Síntese e atividade biológica do derivado 6-formil-oxamniquina
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | , , , , , |
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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Repositório Institucional da UNESP |
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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/openAccess2024-06-24T13:45:05Zoai:repositorio.unesp.br:11449/70603Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T14:41:16.886122Repositório 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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1808128401820614656 |