Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/14049
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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.identifier.issn18117775
dc.identifier.other2-s2.0-84878828933
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/14049-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84878828933&doi=10.3923%2fijp.2013.170.175&partnerID=40&md5=80a8a2ebf24a7c99612afad3630a221b
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.subject5 nitrouracil
dc.subject8 quinolinol
dc.subject8 quinolinol copper 5 iodouracil
dc.subject8 quinolinol copper 5 nitrouracil
dc.subject8 quinolinol derivative
dc.subject8 quinolinol manganese 5 iodouracil
dc.subject8 quinolinol manganese 5 nitrouracil
dc.subject8 quinolinol nickel 5 iodouracil
dc.subject8 quinolinol nickel 5 nitrouracil
dc.subjectampicillin
dc.subjectantiinfective agent
dc.subjectcopper
dc.subjectheterocyclic compound
dc.subjectiodouracil
dc.subjectmanganese
dc.subjectnatural product
dc.subjectnickel
dc.subjectnitrogen oxide
dc.subjecttransition element
dc.subjectunclassified drug
dc.subjecturacil
dc.subjecturacil derivative
dc.subjectantimicrobial activity
dc.subjectarticle
dc.subjectbacterial strain
dc.subjectCandida albicans
dc.subjectcomplex formation
dc.subjectcontrolled study
dc.subjectdrug design
dc.subjectdrug potency
dc.subjectdrug structure
dc.subjectdrug synthesis
dc.subjectEnterococcus faecalis
dc.subjectGram negative bacterium
dc.subjectGram positive bacterium
dc.subjectgrowth inhibition
dc.subjectminimum inhibitory concentration
dc.subjectnonhuman
dc.subjectStaphylococcus aureus
dc.titleAntimicrobial activity of 8-hydroxyquinoline and transition metal complexes
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationInternational Journal of Pharmacology. Vol 9, No.2 (2013), p.170-175
dc.identifier.doi10.3923/ijp.2013.170.175
Appears in Collections:Scopus 1983-2021

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