Synthesis of a Non-Symmetrical Disorazole C1-Analogue and Its Biological Activity

Author:

Lizzadro Luca1,Spieß Oliver2,Reinecke Silke3,Stadler Marc34ORCID,Schinzer Dieter2

Affiliation:

1. Medicinal Chemistry and Chemical Biology Laboratory, School of Pharmacy, University of California San Francisco, 600 16th St., San Francisco, CA 94158, USA

2. Chemisches Institut, Otto-von-Guericke-Universität, Universitätsplatz 2, 39106 Magdeburg, Germany

3. Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstraße 7, 38124 Braunschweig, Germany

4. Institute of Microbiology, Technische Universität Braunschweig, Spielmannstraße 7, 38106 Braunschweig, Germany

Abstract

The synthesis of a novel disorazole C1 analogue is described, and its biological activity as a cytotoxic compound is reported. Based on our convergent and flexible route to the disorazole core, we wish to report a robust strategy to synthesize a non-symmetrical disorazole in which we couple one half of the molecule containing the naturally occurring oxazole heterocycle and the second half of the disorazole macrocycle containing a thiazole heterocycle. This resulted in a very unusual non-symmetrical disorazole C1 analogue containing two different heterocycles, and its biological activity was studied. This provided exciting information about SAR (structure-activity-relationship) for this highly potent class of antitumor compounds.

Funder

Saxony-Anhalt

Publisher

MDPI AG

Reference15 articles.

1. (2024, February 07). Jahresbericht GBF 2001. Available online: https://www.helmholtz-hzi.de/fileadmin/user_upload/Infothek/Ueber_das_HZI/Jahresberichte/Ergebnisberichte/Annual_Report_2001.pdf.

2. Disorazole A1, an Efficient Inhibitor of Eukariotic Organisms Isolated from Myxobacteria;Irschik;J. Antibiot.,1995

3. Myxobacterial secondary metabolites: Bioactivities and modes-of-action;Weissman;Nat. Prod. Rep.,2010

4. Disorazoles, Highly Cytotoxyc Metabolites from the Sorangicin–Producing Bacterium Sorangium cellulosum;Jansen;Liebigs Ann. Chem.,1994

5. Disorazol A1, a highly effective antimitotic agent acting on tubulin polymerization and inducing apoptosis in mammalian cells;Elnakady;Biochem. Pharmacol.,2004

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