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Paullones as Inhibitors of Protein Kinases

[ Vol. 11 , Issue. 11 ]

Author(s):

Nadine Tolle and Conrad Kunick   Pages 1320 - 1332 ( 13 )

Abstract:


Paullones are a class of molecules structurally based on the 7,12-dihydroindolo[3,2-d][1]benzazepin-6(5H)-one parent scaffold. Many of these structures are inhibitors of certain protein kinases, namely cyclin-dependent kinases and glycogen synthase kinase-3. Being well referenced in the literature on the one hand and commercially available on the other hand, paullones have been used as biochemical tools in basic research and drug development for more than a decade. This review gives an overview over the published reports regarding chemistry, biological activity and pharmacological applications of paullone derivatives.

Keywords:

Azepinones, cyclin dependent kinases, GSK-3, indoles, paullones, protein kinase inhibitors, cancer, glycogen synthase kinase-3, screening project, antiproliferative activity, COMPARE, chemotypes inhibiting cyclin-dependent kinases (CDKs)

Affiliation:

Technische Universitat Braunschweig, Institut für Pharmazeutische Chemie, Beethovenstrasse 55, D-38106 Braunschweig, Germany.



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