FIELD: pharmaceutics.
SUBSTANCE: invention relates to a compound which is a compound of formula (1) or a pharmaceutically acceptable salt thereof, wherein: X1 and X2 are saturated hydrocarbon groups, which together contain a total of five to nine carbon atoms and none or one oxygen atom and which are connected to each other in such a way that the functional group (a) forms a monocyclic or bicyclic ring system; R1 is selected from OR5; NR5R6; COOR5; CONR5R6; CONR5OR6; C(=NOR5)R6; CH2NR7COR5; C1-3alkyl group, which is substituted with one to three fluorine atoms; and 5-member ring containing 2 heteroatoms selected from N and S, substituted with methyl; R4 is H or C1-3 alkyl group; and R5, R6 and R7 are identical or different, and each of them is independently selected from hydrogen, a non-aromatic C1-6saturated hydrocarbon group, optionally substituted with one or more fluorine atoms or optionally substituted with a phenyl ring; or R5 and R6 can be bonded to each other to form a monocyclic or bicyclic ring containing 1 or 2 heteroatoms selected from O and N, optionally substituted with methyl; or ethyl 4-[(1R,5S,6r)-6-(diethylcarbamoyl)-3-azabicyclo[3.1.0]hexan-3-yl]piperidine-1-carboxylate or a pharmaceutically acceptable salt thereof. Invention also relates to a pharmaceutical composition for treating a disease or condition mediated by muscarinic receptors M1 and/or M4, containing a compound of the invention and a pharmaceutically acceptable excipient.
(1),
(а)
EFFECT: compounds having muscarinic receptor agonist activity M1 and/or M4, and intended for use in treating a cognitive disorder or psychotic disorder or for treating or reducing the severity of acute, chronic, neuropathic or inflammatory pain.
15 cl, 4 tbl, 52 ex
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Authors
Dates
2022-03-22—Published
2018-06-18—Filed