New geldanamycin derivatives with anti Hsp properties by mutasynthesis.
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Authors
Hermane, JekaterinaEichner, Simone
Mancuso, Lena
Schröder, Benjamin
Sasse, Florenz
Zeilinger, Carsten
Kirschning, Andreas
Issue Date
2019-05-29
Metadata
Show full item recordAbstract
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.Citation
Org Biomol Chem. 2019 May 29;17(21):5269-5278. doi: 10.1039/c9ob00892f.Affiliation
HZI,Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7,38124 Braunschweig, Germany.Publisher
Royal Society of ChemistryPubMed ID
31089638Type
ArticleISSN
1477-0539ae974a485f413a2113503eed53cd6c53
10.1039/c9ob00892f
Scopus Count
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