FIELD: medicine.
SUBSTANCE: invention relates to a compound of the formula (I), its enantiomer, diastereomer or their pharmaceutically acceptable salts. In the formula (I), R1 is hydrogen; R2 is hydrogen or C1-4 linear alkyl; R3 is selected from hydrogen, halogen, CN or OR8; R4 is hydrogen or OR8; R3 and R4 are not hydrogen at the same time; R8 is C3-10 heterocycloalkyl containing 1-4 heteroatoms selected from N, O and S, or C1-4 alkyl substituted with C3-10 heterocycloalkyl containing 1-4 heteroatoms selected from a group of N, O and S; R5 and R6, each independently, is hydrogen, halogen, CN or C1-4 linear alkoxy-group; Y is NH or O; Z1 and Z2, each independently, is CR7 or N: when Z1 is N, Z2 is CR7; and when Z1 is CR7, Z2 is N; W is CR7 or N; R7 is hydrogen or C1-4 linear alkyl. The invention also relates to a pharmaceutical composition based on the compound of the formula (I), to a method for the treatment of a metabolic disorder, and to the use of the compound of the formula (I).
EFFECT: obtaining a compound of the formula (I) having GPR40 agonist properties.
(I)
11 cl, 1 tbl, 28 ex
Title | Year | Author | Number |
---|---|---|---|
NEW HETEROCYCLIC DERIVATIVE | 2019 |
|
RU2792163C2 |
GEMINALLY SUBSTITUTED CYANOETHYLPYRAZOLO PYRIDONES AS JANUS KINASE INHIBITORS | 2014 |
|
RU2664533C2 |
METHODS OF OBTAINING AND PURIFICATION OF HETEROARYL COMPOUNDS | 2010 |
|
RU2557242C2 |
PYRIDINES SUBSTITUTED WITH HETEROARYL AND APPLICATION METHODS | 2017 |
|
RU2756743C2 |
TETRAHYDROPYRIDINE DERIVATIVES AND USE THEREOF AS ANTIBACTERIAL AGENTS | 2017 |
|
RU2722594C1 |
PYRROLO-PYRROLE COMPOSITIONS AS ACTIVATORS OF PYRUVATE KINASE (PKR) | 2018 |
|
RU2736217C2 |
PYRIDAZINONE DERIVATIVES AS PARP INHIBITORS | 2008 |
|
RU2490265C2 |
BROMDOMAIN INHIBITORS | 2012 |
|
RU2671571C1 |
BROMDOMAIN INHIBITORS | 2012 |
|
RU2647592C2 |
5-AMINO-2-(1-HYDROXYETHYL)TETRAHYDROPYRAN DERIVATIVES | 2009 |
|
RU2525541C2 |
Authors
Dates
2021-11-23—Published
2017-12-14—Filed