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dc.provenanceCONICET-
dc.creatorSudarman, Enge-
dc.creatorKuhnert, Eric-
dc.creatorHyde, Kevi D.-
dc.creatorSir, Esteban Benjamin-
dc.creatorSurup, Frank-
dc.creatorStadler, Marc-
dc.date2018-09-06T22:07:35Z-
dc.date2018-09-06T22:07:35Z-
dc.date2016-10-
dc.date2018-09-04T16:35:40Z-
dc.date.accessioned2019-04-29T15:44:44Z-
dc.date.available2019-04-29T15:44:44Z-
dc.date.issued2016-10-
dc.identifierSudarman, Enge; Kuhnert, Eric; Hyde, Kevi D.; Sir, Esteban Benjamin; Surup, Frank; et al.; Truncatones A–D, benzo[j]fluoranthenes from Annulohypoxylon species (Xylariaceae, Ascomycota); Pergamon-Elsevier Science Ltd; Tetrahedron; 72; 41; 10-2016; 6450-6454-
dc.identifier0040-4020-
dc.identifierhttp://hdl.handle.net/11336/58657-
dc.identifierCONICET Digital-
dc.identifierCONICET-
dc.identifier.urihttp://rodna.bn.gov.ar:8080/jspui/handle/bnmm/300918-
dc.descriptionFrom stromata (fruiting bodies) of three xylariaceous fungi belonging to the genus Annulohypoxylon (A. leptascum, A. cf. truncatum and an unidentified Annulohypoxylon sp.), truncatone A (1), three unprecedented derivatives named truncatones B–D (2–4) besides the known 4,5,4′,5′-tetrahydroxy-1,1′-binaphthyl (BNT, 5), hypoxylonol C (6) and hypoxylonol F (7) were isolated. Planar structures of the new benzo[j]fluoranthene derivatives 2–4 were determined on the basis of NMR and HRESIMS data. While the relative configuration of 4 was demonstrated by ROESY NMR data and1H,1H coupling constants, absolute configurations of 1, 2, 4 were determined by CD spectroscopy. Compounds 1, 3 and 4 exhibited cytotoxicity against the mouse fibroblast cell line L929.-
dc.descriptionFil: Sudarman, Enge. Helmoholtz Centre for Infection Research; Alemania-
dc.descriptionFil: Kuhnert, Eric. Helmoholtz Centre for Infection Research; Alemania-
dc.descriptionFil: Hyde, Kevi D.. Mae Fah Luang University; Tailandia-
dc.descriptionFil: Sir, Esteban Benjamin. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán; Argentina. Fundación Miguel Lillo; Argentina-
dc.descriptionFil: Surup, Frank. Helmholtz Centre for Infection Research ; Alemania-
dc.descriptionFil: Stadler, Marc. Helmholtz Centre for Infection Research ; Alemania-
dc.formatapplication/pdf-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherPergamon-Elsevier Science Ltd-
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://dx.doi.org/10.1016/j.tet.2016.08.054-
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0040402016308304-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/-
dc.sourcereponame:CONICET Digital (CONICET)-
dc.sourceinstname:Consejo Nacional de Investigaciones Científicas y Técnicas-
dc.sourceinstacron:CONICET-
dc.source.urihttp://hdl.handle.net/11336/58657-
dc.subjectANNULOHYPOXYLON-
dc.subjectBENZO[J]FLUORANTHENE-
dc.subjectCD-
dc.subjectNMR-
dc.subjectXYLARECEAE-
dc.subjectOtras Ciencias Químicas-
dc.subjectCiencias Químicas-
dc.subjectCIENCIAS NATURALES Y EXACTAS-
dc.titleTruncatones A–D, benzo[j]fluoranthenes from Annulohypoxylon species (Xylariaceae, Ascomycota)-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.typeinfo:ar-repo/semantics/articulo-
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