Influence of the aryl substituent identity in 4-arylamino- 3-nitrocoumarins on their antimicrobial activity

dc.contributor.authorĐekić, Vera
dc.contributor.authorRadulovic, Niko
dc.contributor.authorVukicevic, Rastko
dc.contributor.authorDekić B.
dc.contributor.authorStojanovic-Radic Z.
dc.contributor.authorPalić R.
dc.date.accessioned2020-09-19T18:55:17Z
dc.date.available2020-09-19T18:55:17Z
dc.date.issued2011
dc.description.abstractTwo new and six previously known coumarin derivatives with promising biological properties were synthesized in moderate to good yields by reaction of 4-chloro-3-nitro-coumarin and the appropriate arylamine in ethyl acetate in the presence of triethylamine. The synthesized compounds were evaluated for their in vitro antibacterial and antifungal activities against pathogenic strains. A correlation between the aryl substituent identity and antimicrobial activity was discussed. © 2011 Academic Journals.
dc.identifier.doi10.5897/AJPP10.408
dc.identifier.scopus2-s2.0-79957949391
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/9702
dc.rightsopenAccess
dc.rights.licenseBY-NC-ND
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceAfrican Journal of Pharmacy and Pharmacology
dc.titleInfluence of the aryl substituent identity in 4-arylamino- 3-nitrocoumarins on their antimicrobial activity
dc.typearticle

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