info:eu-repo/semantics/article
Synthesis, analysis, cholinesterase-inhibiting activity and molecular modelling studies of 3-(dialkylamino)-2-hydroxypropyl 4-[(alkoxy-carbonyl)amino]benzoates and their quaternary ammonium salts
Fecha
2017-12Registro en:
Padrtova, Tereza; Marvanova, Pavlina; Odehnalova, Klara; Kubinova, Renata; Parravicini, Oscar; et al.; Synthesis, analysis, cholinesterase-inhibiting activity and molecular modelling studies of 3-(dialkylamino)-2-hydroxypropyl 4-[(alkoxy-carbonyl)amino]benzoates and their quaternary ammonium salts; Molecular Diversity Preservation International; Molecules; 22; 12; 12-2017; 1-21
1420-3049
CONICET Digital
CONICET
Autor
Padrtova, Tereza
Marvanova, Pavlina
Odehnalova, Klara
Kubinova, Renata
Parravicini, Oscar
Garro, Adriana
Enriz, Ricardo Daniel
Humpa, Otakar
Oravec, Michal
Mokry, Petr
Resumen
Tertiary amines 3-(dialkylamino)-2-hydroxypropyl 4-[(alkoxycarbonyl)amino]benzoates and their quaternary ammonium salts were synthesized. The final step of synthesis of quaternary ammonium salts was carried out by microwave-assisted synthesis. Software-calculated data provided the background needed to compare fifteen new resulting compounds by their physicochemical properties. The acid dissociation constant (pKa) and lipophilicity index (log P) of tertiary amines were determined; while quaternary ammonium salts were characterized by software-calculated lipophilicity index and surface tension. Biological evaluation aimed at testing acetylcholinesterase and butyrylcholinesterase-inhibiting activity of synthesized compounds. A possible mechanism of action of these compounds was determined by molecular modelling study using combined techniques of docking; molecular dynamics simulations and quantum mechanics calculations.