dc.contributor.author | Tabanca, Nurhayat | |
dc.contributor.author | Wedge, David E. | |
dc.contributor.author | Ali, Abbas | |
dc.contributor.author | Khan, Ikhlas A. | |
dc.contributor.author | Kaplancıklı, Zafer Asım | |
dc.contributor.author | Altıntop, Mehlika Dilek | |
dc.date.accessioned | 2019-10-19T14:44:29Z | |
dc.date.available | 2019-10-19T14:44:29Z | |
dc.date.issued | 2013 | |
dc.identifier.issn | 1054-2523 | |
dc.identifier.uri | https://dx.doi.org/10.1007/s00044-012-0250-4 | |
dc.identifier.uri | https://hdl.handle.net/11421/13531 | |
dc.description | WOS: 000317988100007 | en_US |
dc.description.abstract | Hydrazone 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.sponsorship | USDA/ARS [56-6402-1-612]; Deployed War-Fighter Protection Research Program; U.S. Department of Defense through the Armed Forces Pest Management Board | en_US |
dc.description.sponsorship | This 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.iso | eng | en_US |
dc.publisher | Springer Birkhauser | en_US |
dc.relation.isversionof | 10.1007/s00044-012-0250-4 | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Hydrazone | en_US |
dc.subject | Fungicide | en_US |
dc.subject | Plant Pathogen | en_US |
dc.subject | Phomopsis Obscurans | en_US |
dc.subject | Phomopsis Viticola | en_US |
dc.subject | Mosquito Control | en_US |
dc.subject | Aedes Aegypti | en_US |
dc.title | Antifungal, mosquito deterrent, and larvicidal activity of N-(benzylidene)-3-cyclohexylpropionic acid hydrazide derivatives | en_US |
dc.type | article | en_US |
dc.relation.journal | Medicinal Chemistry Research | en_US |
dc.contributor.department | Anadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Kimya Anabilim Dalı | en_US |
dc.identifier.volume | 22 | en_US |
dc.identifier.issue | 6 | en_US |
dc.identifier.startpage | 2602 | en_US |
dc.identifier.endpage | 2609 | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.contributor.institutionauthor | Kaplancıklı, Zafer Asım | |
dc.contributor.institutionauthor | Altıntop, Mehlika Dilek | |