Novel Carbocyclic Nucleosides Containing a Cyclopentyl Ring. Adenosine and Uridine Analogues
✍ Scribed by Carmen Balo; Franco Fernández; Evangelina Lens; Carmen López; Graciela Andrei; Robert Snoeck; Jan Balzarini; Erik De Clercq
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 339 KB
- Volume
- 330
- Category
- Article
- ISSN
- 0365-6233
No coin nor oath required. For personal study only.
✦ Synopsis
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.
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Novel Carbocyclic Nucleosides Containing a Cyclobutyl Ring. Guanosine and Adenosine Analogues. -The activity of the title compounds, e.g. (VIII) and (XI), against a variety of DNA and RNA viruses, and their cytotoxicities against several types of host cells, is evaluated. -(BORGES,