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Synthesis and antioxidant evaluation of some novel ortho-hydroxypyridine-4-one iron chelators

A series of ortho-hydroxypyridine-4-ones were prepared in high yields and evaluated for antioxidant and iron chelating activities. N(1)-H hydroxypyridinones Va, Vb, and Ve were the best radical scavengers in DPPH free radical scavenging assay. Compound Vb was proved to be the most potent compound in...

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Autores principales: Mohammadpour, M., Sadeghi, A., Fassihi, A., Saghaei, L., Movahedian, A., Rostami, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501926/
https://www.ncbi.nlm.nih.gov/pubmed/23181095
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author Mohammadpour, M.
Sadeghi, A.
Fassihi, A.
Saghaei, L.
Movahedian, A.
Rostami, M.
author_facet Mohammadpour, M.
Sadeghi, A.
Fassihi, A.
Saghaei, L.
Movahedian, A.
Rostami, M.
author_sort Mohammadpour, M.
collection PubMed
description A series of ortho-hydroxypyridine-4-ones were prepared in high yields and evaluated for antioxidant and iron chelating activities. N(1)-H hydroxypyridinones Va, Vb, and Ve were the best radical scavengers in DPPH free radical scavenging assay. Compound Vb was proved to be the most potent compound in hydrogen peroxide scavenging assay. All of the synthesized compounds had very close chelating ability, compounds containing N(1)-CH3 hydroxypyridinone ring were stronger chelating agents.
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spelling pubmed-35019262012-11-23 Synthesis and antioxidant evaluation of some novel ortho-hydroxypyridine-4-one iron chelators Mohammadpour, M. Sadeghi, A. Fassihi, A. Saghaei, L. Movahedian, A. Rostami, M. Res Pharm Sci Original Article A series of ortho-hydroxypyridine-4-ones were prepared in high yields and evaluated for antioxidant and iron chelating activities. N(1)-H hydroxypyridinones Va, Vb, and Ve were the best radical scavengers in DPPH free radical scavenging assay. Compound Vb was proved to be the most potent compound in hydrogen peroxide scavenging assay. All of the synthesized compounds had very close chelating ability, compounds containing N(1)-CH3 hydroxypyridinone ring were stronger chelating agents. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3501926/ /pubmed/23181095 Text en Copyright: © Journal of Research in Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Mohammadpour, M.
Sadeghi, A.
Fassihi, A.
Saghaei, L.
Movahedian, A.
Rostami, M.
Synthesis and antioxidant evaluation of some novel ortho-hydroxypyridine-4-one iron chelators
title Synthesis and antioxidant evaluation of some novel ortho-hydroxypyridine-4-one iron chelators
title_full Synthesis and antioxidant evaluation of some novel ortho-hydroxypyridine-4-one iron chelators
title_fullStr Synthesis and antioxidant evaluation of some novel ortho-hydroxypyridine-4-one iron chelators
title_full_unstemmed Synthesis and antioxidant evaluation of some novel ortho-hydroxypyridine-4-one iron chelators
title_short Synthesis and antioxidant evaluation of some novel ortho-hydroxypyridine-4-one iron chelators
title_sort synthesis and antioxidant evaluation of some novel ortho-hydroxypyridine-4-one iron chelators
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501926/
https://www.ncbi.nlm.nih.gov/pubmed/23181095
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