abstract |
The present invention relates to compounds of formula (I) below in which: - R 1 and R 3 represent, independently of one another, a methoxy group optionally substituted by one or more fluorine atoms, - R 2 and R 4 represent, independently of one another, a hydrogen atom or a methoxy group optionally substituted by one or more fluorine atoms, - A represents a ring chosen from the group comprising aryl and heteroaryl groups, said ring possibly being substituted by or fused to a heterocycle, - X represents a nitrogen atom or a CH group, and - Z 1 represents a hydrogen atom or a halogen atom, preferably fluorine, and - Z 2 represents a hydrogen atom, a halogen atom, preferably fluorine, a C 1 to C 4 alkyl group, an aryl group or a -CN, -SO 2 NR 12 R 13 , ‑SO 2 R 9 , -COOR 15 or ‑COR 15 group, and also to the pharmaceutically acceptable salts thereof, the isomers thereof and the prodrugs thereof. |