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The Qsar Study of Azole Derivatives Using Molecular Descriptors for Quantum Molecular States

ABSTRACT: Azoles are the main antifungal agents currently used in systemic therapy and local mycoses. The class of azole derivatives has been studied using fingerprint descriptors based on electronegativity of the occupied molecular orbitals (OMO) and unoccupied molecular orbitals (UMO). The Hansch...

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Autores principales: AMZOIU, M.O., CRISTEA, O.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medical University Publishing House Craiova 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256163/
https://www.ncbi.nlm.nih.gov/pubmed/30568822
http://dx.doi.org/10.12865/CHSJ.42.02.02
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author AMZOIU, M.O.
CRISTEA, O.M.
author_facet AMZOIU, M.O.
CRISTEA, O.M.
author_sort AMZOIU, M.O.
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description ABSTRACT: Azoles are the main antifungal agents currently used in systemic therapy and local mycoses. The class of azole derivatives has been studied using fingerprint descriptors based on electronegativity of the occupied molecular orbitals (OMO) and unoccupied molecular orbitals (UMO). The Hansch equations that correlates partition coefficient with chemical structure allows us to identify the nature of the atoms involved in ligand (drug) – receptor interactions, as well as the nature of those interactions. The results indicate that in the most reactive molecular states, such as states HOMO and LUMO, the oxygen atoms are actually involved in the interaction of the ligand - receptor by the transfer of electrons from the biological receptor to the oxygen atoms.
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spelling pubmed-62561632018-12-19 The Qsar Study of Azole Derivatives Using Molecular Descriptors for Quantum Molecular States AMZOIU, M.O. CRISTEA, O.M. Curr Health Sci J Original Paper ABSTRACT: Azoles are the main antifungal agents currently used in systemic therapy and local mycoses. The class of azole derivatives has been studied using fingerprint descriptors based on electronegativity of the occupied molecular orbitals (OMO) and unoccupied molecular orbitals (UMO). The Hansch equations that correlates partition coefficient with chemical structure allows us to identify the nature of the atoms involved in ligand (drug) – receptor interactions, as well as the nature of those interactions. The results indicate that in the most reactive molecular states, such as states HOMO and LUMO, the oxygen atoms are actually involved in the interaction of the ligand - receptor by the transfer of electrons from the biological receptor to the oxygen atoms. Medical University Publishing House Craiova 2016 2016-06-28 /pmc/articles/PMC6256163/ /pubmed/30568822 http://dx.doi.org/10.12865/CHSJ.42.02.02 Text en Copyright © 2016, Medical University Publishing House Craiova http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an open-access article distributed under the terms of a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License, which permits unrestricted use, adaptation, distribution and reproduction in any medium, non-commercially, provided the new creations are licensed under identical terms as the original work and the original work is properly cited.
spellingShingle Original Paper
AMZOIU, M.O.
CRISTEA, O.M.
The Qsar Study of Azole Derivatives Using Molecular Descriptors for Quantum Molecular States
title The Qsar Study of Azole Derivatives Using Molecular Descriptors for Quantum Molecular States
title_full The Qsar Study of Azole Derivatives Using Molecular Descriptors for Quantum Molecular States
title_fullStr The Qsar Study of Azole Derivatives Using Molecular Descriptors for Quantum Molecular States
title_full_unstemmed The Qsar Study of Azole Derivatives Using Molecular Descriptors for Quantum Molecular States
title_short The Qsar Study of Azole Derivatives Using Molecular Descriptors for Quantum Molecular States
title_sort qsar study of azole derivatives using molecular descriptors for quantum molecular states
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6256163/
https://www.ncbi.nlm.nih.gov/pubmed/30568822
http://dx.doi.org/10.12865/CHSJ.42.02.02
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