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.

Pyrimidine 2,4-Diones in the Design of New HIV RT Inhibitors

Romeo, Roberto
Primo
;
Iannazzo, Daniela
Secondo
;
Frezza, Caterina;Marino-Merlo, Francesca
Penultimo
;
Giofrè, Salvatore V
Ultimo
2019-01-01

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.
2019
Inglese
ELETTRONICO
24
9
1
14
14
https://www.mdpi.com/1420-3049/24/9/1718
Internazionale
Esperti anonimi
HIV RT inhibitors, Pyrimidine-2,4-dione derivatives, biological activity, molecular docking, reverse nucleosides
Article number 1718
no
info:eu-repo/semantics/article
Romeo, Roberto; Iannazzo, Daniela; Veltri, Lucia; Gabriele, Bartolo; Macchi, Beatrice; Frezza, Caterina; Marino-Merlo, Francesca; Giofrè, Salvatore V...espandi
14.a Contributo in Rivista::14.a.1 Articolo su rivista
8
262
open
File in questo prodotto:
File Dimensione Formato  
58. molecules-2019.pdf

accesso aperto

Descrizione: Molecules_2019
Tipologia: Versione Editoriale (PDF)
Licenza: Creative commons
Dimensione 931.02 kB
Formato Adobe PDF
931.02 kB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11570/3140101
Citazioni
  • ???jsp.display-item.citation.pmc??? 4
  • Scopus 44
  • ???jsp.display-item.citation.isi??? 39
social impact