Estudo químico de Croton echioides
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Biblioteca Digital de Teses e Dissertações da UFRPE |
Texto Completo: | http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/7040 |
Resumo: | The Croton genus is among the most studied of the Euphorbiaceae family, is the second largest genus in the family and is classified as the 11th largest genus of flowering plants. Belonging to the subfamily Crotonoideae, is represented by about 1,200 species. Among them, the Croton echioides species, popularly known in northeastern Brazil as “caatinga branca", "cinnamon-of-old", "break-knife" or “stench of goat” is restricted to the Caatinga biome. This study aimed to investigate the chemical constituents of the species Croton echioides. The stem bark was extracted with EtOH, the extract was suspended in MeOH: H2O (1: 1), and partitioned with hexane and AcOEt. Fraction of MeOH: H2O were isolated two alkaloids 5,6,6a, 7-tetrahydro-1,11-dihydroxy-2,10-dimethoxy-6,6-dimethyl-4H-5,6,6a dibenzoquinolínium and, 7- tetrahydro-11-hydroxy-1,2,10-trimethoxy-6,6-dimethyl-4H-dibenzoquinolínium (Substances 1 and 2). The hexane fraction were isolated three terpenes, 3β-lup-20 (29)-en-3-ol (Substance 3) 15,16-epoxy-3-13(16)-clerodano-6-ol (Substance 4) and 15,16-epoxy-3-13(16)-clerodano-6,7-ol (Substance 5), the substances were identified by the 1H NMR spectra and APT, including two-dimensional and mass. Four of the isolated compounds are reported for the first time in this species. |
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SILVA, Tania Maria Sarmento daNASCIMENTO, Marcia Silva doCAMARA, Celso de AmorimLINS, Antônio Cláudio da Silvahttp://lattes.cnpq.br/5406132281593591NATIVIDADE, Tamires Botelho da2017-08-02T13:03:04Z2015-02-23NATIVIDADE, Tamires Botelho da. Estudo químico de Croton echioides. 2015. 74 f. Dissertação (Programa de Pós-Graduação em Química) - Universidade Federal Rural de Pernambuco, Recife.http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/7040The Croton genus is among the most studied of the Euphorbiaceae family, is the second largest genus in the family and is classified as the 11th largest genus of flowering plants. Belonging to the subfamily Crotonoideae, is represented by about 1,200 species. Among them, the Croton echioides species, popularly known in northeastern Brazil as “caatinga branca", "cinnamon-of-old", "break-knife" or “stench of goat” is restricted to the Caatinga biome. This study aimed to investigate the chemical constituents of the species Croton echioides. The stem bark was extracted with EtOH, the extract was suspended in MeOH: H2O (1: 1), and partitioned with hexane and AcOEt. Fraction of MeOH: H2O were isolated two alkaloids 5,6,6a, 7-tetrahydro-1,11-dihydroxy-2,10-dimethoxy-6,6-dimethyl-4H-5,6,6a dibenzoquinolínium and, 7- tetrahydro-11-hydroxy-1,2,10-trimethoxy-6,6-dimethyl-4H-dibenzoquinolínium (Substances 1 and 2). The hexane fraction were isolated three terpenes, 3β-lup-20 (29)-en-3-ol (Substance 3) 15,16-epoxy-3-13(16)-clerodano-6-ol (Substance 4) and 15,16-epoxy-3-13(16)-clerodano-6,7-ol (Substance 5), the substances were identified by the 1H NMR spectra and APT, including two-dimensional and mass. Four of the isolated compounds are reported for the first time in this species.O gênero Croton L. encontra-se entre os mais estudados da família Euphorbiaceae, sendo o segundo maior gênero desta família, classificando-se como o 11° maior gênero entre as angiospermas. Pertencente a subfamília Crotonoideae, está representado por aproximadamente 1.200 espécies. Dentre elas, a espécie Croton echioides, popularmente conhecida na região nordeste do Brasil como “caantinga branca”, “canela-de-velho”,“quebra-faca” ou “caatinga de bode” é restrita ao bioma Caatinga. Este trabalho teve como objetivo investigar os constituintes químicos da espécie Croton echioides. A casca do caule foi extraído com EtOH, esse extrato foi suspenso em MeOH:H2O (1:1), e particionado com hexano e AcOEt. Da fração MeOH:H2O foram isolados dois alcaloides, 5,6,6a,7-tetrahidro-1,11-dihidroxi-2,10-dimetoxi-6,6-dimetil-4H-dibenzoquinolínio e 5,6,6a,7-tetrahidro-11-hidroxi-1,2,10-trimetoxi-6,6-dimetil-4H-dibenzoquinolínio (Substâncias 1 e 2). Da fração hexânica foram isolados três terpenos, 3β-lup-20(29)-en-3-ol (Substância 3), 15,16-epoxi-3-13(16)-clerodano-6-ol (Substância 4) e 15,16-epoxi-3-13(16)-clerodano-6,7-ol (Substância 5), as substâncias foram identificadas através dos espectros de RMN de 1H e APT, incluindo bidimensionais e massas. Quatro das substâncias isoladas são relatadas pela primeira vez nesta espécie.Submitted by Mario BC (mario@bc.ufrpe.br) on 2017-08-02T13:03:04Z No. of bitstreams: 1 Tamires Botelho da Natividade.pdf: 2563879 bytes, checksum: 52f923c1e51b91ccac43f0275f4a88e1 (MD5)Made available in DSpace on 2017-08-02T13:03:04Z (GMT). No. of bitstreams: 1 Tamires Botelho da Natividade.pdf: 2563879 bytes, checksum: 52f923c1e51b91ccac43f0275f4a88e1 (MD5) Previous issue date: 2015-02-23Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfporUniversidade Federal Rural de PernambucoPrograma de Pós-Graduação em QuímicaUFRPEBrasilDepartamento de QuímicaEstudo químicoCroton echioidesAngiospermaCIENCIAS EXATAS E DA TERRA::QUIMICAEstudo químico de Croton echioidesinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis1435648362225100898600600600600380641605545709103015717003253031171952075167498588264571info:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UFRPEinstname:Universidade Federal Rural de Pernambuco (UFRPE)instacron:UFRPELICENSElicense.txtlicense.txttext/plain; charset=utf-82165http://www.tede2.ufrpe.br:8080/tede2/bitstream/tede2/7040/1/license.txtbd3efa91386c1718a7f26a329fdcb468MD51ORIGINALTamires Botelho da Natividade.pdfTamires Botelho da Natividade.pdfapplication/pdf2563879http://www.tede2.ufrpe.br:8080/tede2/bitstream/tede2/7040/2/Tamires+Botelho+da+Natividade.pdf52f923c1e51b91ccac43f0275f4a88e1MD52tede2/70402017-08-02 10:03:04.798oai:tede2: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Biblioteca Digital de Teses e Dissertaçõeshttp://www.tede2.ufrpe.br:8080/tede/PUBhttp://www.tede2.ufrpe.br:8080/oai/requestbdtd@ufrpe.br ||bdtd@ufrpe.bropendoar:2024-05-28T12:35:07.716747Biblioteca Digital de Teses e Dissertações da UFRPE - Universidade Federal Rural de Pernambuco (UFRPE)false |
dc.title.por.fl_str_mv |
Estudo químico de Croton echioides |
title |
Estudo químico de Croton echioides |
spellingShingle |
Estudo químico de Croton echioides NATIVIDADE, Tamires Botelho da Estudo químico Croton echioides Angiosperma CIENCIAS EXATAS E DA TERRA::QUIMICA |
title_short |
Estudo químico de Croton echioides |
title_full |
Estudo químico de Croton echioides |
title_fullStr |
Estudo químico de Croton echioides |
title_full_unstemmed |
Estudo químico de Croton echioides |
title_sort |
Estudo químico de Croton echioides |
author |
NATIVIDADE, Tamires Botelho da |
author_facet |
NATIVIDADE, Tamires Botelho da |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
SILVA, Tania Maria Sarmento da |
dc.contributor.referee1.fl_str_mv |
NASCIMENTO, Marcia Silva do |
dc.contributor.referee2.fl_str_mv |
CAMARA, Celso de Amorim |
dc.contributor.referee3.fl_str_mv |
LINS, Antônio Cláudio da Silva |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/5406132281593591 |
dc.contributor.author.fl_str_mv |
NATIVIDADE, Tamires Botelho da |
contributor_str_mv |
SILVA, Tania Maria Sarmento da NASCIMENTO, Marcia Silva do CAMARA, Celso de Amorim LINS, Antônio Cláudio da Silva |
dc.subject.por.fl_str_mv |
Estudo químico Croton echioides Angiosperma |
topic |
Estudo químico Croton echioides Angiosperma CIENCIAS EXATAS E DA TERRA::QUIMICA |
dc.subject.cnpq.fl_str_mv |
CIENCIAS EXATAS E DA TERRA::QUIMICA |
description |
The Croton genus is among the most studied of the Euphorbiaceae family, is the second largest genus in the family and is classified as the 11th largest genus of flowering plants. Belonging to the subfamily Crotonoideae, is represented by about 1,200 species. Among them, the Croton echioides species, popularly known in northeastern Brazil as “caatinga branca", "cinnamon-of-old", "break-knife" or “stench of goat” is restricted to the Caatinga biome. This study aimed to investigate the chemical constituents of the species Croton echioides. The stem bark was extracted with EtOH, the extract was suspended in MeOH: H2O (1: 1), and partitioned with hexane and AcOEt. Fraction of MeOH: H2O were isolated two alkaloids 5,6,6a, 7-tetrahydro-1,11-dihydroxy-2,10-dimethoxy-6,6-dimethyl-4H-5,6,6a dibenzoquinolínium and, 7- tetrahydro-11-hydroxy-1,2,10-trimethoxy-6,6-dimethyl-4H-dibenzoquinolínium (Substances 1 and 2). The hexane fraction were isolated three terpenes, 3β-lup-20 (29)-en-3-ol (Substance 3) 15,16-epoxy-3-13(16)-clerodano-6-ol (Substance 4) and 15,16-epoxy-3-13(16)-clerodano-6,7-ol (Substance 5), the substances were identified by the 1H NMR spectra and APT, including two-dimensional and mass. Four of the isolated compounds are reported for the first time in this species. |
publishDate |
2015 |
dc.date.issued.fl_str_mv |
2015-02-23 |
dc.date.accessioned.fl_str_mv |
2017-08-02T13:03:04Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
NATIVIDADE, Tamires Botelho da. Estudo químico de Croton echioides. 2015. 74 f. Dissertação (Programa de Pós-Graduação em Química) - Universidade Federal Rural de Pernambuco, Recife. |
dc.identifier.uri.fl_str_mv |
http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/7040 |
identifier_str_mv |
NATIVIDADE, Tamires Botelho da. Estudo químico de Croton echioides. 2015. 74 f. Dissertação (Programa de Pós-Graduação em Química) - Universidade Federal Rural de Pernambuco, Recife. |
url |
http://www.tede2.ufrpe.br:8080/tede2/handle/tede2/7040 |
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por |
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por |
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1435648362225100898 |
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600 600 600 600 |
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info:eu-repo/semantics/openAccess |
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openAccess |
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Universidade Federal Rural de Pernambuco |
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Programa de Pós-Graduação em Química |
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UFRPE |
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Brasil |
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Departamento de Química |
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Universidade Federal Rural de Pernambuco |
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