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Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols
New quaternary alkylammonium conjugates of steroids were obtained by two step reaction of sterols (ergosterol, cholesterol, dihydrocholesterol) with bromoacetic acid bromide, followed by bimolecular nucleophilic substitution with a long chain tertiary alkylamine. The structures of products were conf...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270585/ https://www.ncbi.nlm.nih.gov/pubmed/24317524 http://dx.doi.org/10.3390/molecules181214961 |
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author | Brycki, Bogumił Koenig, Hanna Kowalczyk, Iwona Pospieszny, Tomasz |
author_facet | Brycki, Bogumił Koenig, Hanna Kowalczyk, Iwona Pospieszny, Tomasz |
author_sort | Brycki, Bogumił |
collection | PubMed |
description | New quaternary alkylammonium conjugates of steroids were obtained by two step reaction of sterols (ergosterol, cholesterol, dihydrocholesterol) with bromoacetic acid bromide, followed by bimolecular nucleophilic substitution with a long chain tertiary alkylamine. The structures of products were confirmed by spectral ((1)H-NMR, (13)C-NMR, and FT-IR) analysis, mass spectrometry and PM5 semiempirical methods. The pharmacotherapeutic potential of synthesized compounds has been estimated on the basis of Prediction of Activity Spectra for Substances (PASS). |
format | Online Article Text |
id | pubmed-6270585 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62705852018-12-20 Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols Brycki, Bogumił Koenig, Hanna Kowalczyk, Iwona Pospieszny, Tomasz Molecules Article New quaternary alkylammonium conjugates of steroids were obtained by two step reaction of sterols (ergosterol, cholesterol, dihydrocholesterol) with bromoacetic acid bromide, followed by bimolecular nucleophilic substitution with a long chain tertiary alkylamine. The structures of products were confirmed by spectral ((1)H-NMR, (13)C-NMR, and FT-IR) analysis, mass spectrometry and PM5 semiempirical methods. The pharmacotherapeutic potential of synthesized compounds has been estimated on the basis of Prediction of Activity Spectra for Substances (PASS). MDPI 2013-12-05 /pmc/articles/PMC6270585/ /pubmed/24317524 http://dx.doi.org/10.3390/molecules181214961 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Brycki, Bogumił Koenig, Hanna Kowalczyk, Iwona Pospieszny, Tomasz Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols |
title | Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols |
title_full | Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols |
title_fullStr | Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols |
title_full_unstemmed | Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols |
title_short | Synthesis, Spectroscopic and Semiempirical Studies of New Quaternary Alkylammonium Conjugates of Sterols |
title_sort | synthesis, spectroscopic and semiempirical studies of new quaternary alkylammonium conjugates of sterols |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270585/ https://www.ncbi.nlm.nih.gov/pubmed/24317524 http://dx.doi.org/10.3390/molecules181214961 |
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