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Synthesis and Antiviral and Cytostatic Activities of Carbocyclic Nucleosides Incorporating a Modified Cyclobutane Ring

Identifieur interne : 001A13 ( Main/Exploration ); précédent : 001A12; suivant : 001A14

Synthesis and Antiviral and Cytostatic Activities of Carbocyclic Nucleosides Incorporating a Modified Cyclobutane Ring

Auteurs : M. José Figueira [Espagne] ; J. Manuel Blanco [Espagne] ; Olga Caama O ; Franco Fernández [Espagne] ; Xerardo García-Mera [Espagne] ; Carmen L Pez [Espagne] ; Graciela Andrei [Belgique] ; Robert Snoeck [Belgique] ; Elisabeth Padalko [Belgique] ; Johan Neyts [Belgique] ; Jan Balzarini [Belgique] ; Erik De Clercq [Belgique]

Source :

RBID : ISTEX:C0394E5E6D9A4CFFC009A424EFC6BEF534A6957B

English descriptors

Abstract

Five new carbocyclic nucleosides were prepared by constructing a guanine (compounds 3, 5) or 8‐azaguanine (compounds 4, 6, and 7) base on the amino group of (1′S,3′R)‐3‐(3′‐amino‐2′,2′‐dimethylcyclobutyl) propan‐1‐ol (8), and their activities against a variety of viruses and tumor cell lines were determined. Only compounds 3 and 7 showed a detectable activity at subtoxic concentrations against some viruses tested.

Url:
DOI: 10.1002/(SICI)1521-4184(199910)332:10<348::AID-ARDP348>3.0.CO;2-H


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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