Publication:
The synthesis and antitubercular activity of substituted hydrazone,2-pyrazoline-5-one and 2-isoxazoline-5-one derivatives possessing 1,3,4-thiadiazole moiety [1,3,4-Tiyadiazol halkası içeren hidrazon, 2-pirazol-5-on ve 2-izoksazol-5-on türevi bileşiklerin sentezi ve antitüberküler aktiviteleri]

dc.contributor.authorsOral B., Rollas S.
dc.date.accessioned2022-03-15T02:09:38Z
dc.date.accessioned2026-01-10T19:06:50Z
dc.date.available2022-03-15T02:09:38Z
dc.date.issued2012
dc.description.abstractNovel derivatives of substituted hydrazone (2a-e), 2-pyrazoline-5-one (3a-e, 4ae) and 2-isoxazoline-5-one (5a-e) derivatives possessing 1,3,4-thiadiazole moiety were synthesized and evaluated for their antitubercular activity. The highest inhibitions were observed with the synthesized compounds are 87% for 3-methyl-4-[4-(5-cyclohexylamino- 1,3,4-thiadiazole-2-yl)phenylhydrazono]-2-isoxazoline-5-one (5b) and 86% for ethyl 2-[4-(5-cyclohexylamino-1,3,4-thiadiazole-2-yl)phenylhydrazono]-3-oxobutirate (2b). Compounds 2b and 5b could be a good initial point to develop new lead compound.
dc.identifier.doi10.12991/201216402
dc.identifier.issn13090801
dc.identifier.urihttps://hdl.handle.net/11424/247233
dc.language.isoeng
dc.publisherMarmara University
dc.relation.ispartofMarmara Pharmaceutical Journal
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subject1,3,4-thiadiazole
dc.subject2-isoxazoline-5-one
dc.subject2-pyrazolin-5-one
dc.subjectHydrazone and antitubercular activity
dc.titleThe synthesis and antitubercular activity of substituted hydrazone,2-pyrazoline-5-one and 2-isoxazoline-5-one derivatives possessing 1,3,4-thiadiazole moiety [1,3,4-Tiyadiazol halkası içeren hidrazon, 2-pirazol-5-on ve 2-izoksazol-5-on türevi bileşiklerin sentezi ve antitüberküler aktiviteleri]
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage228
oaire.citation.issue3
oaire.citation.startPage222
oaire.citation.titleMarmara Pharmaceutical Journal
oaire.citation.volume16

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