Clinical Candidate VT-1161's Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi

Detalhes bibliográficos
Autor(a) principal: Hoekstra, William J.
Data de Publicação: 2016
Outros Autores: Hargrove, Tatiana Y., Wawrzak, Zdzislaw, Batista, Denise da Gama Jaen, Silva, Cristiane F. da, Nefertiti, Aline S. G., Rachakonda, Girish, Schotzinger, Robert J., Villalta, Fernando, Soeiro, Maria de Nazaré C., Lepesheva, Galina I.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da FIOCRUZ (ARCA)
Texto Completo: https://www.arca.fiocruz.br/handle/icict/23847
Resumo: Viamet Pharmaceuticals, Inc.. Durham, North Carolina, USA.;
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spelling Hoekstra, William J.Hargrove, Tatiana Y.Wawrzak, ZdzislawBatista, Denise da Gama JaenSilva, Cristiane F. daNefertiti, Aline S. G.Rachakonda, GirishSchotzinger, Robert J.Villalta, FernandoSoeiro, Maria de Nazaré C.Lepesheva, Galina I.2018-01-02T16:44:44Z2018-01-02T16:44:44Z2016HOEKSTRA, William J. et al. Clinical Candidate VT-1161’s Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi. Antimicrobial Agents and Chemotherapy, v.60, n.2, p.1058-1066, Feb. 2016.0066-4804https://www.arca.fiocruz.br/handle/icict/2384710.1128/AAC.02287-151098-6596engAmerican Society for MicrobiologyDoença de ChagasTrypanosoma cruziTratamentoMeidcamentos AntifúngicosChagas DiseaseTrypanosoma cruziVT-1161TreatmentMurine ModelTarget Enzyme CYP51Clinical Candidate VT-1161's Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruziinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleViamet Pharmaceuticals, Inc.. Durham, North Carolina, USA.;Vanderbilt University School of Medicine. Department of Biochemistry. Nashville, Tennessee, USA.Northwestern University. Life Science Collaborative Access Team. Synchrotron Research Center. Argonne, Illinois, USA.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Biologia Celular Rio de Janeiro, RJ. Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Biologia Celular Rio de Janeiro, RJ. Brasil.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Biologia Celular Rio de Janeiro, RJ. Brasil.Meharry Medical College. Department of Microbiology and Immunology. Nashville, Tennessee, USA.Viamet Pharmaceuticals, Inc.. Durham, North Carolina, USA.;Meharry Medical College. Department of Microbiology and Immunology. Nashville, Tennessee, USA.Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Biologia Celular Rio de Janeiro, RJ. Brasil.Vanderbilt University School of Medicine. Department of Biochemistry. Nashville, Tennessee, USA / Vanderbilt University. Center for Structural Biology. Nashville, Tennessee, USA.A novel antifungal drug candidate, the 1-tetrazole-based agent VT-1161 [(R)-2-(2,4-difluorophenyl)-1,1-difluoro-3-(1H-tetrazol-1-yl)-1-{5-[4-(2,2,2-trifluoroethoxy)phenyl]pyridin-2-yl}propan-2-ol], which is currently in two phase 2b antifungal clinical trials, was found to be a tight-binding ligand (apparent dissociation constant [Kd], 24 nM) and a potent inhibitor of cytochrome P450 sterol 14α-demethylase (CYP51) from the protozoan pathogen Trypanosoma cruzi. Moreover, VT-1161 revealed a high level of antiparasitic activity against amastigotes of the Tulahuen strain of T. cruzi in cellular experiments (50% effective concentration, 2.5 nM) and was active in vivo, causing >99.8% suppression of peak parasitemia in a mouse model of infection with the naturally drug-resistant Y strain of the parasite. The data strongly support the potential utility of VT-1161 in the treatment of Chagas disease. The structural characterization of T. cruzi CYP51 in complex with VT-1161 provides insights into the molecular basis for the compound's inhibitory potency and paves the way for the further rational development of this novel, tetrazole-based inhibitory chemotype both for antiprotozoan chemotherapy and for antifungal chemotherapy.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/23847/1/license.txt5a560609d32a3863062d77ff32785d58MD51ORIGINALcristiane_silva_etal_IOC_2015.pdfcristiane_silva_etal_IOC_2015.pdfapplication/pdf5445844https://www.arca.fiocruz.br/bitstream/icict/23847/2/cristiane_silva_etal_IOC_2015.pdf440afb546bec46bb94db09cbd9ea5376MD52TEXTcristiane_silva_etal_IOC_2015.pdf.txtcristiane_silva_etal_IOC_2015.pdf.txtExtracted 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dc.title.pt_BR.fl_str_mv Clinical Candidate VT-1161's Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi
title Clinical Candidate VT-1161's Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi
spellingShingle Clinical Candidate VT-1161's Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi
Hoekstra, William J.
Doença de Chagas
Trypanosoma cruzi
Tratamento
Meidcamentos Antifúngicos
Chagas Disease
Trypanosoma cruzi
VT-1161
Treatment
Murine Model
Target Enzyme CYP51
title_short Clinical Candidate VT-1161's Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi
title_full Clinical Candidate VT-1161's Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi
title_fullStr Clinical Candidate VT-1161's Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi
title_full_unstemmed Clinical Candidate VT-1161's Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi
title_sort Clinical Candidate VT-1161's Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi
author Hoekstra, William J.
author_facet Hoekstra, William J.
Hargrove, Tatiana Y.
Wawrzak, Zdzislaw
Batista, Denise da Gama Jaen
Silva, Cristiane F. da
Nefertiti, Aline S. G.
Rachakonda, Girish
Schotzinger, Robert J.
Villalta, Fernando
Soeiro, Maria de Nazaré C.
Lepesheva, Galina I.
author_role author
author2 Hargrove, Tatiana Y.
Wawrzak, Zdzislaw
Batista, Denise da Gama Jaen
Silva, Cristiane F. da
Nefertiti, Aline S. G.
Rachakonda, Girish
Schotzinger, Robert J.
Villalta, Fernando
Soeiro, Maria de Nazaré C.
Lepesheva, Galina I.
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Hoekstra, William J.
Hargrove, Tatiana Y.
Wawrzak, Zdzislaw
Batista, Denise da Gama Jaen
Silva, Cristiane F. da
Nefertiti, Aline S. G.
Rachakonda, Girish
Schotzinger, Robert J.
Villalta, Fernando
Soeiro, Maria de Nazaré C.
Lepesheva, Galina I.
dc.subject.other.pt_BR.fl_str_mv Doença de Chagas
Trypanosoma cruzi
Tratamento
Meidcamentos Antifúngicos
topic Doença de Chagas
Trypanosoma cruzi
Tratamento
Meidcamentos Antifúngicos
Chagas Disease
Trypanosoma cruzi
VT-1161
Treatment
Murine Model
Target Enzyme CYP51
dc.subject.en.pt_BR.fl_str_mv Chagas Disease
Trypanosoma cruzi
VT-1161
Treatment
Murine Model
Target Enzyme CYP51
description Viamet Pharmaceuticals, Inc.. Durham, North Carolina, USA.;
publishDate 2016
dc.date.issued.fl_str_mv 2016
dc.date.accessioned.fl_str_mv 2018-01-02T16:44:44Z
dc.date.available.fl_str_mv 2018-01-02T16:44:44Z
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 HOEKSTRA, William J. et al. Clinical Candidate VT-1161’s Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi. Antimicrobial Agents and Chemotherapy, v.60, n.2, p.1058-1066, Feb. 2016.
dc.identifier.uri.fl_str_mv https://www.arca.fiocruz.br/handle/icict/23847
dc.identifier.issn.pt_BR.fl_str_mv 0066-4804
dc.identifier.doi.none.fl_str_mv 10.1128/AAC.02287-15
dc.identifier.eissn.none.fl_str_mv 1098-6596
identifier_str_mv HOEKSTRA, William J. et al. Clinical Candidate VT-1161’s Antiparasitic Effect In Vitro, Activity in a Murine Model of Chagas Disease, and Structural Characterization in Complex with the Target Enzyme CYP51 from Trypanosoma cruzi. Antimicrobial Agents and Chemotherapy, v.60, n.2, p.1058-1066, Feb. 2016.
0066-4804
10.1128/AAC.02287-15
1098-6596
url https://www.arca.fiocruz.br/handle/icict/23847
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv American Society for Microbiology
publisher.none.fl_str_mv American Society for Microbiology
dc.source.none.fl_str_mv reponame:Repositório Institucional da FIOCRUZ (ARCA)
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collection Repositório Institucional da FIOCRUZ (ARCA)
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