Comparative analysis of stability of tricyclic analogues of acyclovir in an acidic environment.
[ 1 ] Instytut Chemii Bioorganicznej Polskiej Akademii Nauk, Polska Akademia Nauk | [ P ] pracownik
2019
artykuł naukowy
angielski
EN In the presented studies, the effect of hydrogen ions on the stability of the tricyclic aciclovir derivative (i.e. 3,9-dihydro-3-[(2-hydroxyethoxy)methyl]-6-(4-methoxyphenyl)-9-oxo-5H-imidazo[1,2-a]purine; 6-(4-MeOPh)-TACV) and its esters (acetyl (Ac-), iso-butyryl (iBut-), pivaloyl (Piv-), ethoxycarbonyl (Etc-) and nicotinoyl (Nic-)) has been assessed. The HPLC chromatographic method (Lichrospher RP-18 column, 5m, 250mm x 4mm) with UV detection (262nm) was used to observe changes in the concentration of the tested compounds. The mobile phase consisted of acetonitrile-phosphate buffer (pH 6; 20mM; 17mM KH2PO4, 3mM K2HPO4) (35:65, v/v). The studies were carried out in the pH range 0.42-1.38 in the water-organic environment at constant ionic strength (0.50M). The observed rate constants of the degradation reactions of the tested compounds were determined, kinetic equations describing the dependence of k(pH) as a function of pH for the proper acid catalysis were determined and the parameters of the equations describing the reaction of formation the observed product were determined. The dependence of durability on the chemical structure of the tested compounds was indicated and the mechanism of observed reactions was proposed.
283 - 299
CC BY-NC-SA (uznanie autorstwa - użycie niekomercyjne - na tych samych warunkach)
ostateczna wersja opublikowana
03.2019
przed opublikowaniem
40
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