FIELD: chemistry.
SUBSTANCE: invention relates to organic and medicinal chemistry, pharmacology and medicine, specifically to a compound of general formula (I) or a pharmaceutically acceptable salt thereof, where R1 is selected independently and represents: NH-(C1-5-alkyl)-(1-adamantyl); NH-(C1-5-alkyl)-(2-adamantyl); NH-(C1-5-alkyl)-OH; ; R2 is selected independently and represents: C3-6-cycloalkyl, isopropyl, alternatively R2 is methyl, if R1 is
; n takes values 0-2. Invention also relates to a compound of general formula (II) or a pharmaceutically acceptable salt thereof, where if R'1 is selected independently and represents: NH-(C1-5-alkyl)-(1-adamantyl); NH-(C1-5-alkyl)-(2-adamantyl); then R'2 is selected independently and represents hydrogen, methyl, -NH2, halogen; alternatively, if R'1 is selected independently and represents:
;
;
; then R'2 is selected independently and represents methyl, -NH2, halogen; n takes values 0-2. Invention also relates to a pharmaceutical composition based on said compounds and use thereof as an inhibitor of reproduction of a virus belonging to the genus Orthoflavivirus.
EFFECT: design and production of compounds characterized by high efficiency in inhibiting reproduction of viruses of the genus Orthoflavivirus, particularly tick-borne encephalitis virus, yellow fever virus, West Nile virus and others.
11 cl, 4 tbl
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RU2130011C1 |
METHOD OF PRODUCING N-ADAMANTYLATED AMIDES | 2013 |
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RU2549901C1 |
METHOD FOR PREPARING 5,8,9,10-TETRAHYDROPYRIMIDINO[4,5-d]AZOCINE DERIVATIVES HAVING TRIFLATE, SECONDARY AND TERTIARY AMINO GROUPS IN 4-TH POSITION | 2011 |
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Authors
Dates
2024-12-02—Published
2023-11-02—Filed