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Synthesis and Biological Activity of 2-Aminopurine Methylenecyclopropane Analogues of Nucleosides.

โœ 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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โœฆ 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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