Abstract
N-Methanocarbathymidine [(N)-MCT], a thymidine analogue, exhibits potent activity in cell culture against herpes simplex virus1 (HSV-1). (N)-MCT showed higher antiviral activity than ganciclovir (GCV). Continuous treatment of Vero cells with (N)-MCT immediately or 10 h post-infection (p.i.) fully prevented the development of viral infection. However, when infected cells were treated with (N)-MCT at 12 h p.i., there was only a partial inhibition (ca. 50%). Additionally, continuous treatment of infected cells with (N)-MCT for about 48 h was sufficient to achieve full prevention of viral infection without further treatment. These findings suggest the complete loss of herpes simplex thymidine kinase (HSV-tk) activity occurs after 48 h of treatment with (N)-MCT. This study helps to understand the mechanism and dynamics of antiHSV activity of (N)-MCT, which is necessary for its future development as an antiviral drug.
Original language | English |
---|---|
Pages (from-to) | 427-432 |
Number of pages | 6 |
Journal | International Journal of Antimicrobial Agents |
Volume | 25 |
Issue number | 5 |
DOIs | |
State | Published - 1 Jan 2005 |
Keywords
- Antiviral activity
- Ganciclovir
- Herpes simplex thymidine kinase
- Herpes simplex virus
- N- Methanocarbathymidine
- Phosphorylation
ASJC Scopus subject areas
- Microbiology (medical)
- Infectious Diseases
- Pharmacology (medical)