Publication:
Synthesis and biological activity of 4-thiazolidinones, thiosemicarbazides derived from diflunisal hydrazide

dc.contributor.authorsKucukguzel, G; Kocatepe, A; De Clercq, E; Sahin, F; Gulluce, M
dc.date.accessioned2022-03-12T17:22:48Z
dc.date.accessioned2026-01-11T17:13:32Z
dc.date.available2022-03-12T17:22:48Z
dc.date.issued2006
dc.description.abstractTwo novel series of 4-thiazolidinone derivatives, namely 2',4'-difluoro-4-hydroxybiphenyl-3-carboxylic acid [2-(5-nitro-2-furyl/substituted phenyl)-4-thiazol idinone-3 -y1jam ides (5a-g) and 2-(2',4'-difluoro4-hydroxybipheiiyl-3-carbonylhydrazono)-3-alkyl/ary1-4-thiazolidinones (6ae) together with 5-(2',4'-difluoro4-hydroxybiphenyl-5-yi)-2-cyclohexylamino-1,3,4-oxadiazole (7a) have been synthesized as title compounds. 1-(2',4'-Difluoro-4-hydroxybiphenyl-3-carbonyl)4-alkyl/atylthiosemicarbazides (4a-g) were also obtained and used as intermediate to give the title compounds. All synthesized compounds were screened for their antimycobacterial activity against Mycobacterium tuberculosis H37Rv, antiviral and antimicrobial activities against various virus, bacteria and fungi strains. (c) 2006 Elsevier SAS. All rights reserved.
dc.identifier.doi10.1016/j.ejmech.2005.11.005
dc.identifier.issn0223-5234
dc.identifier.pubmed16414150
dc.identifier.urihttps://hdl.handle.net/11424/228447
dc.identifier.wosWOS:000237184000007
dc.language.isoeng
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
dc.relation.ispartofEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subject4-thiazolidinone
dc.subjectanti-HIV activity
dc.subjectdiflunisal
dc.subjectthiosemicarbazide
dc.subjectMYCOBACTERIUM-TUBERCULOSIS
dc.subjectDERIVATIVES
dc.subjectTHIAZOLIDINONES
dc.subject1,3,4-OXADIAZOLES
dc.subjectHYDRAZONES
dc.subjectINHIBITORS
dc.subjectAGENTS
dc.subjectASSAY
dc.subjectAIDS
dc.titleSynthesis and biological activity of 4-thiazolidinones, thiosemicarbazides derived from diflunisal hydrazide
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage359
oaire.citation.issue3
oaire.citation.startPage353
oaire.citation.titleEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
oaire.citation.volume41

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