Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae)

Detalhes bibliográficos
Ano de defesa: 2003
Autor(a) principal: Alves, Cassia Cristina Fernandes lattes
Orientador(a): Carvalho, Mario Geraldo de lattes
Banca de defesa: Carvalho, Mario Geraldo de, Schripsema, Jan, Leit?o, Gilda G., Castro, Rosane Nora, Lima, Marco Edilson Freire de
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal Rural do Rio de Janeiro
Programa de Pós-Graduação: Programa de P?s-Gradua??o em Qu?mica
Departamento: Instituto de Ci?ncias Exatas
País: Brasil
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: https://tede.ufrrj.br/jspui/handle/jspui/4306
Resumo: The analysis of the fractions from the chromatographic fractionation of lhe extracts from Luxemburgia ocrandra (Ochnaceae), latex from Parahancomia amapa (Apocynaceae), Lasegue erecra (Apocynaceae) and from Solanum crinitum (Solanaceae) led to the isolation of some chemical constituents which belong to different classes of special metabolites. From the branches of L. octandra were isolated sitosterol, stigmasterol, lupeol, betulinic acid, chalcone, isoliquiritigenin (2,4,4'trihydroxychalcone), 3,4,3',4'-tetrahydroxychalcone, a mixture of two Cglucopiranosylflavone, 8-C-glucopiranosilluteolin and 8-C-glucopiranosyl-7-methylluteolin, and two biflavoooids, 2",3"-dihydroochnaflavone [5,7,4'-trihydroxychalcone(4'-0-3"')-2",4"-dihydroxychalcone. From the latex of P. amapa were isolated three phenylethanoids, comoside [4-hydroxy-4-(2-0 -P-D-glycopiranosyl-ethylene) cyclohexadienone ), 2-p-hydroxyphenylethanol and 2-( 4-hydroxy-3-methoxyphenyl)ethanol and a mixture of acyl esters of lupool, a-amyrio and P-amyrin. From the wood of L. erecla were isolated scopoletin, the lignoid pinoresinol and the saponin digitoxigenin. Toe steroidal alcaloid solasonin and the flavonoid tiliroside [3-0-(?-D-glucopiranosyl-6'-coumaroil)-kanferol) were isolated, respectively, from the fruits and from the tricomes of S. crinilum. The structures were determined by IR, MS and 1H and 13C NMR spectra analysis. Besides the identification of the new bichalcone, named luxenchalcone, new derivatives, luxenchalcone-trimethylether, luxenchalcone-permethylether, luxenchalcone-peracetylester, tetraacetyl-comoside and peracetylsolasonine were also prepared. Toe general toxicity was eralvated against Artemia salina. Toe anti-helmintic activity of extracts from L. octandra was also studied. Furthermore, the cytotoxic activity against Ehrlich carcinoma and K 562 human leukemia of solasonine, total glycoalkaloids, tiliroside, luxencbalcone and its derivatives was carrie<I onl Finally, the total glycoalkaloids and solasonine were also teste<! for alelopathic activity and were found to be quite active.
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spelling Carvalho, Mario Geraldo dehttp://lattes.cnpq.br/9794451665032168Carvalho, Mario Geraldo deSchripsema, JanLeit?o, Gilda G.Castro, Rosane NoraLima, Marco Edilson Freire dehttp://lattes.cnpq.br/6968560510108605Alves, Cassia Cristina Fernandes2020-12-29T15:22:53Z2003-10-24ALVES, Cassia Cristina Fernandes. Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae). 2003. 197 f. Tese (Doutorado em Qu?mica) - Instituto de Ci?ncias Exatas, Universidade Federal Rural do Rio de Janeiro, Serop?dica-RJ, 2003.https://tede.ufrrj.br/jspui/handle/jspui/4306The analysis of the fractions from the chromatographic fractionation of lhe extracts from Luxemburgia ocrandra (Ochnaceae), latex from Parahancomia amapa (Apocynaceae), Lasegue erecra (Apocynaceae) and from Solanum crinitum (Solanaceae) led to the isolation of some chemical constituents which belong to different classes of special metabolites. From the branches of L. octandra were isolated sitosterol, stigmasterol, lupeol, betulinic acid, chalcone, isoliquiritigenin (2,4,4'trihydroxychalcone), 3,4,3',4'-tetrahydroxychalcone, a mixture of two Cglucopiranosylflavone, 8-C-glucopiranosilluteolin and 8-C-glucopiranosyl-7-methylluteolin, and two biflavoooids, 2",3"-dihydroochnaflavone [5,7,4'-trihydroxychalcone(4'-0-3"')-2",4"-dihydroxychalcone. From the latex of P. amapa were isolated three phenylethanoids, comoside [4-hydroxy-4-(2-0 -P-D-glycopiranosyl-ethylene) cyclohexadienone ), 2-p-hydroxyphenylethanol and 2-( 4-hydroxy-3-methoxyphenyl)ethanol and a mixture of acyl esters of lupool, a-amyrio and P-amyrin. From the wood of L. erecla were isolated scopoletin, the lignoid pinoresinol and the saponin digitoxigenin. Toe steroidal alcaloid solasonin and the flavonoid tiliroside [3-0-(?-D-glucopiranosyl-6'-coumaroil)-kanferol) were isolated, respectively, from the fruits and from the tricomes of S. crinilum. The structures were determined by IR, MS and 1H and 13C NMR spectra analysis. Besides the identification of the new bichalcone, named luxenchalcone, new derivatives, luxenchalcone-trimethylether, luxenchalcone-permethylether, luxenchalcone-peracetylester, tetraacetyl-comoside and peracetylsolasonine were also prepared. Toe general toxicity was eralvated against Artemia salina. Toe anti-helmintic activity of extracts from L. octandra was also studied. Furthermore, the cytotoxic activity against Ehrlich carcinoma and K 562 human leukemia of solasonine, total glycoalkaloids, tiliroside, luxencbalcone and its derivatives was carrie<I onl Finally, the total glycoalkaloids and solasonine were also teste<! for alelopathic activity and were found to be quite active.A an?lise das fra??es obtidas do processamento cromatogr?fico dos extratos das esp?cies Luxemburgia ocrandra (Ochnaceae), l?tex de Parahancorn?a amapa (Apocynaceae), Laseguea erecta (Apocynaceae) e Solanum crinitum (Solanaceae) conduziu ao isolamento de constituintes de diferentes classes de metab?litos especiais. De Luxemburgia octandra foram isolados os ester?ides, sitosterol e estigmasterol, dois triterpenos, lupcol e ?cido betul?nico, uma chalcona sem substituintes, a isoliquiritigenina (2,4,4'-triidroxichalcona) e a 2,4,3',4'-tetraidroxichalcona, uma mistura de C.glicosilflavon?ides, 8-C-glicopiranosilluteolina (5,7,3',4'-tetraidroxi-8-Cglicopiranosil-flavona) e a 8-C-glicopiranosil-7-metil-luteolina, e dois bisflavon?ides, 2",3' -diidroochnaflavona [5,7,4'-triidroxiflavona-(3'-0-4''')-5'',7"-diidroxiflavanona] e 2.4,3'-triidroxichalcona-(4'-0-3'")-2",4"-diidroxichalcona. Do l?tex de P. amapa foram isolados tr?s feniletan?ides, cornos?deo {4-hidroxi-4-(2-O-13-D-glicopiranosil-etileno) cicloexadienona], 2-p-hidroxifeniletanol e 2-(4-hidroxi-3-metoxifenil~tanol e uma mistura de ?steres acil-lupeol, acil-a.-amirina e acil-13-amirina. Do caule de Laseguea erecta foram isolados a cumarina (escopoletina), o lign?ide pinoresinol e a saponina digitoxigenina (?-L-tevetos?deo). Dos frutos de S. crinilum foi isolado o alcal?ide esteroidal solasonina e dos tricomas dos frutos isolou-se o flavon?ide tiliros?deo [3-O-(?-D-glicopiranosil-6'-cumaroil)-canferol]. As estruturas foram identificadas atrav?s da an?lise de espectros IV, massas e RMN1H e 13C, incluindo t?cnicas especiais 1D e 2D de intera??o homonuclear (1Hx1HCOSY) e heteronuclear (1Hx 13C-COSY) das subst?ncias naturais e derivados meti lados e acetilados. Al?m da identifica??o de uma nova bichalcona natural que foi denominada luxenchalcona, foram preparados novos derivados desta subst?ncia, o trimetil?ter, o permetil?ter e o peracetil ?ster, al?m do tetraacetil-cornos?deo e da solasoninaperacetilada. Realizaram-se os testes biol?gicos: toxidade com Artemia salina, atividade antihelm?ntica com extratos de Luxemburgi.a octandra. Atividade citot?xica contra carcinoma de Ehrlich e leucemia humana K562 foram feitos com a solasonina, os glicoalcal?ides totais e o tilirosideo de Solanum crinirum e da Juxenchalcona e seus derivados. Os glicoalcal?ides totais e a solasonina foram avaliados quanto ? atividade alelop?tica.Submitted by Celso Magalhaes (celsomagalhaes@ufrrj.br) on 2020-12-29T15:22:53Z No. of bitstreams: 1 2003 - Cassia Cristina Fernandes Alves.pdf: 7802016 bytes, checksum: 2a5f3e268396740c9f559db850420361 (MD5)Made available in DSpace on 2020-12-29T15:22:53Z (GMT). No. of bitstreams: 1 2003 - Cassia Cristina Fernandes Alves.pdf: 7802016 bytes, checksum: 2a5f3e268396740c9f559db850420361 (MD5) Previous issue date: 2003-10-24Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior - CAPESConselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico - CNPqFunda??o de Amparo ? Pesquisa do Estado do Rio de Janeiro - FAPERJapplication/pdfhttps://tede.ufrrj.br/retrieve/63673/2003%20-%20Cassia%20Cristina%20Fernandes%20Alves.pdf.jpgporUniversidade Federal Rural do Rio de JaneiroPrograma de P?s-Gradua??o em Qu?micaUFRRJBrasilInstituto de Ci?ncias ExatasFlavon?idesterpenosfeniletan?idesflavonoidsterpenoidsphenylethanoidsQu?micaMetab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae)info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UFRRJinstname:Universidade Federal Rural do Rio de Janeiro (UFRRJ)instacron:UFRRJTHUMBNAIL2003 - Cassia Cristina Fernandes Alves.pdf.jpg2003 - Cassia Cristina Fernandes Alves.pdf.jpgimage/jpeg3585http://localhost:8080/tede/bitstream/jspui/4306/4/2003+-+Cassia+Cristina+Fernandes+Alves.pdf.jpg0513681a10784e2ee6029b5d4eb3ee9bMD54TEXT2003 - Cassia Cristina Fernandes Alves.pdf.txt2003 - Cassia Cristina Fernandes Alves.pdf.txttext/plain221http://localhost:8080/tede/bitstream/jspui/4306/3/2003+-+Cassia+Cristina+Fernandes+Alves.pdf.txt0c286e7688cb586078b131fba54f243dMD53ORIGINAL2003 - Cassia Cristina Fernandes Alves.pdf2003 - Cassia Cristina Fernandes Alves.pdfapplication/pdf7802016http://localhost:8080/tede/bitstream/jspui/4306/2/2003+-+Cassia+Cristina+Fernandes+Alves.pdf2a5f3e268396740c9f559db850420361MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-82089http://localhost:8080/tede/bitstream/jspui/4306/1/license.txt7b5ba3d2445355f386edab96125d42b7MD51jspui/43062021-06-03 20:17:49.523oai:localhost: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Biblioteca Digital de Teses e Dissertaçõeshttps://tede.ufrrj.br/PUBhttps://tede.ufrrj.br/oai/requestbibliot@ufrrj.br||bibliot@ufrrj.bropendoar:2021-06-03T23:17:49Biblioteca Digital de Teses e Dissertações da UFRRJ - Universidade Federal Rural do Rio de Janeiro (UFRRJ)false
dc.title.por.fl_str_mv Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae)
title Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae)
spellingShingle Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae)
Alves, Cassia Cristina Fernandes
Flavon?ides
terpenos
feniletan?ides
flavonoids
terpenoids
phenylethanoids
Qu?mica
title_short Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae)
title_full Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae)
title_fullStr Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae)
title_full_unstemmed Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae)
title_sort Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae)
author Alves, Cassia Cristina Fernandes
author_facet Alves, Cassia Cristina Fernandes
author_role author
dc.contributor.advisor1.fl_str_mv Carvalho, Mario Geraldo de
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/9794451665032168
dc.contributor.referee1.fl_str_mv Carvalho, Mario Geraldo de
dc.contributor.referee2.fl_str_mv Schripsema, Jan
dc.contributor.referee3.fl_str_mv Leit?o, Gilda G.
dc.contributor.referee4.fl_str_mv Castro, Rosane Nora
dc.contributor.referee5.fl_str_mv Lima, Marco Edilson Freire de
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/6968560510108605
dc.contributor.author.fl_str_mv Alves, Cassia Cristina Fernandes
contributor_str_mv Carvalho, Mario Geraldo de
Carvalho, Mario Geraldo de
Schripsema, Jan
Leit?o, Gilda G.
Castro, Rosane Nora
Lima, Marco Edilson Freire de
dc.subject.por.fl_str_mv Flavon?ides
terpenos
feniletan?ides
topic Flavon?ides
terpenos
feniletan?ides
flavonoids
terpenoids
phenylethanoids
Qu?mica
dc.subject.eng.fl_str_mv flavonoids
terpenoids
phenylethanoids
dc.subject.cnpq.fl_str_mv Qu?mica
description The analysis of the fractions from the chromatographic fractionation of lhe extracts from Luxemburgia ocrandra (Ochnaceae), latex from Parahancomia amapa (Apocynaceae), Lasegue erecra (Apocynaceae) and from Solanum crinitum (Solanaceae) led to the isolation of some chemical constituents which belong to different classes of special metabolites. From the branches of L. octandra were isolated sitosterol, stigmasterol, lupeol, betulinic acid, chalcone, isoliquiritigenin (2,4,4'trihydroxychalcone), 3,4,3',4'-tetrahydroxychalcone, a mixture of two Cglucopiranosylflavone, 8-C-glucopiranosilluteolin and 8-C-glucopiranosyl-7-methylluteolin, and two biflavoooids, 2",3"-dihydroochnaflavone [5,7,4'-trihydroxychalcone(4'-0-3"')-2",4"-dihydroxychalcone. From the latex of P. amapa were isolated three phenylethanoids, comoside [4-hydroxy-4-(2-0 -P-D-glycopiranosyl-ethylene) cyclohexadienone ), 2-p-hydroxyphenylethanol and 2-( 4-hydroxy-3-methoxyphenyl)ethanol and a mixture of acyl esters of lupool, a-amyrio and P-amyrin. From the wood of L. erecla were isolated scopoletin, the lignoid pinoresinol and the saponin digitoxigenin. Toe steroidal alcaloid solasonin and the flavonoid tiliroside [3-0-(?-D-glucopiranosyl-6'-coumaroil)-kanferol) were isolated, respectively, from the fruits and from the tricomes of S. crinilum. The structures were determined by IR, MS and 1H and 13C NMR spectra analysis. Besides the identification of the new bichalcone, named luxenchalcone, new derivatives, luxenchalcone-trimethylether, luxenchalcone-permethylether, luxenchalcone-peracetylester, tetraacetyl-comoside and peracetylsolasonine were also prepared. Toe general toxicity was eralvated against Artemia salina. Toe anti-helmintic activity of extracts from L. octandra was also studied. Furthermore, the cytotoxic activity against Ehrlich carcinoma and K 562 human leukemia of solasonine, total glycoalkaloids, tiliroside, luxencbalcone and its derivatives was carrie<I onl Finally, the total glycoalkaloids and solasonine were also teste<! for alelopathic activity and were found to be quite active.
publishDate 2003
dc.date.issued.fl_str_mv 2003-10-24
dc.date.accessioned.fl_str_mv 2020-12-29T15:22:53Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.citation.fl_str_mv ALVES, Cassia Cristina Fernandes. Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae). 2003. 197 f. Tese (Doutorado em Qu?mica) - Instituto de Ci?ncias Exatas, Universidade Federal Rural do Rio de Janeiro, Serop?dica-RJ, 2003.
dc.identifier.uri.fl_str_mv https://tede.ufrrj.br/jspui/handle/jspui/4306
identifier_str_mv ALVES, Cassia Cristina Fernandes. Metab?litos especiais isolados de Luxemburgia octandra (Ochnaceae), Laseguea erecta (Apocynaceae), do l?tex de Parahancornia amapa (Apocynaceae) e de Solanum crinitum (Solanaceae). 2003. 197 f. Tese (Doutorado em Qu?mica) - Instituto de Ci?ncias Exatas, Universidade Federal Rural do Rio de Janeiro, Serop?dica-RJ, 2003.
url https://tede.ufrrj.br/jspui/handle/jspui/4306
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Universidade Federal Rural do Rio de Janeiro
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