Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/80029
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorFang, Z-
dc.creatorBan, L-
dc.creatorLi, Y-
dc.creatorYuan, W-
dc.creatorLiu, Z-
dc.creatorLiu, T-
dc.creatorLi, X-
dc.creatorWong, KY-
dc.creatorLu, Y-
dc.creatorSun, N-
dc.creatorYao, X-
dc.date.accessioned2018-12-21T07:14:42Z-
dc.date.available2018-12-21T07:14:42Z-
dc.identifier.issn1347-8613-
dc.identifier.urihttp://hdl.handle.net/10397/80029-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rights© 2018 The Authors. Production and hosting by Elsevier B.V. on behalf of Japanese Pharmacological Society. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication Fang, Z., Ban, L., Li, Y., Yuan, W., Liu, Z., Liu, T., . . . Yao, X. (2018). A quinoline-based FtsZ inhibitor for the study of antimicrobial activity and synergistic effects with β-lactam antibiotics. Journal of Pharmacological Sciences, 137(3), 283-289 is available at https://dx.doi.org/10.1016/j.jphs.2018.07.005en_US
dc.subjectAntibacterial activityen_US
dc.subjectBacterial resistanceen_US
dc.subjectCell divisionen_US
dc.subjectFtsZ inhibitoren_US
dc.subjectSynergistic effecten_US
dc.titleA quinoline-based FtsZ inhibitor for the study of antimicrobial activity and synergistic effects with β-lactam antibioticsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage283-
dc.identifier.epage289-
dc.identifier.volume137-
dc.identifier.issue3-
dc.identifier.doi10.1016/j.jphs.2018.07.005-
dcterms.abstractThe antibacterial activity and the synergistic effect with β-lactam antibiotics of a new 1-methylquinolinium iodide derivative were investigated. The experimental results indicate that the compound possesses a strong antibacterial activity against a panel of bacteria including methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus and NDM-1 Escherichia coli with the MIC values from 0.75 μg/mL to 6 μg/mL. In addition, this compound combined with β-lactam antibiotics shows strong synergistic antimicrobial activities against antibiotic-resistant strains of S. aureus. The results of biochemical studies also reveal that this compound can effectively disrupt GTPase activity, polymerization of FtsZ, and cell division to cause cell death. The compound shows high potential for further development as a new generation of antibacterial agents to fight against the emergence of multidrug-resistant bacteria.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of pharmacological sciences, 2018, v. 137, no. 3, p. 283-289-
dcterms.isPartOfJournal of pharmacological sciences-
dcterms.issued2018-
dc.identifier.scopus2-s2.0-85050403272-
dc.identifier.eissn1347-8648-
dc.description.validate201812 bcrc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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