FIELD: chemistry.
SUBSTANCE: in formula (I) X1 is O; R1 is hydrogen; R2 is hydrogen or C1-7-alkyl, R3 is hydrogen or C1-7-alkyl; R4 and R8 are independently selected from a group consisting of hydrogen, C1-7-alkyl and halogen; R5, R6 and R7 are independently selected from a group consisting of hydrogen and halogen; and one of R5, R6 and R7 is a group, where X2 is selected from a group consisting of S, O, NR9 and (CH2)pNR9CO; R9 is selected from a group consisting of hydrogen and C1-7-alkyl; R10 is C1-7-alkyl; R11 is selected from a group consisting of hydrogen and C1-7-alkyl; or R10 and R11 together with the carbon atom with which they are bonded form a C3-6-cycloalkyl ring; o equals 0, 1 or 2; n equals 0, 1, 2 or 3; p equals 0 or 1; and the sum of m, n and o assumes values from 1 to 5; R12 is phenyl optionally substituted with fluoro-C1-7-alkoxy, halogen, C1-7-alkoxy, fluro-C1-7-alkyl; or R12 is pyridine or pyrimidine substituted with fluoro-C1-7-alkyl; and their pharmaceutically acceptable salts and/or esters. Present invention also relates to pharmaceutical compositions which have agonistic effect on PPARδ and/or PPARα containing such compounds.
EFFECT: new compounds have useful biological properties.
20 cl, 36 ex
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Authors
Dates
2010-03-20—Published
2005-06-21—Filed