Síntese e atividade biológica do derivado 6-formil-oxamniquina

Detalhes bibliográficos
Autor(a) principal: Almeida, Adelia Emilia de [UNESP]
Data de Publicação: 2008
Outros Autores: De Souza, Ana Luiza Ribeiro [UNESP], Allegretti, Silmara Marques, Frezza, Tarsila Ferraz, Pinto, Mara Cristina [UNESP], Ferreira, Antônio Gilberto, Chin, Chung Man [UNESP]
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S1516-93322008000400022
http://hdl.handle.net/11449/70603
Resumo: Schistosomiasis, an important disease in Brazil, is caused by a trematode of the genus Schistosoma, reaching millions of person in one of the most endemic region of this disease in the whole globe. The main goal of this work was to syntetize the 6-formyl- oxamniquine derivative and evaluate its biological activity. The 6-formyl-oxamniquine derivative was obtained by the oxidation of oxamniquine with MnO 2, applying CH 2Cl 2 as solvent at room temperature for 24 hours. The obtaintion of 6-formyl-oxamniquine derivative compound was confirmed by IR spectroscopy and 13C NMR and 1H NMR, presenting similar activity when compared to the commercial oxamniquine (Mansil®).
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spelling Síntese e atividade biológica do derivado 6-formil-oxamniquinaSynthesis and biological activity of 6-formyl-oxamniquine derivativeOoxamniquineSchistosoma mansoniSchistosomiasis6 formyl oxamniquine derivativemanganese oxideoxamniquineunclassified drugBrazilcarbon nuclear magnetic resonancedrug activitydrug structuredrug synthesisinfrared spectroscopyproton nuclear magnetic resonanceschistosomiasisSchistosomiasis, an important disease in Brazil, is caused by a trematode of the genus Schistosoma, reaching millions of person in one of the most endemic region of this disease in the whole globe. The main goal of this work was to syntetize the 6-formyl- oxamniquine derivative and evaluate its biological activity. The 6-formyl-oxamniquine derivative was obtained by the oxidation of oxamniquine with MnO 2, applying CH 2Cl 2 as solvent at room temperature for 24 hours. The obtaintion of 6-formyl-oxamniquine derivative compound was confirmed by IR spectroscopy and 13C NMR and 1H NMR, presenting similar activity when compared to the commercial oxamniquine (Mansil®).Laboratório de Pesquisa e Desenvolvimento de Fármacos Departamento de Fármacos e Medicamentos Universidade Estadual Paulista Júlio de Mesquita FilhoDepartamento de Fármacos e Medicamentos Faculdade Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista Júlio de Mesquita FilhoLaboratório de Helmintologia Departamento de Parasitologia Universidade Estadual de CampinasLaboratório de Parasitologia Departamento de Ciências Biológicas Universidade Estadual Paulista Júlio de Mesquita FilhoDepartamento de Química Orgânica Universidade Federal de São CarlosFaculdade de Ciências Farmacêuticas UNESP, Rod. Araraquara-Jaú, km. 01, 14801-902 - Araraquara - SPLaboratório de Pesquisa e Desenvolvimento de Fármacos Departamento de Fármacos e Medicamentos Universidade Estadual Paulista Júlio de Mesquita FilhoDepartamento de Fármacos e Medicamentos Faculdade Faculdade de Ciências Farmacêuticas Universidade Estadual Paulista Júlio de Mesquita FilhoLaboratório de Parasitologia Departamento de Ciências Biológicas Universidade Estadual Paulista Júlio de Mesquita FilhoFaculdade de Ciências Farmacêuticas UNESP, Rod. Araraquara-Jaú, km. 01, 14801-902 - Araraquara - SPUniversidade Estadual Paulista (Unesp)Universidade Estadual de Campinas (UNICAMP)Universidade Federal de São Carlos (UFSCar)Almeida, Adelia Emilia de [UNESP]De Souza, Ana Luiza Ribeiro [UNESP]Allegretti, Silmara MarquesFrezza, Tarsila FerrazPinto, Mara Cristina [UNESP]Ferreira, Antônio GilbertoChin, Chung Man [UNESP]2014-05-27T11:23:41Z2014-05-27T11:23:41Z2008-10-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article749-754application/pdfhttp://dx.doi.org/10.1590/S1516-93322008000400022Revista Brasileira de Ciencias Farmaceuticas/Brazilian Journal of Pharmaceutical Sciences, v. 44, n. 4, p. 749-754, 2008.1516-9332http://hdl.handle.net/11449/7060310.1590/S1516-93322008000400022S1516-93322008000400022WOS:0002638045000222-s2.0-596491082902-s2.0-59649108290.pdf822173749159841597343336079754130000-0003-4141-0455Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporRevista Brasileira de Ciencias Farmaceuticas/Brazilian Journal of Pharmaceutical Sciencesinfo:eu-repo/semantics/openAccess2023-10-12T06:06:50Zoai:repositorio.unesp.br:11449/70603Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-12T06:06:50Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Síntese e atividade biológica do derivado 6-formil-oxamniquina
Synthesis and biological activity of 6-formyl-oxamniquine derivative
title Síntese e atividade biológica do derivado 6-formil-oxamniquina
spellingShingle Síntese e atividade biológica do derivado 6-formil-oxamniquina
Almeida, Adelia Emilia de [UNESP]
Ooxamniquine
Schistosoma mansoni
Schistosomiasis
6 formyl oxamniquine derivative
manganese oxide
oxamniquine
unclassified drug
Brazil
carbon nuclear magnetic resonance
drug activity
drug structure
drug synthesis
infrared spectroscopy
proton nuclear magnetic resonance
schistosomiasis
title_short Síntese e atividade biológica do derivado 6-formil-oxamniquina
title_full Síntese e atividade biológica do derivado 6-formil-oxamniquina
title_fullStr Síntese e atividade biológica do derivado 6-formil-oxamniquina
title_full_unstemmed Síntese e atividade biológica do derivado 6-formil-oxamniquina
title_sort Síntese e atividade biológica do derivado 6-formil-oxamniquina
author Almeida, Adelia Emilia de [UNESP]
author_facet Almeida, Adelia Emilia de [UNESP]
De Souza, Ana Luiza Ribeiro [UNESP]
Allegretti, Silmara Marques
Frezza, Tarsila Ferraz
Pinto, Mara Cristina [UNESP]
Ferreira, Antônio Gilberto
Chin, Chung Man [UNESP]
author_role author
author2 De Souza, Ana Luiza Ribeiro [UNESP]
Allegretti, Silmara Marques
Frezza, Tarsila Ferraz
Pinto, Mara Cristina [UNESP]
Ferreira, Antônio Gilberto
Chin, Chung Man [UNESP]
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidade Estadual de Campinas (UNICAMP)
Universidade Federal de São Carlos (UFSCar)
dc.contributor.author.fl_str_mv Almeida, Adelia Emilia de [UNESP]
De Souza, Ana Luiza Ribeiro [UNESP]
Allegretti, Silmara Marques
Frezza, Tarsila Ferraz
Pinto, Mara Cristina [UNESP]
Ferreira, Antônio Gilberto
Chin, Chung Man [UNESP]
dc.subject.por.fl_str_mv Ooxamniquine
Schistosoma mansoni
Schistosomiasis
6 formyl oxamniquine derivative
manganese oxide
oxamniquine
unclassified drug
Brazil
carbon nuclear magnetic resonance
drug activity
drug structure
drug synthesis
infrared spectroscopy
proton nuclear magnetic resonance
schistosomiasis
topic Ooxamniquine
Schistosoma mansoni
Schistosomiasis
6 formyl oxamniquine derivative
manganese oxide
oxamniquine
unclassified drug
Brazil
carbon nuclear magnetic resonance
drug activity
drug structure
drug synthesis
infrared spectroscopy
proton nuclear magnetic resonance
schistosomiasis
description Schistosomiasis, an important disease in Brazil, is caused by a trematode of the genus Schistosoma, reaching millions of person in one of the most endemic region of this disease in the whole globe. The main goal of this work was to syntetize the 6-formyl- oxamniquine derivative and evaluate its biological activity. The 6-formyl-oxamniquine derivative was obtained by the oxidation of oxamniquine with MnO 2, applying CH 2Cl 2 as solvent at room temperature for 24 hours. The obtaintion of 6-formyl-oxamniquine derivative compound was confirmed by IR spectroscopy and 13C NMR and 1H NMR, presenting similar activity when compared to the commercial oxamniquine (Mansil®).
publishDate 2008
dc.date.none.fl_str_mv 2008-10-01
2014-05-27T11:23:41Z
2014-05-27T11:23:41Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S1516-93322008000400022
Revista Brasileira de Ciencias Farmaceuticas/Brazilian Journal of Pharmaceutical Sciences, v. 44, n. 4, p. 749-754, 2008.
1516-9332
http://hdl.handle.net/11449/70603
10.1590/S1516-93322008000400022
S1516-93322008000400022
WOS:000263804500022
2-s2.0-59649108290
2-s2.0-59649108290.pdf
8221737491598415
9734333607975413
0000-0003-4141-0455
url http://dx.doi.org/10.1590/S1516-93322008000400022
http://hdl.handle.net/11449/70603
identifier_str_mv Revista Brasileira de Ciencias Farmaceuticas/Brazilian Journal of Pharmaceutical Sciences, v. 44, n. 4, p. 749-754, 2008.
1516-9332
10.1590/S1516-93322008000400022
S1516-93322008000400022
WOS:000263804500022
2-s2.0-59649108290
2-s2.0-59649108290.pdf
8221737491598415
9734333607975413
0000-0003-4141-0455
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Revista Brasileira de Ciencias Farmaceuticas/Brazilian Journal of Pharmaceutical Sciences
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 749-754
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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