Logo do repositório
 

Aromatic compounds produced by Periconia atropurpurea, an endophytic fungus associated with Xylopia aromatica

dc.contributor.authorTeles, Helder Lopes
dc.contributor.authorSordi, Renata
dc.contributor.authorSilva, Geraldo Humberto
dc.contributor.authorCastro-Gamboa, Ian
dc.contributor.authorBolzani, Vanderlan da Silva [UNESP]
dc.contributor.authorPfenning, Ludwig Heinrich
dc.contributor.authorde Abreu, Lucas Magalhaes
dc.contributor.authorCosta-Neto, Claudio Miguel
dc.contributor.authorMarx Young, Maria Claudia
dc.contributor.authorAraújo, Angela Regina [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Federal de Lavras (UFLA)
dc.contributor.institutionInst Bot
dc.contributor.institutionUniversidade Federal de Sergipe (UFS)
dc.date.accessioned2014-05-20T15:25:55Z
dc.date.available2014-05-20T15:25:55Z
dc.date.issued2006-12-01
dc.description.abstract6,8-Dimethoxy-3-(2'-oxo-propyl)-coumarin (1) and 2,4-dihydroxy-6-[(1'E,3'E)-penta-1', 3'-dienyl]-benzaldehyde (2), in addition to the known compound periconicin B (3), were isolated from the ethyl acetate extract of Periconia atropurpurea, an endophytic fungus obtained from the leaves of Xylopia aromatica, a native plant of the Brazilian Cerrado. Their chemical structures were assigned based on analyses of MS, 1D and 2D-NMR spectroscopic experiments. Biological analyses were performed using two mammalian cell lines, human cervix carcinoma (HeLa) and Chinese hamster ovary (CHO). The results showed that compound I had no effect when compared to the control group, which was treated with the vehicle (DMSO). Compound 2 was able to induce a slight increase in cell proliferation of HeLa (37% of increase) and CHO (38% of increase) cell lines. Analysis of compound 3 showed that it has potent cytotoxic activity against both cell lines, with an IC50 of 8.0 mu M. Biological analyses using the phytopathogenic fungi Cladosporium sphaerospermum and C. cladosporioides revealed that also 2 showed potent antifungal activity compared to nystatin. (c) 2006 Elsevier Ltd. All rights reserved.en
dc.description.affiliationUniv Estadual Paulista, Inst Quim, NuBBE Nucleo Bioensaio Biossintese & Ecofis Produ, BR-14801970 Araraquara, SP, Brazil
dc.description.affiliationUniv São Paulo, Fac Med Ribeirao Preto, Dept Bioquim & Imunol, BR-14049900 Ribeirao Preto, Brazil
dc.description.affiliationUniv Fed Lavras, Dept Fitopatol, BR-37200000 Lavras, MG, Brazil
dc.description.affiliationInst Bot, Seccao Fisiol & Bioquim Plantas, BR-01061970 São Paulo, Brazil
dc.description.affiliationUniv Fed Sergipe, Dept Quim, METABIO, BR-49100000 Sao Cristovao, SE, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Inst Quim, NuBBE Nucleo Bioensaio Biossintese & Ecofis Produ, BR-14801970 Araraquara, SP, Brazil
dc.format.extent2686-2690
dc.identifierhttp://dx.doi.org/10.1016/j.phytochem.2006.09.005
dc.identifier.citationPhytochemistry. Oxford: Pergamon-Elsevier B.V., v. 67, n. 24, p. 2686-2690, 2006.
dc.identifier.doi10.1016/j.phytochem.2006.09.005
dc.identifier.issn0031-9422
dc.identifier.lattes4484083685251673
dc.identifier.lattes0037579054083160
dc.identifier.orcid0000-0001-7616-9652
dc.identifier.urihttp://hdl.handle.net/11449/36233
dc.identifier.wosWOS:000242954800013
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofPhytochemistry
dc.relation.ispartofjcr3.186
dc.relation.ispartofsjr1,048
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectPericonia atropurpureapt
dc.subjectendophytic fungipt
dc.subjectcoumarinpt
dc.subjectbenzaldehydept
dc.subjectantifungalpt
dc.subjectcell proliferationpt
dc.titleAromatic compounds produced by Periconia atropurpurea, an endophytic fungus associated with Xylopia aromaticaen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.lattes4484083685251673
unesp.author.lattes0037579054083160[10]
unesp.author.orcid0000-0001-7616-9652[10]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

Arquivos

Licença do pacote

Agora exibindo 1 - 1 de 1
Carregando...
Imagem de Miniatura
Nome:
license.txt
Tamanho:
1.71 KB
Formato:
Item-specific license agreed upon to submission
Descrição: