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Conformational analysis of flephedrone using quantum mechanical models

Flephedrone is an analogue of cathinone - chemically similar to ephedrine, cathine and other amphetamines. Conformations of all isomers of flephedrone have been studied at the quantum-chemical level. Calculations have been performed using DFT and MP2 methods with two basis sets - 6-31G and 6-31G(d,p...

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Autores principales: Kolodziejczyk, Wojciech, Jodkowski, Jerzy, Holmes, Tiffani M., Hill, Glake A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3578731/
https://www.ncbi.nlm.nih.gov/pubmed/23239394
http://dx.doi.org/10.1007/s00894-012-1673-z
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author Kolodziejczyk, Wojciech
Jodkowski, Jerzy
Holmes, Tiffani M.
Hill, Glake A.
author_facet Kolodziejczyk, Wojciech
Jodkowski, Jerzy
Holmes, Tiffani M.
Hill, Glake A.
author_sort Kolodziejczyk, Wojciech
collection PubMed
description Flephedrone is an analogue of cathinone - chemically similar to ephedrine, cathine and other amphetamines. Conformations of all isomers of flephedrone have been studied at the quantum-chemical level. Calculations have been performed using DFT and MP2 methods with two basis sets - 6-31G and 6-31G(d,p). Results show that there are low energy conformers for the ortho, meta, and para isomers that are connected by way of low-barrier transition states. Boltzmann distribution of population predicts the highest population for the 1-meta conformer with a 10 % increase in solution. The molecular electrostatic potential surface data for each molecule has been calculated revealing likely reaction sites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00894-012-1673-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-35787312013-02-26 Conformational analysis of flephedrone using quantum mechanical models Kolodziejczyk, Wojciech Jodkowski, Jerzy Holmes, Tiffani M. Hill, Glake A. J Mol Model Original Paper Flephedrone is an analogue of cathinone - chemically similar to ephedrine, cathine and other amphetamines. Conformations of all isomers of flephedrone have been studied at the quantum-chemical level. Calculations have been performed using DFT and MP2 methods with two basis sets - 6-31G and 6-31G(d,p). Results show that there are low energy conformers for the ortho, meta, and para isomers that are connected by way of low-barrier transition states. Boltzmann distribution of population predicts the highest population for the 1-meta conformer with a 10 % increase in solution. The molecular electrostatic potential surface data for each molecule has been calculated revealing likely reaction sites. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00894-012-1673-z) contains supplementary material, which is available to authorized users. Springer-Verlag 2012-12-14 2013 /pmc/articles/PMC3578731/ /pubmed/23239394 http://dx.doi.org/10.1007/s00894-012-1673-z Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/2.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Kolodziejczyk, Wojciech
Jodkowski, Jerzy
Holmes, Tiffani M.
Hill, Glake A.
Conformational analysis of flephedrone using quantum mechanical models
title Conformational analysis of flephedrone using quantum mechanical models
title_full Conformational analysis of flephedrone using quantum mechanical models
title_fullStr Conformational analysis of flephedrone using quantum mechanical models
title_full_unstemmed Conformational analysis of flephedrone using quantum mechanical models
title_short Conformational analysis of flephedrone using quantum mechanical models
title_sort conformational analysis of flephedrone using quantum mechanical models
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3578731/
https://www.ncbi.nlm.nih.gov/pubmed/23239394
http://dx.doi.org/10.1007/s00894-012-1673-z
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