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dc.contributor.authorTabanca, Nurhayat
dc.contributor.authorWedge, David E.
dc.contributor.authorAli, Abbas
dc.contributor.authorKhan, Ikhlas A.
dc.contributor.authorKaplancıklı, Zafer Asım
dc.contributor.authorAltıntop, Mehlika Dilek
dc.date.accessioned2019-10-19T14:44:29Z
dc.date.available2019-10-19T14:44:29Z
dc.date.issued2013
dc.identifier.issn1054-2523
dc.identifier.urihttps://dx.doi.org/10.1007/s00044-012-0250-4
dc.identifier.urihttps://hdl.handle.net/11421/13531
dc.descriptionWOS: 000317988100007en_US
dc.description.abstractHydrazone derivatives possess good antifungal and insecticidal activities and their structures are used in pesticide design. In the present study, for the first time, ten hydrazone derivatives (1-10) were evaluated for their antifungal activity against Colletotrichum, Botrytis, Fusarium, and Phomopsis species and for their biting deterrent and larvicidal activity against Aedes aegypti, the yellow mosquito. The 96-well microbioassay revealed that compounds 3, 5, 7, and 9 showed strong antifungal activity at 30 mu M against Phomopsis obscurans, whereas only two compounds (5 and 9) demonstrated strong antifungal activity against Phomopsis viticola. Compound 5 showed the highest biting deterrent activity against Ae. aegypti when compared with N,N-diethyl-meta-toluamide, the positive control at 25 nmol/cm(2). Compound 9 exhibited the highest larvicidal activity in toxicity bioassay with LD50 values of 57.4 and 4.35 ppm and LD90 values of 297.8 and 19.1 ppm, respectively, at 24 and 48 h post treatment. Compounds 5 bearing 4-fluoro substituent on benzene ring and 9 carrying a 4-isopropyl group on the benzene ring were found to be the most active compounds in both bioassays. These results could be useful information for development of new effective fungicides and insecticides in the near future.en_US
dc.description.sponsorshipUSDA/ARS [56-6402-1-612]; Deployed War-Fighter Protection Research Program; U.S. Department of Defense through the Armed Forces Pest Management Boarden_US
dc.description.sponsorshipThis study was supported in part by USDA/ARS Grant No. 56-6402-1-612 and Deployed War-Fighter Protection Research Program Grant funded by the U.S. Department of Defense through the Armed Forces Pest Management Board. We thank Ms. J. L. Robertson, Ms. R. Pace and Ms. S. R. Weerasooriya for the bioassays and Dr. James J. Becnel, Mosquito and Fly Research Unit, Center for Medical, Agricultural and Veterinary Entomology, USDA-ARS, Gainesville, for supplying Ae. aegypti eggs.en_US
dc.language.isoengen_US
dc.publisherSpringer Birkhauseren_US
dc.relation.isversionof10.1007/s00044-012-0250-4en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectHydrazoneen_US
dc.subjectFungicideen_US
dc.subjectPlant Pathogenen_US
dc.subjectPhomopsis Obscuransen_US
dc.subjectPhomopsis Viticolaen_US
dc.subjectMosquito Controlen_US
dc.subjectAedes Aegyptien_US
dc.titleAntifungal, mosquito deterrent, and larvicidal activity of N-(benzylidene)-3-cyclohexylpropionic acid hydrazide derivativesen_US
dc.typearticleen_US
dc.relation.journalMedicinal Chemistry Researchen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Kimya Anabilim Dalıen_US
dc.identifier.volume22en_US
dc.identifier.issue6en_US
dc.identifier.startpage2602en_US
dc.identifier.endpage2609en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorKaplancıklı, Zafer Asım
dc.contributor.institutionauthorAltıntop, Mehlika Dilek


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