FIELD: chemistry.
SUBSTANCE: group of inventions relates to organic chemistry, pharmacology and medicine and includes a compound of formula (I), pharmaceutically acceptable salts thereof, a pharmaceutical composition containing it, use, a method for reducing the level of aldosterone and a method of treating. In formula (I) Q1, Q2, Q3, Q4 is selected independently and represents CH or N; if R1 is hydrogen, then R2 is 6-member heterocyclyl containing 2 nitrogen atoms, necessarily substituted with an oxo group, or -(C1-C3)-alkyl-(C3-C6)-cycloalkyl, as well as optionally substituted with 1 substituent selected from (C1-C5)-alkyl; if R1 is -C(=O)-NH-(C1-C5)-alkyl, then R2 is NRcRd, where Rc and Rd together with the nitrogen atom to which they are attached form 8-membered bicyclic heterocyclyl containing 1-2 nitrogen atoms, optionally substituted with 1 substitute selected from (C1-C5) -alkyl.
EFFECT: compound of formula (I) for inhibiting human cytochrome P450 11B2 (CYP11B2) activity and use in treating and/or preventing diseases and disorders which are mediated or supported by the activity of the hormone aldosterone.
14 cl, 2 tbl, 3 ex
Title | Year | Author | Number |
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HUMAN CYTOCHROME 11B2 INHIBITORS | 2022 |
|
RU2800378C1 |
HUMAN ALDOSTERONE SYNTHASE (CYP11B2) INHIBITORS | 2022 |
|
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HUMAN CYTOCHROME 11B2 INHIBITORS | 2022 |
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HUMAN CYTOCHROME 11B2 INHIBITORS | 2021 |
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Authors
Dates
2024-08-07—Published
2023-04-10—Filed