Publication:
Aspochalamins A similar to D and aspochalasin Z produced by the endosymbiotic fungus Aspergillus niveus LU 9575 II. Structure elucidation

dc.bibliographiccitation.firstpage715
dc.bibliographiccitation.issue11
dc.bibliographiccitation.journalThe Journal of Antibiotics
dc.bibliographiccitation.lastpage720
dc.bibliographiccitation.volume57
dc.contributor.authorHoltzel, A.
dc.contributor.authorSchmid, D. G.
dc.contributor.authorNicholson, G. J.
dc.contributor.authorKrastel, P.
dc.contributor.authorZeeck, Axel
dc.contributor.authorGebhardt, Klaus
dc.contributor.authorFiedler, H. P.
dc.contributor.authorJung, G.
dc.date.accessioned2018-11-07T10:44:20Z
dc.date.available2018-11-07T10:44:20Z
dc.date.issued2004
dc.description.abstractThe structures of new cytochalasan fungal metabolites aspochalamins Asimilar toD have been elucidated by ESI-FTICR-MS, NMR spectroscopy, and chiral amino acid analysis. Aspochalamins Asimilar toD consist of different aspochalasin skeletons connected at position C-19 to the N terminus of the tripeptidic moiety amide anthranoyl-L-alanine-E-didehydrotryptamide. Furthermore, the structure of a new aspochalasin analog, aspochalasin Z, was derived from its molecular mass and NMR data as 10-isopropyl-14-methyl[11]-cytochalasa-6Z, 13E, 19E-triene-1,21-dione.
dc.identifier.isi000225409000002
dc.identifier.pmid15712665
dc.identifier.urihttps://resolver.sub.uni-goettingen.de/purl?gro-2/47247
dc.notes.statuszu prüfen
dc.notes.submitterNajko
dc.publisherJapan Antibiotics Research Assoc
dc.relation.issn0021-8820
dc.titleAspochalamins A similar to D and aspochalasin Z produced by the endosymbiotic fungus Aspergillus niveus LU 9575 II. Structure elucidation
dc.typejournal_article
dc.type.internalPublicationyes
dc.type.peerReviewedyes
dc.type.statuspublished
dspace.entity.typePublication

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