Title of article :
Are 5′-O-Carbamate-2′,3′-dideoxythiacytidine New Anti-HIV and Anti-HBV nucleoside Drugs or Prodrugs?
Author/Authors :
Carole Anastasi، نويسنده , , Patrick Vlieghe، نويسنده , , Olivier Hantz، نويسنده , , Olivier Schorr، نويسنده , , Christophe Pannecouque، نويسنده , , Myriam Witvrouw، نويسنده , , Erik De Clercq، نويسنده , , Pascal Clayette، نويسنده , , Nathalie Dereuddre-Bosquet، نويسنده , , Dominique Dormont، نويسنده , , Françoise Gondois-Rey، نويسنده , , Ivan Hirsch، نويسنده , , Jean-Louis Kraus، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Pages :
5
From page :
2459
To page :
2463
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.
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
2003
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
793377
Link To Document :
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