Article
Stereoselective synthesis and antiviral activity of D-2',3'-didehydro-2',3'-dideoxy-2'-fluoro-4'-thionucleosides.
Journal of medicinal chemistry - 24 Oct 2002
Chong Youhoon, Choo Hyunah, Choi Yongseok, Mathew Judy, Schinazi Raymond F, Chu Chung K
Abstract excerpt
As 2',3'-didehydro-2',3'-dideoxy-2'-fluoronucleosides have exhibited interesting antiviral effects against HIV-1 as well as HBV, it is of interest to synthesize the isosterically substituted 4'-thionucleosides in which 4'-oxygen is replaced by a sulfur atom. To study structure-activity relationships, various pyrimidine and purine nucleosides were synthesized from the key intermediate...
Topics
- Animals
- Anti-HIV Agents
- Antiviral Agents
- Binding Sites
- Cell Line
- Chlorocebus aethiops
- Drug Resistance, Viral
- HIV Reverse Transcriptase
- HIV-1
- Humans
- Lamivudine
