FIELD: chemistry.
SUBSTANCE: invention relates to a compound of formula I or a physiologically acceptable salt thereof, where A denotes an O atom; X denotes (C3-C7)-cycloalkanediiyl; R1 denotes a hydrogen atom; R2a, R2b and R2c denote hydrogen atoms or (C1-C4)-alkyls; R3 is a radical of unsaturated 6-membered monocycle, wherein one or more carbon atoms contained in cycle optionally have identical or different substitutes R31 or R3 represents a (C3-C7)-cycloalkyl-CuH2u, where u is selected from 1 and 2; R31 denotes a halogen atom or (C1-C4)-alkyl; wherein all alkyls, independently from each other and from other substitutes, can optionally have one or more substitutes in form of fluorine atoms. Invention also relates to a pharmaceutical composition for activation of EDG-1 receptors, containing at least one compound of formula I or its physiologically acceptable salt and pharmaceutically acceptable carrier.
EFFECT: technical result is derivatives of carboxylic acids having[4,5-D]pyrimidine ring for use as a medicinal agent for EDG-1 receptor activation.
5 cl, 2 tbl, 2 ex
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Authors
Dates
2017-01-30—Published
2012-07-06—Filed