FIELD: medicine.
SUBSTANCE: present invention relates to a compound having a structure of the Formula (1) or to its pharmaceutically acceptable salt, having immunomodulating properties, which act through TLR, and which are useful in the treatment of viral infections and cancer diseases.
,
where R1a is selected from a group consisting of H, C1-C4 alkyl, and A, where alkyl is optionally substituted with -COOH, -SO2CH3, -SCH3, -OCH3, or A; R1b is C2-C5 alkyl; X is C1-C4 alkyl, where alkyl is optionally substituted with A or -OH; L1 is selected from a group consisting of a bond, -CH2-, -O- and -CH2CH2-; Y is selected from a group consisting of C1-C3 alkyl and C6 aryl, where C6 aryl is optionally substituted with 1-5 substituents, which are independently selected from A, C1-C3 alkyl, and C1-C3 alkoxy; A is selected from a group consisting of , , , , and ; L2 is selected from a group consisting of a bond, -(CH2)n-, -C(O)NH(CH2)n-, , and ; m is an integer from zero to four; n is an integer from one to four; where the compound is substituted with at least one A. In this case, following conditions are satisfied: when X is -CH3, L1 is -CH2-, Y is C6 aryl substituted with A, and L2 is -CH2-, then A is not -L2-COOH, except for cases, when R1a contains -COOH or -SO2CH3; and, when X is -CH3, L1 is -CH2-, Y is C6 aryl substituted with A, L2 is -CH2-, and A is , then A and L1 are not in a pair position relatively to each other.
EFFECT: obtaining a compound for the treatment of viral infections and cancer diseases.
55 cl, 1 tbl, 53 ex
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Authors
Dates
2022-10-21—Published
2017-12-04—Filed