Publication:
Anticonvulsant activity of some substituted 1,3,4-thiadiazoles

dc.contributor.authorsGülerman N.N., Rollas S., Ekinci A.C., Vidin A.
dc.date.accessioned2022-03-28T14:50:57Z
dc.date.accessioned2026-01-10T16:51:08Z
dc.date.available2022-03-28T14:50:57Z
dc.date.issued2001
dc.description.abstractSome 5-[4-(benzoylamino)phenyl]-2 substituted amino-1,3,4-thiadiazoles have been synthesized previously in our laboratory. The structures of these compounds were elucidated using UV, IR and Mass spectroscopic methods besides elemental analyses. In the present work, the structures of these compounds have also been supported by 1H-NMR and their anticonvulsant activities against pentylenetetrazole induced seizures in male and female Albino Swiss mice have been investigated. All the compounds showed protections ranging from 10 to 60% at a dose of l00 mg.kg-1 and among them, 2-allylamino-5-[4-(benzoylamino)phenyl]-l,3,4-thiadizole was found to posses significant protection against pentylenetetrazole shock.
dc.identifier.issn1300638X
dc.identifier.urihttps://hdl.handle.net/11424/255576
dc.language.isoeng
dc.relation.ispartofActa Pharmaceutica Turcica
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subject2,5-disubstituted-1,3,4-thiadiazoles
dc.subjectAnticonvulsant activity
dc.titleAnticonvulsant activity of some substituted 1,3,4-thiadiazoles
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage163
oaire.citation.issue3-4
oaire.citation.startPage161
oaire.citation.titleActa Pharmaceutica Turcica
oaire.citation.volume43

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