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Are 5'-O-carbamate-2',3'-dideoxythiacytidine new anti-HIV and anti-HBV nucleoside drugs or prodrugs?
- Source :
-
Bioorganic & medicinal chemistry letters [Bioorg Med Chem Lett] 2003 Aug 04; Vol. 13 (15), pp. 2459-63. - Publication Year :
- 2003
-
Abstract
- In contrast to 5'-O-carbonate 3TC derivatives (23, 24), which are clearly 3TC prodrugs, the corresponding 3TC carbamates (15-21 and 25), found to be very stable compounds with respect to enzymatic hydrolysis (cellular lysates and culture cell media) and still active on both HIV-1 and HBV infected cells, may not be 3TC prodrugs. The antiviral properties as well as the mechanism of action of 3TC analogues have been studied and evaluated.
- Subjects :
- Anti-HIV Agents metabolism
Antiviral Agents metabolism
Cell Line
Culture Media
Deoxycytidine analogs & derivatives
Deoxycytidine metabolism
HIV-1 drug effects
Humans
Prodrugs metabolism
Anti-HIV Agents pharmacology
Antiviral Agents pharmacology
Deoxycytidine pharmacology
Hepatitis B virus drug effects
Prodrugs pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 0960-894X
- Volume :
- 13
- Issue :
- 15
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry letters
- Publication Type :
- Academic Journal
- Accession number :
- 12852943
- Full Text :
- https://doi.org/10.1016/s0960-894x(03)00496-7