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dc.creatorTunç, Turgay
dc.date2019-12-16
dc.date.accessioned2020-01-06T20:13:31Z
dc.date.available2020-01-06T20:13:31Z
dc.identifierhttp://www.jcchems.com/index.php/JCCHEMS/article/view/959
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/122362
dc.descriptionThree new Schiff bases bearing benzimidazole and p-toluen sulfonamide moiety were synthesized. Their structures were characterized by elemental analysis, FTIR, NMR and LCMS methods. The antimicrobial properties of the compounds were also evaluated. All compounds exhibit higher antimicrobial activity against all bacteria, Schiff bases (4a-4c) shows more activity than the parent aldehyde (3). 4c displays higher antibacterial activity against P. aeruginosa compare to reference drug Sulfioxazole. The compounds were found more potent against Gram-negative than Gram positive bacteria. One more free phenyl group increase the activity in 4c, but one more phenyl ring in 4b does not.In vitro antifungal activity of the compounds was also tested on fungi C. albicans C. tropicalis and C. krusei. However, our compounds exhibit no antifungal activity against three fungi.  en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherSociedad Chilena de Químicaen-US
dc.relationhttp://www.jcchems.com/index.php/JCCHEMS/article/view/959/342
dc.rightsCopyright (c) 2019 Journal of the Chilean Chemical Societyen-US
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/4.0en-US
dc.sourceJournal of the Chilean Chemical Society; Vol 64 No 4 (2019): Journal of the Chilean Chemical Society; 4590-4592en-US
dc.source0717-9707
dc.source0717-9324
dc.subjectBenzimidazoleen-US
dc.subjectSchiff basesen-US
dc.subjectantimicrobial activity.en-US
dc.titleSYNTHESIS AND ANTIMICROBIAL STUDY OF NEW BENZIMIDAZOLE SCHIFF BASES BEARING P-TOLUENE SULFONAMIDE MOIETYen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion


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