Cargando…

Synthesis, Analysis, Cholinesterase-Inhibiting Activity and Molecular Modelling Studies of 3-(Dialkylamino)-2-hydroxypropyl 4-[(Alkoxy-carbonyl)amino]benzoates and Their Quaternary Ammonium Salts

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Padrtova, Tereza, Marvanova, Pavlina, Odehnalova, Klara, Kubinova, Renata, Parravicini, Oscar, Garro, Adriana, Enriz, Ricardo D., Humpa, Otakar, Oravec, Michal, Mokry, Petr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149889/
https://www.ncbi.nlm.nih.gov/pubmed/29168793
http://dx.doi.org/10.3390/molecules22122048
_version_ 1783356890426638336
author Padrtova, Tereza
Marvanova, Pavlina
Odehnalova, Klara
Kubinova, Renata
Parravicini, Oscar
Garro, Adriana
Enriz, Ricardo D.
Humpa, Otakar
Oravec, Michal
Mokry, Petr
author_facet Padrtova, Tereza
Marvanova, Pavlina
Odehnalova, Klara
Kubinova, Renata
Parravicini, Oscar
Garro, Adriana
Enriz, Ricardo D.
Humpa, Otakar
Oravec, Michal
Mokry, Petr
author_sort Padrtova, Tereza
collection PubMed
description 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 (pK(a)) 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.
format Online
Article
Text
id pubmed-6149889
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-61498892018-11-13 Synthesis, Analysis, Cholinesterase-Inhibiting Activity and Molecular Modelling Studies of 3-(Dialkylamino)-2-hydroxypropyl 4-[(Alkoxy-carbonyl)amino]benzoates and Their Quaternary Ammonium Salts Padrtova, Tereza Marvanova, Pavlina Odehnalova, Klara Kubinova, Renata Parravicini, Oscar Garro, Adriana Enriz, Ricardo D. Humpa, Otakar Oravec, Michal Mokry, Petr Molecules Article 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 (pK(a)) 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. MDPI 2017-11-23 /pmc/articles/PMC6149889/ /pubmed/29168793 http://dx.doi.org/10.3390/molecules22122048 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Padrtova, Tereza
Marvanova, Pavlina
Odehnalova, Klara
Kubinova, Renata
Parravicini, Oscar
Garro, Adriana
Enriz, Ricardo D.
Humpa, Otakar
Oravec, Michal
Mokry, Petr
Synthesis, Analysis, Cholinesterase-Inhibiting Activity and Molecular Modelling Studies of 3-(Dialkylamino)-2-hydroxypropyl 4-[(Alkoxy-carbonyl)amino]benzoates and Their Quaternary Ammonium Salts
title Synthesis, Analysis, Cholinesterase-Inhibiting Activity and Molecular Modelling Studies of 3-(Dialkylamino)-2-hydroxypropyl 4-[(Alkoxy-carbonyl)amino]benzoates and Their Quaternary Ammonium Salts
title_full Synthesis, Analysis, Cholinesterase-Inhibiting Activity and Molecular Modelling Studies of 3-(Dialkylamino)-2-hydroxypropyl 4-[(Alkoxy-carbonyl)amino]benzoates and Their Quaternary Ammonium Salts
title_fullStr Synthesis, Analysis, Cholinesterase-Inhibiting Activity and Molecular Modelling Studies of 3-(Dialkylamino)-2-hydroxypropyl 4-[(Alkoxy-carbonyl)amino]benzoates and Their Quaternary Ammonium Salts
title_full_unstemmed Synthesis, Analysis, Cholinesterase-Inhibiting Activity and Molecular Modelling Studies of 3-(Dialkylamino)-2-hydroxypropyl 4-[(Alkoxy-carbonyl)amino]benzoates and Their Quaternary Ammonium Salts
title_short Synthesis, Analysis, Cholinesterase-Inhibiting Activity and Molecular Modelling Studies of 3-(Dialkylamino)-2-hydroxypropyl 4-[(Alkoxy-carbonyl)amino]benzoates and Their Quaternary Ammonium Salts
title_sort synthesis, analysis, cholinesterase-inhibiting activity and molecular modelling studies of 3-(dialkylamino)-2-hydroxypropyl 4-[(alkoxy-carbonyl)amino]benzoates and their quaternary ammonium salts
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149889/
https://www.ncbi.nlm.nih.gov/pubmed/29168793
http://dx.doi.org/10.3390/molecules22122048
work_keys_str_mv AT padrtovatereza synthesisanalysischolinesteraseinhibitingactivityandmolecularmodellingstudiesof3dialkylamino2hydroxypropyl4alkoxycarbonylaminobenzoatesandtheirquaternaryammoniumsalts
AT marvanovapavlina synthesisanalysischolinesteraseinhibitingactivityandmolecularmodellingstudiesof3dialkylamino2hydroxypropyl4alkoxycarbonylaminobenzoatesandtheirquaternaryammoniumsalts
AT odehnalovaklara synthesisanalysischolinesteraseinhibitingactivityandmolecularmodellingstudiesof3dialkylamino2hydroxypropyl4alkoxycarbonylaminobenzoatesandtheirquaternaryammoniumsalts
AT kubinovarenata synthesisanalysischolinesteraseinhibitingactivityandmolecularmodellingstudiesof3dialkylamino2hydroxypropyl4alkoxycarbonylaminobenzoatesandtheirquaternaryammoniumsalts
AT parravicinioscar synthesisanalysischolinesteraseinhibitingactivityandmolecularmodellingstudiesof3dialkylamino2hydroxypropyl4alkoxycarbonylaminobenzoatesandtheirquaternaryammoniumsalts
AT garroadriana synthesisanalysischolinesteraseinhibitingactivityandmolecularmodellingstudiesof3dialkylamino2hydroxypropyl4alkoxycarbonylaminobenzoatesandtheirquaternaryammoniumsalts
AT enrizricardod synthesisanalysischolinesteraseinhibitingactivityandmolecularmodellingstudiesof3dialkylamino2hydroxypropyl4alkoxycarbonylaminobenzoatesandtheirquaternaryammoniumsalts
AT humpaotakar synthesisanalysischolinesteraseinhibitingactivityandmolecularmodellingstudiesof3dialkylamino2hydroxypropyl4alkoxycarbonylaminobenzoatesandtheirquaternaryammoniumsalts
AT oravecmichal synthesisanalysischolinesteraseinhibitingactivityandmolecularmodellingstudiesof3dialkylamino2hydroxypropyl4alkoxycarbonylaminobenzoatesandtheirquaternaryammoniumsalts
AT mokrypetr synthesisanalysischolinesteraseinhibitingactivityandmolecularmodellingstudiesof3dialkylamino2hydroxypropyl4alkoxycarbonylaminobenzoatesandtheirquaternaryammoniumsalts