FIELD: chemistry.
SUBSTANCE: invention relates to a compound represented by the following formula:
[Structural Formula 1]
or a pharmaceutically acceptable salt thereof. In Formula 1, ring P is pyridine; W is methylene; pyridine together with the adjacent ring forms a substituted tetrahydronaphthyridine; ring A is piperidine, azetidine or pyrrolidine; ring B is (1) a benzene ring optionally substituted with 1 to 4 substituents selected from a halogen atom, C3-10 cycloalkyl group, C1-6 alkoxy group and C6-14 aryl group, optionally substituted with 1 to 3 halogen atoms, or (2) pyridine, indole or pyrazole, each optionally substituted with 1 to 3 substituents selected from C1-6 alkyl group, C3-10 cycloalkyl group, C1-6 alkoxy groups and C6-14 aryl group optionally substituted with 1 to 3 halogen atoms; R1 represents a hydrogen atom or COOH; R2 represents a hydrogen atom, C1-6 alkyl group optionally substituted with C1-6 alkoxy group, C3-10 cycloalkyl group or COOH; and one of R1 and R2 is COOH, and each of R3, R4, R5 and R6 represents a hydrogen atom. Medicament, a method for the prevention or treatment of diabetes mellitus, a method for antagonising somatostatin receptor subtype 5, and the use of a compound of formula 1 are also disclosed.
EFFECT: present compound has the action of an SSTR5 antagonist and can be used as a medicament for the prevention or treatment of diabetes mellitus.
17 cl, 5 tbl, 89 ex
Title | Year | Author | Number |
---|---|---|---|
HALOGEN SUBSTITUTED HETEROCYCLIC COMPOUND SALT | 2015 |
|
RU2689315C2 |
TRICYCLIC COMPOUND AND JAK INHIBITOR | 2015 |
|
RU2674262C2 |
NOVEL TRICYCLIC DERIVATIVE AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF, METHOD FOR PRODUCTION THEREOF AND PHARMACEUTICAL COMPOSITION CONTAINING SAID DERIVATIVE | 2009 |
|
RU2470934C1 |
NITROIMIDAZOLE DERIVATIVE AGAINST PULMONARY TUBERCULOSIS | 2016 |
|
RU2675622C1 |
TRKA KINASE INHIBITORS, COMPOSITIONS BASED THEREON AND METHODS | 2015 |
|
RU2672583C2 |
COMPOUND BASED ON DIHYDRONAPTHYRIDINONE, METHOD OF ITS OBTAINING, AND ITS USE IN MEDICINE | 2021 |
|
RU2809869C1 |
AVB6 INTEGRIN INHIBITORS | 2018 |
|
RU2769702C2 |
CONDENSED HETEROCYCLIC NITROGEN COMPOUNDS AND USING THEM AS INHIBITORS OF AMYLOID BETA PRODUCTION | 2010 |
|
RU2515976C2 |
TRICYCLIC HETEROCYCLIC COMPOUNDS AND JAK INHIBITORS | 2012 |
|
RU2632870C2 |
NOVEL HETEROCYCLIC COMPOUND OR SALT THEREOF AND INTERMEDIATE COMPOUND THEREOF | 2007 |
|
RU2434868C2 |
Authors
Dates
2018-11-08—Published
2014-10-06—Filed