Oxindoles which are inhibitors of CDK-1 and their application in therapeutics

Abstract

The present invention relates to a compound of formula (I): 1 wherein R5 is selected from the group consisting of 3-pyridyl, 5-pyrimidinyl, —CONH—(C1-C4 alkyl), —NHCO—(C1-C4 alkyl), halogen, —SO2NH2, —NO2, —CF3 or thien-2-ylcarbonyl 2 and —CO2R where R can be hydrogen or C1-C4 alkyl; and Ar is selected from the group consisting of 5-imidazolyl, 2-pyrrolyl optionally substituted by a C1-C4 alkyl radical, 2-furyl or 2-thiazolyl, in the E or Z geometrical isomeric form or a mixture of the two geometrical isomeric forms. The invention is also directed to a method of treating primary and secondary tumours in a patient in need thereof comprising administering to the patient a therapeutically effective amount of a compound of formula I. The invention is also directed to a method of using a compound of formula I to treat cancer, inhibit the proliferation of a cell and induce cell apoptosis, comprising contacting a cell with an effective amount of the compound of formula I., The invention is also directed to a method of preparing the compound of formula I.

Dependencies are inferred from the claim text.