FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to tricyclic spiro-derivatives of formula (I') wherein: R1 means H, C1-C6-alkyl, C1-C6-alkoxy, halogen-C1-C6-alkyl, halogen-C1-C6-alkoxy, halogen; m is equal to 0-4; R2 means A; A means , : n is equal to 1-4; R4 means C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C6-C10-aryl, 5, 6-member heteroaryl containing one, two and three heteroatoms independently specified in N, O, S, which may be condensed with a benzene ring; R4 may be substituted by one or more groups R6; R6 means C1-C6-alkyl, C1-C6-alkoxy, C6-C10-aryl, C6-C10-aryl-C1-C6-alkyl, C3-C8-cycloalkyl, CN, halogen, aminocarbonyl, C1-C6-acylamino, C1-C6-alkylsulphonyl, trihalogen-C1-C6-alkyl, -O-phenyl wherein phenyl may be substituted by one or two substituted specified in halogen, C1-C6-alkoxy; R7 means H, and C1-C6-alkyl; R means B; B means: , n is equal to 1-4; R5 means COOH, tetrazole; X means CH2, NH; Y means C(O); Z means C(O); as well as its geometric isomers, optically active forms, such as enantiomers, diastereomers, its racemate forms, or its pharmaceutically acceptable salts.
EFFECT: compounds are used for treating and/or preventing allergic diseases, inflammatory dermatoses and other diseases with an inflammatory component.
23 cl, 3 tbl, 125 ex
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Authors
Dates
2013-04-10—Published
2006-05-23—Filed