Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60505
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dc.contributor.authorChavan, Harshal-
dc.contributor.authorShirodkar, Prutha-
dc.contributor.authorMogal, Rajendra-
dc.contributor.authorAmrutkar, Sunil-
dc.date.accessioned2022-09-19T10:01:38Z-
dc.date.available2022-09-19T10:01:38Z-
dc.date.issued2022-09-
dc.identifier.issn2583-1321 (Online); 0019-5103 (Print)-
dc.identifier.urihttp://nopr.niscpr.res.in/handle/123456789/60505-
dc.description994-998en_US
dc.description.abstractCurrent research work is focused on incorporation of thiosemicarbazide, triazole in one framework and observed for antifungal, antibacterial and anthelmintic activities. Derivatives of 1,2,4-triazole-3-thiol are synthesized with thiosemicarbazide and semicarbazide as a starting material. Thiosemicarbazide are subjected to intermolecular cyclization in alkaline medium followed by acidification to give 1,2,4-triazole-3-thiol. Equimolar mixture of thiosemicarbazide and different consecutive acids are heated, fusion occurred to give different triazoles derivatives. The minimum inhibitory concentrations for synthesized compounds are in the range of 3.12-25 μg/mL.en_US
dc.language.isoenen_US
dc.publisherNIScPR-CSIR,Indiaen_US
dc.sourceIJC Vol.61(09) [Sep 2022]en_US
dc.subjectThiosemicarbazideen_US
dc.subject1,2,4-triazoleen_US
dc.subjectantimicrobial activityen_US
dc.subjectantifungal activityen_US
dc.subjectanthelmintic activityen_US
dc.titleSynthesis and evaluation of 1,2,4-triazole derivatives as antimicrobial, antifungal and anthelmintic agentsen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.56042/ijc.v61i9.66354en_US
Appears in Collections:IJC Vol.61(09) [Sep 2022]

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