FIELD: organic chemistry, medicine, pharmacy.
SUBSTANCE: invention relates to new derivatives of benzophenone of the general formula (I): or their pharmaceutically acceptable salts and N-oxides, i. e. compounds wherein nitrogen atom at heterocyclic substitute can be oxidized. Compounds show property of inhibitor of interleukin (IL-1β) or alpha-tumor necrosis factor (TNF-α) and can be used in treatment of inflammatory diseases and states. In compound of the general formula (I) R1 represents (C1-C6)-alkyl; R2 represents one or some similar or different substitutes taken among the group consisting of hydrogen, halogen atom, (C1-C6)-alkyl, (C1-C6)-alkoxy-group; R3 represents one substitute at ortho-position taken among the group consisting of hydrogen, halogen atom; R4 represents hydrogen atom; R5 represents nitrogen-containing heteroaromatic mono- or bicyclic system comprising 1-4 heteroatoms taken among nitrogen (N), sulfur (S) or oxygen (O) atoms wherein each ring comprises 5 or 6 atoms in ring with exception for triazine being indicated mono- or bicyclic system is substituted optionally with hydrogen, halogen atom, halidealkyl, cyano-, carboxy-, nitro-group, (C1-C6)-alkyl, (C1-C6)-alkoxy-group, (C1-C6)-alkoxycarbonyl, -NR9R10 wherein R9 and R10 represent hydrogen atom; X represents oxygen atom. Also, invention relates to a pharmaceutical composition and to a method for treatment and prophylaxis of diseases.
EFFECT: improved treatment method, valuable medicinal properties of compounds.
20 cl, 3 tbl, 83 ex
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Authors
Dates
2006-02-20—Published
2001-05-18—Filed