PL
Zbadano 9 nowo zsyntetyzowanych N-benzoilofenyloserynianów seskwiterpenów o budowie analogicznej do taksolu w kierunku ich przeciwwirusowej aktywności. Badania przeprowadzono w układzie in vitro na modelu zakażeń hodowli komórkowej Vero wirusem HSV-1Mc oraz w układzie in vivo, badając wpływ związków na przebieg zakażenia myszy retrowirusem Mo- MSV.
EN
The study comprised newly synthesized sesquiterpenoid analogs of taxol. The synthesis of the compounds was performed at the Institute of Organic Chemistry, Polish Academy of Sciences. Cytotoxicity of the compound was assessed using formazan method. In in vitro studies the cell cultures were infected with HSV-1Mc. The tested compounds were added in different concentrations to the cell culture after viral infection. Titer of the virus was expressed in TCIDW50/ml at particular stages of the experiments. In in vivo experiments NMRI mice were infected intramuscularly with a Moloney murine sarcoma virus (Mo-MSV). Tested compounds were administered to the mice intravenously on the day of virus inoculation. In Mo-MSV-infected mice dynamics of tumor progression and regression was assessed, as well as a mean time interval of tumor disappearance. Among the compounds tested: isovellerol-13-N-benzoyl-(2'R,3'S)-3'-phenylisoserinate, 5-deoxy-lactarolid B 8-[N-benzoyl-(2'R,3'S)-3'-phenylisoserinate] and isolactarorufin 8-epi-[N-benzoyl-(2'R,3'S)-3'-phenylisoserinate] showed significant antiviral activity in in vitro experiments. In in vivo experiments only lactarorufin A 8-[N-benzoyl-(2'R,3'S)-3'-phenylisoserinate] significantly inhibited the development of tumors and shortened the time of their total regression in the course of Mo-MSV infection.