1-Azabicyclo[2.2.2]octan-3-one derivatives and maleimide derivatives and their use for treating cancer tumors
The present invention provides novel compounds, corresponding to formulae I and II, respectively, which are able to reactivate the apoptosis-inducing function of mutant p53 proteins. This reactivation is provided by restoration of sequence-specific DNA-binding activity and transcriptional transactivation function to mutant p53 proteins, and modulation of the conformation-dependent epitopes of the p53 protein. Accordingly, the substances according to the invention will be used in pharmaceutical compositions and methods for treatment of patients suffering from various types of tumors.
1. A method of treating cancer, comprising administering to a mammal in need thereof a therapeutically effective amount of a compound having the formula I
wherein
R 2 or R 3 are the same or different and are chosen from the group of hydrogen, C1-15 alkyl, C2-15 alkenyl, C2-15 alkynyl, C1-15 alkoxy, C1-15 alkylamino, aryl, C6-15 aryl alkyl, C1-15 alkyl carboxy, C2-15 alkyl alkyl carboxylate, C1-15 alkylthio, C1-15 alkyl hydroxy, wherein said groups optionally can be substituted with halogen or from 2-hydroxymethyl-3,3-dihydroxy-1-azabicyclo[2,2,2]octane [[and from compounds having the formula II
wherein
R 1 is chosen from the group of hydrogen, C1-15 alkyl, C1-15 alkenyl, C1-15 alkynyl, C1-15 alkoxy, C1-15 alkylamino, aryl, C6-15 aryl alkyl, C1-15 alkyl carboxy, C2-15 alkyl alkyl carboxylate, C1-15 alkylthio, C1-15 alkyl hydroxyl, wherein said groups optionally can be substituted with halogen, for the preparation of a pharmaceutical for the treatment of conditions caused by mutant p53 protein]].
2. A method of treating cancer, comprising administering to a mammal in need thereof a pharmaceutically effective amount of 2,2-bis(hydroxymethyl)-1-azabicyclo[2,2,2]octan-3-one, 2-[(6-chloro-9-H-purin-9-yl)methyl-1-azabicyclo[2.2.2]octan-3-one or 2-hydroxymethyl-3,3-dihydroxy-1-azabicyclo[2,2,2]octane.