New geldanamycin derivatives with anti Hsp properties by mutasynthesis

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dc.identifier.uri http://dx.doi.org/10.15488/10458
dc.identifier.uri https://www.repo.uni-hannover.de/handle/123456789/10533
dc.contributor.author Hermane, Jekaterina
dc.contributor.author Eichner, Simone
dc.contributor.author Mancuso, Lena
dc.contributor.author Schröder, Benjamin
dc.contributor.author Sasse, Florenz
dc.contributor.author Zeilinger, Carsten
dc.contributor.author Kirschning, Andreas
dc.date.accessioned 2021-02-24T10:00:45Z
dc.date.available 2021-02-24T10:00:45Z
dc.date.issued 2019
dc.identifier.citation Hermane, J.; Eichner, S.; Mancuso, L.; Schröder, B.; Sasse, F. et al.: New geldanamycin derivatives with anti Hsp properties by mutasynthesis. In: Organic and Biomolecular Chemistry 17 (2019), Nr. 21, S. 5269-5278. DOI: https://doi.org/10.1039/c9ob00892f
dc.description.abstract Mutasynthetic supplementation of the AHBA blocked mutant strain of S. hygroscopicus, the geldanamycin producer, with 21 aromatic and heteroaromatic amino acids provided new nonquinoid geldanamycin derivatives. Large scale (5 L) fermentation provided four new derivatives in sufficient quantity for full structural characterisation. Among these, the first thiophene derivative of reblastatin showed strong antiproliferative activity towards several human cancer cell lines. Additionally, inhibitory effects on human heat shock protein Hsp90α and bacterial heat shock protein from H. pylori HpHtpG were observed, revealing strong displacement properties for labelled ATP and demonstrating that the ATP-binding site of Hsps is the target site for the new geldanamycin derivatives. © 2019 The Royal Society of Chemistry. eng
dc.language.iso eng
dc.publisher Cambridge : Royal Society of Chemistry
dc.relation.ispartofseries Organic and Biomolecular Chemistry 17 (2019), Nr. 21
dc.rights CC BY-NC 3.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by-nc/3.0/
dc.subject.ddc 540 | Chemie ger
dc.title New geldanamycin derivatives with anti Hsp properties by mutasynthesis
dc.type Article
dc.type Text
dc.relation.issn 1477-0520
dc.relation.doi https://doi.org/10.1039/c9ob00892f
dc.bibliographicCitation.issue 21
dc.bibliographicCitation.volume 17
dc.bibliographicCitation.firstPage 5269
dc.bibliographicCitation.lastPage 5278
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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