Publication:
Antimicrobial activity of 8-hydroxyquinoline and transition metal complexes

dc.contributor.authorSrisung S.
dc.contributor.authorSuksrichavalit T.
dc.contributor.authorPrachayasittikul S.
dc.contributor.authorRuchirawat S.
dc.contributor.authorPrachayasittikul V.
dc.date.accessioned2021-04-05T03:32:59Z
dc.date.available2021-04-05T03:32:59Z
dc.date.issued2013
dc.date.issuedBE2556
dc.description.abstractHeterocyclic compounds like 8-hydroxyquinoline (8HQ) and derivatives have been found in natural products and therapeutics. Herein 8HQ and metal complexes of 8HQ-5-substituted (X) uracils, X = I, N02 (1-6) were investigated for their antimicrobial potency. The complexes 1 -6 exhibited growth inhibition against many strains of gram-positive and gram-negative bacteria with minimum inhibitory concentrations (MICs) of 575.71-718.76 uM. The investigated compound 8HQ was shown to be a very strong antimicrobial agent with the MIC of 27.58 uM that comparable to ampicillin (MIC 26.93 uM), the reference drug. The activity of 8HQ mostly was observed for resistant pathogens, gram- positive bacteria e.g. Staphylococcus aureus, Enterococcus faecalis and diploid fungus, Candida albicans. The findings reveal 8HQ as the very potent antimicrobial agent and a series of 8HQ transition metal complexes as novel antimicrobials as well as the applications of 8HQ for the design and synthesis of new and potential therapeutic lead compounds. © 2013 Asian Network for Scientific Information.
dc.format.mimetypeapplication/pdf
dc.identifier.citationInternational Journal of Pharmacology. Vol 9, No.2 (2013), p.170-175
dc.identifier.doi10.3923/ijp.2013.170.175
dc.identifier.issn18117775
dc.identifier.other2-s2.0-84878828933
dc.identifier.urihttps://hdl.handle.net/20.500.14740/6640
dc.rights.holderScopus
dc.subject.other5 nitrouracil
dc.subject.other8 quinolinol
dc.subject.other8 quinolinol copper 5 iodouracil
dc.subject.other8 quinolinol copper 5 nitrouracil
dc.subject.other8 quinolinol derivative
dc.subject.other8 quinolinol manganese 5 iodouracil
dc.subject.other8 quinolinol manganese 5 nitrouracil
dc.subject.other8 quinolinol nickel 5 iodouracil
dc.subject.other8 quinolinol nickel 5 nitrouracil
dc.subject.otherAmpicillin
dc.subject.otherAntiinfective agent
dc.subject.otherCopper
dc.subject.otherHeterocyclic compound
dc.subject.otherIodouracil
dc.subject.otherManganese
dc.subject.otherNatural product
dc.subject.otherNickel
dc.subject.otherNitrogen oxide
dc.subject.otherTransition element
dc.subject.otherUnclassified drug
dc.subject.otherUracil
dc.subject.otherUracil derivative
dc.subject.otherAntimicrobial activity
dc.subject.otherArticle
dc.subject.otherBacterial strain
dc.subject.otherCandida albicans
dc.subject.otherComplex formation
dc.subject.otherControlled study
dc.subject.otherDrug design
dc.subject.otherDrug potency
dc.subject.otherDrug structure
dc.subject.otherDrug synthesis
dc.subject.otherEnterococcus faecalis
dc.subject.otherGram negative bacterium
dc.subject.otherGram positive bacterium
dc.subject.otherGrowth inhibition
dc.subject.otherMinimum inhibitory concentration
dc.subject.otherNonhuman
dc.subject.otherStaphylococcus aureus
dc.titleAntimicrobial activity of 8-hydroxyquinoline and transition metal complexes
dc.typeArticle
dspace.entity.typePublication
swu.datasource.scopushttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84878828933&doi=10.3923%2fijp.2013.170.175&partnerID=40&md5=80a8a2ebf24a7c99612afad3630a221b

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