FIELD: organic chemistry, medicine.
SUBSTANCE: invention relates to new substituted 3-pyridyl-4-arylpyrroles of the formula (I):
wherein R1 means hydrogen atom (H), (C1-C5)-alkyl, (C1-C5)-alkylamino-group, amino-group which are substituted with dimethyl, N-containing (C1-C5)-alkylheterocycle taken among methyl-substituted piperidine, morpholine, pyrrolidine, thiazine, methyl-substituted pyrrole. Phenyl, phenyl substituted with one or more (C1-C5)-alkyl, amino-group, NHAc, Nitro-group, nitrile and sulfone and pyridine; R2 means hydrogen atom (H), (CH2)3OH, unsubstituted (C1-C5)-alkylphenyl and morpholine; R3 represents one or more substituents taken independently among the group consisting of hydrogen, halogen atom, methoxy-group, trifluoromethyl, hydroxy-group, dimethylamino-group; X represents either carbon atom © or nitrogen atom (N), or its pharmaceutically acceptable salt. Compound of the formula (I) inhibit producing TNF-α that allows their using in pharmaceutical composition for treatment of inflammatory disorders mediated by inhibition in producing TNF-α and/or activity of p38.
EFFECT: valuable medicinal properties of compounds.
19 cl, 6 sch, 5 tbl
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Authors
Dates
2004-10-27—Published
2000-04-28—Filed