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Copper complexes of pyridine derivatives with superoxide scavenging and antimicrobial activities

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dc.contributor.author Suksrichavalit T.
dc.contributor.author Prachayasittikul S.
dc.contributor.author Nantasenamat C.
dc.contributor.author Isarankura-Na-Ayudhya C.
dc.contributor.author Prachayasittikul V.
dc.date.accessioned 2021-04-05T04:32:24Z
dc.date.available 2021-04-05T04:32:24Z
dc.date.issued 2009
dc.identifier.issn 2235234
dc.identifier.other 2-s2.0-67349216170
dc.identifier.uri https://ir.swu.ac.th/jspui/handle/123456789/15043
dc.identifier.uri https://www.scopus.com/inward/record.uri?eid=2-s2.0-67349216170&doi=10.1016%2fj.ejmech.2009.03.033&partnerID=40&md5=73f0d3868a1c097b7b3c7acf01ce1bec
dc.description.abstract Superoxide anions are reactive oxygen species that can attack biomolecules such as DNA, lipids and proteins to cause many serious diseases. This study reports the synthesis of copper complexes of nicotinic acid with related pyridine derivatives. The copper complexes were shown to possess superoxide dismutase (SOD) and antimicrobial activities. The copper complexes exerted SOD activity in range of 49.07-130.23 μM. Particularly, copper complex of nicotinic acid with 2-hydroxypyridine was the most potent SOD mimic with an IC50 of 49.07 μM. In addition, the complexes exhibited antimicrobial activity against Bacillus subtilis ATCC 6633 and Candida albicans ATCC 90028 with MIC range of 128-256 μg/mL. The SOD activities were well correlated with the theoretical parameters as calculated by density functional theory at the B3LYP/LANL2DZ level of theory. Interestingly, the SOD activity of the copper complexes was demonstrated to be inversely correlated with the electron affinity, but was well correlated with both HOMO and LUMO energies. The vitamin-metal complexes described in this report are great examples of the value-added benefits of vitamins for medicinal applications. © 2009 Elsevier Masson SAS. All rights reserved.
dc.subject 2 aminopyridine
dc.subject ampicillin
dc.subject copper complex
dc.subject nicotinic acid
dc.subject nicotinic acid 2 aminopyridine copper complex
dc.subject nicotinic acid 2 hydroxypyridine copper complex
dc.subject nicotinic acid picolinic acid copper complex
dc.subject picolinic acid
dc.subject pyridine derivative
dc.subject reactive oxygen metabolite
dc.subject superoxide
dc.subject superoxide dismutase
dc.subject unclassified drug
dc.subject Aeromonas hydrophila
dc.subject antimicrobial activity
dc.subject antioxidant activity
dc.subject article
dc.subject Bacillus cereus
dc.subject Bacillus subtilis
dc.subject Candida albicans
dc.subject Citrobacter freundii
dc.subject density functional theory
dc.subject drug synthesis
dc.subject enzyme activity
dc.subject IC 50
dc.subject infrared spectroscopy
dc.subject Listeria monocytogenes
dc.subject minimum inhibitory concentration
dc.subject molecular model
dc.subject Morganella morganii
dc.subject nonhuman
dc.subject Plesiomonas shigelloides
dc.subject quantum chemistry
dc.subject Salmonella enteritidis
dc.subject Shigella dysenteriae
dc.subject Streptococcus pyogenes
dc.subject Anti-Infective Agents
dc.subject Bacteria
dc.subject Biomimetics
dc.subject Copper
dc.subject Free Radical Scavengers
dc.subject Inhibitory Concentration 50
dc.subject Models, Molecular
dc.subject Molecular Conformation
dc.subject Organometallic Compounds
dc.subject Pyridines
dc.subject Quantum Theory
dc.subject Spectrophotometry, Infrared
dc.subject Superoxide Dismutase
dc.subject Superoxides
dc.subject Yeasts
dc.title Copper complexes of pyridine derivatives with superoxide scavenging and antimicrobial activities
dc.type Article
dc.rights.holder Scopus
dc.identifier.bibliograpycitation European Journal of Medicinal Chemistry. Vol 44, No.8 (2009), p.3259-3265
dc.identifier.doi 10.1016/j.ejmech.2009.03.033


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