FIELD: organic chemistry, biochemistry, medicine, pharmacy.
SUBSTANCE: invention describes derivatives of naphthyridine of the general formula (I) or their pharmaceutically acceptable salts:
wherein: R1: -R0 or -lower alkylene-cycloalkyl; R0: -lower alkyl; R2: -R0, -halogen atom, -lower alkylene-OH, -S-Ro, -NHR0 or -CH=N-OR9 that can be similar or distinct of one another; R3 and R4: -H; R9: -H; R5: cyclohexyl, thienyl or phenyl that can be substituted with group taken among lower alkyl and halogen atom; R6: -OH, -OR7, -COOH, -CONH2, -CON(R7)2, -O-COR7, -O-COOR7, -COR7, -NH2, -N(R7)2, -N(R7)COR7, -N(R7)SO2R7, -C(NH)NH2, -NHC(NH)NH2 or group of the formula: -Y-R8; R7: lower alkyl that can be substituted with group -CO2R0; R8: phenyl that can be substituted with group taken among R10, or heterocyclic group taken among morpholinyl, tetrazolyl, imidazolyl, pyridyl, piperidyl, thiazolyl, piperazyl, pyrrolidyl or imidazo[1,2-a]pyridyl that can be substituted with group taken among R10; R10: -halogen atom, -CO2H, -NH2 or -COR0, or group described as R7; Y: a bind or -CO-; X: a bind or lower alkylene. These compounds can be used as prophylactic or curative agents in treatment of respiratory diseases associated with inhibition of activity of phosphodiesterase-IV.
EFFECT: valuable medicinal properties of compounds and composition.
7 cl, 6 tbl, 57 ex
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Authors
Dates
2004-11-20—Published
2000-10-24—Filed