Publication:
Copper complexes of nicotinic-aromatic carboxylic acids as superoxide dismutase mimetics

dc.contributor.authorSuksrichavalit T.
dc.contributor.authorPrachayasittikul S.
dc.contributor.authorPiacham T.
dc.contributor.authorIsarankura-Na-Ayudhya C.
dc.contributor.authorNantasenamat C.
dc.contributor.authorPrachayasittikul V.
dc.date.accessioned2021-04-05T04:31:57Z
dc.date.available2021-04-05T04:31:57Z
dc.date.issued2008
dc.date.issuedBE2551
dc.description.abstractNicotinic acid (also known as vitamin B3) is a dietary element essential for physiological and antihyperlipidemic functions. This study reports the synthesis of novel mixed ligand complexes of copper with nicotinic and other select carboxylic acids (phthalic, salicylic and anthranilic acids). The tested copper complexes exhibited superoxide dismutase (SOD) mimetic activity and antimicrobial activity against Bacillus subtilis ATCC 6633, with a minimum inhibition concentration of 256 μg/mL. Copper complex of nicotinic-phthalic acids (CuNA/Ph) was the most potent with a SOD mimetic activity of IC 50 34.42 μM. The SOD activities were observed to correlate well with the theoretical parameters as calculated using density functional theory (DFT) at the B3LYP/LANL2DZ level of theory. Interestingly, the SOD activity of the copper complex CuNA/Ph was positively correlated with the electron affinity (EA) value. The two quantum chemical parameters, highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO), were shown to be appropriate for understanding the mechanism of the metal complexes as their calculated energies show good correlation with the SOD activity. Moreover, copper complex with the highest SOD activity were shown to possess the lowest HOMO energy. These findings demonstrate a great potential for the development of value-added metallovitamin-based therapeutics. © 2008 by the authors; licensee Molecular Diversity Preservation International.
dc.format.mimetypeapplication/pdf
dc.identifier.citationMolecules. Vol 13, No.12 (2008), p.3040-3056
dc.identifier.doi10.3390/molecules13123040
dc.identifier.issn14203049
dc.identifier.other2-s2.0-58149292064
dc.identifier.urihttps://hdl.handle.net/20.500.14740/3811
dc.rights.holderScopus
dc.subject.otherAntiinfective agent
dc.subject.otherAromatic hydrocarbon
dc.subject.otherBiomimetic material
dc.subject.otherCarboxylic acid
dc.subject.otherCopper
dc.subject.otherLigand
dc.subject.otherNicotinic acid
dc.subject.otherScavenger
dc.subject.otherSuperoxide
dc.subject.otherSuperoxide dismutase
dc.subject.otherArticle
dc.subject.otherBacterium
dc.subject.otherChemical structure
dc.subject.otherChemistry
dc.subject.otherDrug effect
dc.subject.otherFungus
dc.subject.otherInfrared spectrophotometry
dc.subject.otherMetabolism
dc.subject.otherMicrobiological examination
dc.subject.otherAnti-Infective Agents
dc.subject.otherBacteria
dc.subject.otherBiomimetic Materials
dc.subject.otherCarboxylic Acids
dc.subject.otherCopper
dc.subject.otherFree Radical Scavengers
dc.subject.otherFungi
dc.subject.otherHydrocarbons, Aromatic
dc.subject.otherLigands
dc.subject.otherMicrobial Sensitivity Tests
dc.subject.otherModels, Molecular
dc.subject.otherNiacin
dc.subject.otherSpectrophotometry, Infrared
dc.subject.otherSuperoxide Dismutase
dc.subject.otherSuperoxides
dc.titleCopper complexes of nicotinic-aromatic carboxylic acids as superoxide dismutase mimetics
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-58149292064&doi=10.3390%2fmolecules13123040&partnerID=40&md5=3038492ac5cbd296eda8b53663483bda

Files