Novel macrocycles for the treatment of cancer diseases
The present invention relates to novel macrocycles of the general formula (I) and to the use thereof in the treatment of cancer diseases.
1 . Compounds of the general formula (I):
wherein
R 1 is a C 1-6 alkyl, a C 2-6 alkynyl or a C 2-6 alkenyl radical,
R 2 is a hydrogen atom or a C 1-6 alkyl radical,
X—Y is selected from the following groups:
R 3 is a halogen atom or a C 1-6 alkyl, a C 2-6 alkenyl or a C 1-6 heteroalkyl radical,
R 4 is a bicycloaryl radical, a bicycloheteroaryl radical or a group of formula —C(R 5 )═CHR 6 ,
R 5 is a hydrogen atom or a methyl group and
R 6 is an optionally substituted aryl or heteroaryl group,
or a pharmacologically acceptable salt, solvate, hydrate or a pharmacologically acceptable formulation thereof.
2 . Compounds of formula (I), wherein R 1 is a methyl group.
3 . Compounds according to claim 1 , wherein R 2 is a hydrogen atom or a methyl group.
4 . Compounds according to claim 1 , wherein R 3 is a methyl group, a trifluoromethyl group or a group of formula COOH.
5 . Compounds according to claim 1 , wherein R 3 is a trifluoromethyl group.
6 . Compounds according to claim 1 , wherein R 6 is an optionally substituted 5- or 6-membered heteroaryl radical having 1, 2 or 3 hetero atoms selected from S, N and O.
7 . Compounds according to claim 1 , wherein R 6 is an optionally substituted thiazole ring or pyridine ring.
8 . Compounds according to claim 1 , wherein R 4 is a group having the following formula:
9 . Pharmaceutical composition, which contains a compound according to claim 1 and optionally one or more carriers and/or one or more adjuvants.
10 . Use of a compound or a pharmaceutical composition according to claim 1 in the treatment of cancer diseases.