| 摘要 |
The invention relates to formula (I)in which R is a hydrogen or halogen atom or a (C-C)alkyl group; X is one or more substituents selected from a hydrogen or halogen atom, a (C-C)alkyl, halo(C-C)alkyl, (C-C)alkoxy, halo(C-C)alkoxy, cyano, hydroxy, or hydroxy(C-C)alkyl group; Y is a hydrogen or halogen atom or a (C-C)alkyl group; R1 is an NR2R3 or OR4 group; R2 and R3 independently are a hydrogen atom, a (C-C)alkyl, hydroxy(C-C)alkyl or oxo(C-C)alkyl group, or R2 and R3, together with the nitrogen atom supporting the same, form a heterocycle optionally substituted by a (C-C)alkyl, hydroxy, or oxo group; R4 is a (C-C)alkyl, hydroxy(C-C)alkyl, or oxo(C-C)alkyl group, in the base or acid addition salt state. Said formula can be used therapeutically for treating or preventing diseases linked to the nuclear receptors Nurr-1, also known as NR4A2, NOT, TINUR, RNR-1, and HZF3. |
