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The novel hybrid antitumor compound premithramycinone H provides indirect evidence for a tricyclic intermediate of the biosynthesis of the aureolic acid antibiotic mithramycin

dc.contributor.authorLombó Brugos, Felipe 
dc.contributor.authorKünzel, Eva
dc.contributor.authorPrado Álvarez, Laura 
dc.contributor.authorFernández Braña, Alfredo Javier 
dc.contributor.authorBindseil, K. U.
dc.contributor.authorFrevert, J.
dc.contributor.authorBearden, D. W.
dc.contributor.authorMéndez Fernández, María del Carmen 
dc.contributor.authorSalas Fernández, José Antonio 
dc.contributor.authorRohr, Jürgen
dc.date.accessioned2017-02-16T08:46:55Z
dc.date.available2017-02-16T08:46:55Z
dc.date.issued2000
dc.identifier.citationAngewandte Chemie - International Edition, 39, 4, p. 796-799 (2000); doi:10.1002/(SICI)1521-3773(20000218)39:4<796
dc.identifier.issn1433-7851
dc.identifier.urihttp://hdl.handle.net/10651/40167
dc.description.sponsorshipThis work was supported by the European Union (BIO4-CT96-0068), the Medical University of South Carolina (Institutional Research Funds of 1999-2 000), and the Spanish Ministry of Education and Culture (BIO97-0771). Dr. M. Walla and Dr. W. Cotham (University of South Carolina) are acknowledged for excellent mass spectra.
dc.format.extentp. 796-799
dc.language.isoeng
dc.relation.ispartofAngewandte Chemie - International Edition
dc.rights© WILEY-VCH
dc.sourceScopus
dc.titleThe novel hybrid antitumor compound premithramycinone H provides indirect evidence for a tricyclic intermediate of the biosynthesis of the aureolic acid antibiotic mithramycineng
dc.typejournal article
dc.identifier.doi10.1002/(SICI)1521-3773(20000218)39:4<796::AID-ANIE796>3.0.CO;2-N
dc.relation.projectIDEU / BIO4-CT96-0068
dc.relation.projectIDMEC / BIO97-0771
dc.relation.publisherversionhttp://dx.doi.org/10.1002/(SICI)1521-3773(20000218)39:4<796::AID-ANIE796>3.0.CO;2-N


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