SYNTHESIS AND EVALUATION OF THE ANTIVIRAL ACTIVITY OF ACYCLIC NUCLEOSIDES CARRYING FLUORINE AND SULFUR SUBSTITUENTS

Citation
P. Bravo et al., SYNTHESIS AND EVALUATION OF THE ANTIVIRAL ACTIVITY OF ACYCLIC NUCLEOSIDES CARRYING FLUORINE AND SULFUR SUBSTITUENTS, Il Farmaco, 48(8), 1993, pp. 1113-1120
Citations number
14
Categorie Soggetti
Pharmacology & Pharmacy
Journal title
ISSN journal
0014827X
Volume
48
Issue
8
Year of publication
1993
Pages
1113 - 1120
Database
ISI
SICI code
0014-827X(1993)48:8<1113:SAEOTA>2.0.ZU;2-#
Abstract
-2',3'-Seco nucleosides 5 carrying fluorine and sulfur substituents at C-3' and C-5, respectively, of acyclic sugar moiety were synthesized in enantiomerically and diastereoisomerically pure form. These product s and some structurally similar 1',2'-seco-2'-nor-and 1',2'-seco-nucle osides 3 and 4 were tested in vitro for cytotoxicity and antiviral act ivity. At non-cytotoxic concentrations the compounds were inactive aga inst human immunodeficiency virus and herpes simplex virus type-1.