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DIPHENYL-PYRAZOLOPYRDINE DERIVATIVES, PREPARATION THEREOF, AND USE THEREOF AS NUCLEAR RECEPTOR NOT MODULATORS
专利权人:
SANOFI
发明人:
AUGER, FLORIAN,EVEN, LUC
申请号:
SG2012039749
公开号:
SG181138A1
申请日:
2010.12.03
申请国别(地区):
SG
年份:
2012
代理人:
摘要:
WO 2011/067544 -38 - PCl/F122010/052605AbstractDIPHENYL-PYRAZOLOPYRIDINE DERIVATIVES, PREPARATION THEREOF, AND USE THEREOF AS NUCLEAR RECEPTOR NOT MODULATORSThe invention relates to a formula (I), in which R is a hydrogen or halogen atom or a (C1-C6) alkyl group; X is one or more substituents selected from a hydrogen or halogen 5 atom, a (C1-C6)allcyl, halo(CI-C6)allcyl, (C1-C6)alkoxy, halo(C1-C6)alkoxy, cyano, hydroxy, or hydroxy(C1-C6)alkyl group; Y is a hydrogen or halogen atom or a (C1-C6)allcyl group; RI is an NR2R3 or OR4 group; R2 and R3 independently are a hydrogen atom, a (C1-C6)allcyl, hydroxy(C1-C6)allcyl or oxo(C I -C6)alkyl group or R2 and R3, together with the nitrogen atom supporting the same, form a heterocycle optionally substituted by a (C1- 10 C6)allcyl, hydroxy or oxo group; and R4 is a (C1-C6)allcyl, hydroxy(C 1 -C6)allcyl, or oxo(C1-C6)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 Nun- 1, also known as NR4A2, NOT, T1NUR, RNR-1, and HZE3.
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