QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da FIOCRUZ (ARCA) |
Texto Completo: | https://www.arca.fiocruz.br/handle/icict/19408 |
Resumo: | 2016-01-01 |
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Melo Filho, Cleber C.Dantas, Rafael F.Braga, Rodolpho C.Neves, Bruno J.Senger, Mario R.Valente, Walter C. G.Rezende.Neto, João M.Chaves, Willian T.Muratov, Eugene N.Paveley, Ross A.Furnham, NicholasKamentsky, LeeCarpenter, Anne E.Silva.Junior, Floriano P.Andrade, Carolina H.2017-06-19T17:45:23Z2017-06-19T17:45:23Z2016MELO FILHO, Cleber C. et al. QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni. J. Chem. Inf. Model., v.56, p.1357−1372, June 2016.1549-9596https://www.arca.fiocruz.br/handle/icict/1940810.1021/acs.jcim.6b000551549-960XengAmerican Chemical SocietySchistosoma mansoniRelação Quantitativa Estrutura-AtividadeNovos suportes químicosSchistosoma mansoniQSARNovel Chemical ScaffoldsQSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoniinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2016-01-01Universidade Federal de Goiás. Faculdade de Farmácia. Laboratório de Planejamento de Fármacos e Modelagem Molecular (LabMol). Goiânia, GO, Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Bioquímica Experimental e Computacional de Fármacos. Rio de Janeiro, RJ. Brasil.Universidade Federal de Goiás. Faculdade de Farmácia. Laboratório de Planejamento de Fármacos e Modelagem Molecular (LabMol). Goiânia, GO, Brasil.Universidade Federal de Goiás. Faculdade de Farmácia.Laboratório de Planejamento de Fármacos e Modelagem Molecular (LabMol). Goiânia, GO, Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Bioquímica Experimental e Computacional de Fármacos. Rio de Janeiro, RJ. Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Bioquímica Experimental e Computacional de Fármacos. Rio de Janeiro, RJ. Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Bioquímica Experimental e Computacional de Fármacos. Rio de Janeiro, RJ. Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Bioquímica Experimental e Computacional de Fármacos. Rio de Janeiro, RJ. Brasil.University of North Carolina. Eshelman School of Pharmacy. Division of Chemical Biology and Medicinal Chemistry. Laboratory for Molecular Modeling. Chapel Hill, North Carolina, USA / Odessa National Polytechnic University. Department of Chemical Technology. Odessa, Ukraine.London School of Hygiene and Tropical Medicine. Department of Pathogen Molecular Biology & Department of Infection and Immunity. London, United Kingdom.London School of Hygiene and Tropical Medicine. Department of Pathogen Molecular Biology & Department of Infection and Immunity. London, United Kingdom.Broad Institute of Massachusetts Institute of Technology and Harvard. Imaging Platform.Cambridge, Massachusetts, USA.Broad Institute of Massachusetts Institute of Technology and Harvard. Imaging Platform.Cambridge, Massachusetts, USA.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Bioquímica Experimental e Computacional de Fármacos. Rio de Janeiro, RJ. Brasil.Universidade Federal de Goiás. Faculdade de Farmácia. Laboratório de Planejamento de Fármacos e Modelagem Molecular (LabMol). Goiânia, GO, Brasil.Schistosomiasis is a neglected tropical disease that affects millions of people worldwide. Thioredoxin glutathione reductase of Schistosoma mansoni (SmTGR) is a validated drug target that plays a crucial role in the redox homeostasis of the parasite. We report the discovery of new chemical scaffolds against S. mansoni using a combi-QSAR approach followed by virtual screening of a commercial database and confirmation of top ranking compounds by in vitro experimental evaluation with automated imaging of schistosomula and adult worms. We constructed 2D and 3D quantitative structure-activity relationship (QSAR) models using a series of oxadiazoles-2-oxides reported in the literature as SmTGR inhibitors and combined the best models in a consensus QSAR model. This model was used for a virtual screening of Hit2Lead set of ChemBridge database and allowed the identification of ten new potential SmTGR inhibitors. Further experimental testing on both shistosomula and adult worms showed that 4-nitro-3,5-bis(1-nitro-1H-pyrazol-4-yl)-1H-pyrazole (LabMol-17) and 3-nitro-4-{[(4-nitro-1,2,5-oxadiazol-3-yl)oxy]methyl}-1,2,5-oxadiazole (LabMol-19), two compounds representing new chemical scaffolds, have high activity in both systems. These compounds will be the subjects for additional testing and, if necessary, modification to serve as new schistosomicidal agents.info:eu-repo/semantics/openAccessreponame:Repositório Institucional da FIOCRUZ (ARCA)instname:Fundação Oswaldo Cruz (FIOCRUZ)instacron:FIOCRUZLICENSElicense.txtlicense.txttext/plain; charset=utf-82991https://www.arca.fiocruz.br/bitstream/icict/19408/1/license.txt5a560609d32a3863062d77ff32785d58MD51ORIGINALmario2_senger_etal_IOC_2016.pdfmario2_senger_etal_IOC_2016.pdfapplication/pdf8232715https://www.arca.fiocruz.br/bitstream/icict/19408/2/mario2_senger_etal_IOC_2016.pdf18b8f8061c2200055931f3faf0acbbaeMD52TEXTmario2_senger_etal_IOC_2016.pdf.txtmario2_senger_etal_IOC_2016.pdf.txtExtracted texttext/plain68812https://www.arca.fiocruz.br/bitstream/icict/19408/3/mario2_senger_etal_IOC_2016.pdf.txtc46332cf23a0cbf4090a0a4b605da91dMD53icict/194082021-03-24 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dc.title.pt_BR.fl_str_mv |
QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni |
title |
QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni |
spellingShingle |
QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni Melo Filho, Cleber C. Schistosoma mansoni Relação Quantitativa Estrutura-Atividade Novos suportes químicos Schistosoma mansoni QSAR Novel Chemical Scaffolds |
title_short |
QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni |
title_full |
QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni |
title_fullStr |
QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni |
title_full_unstemmed |
QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni |
title_sort |
QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni |
author |
Melo Filho, Cleber C. |
author_facet |
Melo Filho, Cleber C. Dantas, Rafael F. Braga, Rodolpho C. Neves, Bruno J. Senger, Mario R. Valente, Walter C. G. Rezende.Neto, João M. Chaves, Willian T. Muratov, Eugene N. Paveley, Ross A. Furnham, Nicholas Kamentsky, Lee Carpenter, Anne E. Silva.Junior, Floriano P. Andrade, Carolina H. |
author_role |
author |
author2 |
Dantas, Rafael F. Braga, Rodolpho C. Neves, Bruno J. Senger, Mario R. Valente, Walter C. G. Rezende.Neto, João M. Chaves, Willian T. Muratov, Eugene N. Paveley, Ross A. Furnham, Nicholas Kamentsky, Lee Carpenter, Anne E. Silva.Junior, Floriano P. Andrade, Carolina H. |
author2_role |
author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Melo Filho, Cleber C. Dantas, Rafael F. Braga, Rodolpho C. Neves, Bruno J. Senger, Mario R. Valente, Walter C. G. Rezende.Neto, João M. Chaves, Willian T. Muratov, Eugene N. Paveley, Ross A. Furnham, Nicholas Kamentsky, Lee Carpenter, Anne E. Silva.Junior, Floriano P. Andrade, Carolina H. |
dc.subject.other.pt_BR.fl_str_mv |
Schistosoma mansoni Relação Quantitativa Estrutura-Atividade Novos suportes químicos |
topic |
Schistosoma mansoni Relação Quantitativa Estrutura-Atividade Novos suportes químicos Schistosoma mansoni QSAR Novel Chemical Scaffolds |
dc.subject.en.pt_BR.fl_str_mv |
Schistosoma mansoni QSAR Novel Chemical Scaffolds |
description |
2016-01-01 |
publishDate |
2016 |
dc.date.issued.fl_str_mv |
2016 |
dc.date.accessioned.fl_str_mv |
2017-06-19T17:45:23Z |
dc.date.available.fl_str_mv |
2017-06-19T17:45:23Z |
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.citation.fl_str_mv |
MELO FILHO, Cleber C. et al. QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni. J. Chem. Inf. Model., v.56, p.1357−1372, June 2016. |
dc.identifier.uri.fl_str_mv |
https://www.arca.fiocruz.br/handle/icict/19408 |
dc.identifier.issn.pt_BR.fl_str_mv |
1549-9596 |
dc.identifier.doi.none.fl_str_mv |
10.1021/acs.jcim.6b00055 |
dc.identifier.eissn.none.fl_str_mv |
1549-960X |
identifier_str_mv |
MELO FILHO, Cleber C. et al. QSAR-Driven Discovery of Novel Chemical Scaffolds Active against Schistosoma mansoni. J. Chem. Inf. Model., v.56, p.1357−1372, June 2016. 1549-9596 10.1021/acs.jcim.6b00055 1549-960X |
url |
https://www.arca.fiocruz.br/handle/icict/19408 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
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openAccess |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da FIOCRUZ (ARCA) instname:Fundação Oswaldo Cruz (FIOCRUZ) instacron:FIOCRUZ |
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FIOCRUZ |
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Repositório Institucional da FIOCRUZ (ARCA) |
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