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Synthesis and antiviral activities of 3-deaza-3-fluoroaristeromycin and its 5' analogues.

Authors :
Chen Q
Liu C
Komazin G
Bowlin TL
Schneller SW
Source :
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2014 Dec 15; Vol. 22 (24), pp. 6961-4. Date of Electronic Publication: 2014 Nov 06.
Publication Year :
2014

Abstract

The naturally occurring adenine based carbocyclic nucleosides aristeromycin and neplanocin A and their 3-deaza analogues have found a prominent place in the search for diverse antiviral activity agent scaffolds because of their ability to inhibit S-adenosylhomocysteine (AdoHcy) hydrolase. Following the lead of these compounds, their 3-deaza-3-fluoroaristeromycin analogues have been synthesized and their effect on S-adenosylhomocysteine hydrolase and RNA and DNA viruses determined.<br /> (Copyright © 2014 Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1464-3391
Volume :
22
Issue :
24
Database :
MEDLINE
Journal :
Bioorganic & medicinal chemistry
Publication Type :
Academic Journal
Accession number :
25456389
Full Text :
https://doi.org/10.1016/j.bmc.2014.10.014