Conformational mimetics of the α-methyl chalcone TUB091 binding tubulin: Design, synthesis and antiproliferative activity

• Published in: European journal of medicinal chemistry 2018-03, Vol.148, p.337-348
• Main Authors: Bueno, Oskía, Tobajas, Gloria, Quesada, Ernesto, Estévez-Gallego, Juan, Noppen, Sam, Camarasa, María-José, Díaz, José-Fernando, Liekens, Sandra, Priego, Eva-María, Pérez-Pérez, María-Jesús
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic Agents - chemical synthesis; Antineoplastic Agents - chemistry; Antineoplastic Agents - pharmacology; Antiproliferative activity; Benzodioxoles - metabolism; Binding Sites; Biomimetics; Cell Line; Cell Proliferation - drug effects; Chalcones; Chalcones - metabolism; Drug Design; Endothelial Cells - drug effects; Humans; Molecular modeling; Neoplasms - drug therapy; Neoplasms - pathology; Protein Conformation; Tubulin; Tubulin - metabolism; Tubulin Modulators
• ISSN: 0223-5234; 1768-3254
• DOI: 10.1016/j.ejmech.2018.02.019

Based on the conformation of the α-methyl chalcone TUB091 in its complex with tubulin, a series of conformational mimetics have been designed and synthesized where the methyl group of the chalcone has been fused to phenyl ring B resulting in 1,2,3,4-tetrahydronaphthalen-2-yl aryl ketones. Among the synthesized compounds, the 5-amino-6-methoxy derivative, with a similar substitution pattern to that of TUB091, showed antiproliferative activity around 20 nM against tumor and endothelial cells. Tubulin binding experiments confirmed its binding to tubulin at the colchicine site with a Kb of 2.4 × 106 M−1 resulting in the inhibition of the in vitro assembly of purified tubulin. Moreover, based on the recently reported complex of combretastatin A4 (CA4) with tubulin, a comparative analysis of the binding mode of CA4 and the α-methyl chalcone to tubulin has been performed. [Display omitted] •Novel 1,2,3,4-tetrahydronaphthalen-2-yl aryl ketones have been synthesized.•These derivatives are proposed to mimic the conformation of α-methyl chalcones.•The most potent derivative has antiproliferative activity around 20 nM.•The binding mode of CA4 and the α-methyl chalcone to tubulin has been compared.