Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/15043
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dc.contributor.authorSuksrichavalit T.
dc.contributor.authorPrachayasittikul S.
dc.contributor.authorNantasenamat C.
dc.contributor.authorIsarankura-Na-Ayudhya C.
dc.contributor.authorPrachayasittikul V.
dc.date.accessioned2021-04-05T04:32:24Z-
dc.date.available2021-04-05T04:32:24Z-
dc.date.issued2009
dc.identifier.issn2235234
dc.identifier.other2-s2.0-67349216170
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/15043-
dc.identifier.urihttps://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.abstractSuperoxide 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.subject2 aminopyridine
dc.subjectampicillin
dc.subjectcopper complex
dc.subjectnicotinic acid
dc.subjectnicotinic acid 2 aminopyridine copper complex
dc.subjectnicotinic acid 2 hydroxypyridine copper complex
dc.subjectnicotinic acid picolinic acid copper complex
dc.subjectpicolinic acid
dc.subjectpyridine derivative
dc.subjectreactive oxygen metabolite
dc.subjectsuperoxide
dc.subjectsuperoxide dismutase
dc.subjectunclassified drug
dc.subjectAeromonas hydrophila
dc.subjectantimicrobial activity
dc.subjectantioxidant activity
dc.subjectarticle
dc.subjectBacillus cereus
dc.subjectBacillus subtilis
dc.subjectCandida albicans
dc.subjectCitrobacter freundii
dc.subjectdensity functional theory
dc.subjectdrug synthesis
dc.subjectenzyme activity
dc.subjectIC 50
dc.subjectinfrared spectroscopy
dc.subjectListeria monocytogenes
dc.subjectminimum inhibitory concentration
dc.subjectmolecular model
dc.subjectMorganella morganii
dc.subjectnonhuman
dc.subjectPlesiomonas shigelloides
dc.subjectquantum chemistry
dc.subjectSalmonella enteritidis
dc.subjectShigella dysenteriae
dc.subjectStreptococcus pyogenes
dc.subjectAnti-Infective Agents
dc.subjectBacteria
dc.subjectBiomimetics
dc.subjectCopper
dc.subjectFree Radical Scavengers
dc.subjectInhibitory Concentration 50
dc.subjectModels, Molecular
dc.subjectMolecular Conformation
dc.subjectOrganometallic Compounds
dc.subjectPyridines
dc.subjectQuantum Theory
dc.subjectSpectrophotometry, Infrared
dc.subjectSuperoxide Dismutase
dc.subjectSuperoxides
dc.subjectYeasts
dc.titleCopper complexes of pyridine derivatives with superoxide scavenging and antimicrobial activities
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationEuropean Journal of Medicinal Chemistry. Vol 44, No.8 (2009), p.3259-3265
dc.identifier.doi10.1016/j.ejmech.2009.03.033
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