FIELD: chemistry.
SUBSTANCE: invention relates to new derivatives of aminobenzophenones with general formula I with inhibition properties towards interleukin-1β(IL-1β) and tumour necrosis factor (TNF-α). In general formula I X is oxygen; R1 is (C1-C3)alkyl, R2 is one or more, identical or different substitutes, chosen from a group containing hydrogen and halogen; R3 is one or more, identical or different substitutes, chosen from a group containing hydrogen and halogen, R4 is hydrogen, R5 is hydrogen, R6 is (C1-C10)alkyl-heterocyclyl, (C1-C10)alkyl, (C2-C10)olefin group, heterocyclyl, Y1R21, Y2R22 or Y4R24; where (C1-C10)alkyl, (C2-C10)olefin group are substituted with one or more identical or different substitutes, represented by R7 and where (C1-C10)alkyl-heterocyclyl, heterocyclyl are optionally substituted with one or more, identical or different substitutes, represented by R7; heterocyclyl itself and in (C1-C10)alkyl-heterocyclyl represents a 5-6-member saturated or partially unsaturated heterocyclyl, possibly condensed with a benzene ring and containing 1-2 heteroatoms, chosen fron nitrogen, oxygen and sulphur.
EFFECT: compounds can be used for making medicinal preparation for curing and preventing diseases, related to cytokine regulation system, such as inflammatory diseases.
13 cl, 4 dwg, 3 tbl, 169 ex
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Authors
Dates
2009-07-20—Published
2002-08-26—Filed