FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to oxazolopyrimidine compounds of formula , wherein A is specified in O or S; X is specified in (C1-C6)-alkanediyl, (C2-C6)-alkenediyl and (C1-C6)-alkanediyl-oxy, wherein an oxygen atom of (C1-C6)-alkanediyl-oxy group is bound to the group R2; Y represents a 4-7-merous saturated monocyclic heterocycle; R1 represents hydrogen; R2 is specified in phenylene, which is optionally substituted by one or two identical or different substitutes R22; R3 is specified in phenylene and thiazole, wherein a ring residue is optionally substituted by identical or different substitutes R31 at one or two carbon atoms of the ring; R22 is specified in halogen and (C1-C4)-alkyl-, which is optionally substituted by 1-3 fluorine atoms; R31 is specified in halogen, (C1-C4)-alkyl and (C1-C4)-alkyloxy. The invention also refers to a method for producing the compounds of formula I and to a pharmaceutical composition applicable for activating EDG-1 receptor.
EFFECT: compounds of formula I applicable for activating EDG-1 receptor and for treating disturbed wound healing and diabetic foot.
18 cl, 2 tbl, 37 ex
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Authors
Dates
2015-08-20—Published
2011-01-12—Filed