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dc.contributor.author
Uppar, Vijayakumar  
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Chandrashekharappa, Sandeep  
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Venugopala, Katharigatta N.  
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Deb, Pran Kishore  
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Kar, Supratik  
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Alwassil, Osama I.  
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Gleiser, Raquel M.  
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Garcia, Daniel Asmed  
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Odhav, Bharti  
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Mohan, Mahendra K.  
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Venugopala, Rashmi  
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Padmashali, Basavaraj  
dc.date.available
2021-02-09T18:08:35Z  
dc.date.issued
2020-08  
dc.identifier.citation
Uppar, Vijayakumar; Chandrashekharappa, Sandeep; Venugopala, Katharigatta N.; Deb, Pran Kishore; Kar, Supratik; et al.; Synthesis and characterization of pyrrolo[1,2-a]quinoline derivatives for their larvicidal activity against Anopheles arabiensis; Springer/Plenum Publishers; Structural Chemistry; 31; 4; 8-2020; 1533-1543  
dc.identifier.issn
1040-0400  
dc.identifier.uri
http://hdl.handle.net/11336/125227  
dc.description.abstract
Certain tetrahydropyrido[1,2-a]quinolines and pyrroloquinoline homologs have shown various biological activities such as antimicrobials, crop-protectings, diuretics, antioxidants, anticoagulants, and antimalarial activities. Keeping this observation in mind, we envisaged to synthesize and characterize a series of novel ethyl 1-(substituted benzoyl)-5-methylpyrrolo[1,2-a]quinoline-3-carboxylates and dimethyl 1-(substituted benzoyl)-5-methylpyrrolo[1,2-a]quinoline-2,3-dicarboxylates (2a-k). Quaternary salts of lepidine such as 1-[2-(substituted phenyl)-2-oxoethyl]-4-methylquinolin-1-ium bromide (1a-f) were obtained by stirring lepidine with different phenacyl bromides in acetone at room temperature separately. These quaternary salts of lepidine (1a-f) were then treated with electron-deficient ethyl propiolate and dimethyl-but-2-yne-dioate separately, in the presence of anhydrous K2CO3 and dimethylformamide (DMF) solvent to obtain ethyl 1-(substituted benzoyl)-5-methylpyrrolo[1,2-a]quinoline-3-carboxylates and dimethyl 1-(substituted benzoyl)-5-methylpyrrolo[1,2-a]quinoline-2,3-dicarboxylates, respectively (2a-k). The newly synthesized compounds were assessed by spectroscopic techniques to determine their structures. Based on our previous study on the similar pharmacophore, the synthesized compounds 2a-k were screened for their larvicidal activity against Anopheles arabiensis using a standard World Health Organization larvicidal assay; compounds 2b and 2e at 8.12 and 9.2 μM exhibited the highest larval mortality at 78 and 89%, respectively, when compared with the negative control acetone, and it demonstrated less activity, which was similar to the positive control, temephos. Finally, the test compound 2e at 9.2 μM, resulted in an 89% mortality rate after 48 h of exposure, followed by compound 2b at 8.12 μM with a 78% mortality rate. Compounds 2f, 2d, and 2c showed intermediate toxicity, and the mortality rate was lower than 60% for larvae exposed to any of the remaining test compounds.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Springer/Plenum Publishers  
dc.rights
info:eu-repo/semantics/restrictedAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
LEPIDINE  
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PYRROLO[1,2-A]QUINOLINE  
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STRUCTURAL ELUCIDATION  
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LARVICIDAL ACTIVITY  
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Otras Ciencias Químicas  
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Ciencias Químicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
Synthesis and characterization of pyrrolo[1,2-a]quinoline derivatives for their larvicidal activity 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
2021-01-18T15:46:58Z  
dc.identifier.eissn
1572-9001  
dc.journal.volume
31  
dc.journal.number
4  
dc.journal.pagination
1533-1543  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
New York  
dc.description.fil
Fil: Uppar, Vijayakumar. Rani Channamma University; India  
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Fil: Chandrashekharappa, Sandeep. National Centre For Biological Sciences; India  
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Fil: Venugopala, Katharigatta N.. King Faisal University; Arabia Saudita. Durban University Of Technology; Sudáfrica  
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Fil: Deb, Pran Kishore. Philadelphia University; Jordania  
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Fil: Kar, Supratik. Jackson State University; Estados Unidos  
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Fil: Alwassil, Osama I.. King Saud Bin Abdulaziz University For Health Sciences; Arabia Saudita  
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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 Evaluación de Recursos Agrícolas y Naturales; Argentina  
dc.description.fil
Fil: Garcia, Daniel Asmed. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones Biológicas y Tecnológicas. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales. Instituto de Investigaciones Biológicas y Tecnológicas; Argentina. Universidad Nacional de Córdoba. Facultad de Ciencias Exactas, Físicas y Naturales. Departamento de Química. Cátedra de Química Biológica; Argentina  
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Fil: Odhav, Bharti. Durban University Of Technology; Sudáfrica  
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Fil: Mohan, Mahendra K.. National Centre For Biological Sciences; India  
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Fil: Venugopala, Rashmi. University of KwaZulu-Natal; Sudáfrica  
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Fil: Padmashali, Basavaraj. Rani Channamma University; India  
dc.journal.title
Structural Chemistry  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://link.springer.com/10.1007/s11224-020-01516-w  
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info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1007/s11224-020-01516-w