NEW COMPOUNDS AND THEIR USE AS PPAR-MODULATORS Russian patent published in 2009 - IPC C07C311/09 C07C311/21 C07C311/51 C07D207/337 C07D207/34 C07D209/26 C07D209/42 C07D295/12 C07D295/13 C07D471/04 C07C63/04 C07C59/205 C07C65/32 A61K31/18 A61K31/40 A61P1/04 A61P9/08 A61P9/10 A61P11/00 A61P13/12 A61P17/06 A61P19/02 A61P35/00 

Abstract RU 2349582 C2

FIELD: chemistry.

SUBSTANCE: present invention pertains to new compounds with general formula (I), in which X1 is phenyl, 9-member bicyclic heteroaryl, containing S or O as heteroatoms, or 5-member heteroaryl, containing S or O as heteroatoms, each of which is optionally substituted with one or more substitutes, chosen from halogen or C1-6alkyl, which is optionally substituted with one or more halogens. X2 is phenyl, which is optionally substituted with one or more substitutes, chosen from halogen, or 5-member heteroaryl, containing S or O as heteroatoms. Ar is phenylene, which is optionally substituted with one or more substitutes, chosen from halogen, or C1-6alkyl, phenyl, C1-6alkoxy, each of which is optionally substituted with one or more halogens. Y1 is O or S, and Y2 represents O, Z represents -(CH2)n-, where n equals 1, 2 or 3. R1 is hydrogen or C1-6alkoxy and R2 is hydrogen, C1-6alkyl. The invention also relates to pharmaceutical salts of these compounds or any of their tautomeric forms, stereoisomers, stereoisomer mixtures, including racemic mixtures.

EFFECT: invention also pertains to use of these compounds as pharmaceutical compositions, with effect on receptors, activated by the peroxisome proliferator PPARδ subtype, and to pharmaceutical compositions, containing these compounds (I).

36 cl, 41 ex

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RU 2 349 582 C2

Authors

Jeppesen Lone

Mogensen Dzhon Patrik

Pettersson Ingrid

Sauerberg Per

Pigera Pavel

Gavranek Miroslav

Dates

2009-03-20Published

2003-10-27Filed