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Antifungal Activities of New Coumarins
Newly synthesized coumarins 4-((5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)-methoxy)-2H-chromen-2-one and 4-((5-(phenylamino)-1,3,4-thiadiazol-2-yl)-methoxy)-2H-chromen-2-one were tested against selected types of fungi and showed significant activities. DFT calculations of the synthesized coumarins w...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268721/ https://www.ncbi.nlm.nih.gov/pubmed/22628043 http://dx.doi.org/10.3390/molecules17055713 |
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author | Al-Amiery, Ahmed A. Kadhum, Abdul Amir Hassan Mohamad, Abu Bakar |
author_facet | Al-Amiery, Ahmed A. Kadhum, Abdul Amir Hassan Mohamad, Abu Bakar |
author_sort | Al-Amiery, Ahmed A. |
collection | PubMed |
description | Newly synthesized coumarins 4-((5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)-methoxy)-2H-chromen-2-one and 4-((5-(phenylamino)-1,3,4-thiadiazol-2-yl)-methoxy)-2H-chromen-2-one were tested against selected types of fungi and showed significant activities. DFT calculations of the synthesized coumarins were performed using molecular structures with optimized geometries. Molecular orbital calculations provide a detailed description of the orbitals, including spatial characteristics, nodal patterns, and the contributions of individual atoms. |
format | Online Article Text |
id | pubmed-6268721 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62687212018-12-20 Antifungal Activities of New Coumarins Al-Amiery, Ahmed A. Kadhum, Abdul Amir Hassan Mohamad, Abu Bakar Molecules Article Newly synthesized coumarins 4-((5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)-methoxy)-2H-chromen-2-one and 4-((5-(phenylamino)-1,3,4-thiadiazol-2-yl)-methoxy)-2H-chromen-2-one were tested against selected types of fungi and showed significant activities. DFT calculations of the synthesized coumarins were performed using molecular structures with optimized geometries. Molecular orbital calculations provide a detailed description of the orbitals, including spatial characteristics, nodal patterns, and the contributions of individual atoms. MDPI 2012-05-14 /pmc/articles/PMC6268721/ /pubmed/22628043 http://dx.doi.org/10.3390/molecules17055713 Text en © 2012 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 Al-Amiery, Ahmed A. Kadhum, Abdul Amir Hassan Mohamad, Abu Bakar Antifungal Activities of New Coumarins |
title | Antifungal Activities of New Coumarins |
title_full | Antifungal Activities of New Coumarins |
title_fullStr | Antifungal Activities of New Coumarins |
title_full_unstemmed | Antifungal Activities of New Coumarins |
title_short | Antifungal Activities of New Coumarins |
title_sort | antifungal activities of new coumarins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268721/ https://www.ncbi.nlm.nih.gov/pubmed/22628043 http://dx.doi.org/10.3390/molecules17055713 |
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