Synthesis, antiproliferative activity and inhibition of tubulin polymerization by anthracenone-based oxime derivatives

Surkau G, Böhm KJ, Müller K, Prinz H

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

A series of anthracenone-based oxime ethers and -esters were synthesized in order to evaluate their antiproliferative activity. Several investigated compounds displayed strong antiproliferative activity against K562 leukemia cells and proved to be strong inhibitors of tubulin polymerization. In this context, anthracenone-based oxime ethers and -esters are considered to contribute to the development of novel antiproliferative drugs, based on tubulin interaction. (C) 2010 Elsevier Masson SAS. All rights reserved.

Details zur Publikation

FachzeitschriftEuropean Journal of Medicinal Chemistry
Jahrgang / Bandnr. / Volume45
Ausgabe / Heftnr. / Issue8
Seitenbereich3354-3364
StatusVeröffentlicht
Veröffentlichungsjahr2010 (31.08.2010)
Sprache, in der die Publikation verfasst istEnglisch
DOI10.1016/j.ejmech.2010.04.019
StichwörterAnthraquinone oximes Anthracenones 10-Hydroxyimino-10H-anthracen-9-ones Tubulin polymerization Antiproliferative activity antimicrotubule agents colchicine site biological evaluation common pharmacophore cancer mechanism cleavage ligands

Autor*innen der Universität Münster

Müller, Klaus
Professur für Pharmazeutische Chemie (Prof. Müller)
Prinz, Helge
Professur für Pharmazeutische Chemie (Prof. Müller)
Surkau, Georg
Institut für Pharmazeutische und Medizinische Chemie