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Synthesis and anti-HIV properties of new carbamate prodrugs of AZT.
- Source :
-
Chemical biology & drug design [Chem Biol Drug Des] 2012 Dec; Vol. 80 (6), pp. 947-52. Date of Electronic Publication: 2012 Oct 09. - Publication Year :
- 2012
-
Abstract
- A series of new 5'-O-carbamate prodrugs of AZT have been prepared. The stability in biological media, anti-HIV properties and pharmacokinetic parameters in dogs were evaluated. The compounds display moderate anti-HIV activity in cell culture. After oral administration of carbamate IV in dogs, both intact prodrug IV and released AZT were discovered in dog blood. Pharmacokinetic parameters of the compound IV were estimated. Half-life (T(1/2)) of AZT released after oral administration of IV in dogs was close to that after administration of AZT itself, and time to the maximum concentration (T(max)) of AZT released from IV was two and three times longer compared with that of AZT and H-phosphonate AZT, respectively. Acute toxicity was more than five times less if compared with AZT. As a result, we consider this series of carbamate derivatives of AZT as perspective for development of anti-HIV agents.<br /> (© 2012 John Wiley & Sons A/S.)
- Subjects :
- Administration, Oral
Animals
Anti-HIV Agents pharmacokinetics
Anti-HIV Agents toxicity
Cell Line
Cell Survival drug effects
Dogs
Half-Life
Humans
Mice
Mice, Inbred BALB C
Prodrugs pharmacokinetics
Prodrugs toxicity
Anti-HIV Agents chemical synthesis
Carbamates chemistry
Prodrugs chemical synthesis
Zidovudine chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1747-0285
- Volume :
- 80
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Chemical biology & drug design
- Publication Type :
- Academic Journal
- Accession number :
- 22958368
- Full Text :
- https://doi.org/10.1111/cbdd.12047