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Recent advances bioactive 1,2,4-triazole-3-thiones

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dc.contributor.authorSÜZGÜN, PELİN
dc.contributor.authorsKucukguzel, S. Guniz; Cikla-Suzgun, Pelin
dc.date.accessioned2022-03-10T15:25:15Z
dc.date.available2022-03-10T15:25:15Z
dc.date.issued2015
dc.description.abstractTriazoles are heterocyclic compounds which have a five-membered ring of two carbon atoms and three nitrogen atoms. These structures have been interest in the development of novel compounds with anticonvulsant, antidepressant, antioxidant, anti-inflammatory, analgesic, antinociceptive, antibacterial, antimycobacterial, antifungal, antiviral, anticancer, anti-parasitic, anti-urease and other activities. Therefore, many researchers have synthesized these compounds as target structures and evaluated their biological activities. This review contains various pharmacological activities of 1,2,4-triazole-3-thiones in one place and it is also the milestone for the new research towards this moiety. (C) 2014 Elsevier Masson SAS. All rights reserved.
dc.identifier.doi10.1016/j.ejmech.2014.11.033
dc.identifier.eissn1768-3254
dc.identifier.issn0223-5234
dc.identifier.pubmed25563511
dc.identifier.urihttps://hdl.handle.net/11424/220176
dc.identifier.wosWOS:000356734600057
dc.language.isoeng
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
dc.relation.ispartofEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subject1,2,4-Triazole-3-thione
dc.subjectRibavirin
dc.subjectFluconazole
dc.subjectAnastrozole
dc.subjectEtodolac 1,2,4-triazole
dc.subjectDiflunisal 1,2,4-triazole
dc.subjectCLASSICAL ANTIEPILEPTIC DRUGS
dc.subjectINDUCED SEIZURE MODEL
dc.subjectANTIMICROBIAL ACTIVITIES
dc.subjectMANNICH-BASES
dc.subject1,3,4-THIADIAZOLE DERIVATIVES
dc.subjectBIOLOGICAL EVALUATION
dc.subjectUREASE INHIBITION
dc.subjectANTIINFLAMMATORY ACTIVITIES
dc.subjectANTICONVULSANT ACTIVITY
dc.subjectANTIBACTERIAL ACTIVITY
dc.titleRecent advances bioactive 1,2,4-triazole-3-thiones
dc.typereview
dspace.entity.typePublication
local.avesis.idf54d25aa-e9e6-47d5-9e8b-66041acf3ea3
local.import.packageSS5
local.indexed.atWOS
local.indexed.atSCOPUS
local.indexed.atPUBMED
local.journal.numberofpages41
oaire.citation.endPage870
oaire.citation.startPage830
oaire.citation.titleEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
oaire.citation.volume97
relation.isAuthorOfPublication6f8a150f-0ec8-4a51-9a1b-b9c26aecdf69
relation.isAuthorOfPublication.latestForDiscovery6f8a150f-0ec8-4a51-9a1b-b9c26aecdf69

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