Synthesis, Antibacterial, Antiurease, and Antioxidant Activities of Some New 1,2,4-Triazole Schiff Base and Amine Derivatives
dc.contributor.author | Sökmen, Bahar Bilgin | |
dc.contributor.author | Gümrükçüoğlu, Nurhan | |
dc.contributor.author | Uğraş, Serpil | |
dc.contributor.author | Şahin, Hüseyin | |
dc.contributor.author | Sağkal, Yasemin | |
dc.contributor.author | Uğraş, Halil İbrahim | |
dc.date.accessioned | 2020-04-30T23:32:28Z | |
dc.date.available | 2020-04-30T23:32:28Z | |
dc.date.issued | 2015 | |
dc.department | DÜ, Ziraat Fakültesi, Tarla Bitkileri Bölümü | en_US |
dc.description | Sahin, Huseyin/0000-0002-6018-1494 | en_US |
dc.description | WOS: 000348103100007 | en_US |
dc.description | PubMed: 25342259 | en_US |
dc.description.abstract | The acylhydrazone compound named ethyl N'-furan-2-carbonylbenzohydrazonate was synthesized by the condensation of ethyl benzimidate hydrochloride with furan-2-carbohydrazide. The treatment of the acylhydrazone with hydrazine hydrate afforded 4-amino-3-furan-2-yl-5-phenyl-1,2,4-triazole. The usage of this compound with various aromatic aldehydes resulted in the formation of 4-arylidenamino-3-furan-2-yl-5-phenyl-1,2,4-triazoles. Sodium borohydride reduction of 4-arylidenamino derivatives afforded 4-alkylamino-3-furan-2-yl-5-phenyl-1,2,4-triazoles. The obtained products were identified by FT-IR, H-1-NMR, C-13-NMR. A series of compounds were evaluated for their antibacterial, antiurease, and antioxidant activities. The results showed that the synthesized new compounds had effective antiurease and antioxidant activities. | en_US |
dc.identifier.doi | 10.1007/s12010-014-1307-2 | en_US |
dc.identifier.endpage | 714 | en_US |
dc.identifier.issn | 0273-2289 | |
dc.identifier.issn | 1559-0291 | |
dc.identifier.issue | 2 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 705 | en_US |
dc.identifier.uri | https://doi.org/10.1007/s12010-014-1307-2 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12684/4727 | |
dc.identifier.volume | 175 | en_US |
dc.identifier.wos | WOS:000348103100007 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Humana Press Inc | en_US |
dc.relation.ispartof | Applied Biochemistry And Biotechnology | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Acyl hydrazone | en_US |
dc.subject | 1,2,4-triazole | en_US |
dc.subject | Schiff base | en_US |
dc.subject | Reduction | en_US |
dc.subject | Urease inhibition activity | en_US |
dc.subject | Antioxidant activity | en_US |
dc.title | Synthesis, Antibacterial, Antiurease, and Antioxidant Activities of Some New 1,2,4-Triazole Schiff Base and Amine Derivatives | en_US |
dc.type | Article | en_US |
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