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Synthesis and antimosquito properties of 2,6-substituted benzo[ d ] thiazole and 2,4-substituted benzo[ d ]thiazole analogues against Anopheles arabiensis

dc.contributor.authorVenugopala, Katharigatta Narayanaswamyen_US
dc.contributor.authorKrishnappa, Krishnappaen_US
dc.contributor.authorNayak, Susanta K.en_US
dc.contributor.authorSubrahmanya, Bhat K.en_US
dc.contributor.authorVaderapura, Jayashankaragowda P.en_US
dc.contributor.authorChalannavar, Raju K.en_US
dc.contributor.authorGleiser, Raquel M.en_US
dc.contributor.authorOdhav, Bhartien_US
dc.date.accessioned2013-08-29T08:03:38Z
dc.date.available2013-08-29T08:03:38Z
dc.date.issued2013-07
dc.description.abstractA novel and efficient one pot synthesis was developed for 2,6-substituted-benzo[d]thiazole analogues 4a–k and 2,4-substituted-benzo[d]thiazole analogues 4l–pvia three component condensation reaction of substituted arylaldehyde, 2-amino-6-halo/4-methyl-benzo[d]thiazole and 2-naphthol or 6-hydroxyquinoline in presence of 10% w/v NaCl in water by microwave method. This method enabled for short reaction times, easy work-up and significant high yields. The title compound 4b was used for single crystal X-ray studies in order to understand its conformation and packing features. The title compounds 4a–p were screened for antimosquito properties such as repellency, insecticidal and larvicidal activity against Anopheles arabiensis by mosquito feeding-probing assay, cone bio-assay and standard WHO larvicidal assay, respectively. Among these analogous 4b, 4d and 4p exhibit the highest repellent activity comparable to the positive control DEET, and 4a and 4k knockdown most mosquitoes on repellent assays.en_US
dc.dut-rims.pubnumDUT-002422en_US
dc.format.extent9 p.en_US
dc.identifier.citationVenugopala, K.N., Krishnappa, M., Nayak, S.K., Subrahmanya, B.K., Vaderapura, J.P., Chalannavar, R.K., Gleiser, R.M. and Odhav, B. 2013. Synthesis and antimosquito properties of 2,6-substituted benzo[ d ] thiazole and 2,4-substituted benzo[ d ]thiazole analogues against Anopheles arabiensis. European Journal of Medicinal Chemistry, 65: 295-303.en_US
dc.identifier.doi10.1016/j.ejmech.2013.04.061
dc.identifier.urihttp://hdl.handle.net/10321/891
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.publisher.urihttp://dx.doi.org/10.1016/j.ejmech.2013.04.061en_US
dc.relation.ispartofEuropean Journal of Medicinal Chemistryen_US
dc.subjectOne pot synthesisen_US
dc.subjectSubstituted benzo[d]thiazoleen_US
dc.subject2-Naphtholen_US
dc.subject6-Hydroxyquinolineen_US
dc.subjectMicrowave irradiationen_US
dc.subjectSingle crystal X-ray studiesen_US
dc.subjectLarvicideen_US
dc.subjectAdulticidal activityen_US
dc.subjectRepellenten_US
dc.subject.lcshInsecticide resistanceen_US
dc.titleSynthesis and antimosquito properties of 2,6-substituted benzo[ d ] thiazole and 2,4-substituted benzo[ d ]thiazole analogues against Anopheles arabiensisen_US
dc.typeArticleen_US

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