential anti-HIV (human immunodeficiency virus) activity. Compounds 6a-c, characterized by the presence of an ethereal group at C-3, show HIV reverse transcriptase (RT) inhibitor activity in the nanomolar range as well as HIV-infection inhibitor activity in the low micromolar with no toxicity. In the same context, compound 7b shows only a negligible inhibition of RT HIV.
Tipologia CRIS:
14.a.1 Articolo su rivista
Keywords:
HIV RT inhibitors, Pyrimidine-2,4-dione derivatives, biological activity, molecular docking, reverse nucleosides
Elenco autori:
Romeo, Roberto; Iannazzo, Daniela; Veltri, Lucia; Gabriele, Bartolo; Macchi, Beatrice; Frezza, Caterina; Marino-Merlo, Francesca; Giofrè, Salvatore V
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