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dc.contributor.author
Venugopala, Katharigatta Narayanaswamy
dc.contributor.author
Krishnappa, Manjula
dc.contributor.author
Nayak, Susanta K.
dc.contributor.author
Subrahmanya, Bhat K.
dc.contributor.author
Vaderapura, Jayashankaragowda P.
dc.contributor.author
Chalannavar, Raju K.
dc.contributor.author
Gleiser, Raquel M.
dc.contributor.author
Odhav, Bharti
dc.date.available
2017-08-16T18:41:05Z
dc.date.issued
2013-05
dc.identifier.citation
Venugopala, Katharigatta Narayanaswamy; Krishnappa, Manjula; Nayak, Susanta K.; Subrahmanya, Bhat K.; Vaderapura, Jayashankaragowda P.; et al.; Synthesis and antimosquito properties of 2,6-substituted benzo[d]thiazole and 2,4-substituted benzo[d]thiazole analogues against Anopheles arabiensis; Elsevier Masson; European Journal Of Medical Chemistry; 65; 5-2013; 295-303
dc.identifier.issn
0223-5234
dc.identifier.uri
http://hdl.handle.net/11336/22527
dc.description.abstract
A novel and efficient one pot synthesis was developed for 2,6-substituted-benzo[d]thiazole analogues 4a ek and 2,4-substituted-benzo[d]thiazole analogues 4lep via three component condensation reaction of substituted arylaldehyde, 2-amino-6-halo/4-methyl-benzo[d]thiazole and 2-naphthol or 6-hydroxy quinoline 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 4aep 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.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Elsevier Masson
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.subject
One Pot Synthesis
dc.subject
Larvicide
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Insecticide
dc.subject
Repellent
dc.subject.classification
Bioquímica y Biología Molecular
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Ciencias Biológicas
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS
dc.title
Synthesis and antimosquito properties of 2,6-substituted benzo[d]thiazole and 2,4-substituted benzo[d]thiazole analogues against Anopheles arabiensis
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2016-12-12T14:16:21Z
dc.journal.volume
65
dc.journal.pagination
295-303
dc.journal.pais
Francia
dc.journal.ciudad
Paris
dc.description.fil
Fil: Venugopala, Katharigatta Narayanaswamy. Durban University of Technology; Sudáfrica
dc.description.fil
Fil: Krishnappa, Manjula. Strides Arcolab; India
dc.description.fil
Fil: Nayak, Susanta K.. Universite de Rennes I; Francia
dc.description.fil
Fil: Subrahmanya, Bhat K.. Strides Arcolab; India
dc.description.fil
Fil: Vaderapura, Jayashankaragowda P.. S.S.M.R.V. College; India
dc.description.fil
Fil: Chalannavar, Raju K.. Durban University of Technology; Sudáfrica
dc.description.fil
Fil: Gleiser, Raquel M.. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Córdoba. Instituto Multidisciplinar de Biología Vegetal (p). Grupo Vinculado Centro de Relevamiento y Evaluacion de Recursos Agricolas y Naturales; Argentina
dc.description.fil
Fil: Odhav, Bharti. Durban University of Technology; Sudáfrica
dc.journal.title
European Journal Of Medical Chemistry
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.ejmech.2013.04.061
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0223523413002936
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