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New microbial source of the antifungal allylamine “Terbinafine”
The isolated active compound “F12” from the culture media of the Streptomyces sp. KH-F12 was identified using different spectroscopic techniques. Both 1D- and 2D-NMR as well as HRESIMS were utilized to characterize the structure of the isolated compound. ‘F12” was found to be the known systemic anti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357105/ https://www.ncbi.nlm.nih.gov/pubmed/28344499 http://dx.doi.org/10.1016/j.jsps.2016.06.006 |
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author | Abdel-Kader, Maged S. Muharram, Magdy M. |
author_facet | Abdel-Kader, Maged S. Muharram, Magdy M. |
author_sort | Abdel-Kader, Maged S. |
collection | PubMed |
description | The isolated active compound “F12” from the culture media of the Streptomyces sp. KH-F12 was identified using different spectroscopic techniques. Both 1D- and 2D-NMR as well as HRESIMS were utilized to characterize the structure of the isolated compound. ‘F12” was found to be the known systemic antifungal drug terbinafine marketed under the name “Lamisil”. Full analysis of the COSY, HSQC and HMBC enables the full assignment of proton and carbon atoms. Terbinafine is a synthetic allylamine and is reported here for the first time from natural source. |
format | Online Article Text |
id | pubmed-5357105 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-53571052017-03-24 New microbial source of the antifungal allylamine “Terbinafine” Abdel-Kader, Maged S. Muharram, Magdy M. Saudi Pharm J Short Communication The isolated active compound “F12” from the culture media of the Streptomyces sp. KH-F12 was identified using different spectroscopic techniques. Both 1D- and 2D-NMR as well as HRESIMS were utilized to characterize the structure of the isolated compound. ‘F12” was found to be the known systemic antifungal drug terbinafine marketed under the name “Lamisil”. Full analysis of the COSY, HSQC and HMBC enables the full assignment of proton and carbon atoms. Terbinafine is a synthetic allylamine and is reported here for the first time from natural source. Elsevier 2017-03 2016-06-24 /pmc/articles/PMC5357105/ /pubmed/28344499 http://dx.doi.org/10.1016/j.jsps.2016.06.006 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Short Communication Abdel-Kader, Maged S. Muharram, Magdy M. New microbial source of the antifungal allylamine “Terbinafine” |
title | New microbial source of the antifungal allylamine “Terbinafine” |
title_full | New microbial source of the antifungal allylamine “Terbinafine” |
title_fullStr | New microbial source of the antifungal allylamine “Terbinafine” |
title_full_unstemmed | New microbial source of the antifungal allylamine “Terbinafine” |
title_short | New microbial source of the antifungal allylamine “Terbinafine” |
title_sort | new microbial source of the antifungal allylamine “terbinafine” |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357105/ https://www.ncbi.nlm.nih.gov/pubmed/28344499 http://dx.doi.org/10.1016/j.jsps.2016.06.006 |
work_keys_str_mv | AT abdelkadermageds newmicrobialsourceoftheantifungalallylamineterbinafine AT muharrammagdym newmicrobialsourceoftheantifungalallylamineterbinafine |