FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a new compound of formula 1, its isomer or pharmaceutically acceptable salt, where A represents -(CH2)m- or -O-, where m is an integer with a value from 1 to 3; R1 is (4–6 membered heterocycloalkyl containing one O)C1-6alkyl heteroatom, or (5-membered heteroaryl containing one or more heteroatoms selected from N and O)C1-6alkyl; R2 is independently either hydrogen or halogen; R3 is hydrogen; R4 is independently either hydrogen, halogen, C1-6alkyl substituted with halogen, or a nitrile group; n is an integer with the value from 1 to 4, where if n is an integer with the value from 2 to 4, each of R2, R3 and R4 may be the same or different from each other; Z1, Z2, Z3 and Z 7 are CH; and Z4, Z5 or Z6 are each independently CH, CF, CCl, CBr or CI; where heterocycloalkyl or heteroaryl is either unsubstituted or substituted with C1-6alkyl. The invention also relates to a pharmaceutical composition containing such a compound and a method of producing such a compound. The technical result of the invention is to obtain a new compound with the activity of a GLP-1 agonist.
[Formula 1]
EFFECT: invention can be used as an agent for the treatment or prevention of various metabolic diseases such as obesity, diabetes and hyperlipidemia.
13 cl, 1 tbl, 37 ex
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Authors
Dates
2023-07-19—Published
2021-03-17—Filed