Publication:
Copper complexes of pyridine derivatives with superoxide scavenging and antimicrobial activities

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.date.issuedBE2552
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.format.mimetypeapplication/pdf
dc.identifier.citationEuropean Journal of Medicinal Chemistry. Vol 44, No.8 (2009), p.3259-3265
dc.identifier.doi10.1016/j.ejmech.2009.03.033
dc.identifier.issn2235234
dc.identifier.other2-s2.0-67349216170
dc.identifier.urihttps://hdl.handle.net/20.500.14740/5927
dc.rights.holderมหาวิทยาลัยศรีนครินทรวิโรฒ
dc.subject.other2 aminopyridine
dc.subject.otherAmpicillin
dc.subject.otherCopper complex
dc.subject.otherNicotinic acid
dc.subject.otherNicotinic acid 2 aminopyridine copper complex
dc.subject.otherNicotinic acid 2 hydroxypyridine copper complex
dc.subject.otherNicotinic acid picolinic acid copper complex
dc.subject.otherPicolinic acid
dc.subject.otherPyridine derivative
dc.subject.otherReactive oxygen metabolite
dc.subject.otherSuperoxide
dc.subject.otherSuperoxide dismutase
dc.subject.otherUnclassified drug
dc.subject.otherAeromonas hydrophila
dc.subject.otherAntimicrobial activity
dc.subject.otherAntioxidant activity
dc.subject.otherArticle
dc.subject.otherBacillus cereus
dc.subject.otherBacillus subtilis
dc.subject.otherCandida albicans
dc.subject.otherCitrobacter freundii
dc.subject.otherDensity functional theory
dc.subject.otherDrug synthesis
dc.subject.otherEnzyme activity
dc.subject.otherIC 50
dc.subject.otherInfrared spectroscopy
dc.subject.otherListeria monocytogenes
dc.subject.otherMinimum inhibitory concentration
dc.subject.otherMolecular model
dc.subject.otherMorganella morganii
dc.subject.otherNonhuman
dc.subject.otherPlesiomonas shigelloides
dc.subject.otherQuantum chemistry
dc.subject.otherSalmonella enteritidis
dc.subject.otherShigella dysenteriae
dc.subject.otherStreptococcus pyogenes
dc.subject.otherAnti-Infective Agents
dc.subject.otherBacteria
dc.subject.otherBiomimetics
dc.subject.otherCopper
dc.subject.otherFree Radical Scavengers
dc.subject.otherInhibitory Concentration 50
dc.subject.otherModels, Molecular
dc.subject.otherMolecular Conformation
dc.subject.otherOrganometallic Compounds
dc.subject.otherPyridines
dc.subject.otherQuantum Theory
dc.subject.otherSpectrophotometry, Infrared
dc.subject.otherSuperoxide Dismutase
dc.subject.otherSuperoxides
dc.subject.otherYeasts
dc.titleCopper complexes of pyridine derivatives with superoxide scavenging and antimicrobial activities
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-67349216170&doi=10.1016%2fj.ejmech.2009.03.033&partnerID=40&md5=73f0d3868a1c097b7b3c7acf01ce1bec

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