FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula I, where R1, R2, R3, X1, Y1, Y2, Y3, Y4 and Y5 have the meanings defined in this use, and a pharmaceutically acceptable salt thereof, as antagonist of MC4R. Pharmaceutical compositions containing such compounds and salts, and the use of such compounds and salts for the treatment of, for example, cachexia, anorexia or anorexia nervosa are also provided.
EFFECT: obtaining spiro compounds as antagonists of melanocortin 4 receptors and their use.
20 cl, 6 dwg, 14 tbl, 201 ex
Title | Year | Author | Number |
---|---|---|---|
COMPOUNDS WITH CONDENSED RINGS | 2019 |
|
RU2783414C2 |
BENZOXAZEPINE PI3K INHIBITORS AND METHODS OF USE | 2010 |
|
RU2600927C2 |
COMPOUNDS OF PYRIDAZINAMIDE AND THEIR USE AS SYNTHETIC SYNECKINASIS INHIBITORS (SYK) | 2013 |
|
RU2627661C2 |
BENZOXAZEPINE PI3 INHIBITORS AND METHODS OF USE | 2010 |
|
RU2654068C1 |
SUBSTITUTED IMIDAZOPYRIDINES AS HDM2 INHIBITORS | 2013 |
|
RU2690663C2 |
CYCLOALKYL NITRILE PYRAZOLO PYRIDONES AS JANUS KINASE INHIBITORS | 2014 |
|
RU2655380C2 |
SPIRO CONDENSED PYRROLIDINE DERIVATIVES AS INHIBITORS OF DEUBIQUITINATING ENZYMES (DUB) | 2017 |
|
RU2730552C2 |
DERIVATIVES OF PYRIDINE AND APPLICATION THEREOF AGAINST MICROBACTERIA | 2015 |
|
RU2664587C1 |
QUINOLINE-2 DERIVATIVES AS C-KIT KINASE INHIBITORS | 2016 |
|
RU2754858C2 |
SUBSTITUTED 1,2-DIHYDRO-3H-PYRAZOLO[3,4-D]PYRIMIDIN-3-ONES | 2019 |
|
RU2812726C2 |
Authors
Dates
2024-02-13—Published
2021-06-07—Filed