FIELD: chemistry, pharmacology.
SUBSTANCE: described are novel pyridopyrrolizine and pyridoindolizine derivatives of general formula I and their pharmaceutically acceptable salts and hydrates, where A is C1-3alkyl; Ar stands for naphtyl or phenyl optionally substituted with one or two groups, selected from halogen, C1-6alkyl or C1-6alkyl haloid; Q stands for COOH; one of X1, X2, X3 or X4 stands for nitrogen, others are independently selected from CH and C-Rg, where Rg stands for C1-6alkyl or S(O)nC1-6alkyl, where n=0, 2; Y1 stands for S or C(O); Y2 stands for (CRdRe)m, where Rd and Re - hydrogen, m is integer 1 or 2; R1, R2, R3 stands for hydrogen, pharmaceutical composition, containing them, and method of treatment of diseases, mediated by prostaglandin D2.
EFFECT: obtaining novel pyridopyrrolizine and pyridoindolizine derivatives which possess useful properties.
22 cl, 2 tbl, 17 ex
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Authors
Dates
2008-12-27—Published
2003-10-28—Filed