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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...

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Detalles Bibliográficos
Autores principales: Al-Amiery, Ahmed A., Kadhum, Abdul Amir Hassan, Mohamad, Abu Bakar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
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.
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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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