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Synthesis and Antibacterial Activity of Novel Curcumin Derivatives Containing Heterocyclic Moiety

A series of curcumin derivatives containing heterocyclic moiety have been synthesized and evaluated for their antibacterial activities. The chemical structures of the synthesized compounds were verified on the basis of spectral data and elemental analyses. Investigation of antimicrobial activity of...

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Autores principales: A. Hamed, Othman, Mehdawi, Noha, Abu Taha, Adham, M. Hamed, Emad, A. Al-Nuri, Mohammed, S. Hussein, Ayman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shaheed Beheshti University of Medical Sciences 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813224/
https://www.ncbi.nlm.nih.gov/pubmed/24250571
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author A. Hamed, Othman
Mehdawi, Noha
Abu Taha, Adham
M. Hamed, Emad
A. Al-Nuri, Mohammed
S. Hussein, Ayman
author_facet A. Hamed, Othman
Mehdawi, Noha
Abu Taha, Adham
M. Hamed, Emad
A. Al-Nuri, Mohammed
S. Hussein, Ayman
author_sort A. Hamed, Othman
collection PubMed
description A series of curcumin derivatives containing heterocyclic moiety have been synthesized and evaluated for their antibacterial activities. The chemical structures of the synthesized compounds were verified on the basis of spectral data and elemental analyses. Investigation of antimicrobial activity of the derivatives demonstrated the ability to inhibit Gram-positive microorganisms with zone of inhibition ranging from 14-18 mm, MIC ranging between 0.0625 and 0.25 mg/mL. Among all tested derivatives, diazepine 4 exhibited remarkable potency against Gram-positive bacteria S. aureus. An extensive study is underway to optimize the effectiveness of diazepine type of compounds and to determine their mode of action.
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spelling pubmed-38132242013-11-18 Synthesis and Antibacterial Activity of Novel Curcumin Derivatives Containing Heterocyclic Moiety A. Hamed, Othman Mehdawi, Noha Abu Taha, Adham M. Hamed, Emad A. Al-Nuri, Mohammed S. Hussein, Ayman Iran J Pharm Res Original Article A series of curcumin derivatives containing heterocyclic moiety have been synthesized and evaluated for their antibacterial activities. The chemical structures of the synthesized compounds were verified on the basis of spectral data and elemental analyses. Investigation of antimicrobial activity of the derivatives demonstrated the ability to inhibit Gram-positive microorganisms with zone of inhibition ranging from 14-18 mm, MIC ranging between 0.0625 and 0.25 mg/mL. Among all tested derivatives, diazepine 4 exhibited remarkable potency against Gram-positive bacteria S. aureus. An extensive study is underway to optimize the effectiveness of diazepine type of compounds and to determine their mode of action. Shaheed Beheshti University of Medical Sciences 2013 /pmc/articles/PMC3813224/ /pubmed/24250571 Text en © 2013 by School of Pharmacy, Shaheed Beheshti University of Medical Sciences and Health Services This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
A. Hamed, Othman
Mehdawi, Noha
Abu Taha, Adham
M. Hamed, Emad
A. Al-Nuri, Mohammed
S. Hussein, Ayman
Synthesis and Antibacterial Activity of Novel Curcumin Derivatives Containing Heterocyclic Moiety
title Synthesis and Antibacterial Activity of Novel Curcumin Derivatives Containing Heterocyclic Moiety
title_full Synthesis and Antibacterial Activity of Novel Curcumin Derivatives Containing Heterocyclic Moiety
title_fullStr Synthesis and Antibacterial Activity of Novel Curcumin Derivatives Containing Heterocyclic Moiety
title_full_unstemmed Synthesis and Antibacterial Activity of Novel Curcumin Derivatives Containing Heterocyclic Moiety
title_short Synthesis and Antibacterial Activity of Novel Curcumin Derivatives Containing Heterocyclic Moiety
title_sort synthesis and antibacterial activity of novel curcumin derivatives containing heterocyclic moiety
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3813224/
https://www.ncbi.nlm.nih.gov/pubmed/24250571
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