A Natural Product Inspired Tetrahydropyran Collection Yields Mitosis Modulators that Synergistically Target CSE1L and Tubulin

Abstract

Eine Prins-Cyclisierung eines polymergebundenen Aldehyds mit einem Homoallylalkohol ist der Schlüsselschritt einer Synthese von Tetrahydropyran-Derivaten. Ein phänotypisches Screening identifizierte Mitose-Inhibitoren (zu erkennen an der Anreicherung runder Zellen mit verdichteter DNA und Membranbläschen; siehe Bild). Diese erhalten den Namen Tubulexine, da sie an das CSE1L-Protein und die Bindungsstelle der Vinca-Alkaloide im Tubulin binden. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.