Synthesis and Biological Activity of 2-Aminopurine Methylenecyclopropane Analogues of Nucleosides.
โ Scribed by Ruifang Wang; Xinchao Chen; John C. Drach; Earl R. Kern; Jiri Zemlicka
- Publisher
- John Wiley and Sons
- Year
- 2003
- Weight
- 130 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0931-7597
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โฆ Synopsis
Synthesis and Biological Activity of 2-Aminopurine Methylenecyclopropane Analogues of Nucleosides. -Racemic 2-aminopurine methylenecyclopropane analogues such as (V) and (VI), as well as the (S)-enantiomer of compound (V) are synthesized and evaluated for their bioactivity. All the racemic compounds are found to be inactive against various virus species, while ((S)-(V)) inhibits replication of HSV-1, possesses moderate activity against VZV and it is a substrate for xanthine oxidase. -(
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Edited By Piet Herdewijn. Includes Bibliographical References And Index.