FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (I) or a pharmaceutically acceptable salt thereof.
The invention also relates to a pharmaceutical composition containing a compound of formula (I) or a pharmaceutically acceptable salt thereof having the property of an inhibitor of lipoprotein-associated phospholipase A2 (Lp-PLA2), and also relates to the use of a compound of formula (I) or a pharmaceutically acceptable salt or pharmaceutical composition thereof for the preparation of Lp-PLA2 inhibitor, also relates to the use of a compound of formula (I) or a pharmaceutically acceptable salt or pharmaceutical composition thereof for the preparation of a medicinal product for the treatment of a neurodegeneration-related disease, also relates to the use of a compound of formula (I) or a pharmaceutically acceptable salt or pharmaceutical composition thereof for the preparation of a medicinal product for the treatment of cardiovascular disease, diabetic macular edema (DME) or prostate disease.
EFFECT: group of inventions ensures the development of the synthesis of new tetracyclic pyrimidinones compounds as alternative inhibitors of lipoprotein-associated phospholipase A2 (Lp-PLA2).
27 cl, 2 tbl, 20 ex
| Title | Year | Author | Number |
|---|---|---|---|
| OBTAINING AND USING A TRICYCLIC PYRIMIDINONE COMPOUND AND A COMPOSITION THEREOF | 2021 |
|
RU2838186C1 |
| OBTAINING AND USING TRICYCLIC PYRIMIDINONE COMPOUND AND COMPOSITION THEREOF | 2021 |
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| PYRANODIPYRIDINE COMPOUND | 2016 |
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| PYRROLIDINE DERIVATIVES AS PPAR AGONISTS | 2017 |
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RU2711991C1 |
| PENTACYCLIC HETEROCYCLIC COMPOUND | 2020 |
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RU2815382C2 |
| LSD1 INHIBITOR, AS WELL AS ITS PRODUCTION METHOD AND ITS APPLICATION | 2018 |
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Authors
Dates
2023-11-15—Published
2020-09-01—Filed