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dc.contributor.authorAtes, O
dc.contributor.authorKucukbasmaci, O
dc.contributor.authorKiraz, M
dc.contributor.authorYegenoglu, Y
dc.contributor.authorUlusoy, N
dc.date.accessioned2021-03-04T12:03:23Z
dc.date.available2021-03-04T12:03:23Z
dc.date.issued2003
dc.identifier.citationUlusoy N., Ates O., Kucukbasmaci O., Kiraz M., Yegenoglu Y., "Synthesis, characterization, and evaluation of antimicrobial activity of some 1,2,4-triazole derivatives bearing an antipyryl moiety", MONATSHEFTE FUR CHEMIE, cilt.134, sa.3, ss.465-474, 2003
dc.identifier.issn0026-9247
dc.identifier.otherav_7579d9ed-37bc-4ccd-af9c-ec05dd8f8687
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/80675
dc.identifier.urihttps://doi.org/10.1007/s00706-002-0546-z
dc.description.abstractSome novel 4-[[2-[[5-(2-furanyl)-4-alkyl/aryl-4H-1,2,4-triazol-3-yl]thio]-acetyl/propionyl] -amino]-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazoles were synthesized and evaluated for in vitro antibacterial activity against Staphylococcus aureus ATCC 29213, Pseudomonas aeruginosa ATCC 27853, Escherichia coli ATCC 25922, and Enterococcus faecalis ATCC 29212 and antifungal activity against Candida albicans ATCC 10231, Candida parapsilosis ATCC 22019, Candida krusei ATCC 6258, Candida parapsilosis, Trichophyton mentagrophytes var. erinacei NCPF 375, Microsporum gypseum NCPF 580, and Trichophyton rubrum using the microbroth dilution method. All of the compounds were found to be ineffective against the above bacteria within the applied MIC ranges. On the other hand, they were effective against fungi to different degrees. Three compounds showed high activity against C. parapsilosis and T mentagrophytes var erinacei NCPF 375 (MIC = 8 mug cm(-3)). The in vitro antimycobacterial activity of the new compounds was also investigated against Mycobacterium tuberculosis H37RV (ATCC 27294) in BACTEC 12B medium using a broth microdilution assay, the Microplate Alamar Blue Assay (MABA). Compounds exhibiting fluorescence were tested in the BACTEC 460 radiometric system. The most active compound was found with 66% inhibition at > 6.25 mug cm(-3).
dc.language.isoeng
dc.subjectTemel Bilimler (SCI)
dc.subjectAlkoloidler
dc.subjectKİMYA, MULTİDİSİPLİNER
dc.subjectKimya
dc.subjectBiyokimya
dc.subjectTemel Bilimler
dc.titleSynthesis, characterization, and evaluation of antimicrobial activity of some 1,2,4-triazole derivatives bearing an antipyryl moiety
dc.typeMakale
dc.relation.journalMONATSHEFTE FUR CHEMIE
dc.contributor.department, ,
dc.identifier.volume134
dc.identifier.issue3
dc.identifier.startpage465
dc.identifier.endpage474
dc.contributor.firstauthorID167750


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