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Trienamine catalyzed asymmetric synthesis and biological investigation of a cytochalasin B-inspired compound collection
Max-Planck-Institute für Molekulare Physiologie, Dortmund, Germany.
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2016 (engelsk)Inngår i: Organic and biomolecular chemistry, ISSN 1477-0520, E-ISSN 1477-0539, Vol. 14, nr 1, s. 50-54Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Due to their enhanced metabolic needs many cancers need a sufficient supply of glucose, and novel inhibitors of glucose import are in high demand. Cytochalasin B (CB) is a potent natural glucose import inhibitor which also impairs the actin cytoskeleton leading to undesired toxicity. With a view to identifying selective glucose import inhibitors we have developed an enantioselective trienamine catalyzed synthesis of a CB-inspired compound collection. Biological analysis revealed that indeed actin impairment can be distinguished from glucose import inhibition and led to the identification of the first selective glucose import inhibitor based on the basic structural architecture of cytochalasin B.

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Royal Society of Chemistry, 2016. Vol. 14, nr 1, s. 50-54
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URN: urn:nbn:se:umu:diva-128758DOI: 10.1039/C5OB02272JISI: 000366861800005PubMedID: 26606903OAI: oai:DiVA.org:umu-128758DiVA, id: diva2:1056264
Tilgjengelig fra: 2016-12-14 Laget: 2016-12-14 Sist oppdatert: 2018-06-09bibliografisk kontrollert

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