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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/68423
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dc.contributor.authorTeles, Helder Lopes-
dc.contributor.authorAraújo, Ângela Regina-
dc.contributor.authorSilva, Geraldo Humberto-
dc.contributor.authorCastro-Gamboa, Ian-
dc.contributor.authorBolzani, Vanderlan da Silva-
dc.contributor.authorPereira, José Odair-
dc.contributor.authorCosta-Neto, Claudio Miguel-
dc.contributor.authorHaddad, Renato-
dc.contributor.authorEberlin, Marcos Nogueira-
dc.contributor.authorYoung, Maria Claudia Marx-
dc.date.accessioned2014-05-27T11:21:38Z-
dc.date.accessioned2016-10-25T18:21:09Z-
dc.date.available2014-05-27T11:21:38Z-
dc.date.available2016-10-25T18:21:09Z-
dc.date.issued2005-10-01-
dc.identifierhttp://dx.doi.org/10.1016/j.phytochem.2005.04.043-
dc.identifier.citationPhytochemistry, v. 66, n. 19, p. 2363-2367, 2005.-
dc.identifier.issn0031-9422-
dc.identifier.urihttp://hdl.handle.net/11449/68423-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/68423-
dc.description.abstractAn isolate of Curvularia sp. was obtained from the leaves of Ocotea corymbosa, a native plant of the Brazilian Cerrado. The ethyl acetate extract from culture of this fungus afforded two benzopyran derivatives: (2′S)-2-(propan-2′-ol)-5-hydroxy-benzopyran-4-one (2) and 2,3-dihydro-2-methyl-benzopyran-4,5-diol (4); and two known benzopyrans: 2-methyl-5-methoxy-benzopyran-4-one (1) and (2R)-2,3-dihydro-2-methyl-5-methoxy- benzopyran-4-one (3). The structures of 2 and 4 were established on the basis of comprehensive spectroscopic analysis, mainly using 1D and 2D NMR experiments. The benzopyrans 1 and 2 showed weak in vitro antifungal activity against Cladosporium sphaerospermum and C. cladosporioides. Analyses of the biological activities were also carried out on HeLa (human cervix tumor) and CHO (Chinese hamster ovary) cells, aiming to evaluate their potential effects on mammalian cell line proliferation. Results from both cell lines indicated that compound 2 was able to induce cell proliferation: 70% on HeLa cells and 25% on CHO cells. © 2005 Elsevier Ltd. All rights reserved.en
dc.format.extent2363-2367-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectBenzopyrans-
dc.subjectCell proliferation-
dc.subjectCurvularia-
dc.subjectEndophytic fungi-
dc.subjectMetabolites-
dc.subjectantifungal agent-
dc.subjectantineoplastic agent-
dc.subjectbenzopyran derivative-
dc.subjectanimal-
dc.subjectAscomycetes-
dc.subjectcell proliferation-
dc.subjectcell survival-
dc.subjectchemical structure-
dc.subjectchemistry-
dc.subjectCricetulus-
dc.subjectdrug effect-
dc.subjectdrug screening-
dc.subjectgrowth, development and aging-
dc.subjecthamster-
dc.subjecthuman-
dc.subjectisolation and purification-
dc.subjectmicrobiology-
dc.subjectOcotea-
dc.subjecttumor cell line-
dc.subjectAnimals-
dc.subjectAntifungal Agents-
dc.subjectAntineoplastic Agents-
dc.subjectAscomycota-
dc.subjectCell Line, Tumor-
dc.subjectCell Proliferation-
dc.subjectCell Survival-
dc.subjectCricetinae-
dc.subjectDrug Screening Assays, Antitumor-
dc.subjectHumans-
dc.subjectMolecular Structure-
dc.subjectCladosporium-
dc.subjectCladosporium cladosporioides-
dc.subjectCladosporium sphaerospermum-
dc.subjectCricetulus griseus-
dc.subjectFungi-
dc.subjectLauraceae-
dc.subjectMagnoliophyta-
dc.subjectMammalia-
dc.subjectOcotea corymbosa-
dc.titleBenzopyrans from Curvularia sp., an endophytic fungus associated with Ocotea corymbosa (Lauraceae)en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Do Amazonas-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionInstituto de Botânica-
dc.description.affiliationNuBBE-Núcleo de Bioensaio, Biossíntese e Ecofisiologia de Produtos Naturais Instituto de Química Universidade Estadual Paulista, CP 355, CEP 14801-970, Araraquara, SP-
dc.description.affiliationFaculdade de Ciências Agrárias Universidade Do Amazonas, CEP 69077-000, Manaus, AM-
dc.description.affiliationDepartamento de Bioquímica e Imunologia Faculdade de Medicina de Ribeirão Preto Universidade de São Paulo, CEP 14049-900, Ribeirao Preto, SP-
dc.description.affiliationThompson Mass Spectroscopy Laboratory Instituto de Química Universidade Estadual de Campinas, CP 6154, CEP 13083-970, Campinas, SP-
dc.description.affiliationSecção de Fisiologia e Bioquímica de Plantas Instituto de Botânica, CP 4009, CEP 01061-970, São Paulo, SP-
dc.description.affiliationUnespNuBBE-Núcleo de Bioensaio, Biossíntese e Ecofisiologia de Produtos Naturais Instituto de Química Universidade Estadual Paulista, CP 355, CEP 14801-970, Araraquara, SP-
dc.identifier.doi10.1016/j.phytochem.2005.04.043-
dc.identifier.wosWOS:000232842000012-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofPhytochemistry-
dc.identifier.scopus2-s2.0-26044472099-
dc.identifier.orcid0000-0001-7616-9652pt
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