Alkaloids from croton echinocarpus baill.: Anti-hiv potential

Detalhes bibliográficos
Autor(a) principal: Ravanelli, N.
Data de Publicação: 2016
Outros Autores: Santos, Kátia P., Motta, Lucimar Barbosa da, Lago, Joao Henrique Ghilardi [UNIFESP], Furlan, Cláudia Maria
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/49647
https://doi.org/10.1016/j.sajb.2015.06.011
Resumo: Croton belongs to the Euphorbiaceae genus, one of the major Angiosperms families, and is widely distributed throughout the world, especially in the tropics. In this study, the hydroalcoholic extract (70% EtOH) of Croton echinocarpus leaves afforded two alkaloids: corydine and norisoboldine, and their structures were established by spectroscopic data interpretation (UV, IR, NMR and LREIMS). Both alkaloids displayed significant in vitro anti-HIV potential, inhibiting 40% of the HIV-1 reverse transcriptase enzyme activity at a concentration of 100 mu g mL(-1) of norisoboldine and 450 mu g mL(-1) of corydine. Corydine showed IC50 of 356.8 mu g mL(-1), while norisoboldine was more efficient on inhibiting the RT activity, showing IC50 of 153.7 mu g mL(-1). (C) 2015 SAAB. Published by Elsevier B.V. All rights reserved.
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spelling Ravanelli, N.Santos, Kátia P.Motta, Lucimar Barbosa daLago, Joao Henrique Ghilardi [UNIFESP]Furlan, Cláudia Maria2019-01-21T10:30:14Z2019-01-21T10:30:14Z2016South African Journal Of Botany. Amsterdam, v. 102, p. 153-156, 2016.0254-6299http://repositorio.unifesp.br/handle/11600/49647https://doi.org/10.1016/j.sajb.2015.06.01110.1016/j.sajb.2015.06.011WOS:000368959100021Croton belongs to the Euphorbiaceae genus, one of the major Angiosperms families, and is widely distributed throughout the world, especially in the tropics. In this study, the hydroalcoholic extract (70% EtOH) of Croton echinocarpus leaves afforded two alkaloids: corydine and norisoboldine, and their structures were established by spectroscopic data interpretation (UV, IR, NMR and LREIMS). Both alkaloids displayed significant in vitro anti-HIV potential, inhibiting 40% of the HIV-1 reverse transcriptase enzyme activity at a concentration of 100 mu g mL(-1) of norisoboldine and 450 mu g mL(-1) of corydine. Corydine showed IC50 of 356.8 mu g mL(-1), while norisoboldine was more efficient on inhibiting the RT activity, showing IC50 of 153.7 mu g mL(-1). (C) 2015 SAAB. Published by Elsevier B.V. All rights reserved.Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [FAPESP 2012/10079-0]Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)Department of Botany, Institute of Bioscience, University of São Paulo, Rua do Matão 277, CEP 05508-090 São Paulo, SP, BrazilUniversidade Paulista, Rua Apeninos 267, CEP 01533-000 São Paulo, SP, BrazilInstituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Rua Prof. Arthur Riedel 275, CEP 09972-270 Diadema, SP, BrazilInstituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Rua Prof. Arthur Riedel 275, CEP 09972-270 Diadema, SP, BrazilFAPESP: 2012/10079-0Web of Science153-156engElsevier science bvSouth African Journal Of BotanyNorisoboldineCorydineCrotonAnti-Hiv ActivityDragons BloodMolecular PhylogeneticsEuphorbiaceaeExtractsIdentificationConstituentsUrucuranaPlantsAlkaloids from croton echinocarpus baill.: Anti-hiv potentialinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/496472021-09-28 16:10:24.306metadata only accessoai:repositorio.unifesp.br:11600/49647Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652021-09-28T19:10:24Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Alkaloids from croton echinocarpus baill.: Anti-hiv potential
title Alkaloids from croton echinocarpus baill.: Anti-hiv potential
spellingShingle Alkaloids from croton echinocarpus baill.: Anti-hiv potential
Ravanelli, N.
Norisoboldine
Corydine
Croton
Anti-Hiv ActivityDragons Blood
Molecular Phylogenetics
Euphorbiaceae
Extracts
Identification
Constituents
Urucurana
Plants
title_short Alkaloids from croton echinocarpus baill.: Anti-hiv potential
title_full Alkaloids from croton echinocarpus baill.: Anti-hiv potential
title_fullStr Alkaloids from croton echinocarpus baill.: Anti-hiv potential
title_full_unstemmed Alkaloids from croton echinocarpus baill.: Anti-hiv potential
title_sort Alkaloids from croton echinocarpus baill.: Anti-hiv potential
author Ravanelli, N.
author_facet Ravanelli, N.
Santos, Kátia P.
Motta, Lucimar Barbosa da
Lago, Joao Henrique Ghilardi [UNIFESP]
Furlan, Cláudia Maria
author_role author
author2 Santos, Kátia P.
Motta, Lucimar Barbosa da
Lago, Joao Henrique Ghilardi [UNIFESP]
Furlan, Cláudia Maria
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Ravanelli, N.
Santos, Kátia P.
Motta, Lucimar Barbosa da
Lago, Joao Henrique Ghilardi [UNIFESP]
Furlan, Cláudia Maria
dc.subject.eng.fl_str_mv Norisoboldine
Corydine
Croton
Anti-Hiv ActivityDragons Blood
Molecular Phylogenetics
Euphorbiaceae
Extracts
Identification
Constituents
Urucurana
Plants
topic Norisoboldine
Corydine
Croton
Anti-Hiv ActivityDragons Blood
Molecular Phylogenetics
Euphorbiaceae
Extracts
Identification
Constituents
Urucurana
Plants
description Croton belongs to the Euphorbiaceae genus, one of the major Angiosperms families, and is widely distributed throughout the world, especially in the tropics. In this study, the hydroalcoholic extract (70% EtOH) of Croton echinocarpus leaves afforded two alkaloids: corydine and norisoboldine, and their structures were established by spectroscopic data interpretation (UV, IR, NMR and LREIMS). Both alkaloids displayed significant in vitro anti-HIV potential, inhibiting 40% of the HIV-1 reverse transcriptase enzyme activity at a concentration of 100 mu g mL(-1) of norisoboldine and 450 mu g mL(-1) of corydine. Corydine showed IC50 of 356.8 mu g mL(-1), while norisoboldine was more efficient on inhibiting the RT activity, showing IC50 of 153.7 mu g mL(-1). (C) 2015 SAAB. Published by Elsevier B.V. All rights reserved.
publishDate 2016
dc.date.issued.fl_str_mv 2016
dc.date.accessioned.fl_str_mv 2019-01-21T10:30:14Z
dc.date.available.fl_str_mv 2019-01-21T10:30:14Z
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 South African Journal Of Botany. Amsterdam, v. 102, p. 153-156, 2016.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/49647
https://doi.org/10.1016/j.sajb.2015.06.011
dc.identifier.issn.none.fl_str_mv 0254-6299
dc.identifier.doi.none.fl_str_mv 10.1016/j.sajb.2015.06.011
dc.identifier.wos.none.fl_str_mv WOS:000368959100021
identifier_str_mv South African Journal Of Botany. Amsterdam, v. 102, p. 153-156, 2016.
0254-6299
10.1016/j.sajb.2015.06.011
WOS:000368959100021
url http://repositorio.unifesp.br/handle/11600/49647
https://doi.org/10.1016/j.sajb.2015.06.011
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv South African Journal Of Botany
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 153-156
dc.publisher.none.fl_str_mv Elsevier science bv
publisher.none.fl_str_mv Elsevier science bv
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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