FIELD: medicine; pharmaceuticals.
SUBSTANCE: invention relates to substituted pyrazolo[1,5-a]pyridine derivatives of formula (IIB) or pharmaceutically acceptable salts thereof, in which E denotes -CH2-; Q is -CH2-; Z is hydrogen or methyl; V denotes CR22 or N; R12 denotes hydrogen; R15 denotes a difluoromethoxy group; R16 denotes hydrogen; R21 denotes hydroxy (C1-Cb) alkyl; or R21 denotes piperidinyl, piperazinyl or morpholinyl, any of these groups may optionally contain one, two or three substitutes independently selected from a group comprising C1-C6-alkyl, C1-C6-alkylsulfonyl, oxo group and carboxy group; R22 denotes hydrogen, halogen or C1-C6-alkyl; and R23 denotes hydrogen, C1-C6-alkyl, trifluoromethyl or C1-C6-alkoxy group. Compounds of formula (IIB) are active modulators of TNFα activity rights and can be used for treating and/or preventing various human diseases, including autoimmune and inflammatory disorders; neurological and neurodegenerative disorders; pain and nociceptive disorders; cardiovascular disorders; metabolic disorders; ophthalmic disorders and oncological disorders
.
EFFECT: most preferably compounds can be used for preparing a drug for treating and/or preventing rheumatoid arthritis or Crohn's disease and in a method of treating or preventing these diseases.
6 cl, 7 ex
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Authors
Dates
2019-04-11—Published
2014-12-08—Filed