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dc.contributor.authorOliveira, Camila M.-
dc.contributor.authorRegasini, Luis O.-
dc.contributor.authorSilva, Geraldo H.-
dc.contributor.authorPfenning, Ludwig H.-
dc.contributor.authorYoung, Maria C. M.-
dc.contributor.authorBerlinck, Roberto G. S.-
dc.contributor.authorBolzani, Vanderlan da Silva-
dc.contributor.authorAraujo, Angela R.-
dc.date.accessioned2014-05-20T14:20:04Z-
dc.date.accessioned2016-10-25T17:41:24Z-
dc.date.available2014-05-20T14:20:04Z-
dc.date.available2016-10-25T17:41:24Z-
dc.date.issued2011-06-15-
dc.identifierhttp://dx.doi.org/10.1016/j.phytol.2010.11.003-
dc.identifier.citationPhytochemistry Letters. Amsterdam: Elsevier B.V., v. 4, n. 2, p. 93-96, 2011.-
dc.identifier.issn1874-3900-
dc.identifier.urihttp://hdl.handle.net/11449/26027-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/26027-
dc.description.abstractThe dihydroisocoumarin (3R, 4R)-3,4-dihydro-4,6-dihydroxy-3-methyl-1-oxo-1H-isochromene-5-carboxylic acid (1) was isolated from Xylaria sp., a fungus associated with Piper aduncum (Piperaceae). Additionally, two known compounds, (R)-7-hydroxymellein (2) and (3R, 4R)-4,7-dihydroxymellein (3), were isolated from Penicillium sp. associated to Alibertia macrophylla (Rubiaceae). The structures of all compounds were elucidated by analysis of spectroscopic data. The dihydrocoumarin derivatives 1-3 showed antifungal and acetylcholinesterase (AChE) inhibitory activities in vitro. (C) 2010 Phytochemical Society of Europe. Published by Elsevier B. V. All rights reserved.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipBiodiversity Virtual Institute-
dc.format.extent93-96-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectDihydroisocoumarinsen
dc.subjectEndophytic fungien
dc.subjectBioactive compoundsen
dc.titleDihydroisocoumarins produced by Xylaria sp and Penicillium sp., endophytic fungi associated with Piper aduncum and Alibertia macrophyllaen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal de Sergipe (UFS)-
dc.contributor.institutionUniversidade Federal de Lavras (UFLA)-
dc.contributor.institutionInst Bot-
dc.description.affiliationUniv Estadual Paulista, NuBBE Nucleo Bioensaios Biossintese & Ecofisiol P, Inst Quim, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUniv Fed Sergipe, Dept Quim, BR-49500000 Itabaiana, SE, Brazil-
dc.description.affiliationUniversidade Federal de Lavras (UFLA), Dept Fitopatol, BR-37200000 Lavras, MG, Brazil-
dc.description.affiliationInst Bot, Seccao Fisiol & Bioquim Plantas, BR-01061970 São Paulo, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, NuBBE Nucleo Bioensaios Biossintese & Ecofisiol P, Inst Quim, BR-14800900 Araraquara, SP, Brazil-
dc.description.sponsorshipIdBiodiversity Virtual Institute: 03/02176-7-
dc.identifier.doi10.1016/j.phytol.2010.11.003-
dc.identifier.wosWOS:000290788100008-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofPhytochemistry Letters-
dc.identifier.orcid0000-0001-7616-9652pt
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