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Novel Carbocyclic Nucleosides Containing a Cyclopentyl Ring. Adenosine and Uridine Analogues

Identifieur interne : 001B74 ( Main/Exploration ); précédent : 001B73; suivant : 001B75

Novel Carbocyclic Nucleosides Containing a Cyclopentyl Ring. Adenosine and Uridine Analogues

Auteurs : Carmen Balo [Espagne] ; Franco Fernández [Espagne] ; Evangelina Lens [Espagne] ; Carmen L Pez [Espagne] ; Graciela Andrei [Belgique] ; Robert Snoeck [Belgique] ; Jan Balzarini [Belgique] ; Erik De Clercq [Belgique]

Source :

RBID : ISTEX:EFFFE6E318D9E96CC5FA6AFD7CCA9371A503B0E5

English descriptors

Abstract

cis‐3‐Aminomethylcyclopentylmethanol (4) was used as a precursor in the synthesis of carbocyclic nucleosides containing adenine, hypoxanthine, 8‐azahypoxanthine, uracil, and 5‐iodouracil bases. None of these compounds had appreciable activity against eighteen viruses in the concentration ranges tested. Two of them showed a weak cytostatic activity against three tumor lines.

Url:
DOI: 10.1002/ardp.19973300807


Affiliations:


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


Le document en format XML

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<div type="abstract" xml:lang="en">cis‐3‐Aminomethylcyclopentylmethanol (4) was used as a precursor in the synthesis of carbocyclic nucleosides containing adenine, hypoxanthine, 8‐azahypoxanthine, uracil, and 5‐iodouracil bases. None of these compounds had appreciable activity against eighteen viruses in the concentration ranges tested. Two of them showed a weak cytostatic activity against three tumor lines.</div>
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