134444-47-6Relevant articles and documents
Chemical and enzymatic synthesis and antiviral properties of 2'-deoxy- 2'-fluoroguanosine
Zaitseva, Galina V.,Zinchenko, Anatoli I.,Barai, Vladimir N.,Pavlova,Boreko, Evgeny I.,Mikhailopulo, Igor A.
, p. 687 - 688 (1999)
Chemical and enzymatic methods were employed for the synthesis of the title compound, 2'F-Guo 7. High antiviral activity of 2'F-Guo was established in chick embryo cells infected with influenza virus FPV/Rostock/34 (H7N1) and herpes simplex virus (HSV) type I (1C strain).
Anti-HCV nucleoside derivatives
-
, (2008/06/13)
The present invention comprises nucleoside derivatives for use in the treatment or prophylaxis of hepatitis C virus infections. In particular, the present invention discloses the novel use of known 2'-deoxy-2'-fluoro nucleoside derivatives as inhibitors of hepatitis C virus (HCV) RNA replication and pharmaceutical compositions of such compounds. The compounds of this invention have potential use as therapeutic agents for the treatment of HCV infections.
Synthesis and biologic activity of purine 2'-deoxy-2'-fluoro- ribonucleosides
Thomas,Tiwari,Clayton,Secrist III,Montgomery
, p. 309 - 323 (2007/10/02)
The synthesis of 3,5-di-O-benzoyl-2-deoxy-2-fluoro-D-ribofuranosyl bromide (8) and its reaction with 2,6-dichloropurine by fusion and with mercuric cyanide catalysis is described. The resulting 2,6-dichloro-9-(3,5-di-O- benzoyl-2-deoxy-2-fluoro-β-D-ribofuranosyl)purine (13) was converted to the 2-fluoroadenine (16), the 2-chloroadenine (17), 2,6-diaminopurine (12), and guanine (14) nucleosides by standard procedures. These nucleosides were cytotoxic to a number of cell lines in culture. The 2-haloadenine nucleosides 16 and 17 gave modest increases in lifespan when tested against the P388 leukemia in mice.