FIELD: medicine; pharmaceutics.
SUBSTANCE: invention relates to TLR7 agonists and pharmaceutically acceptable salts thereof, represented by general formula I, where R1 is -H, -OH, -OC(O)-R6 or -F; R2 is -H or -F; R3 is independently -OH or -OC (O) -R7; R4 is -(C1-C8)alkyl, -(C1-C8)alkenyl, -(C1-C8)alkynyl, -(C1-C8)haloalkyl, -(CH2)n(cycloalkyl), -(CH2)n(aryl) or -(CH2)nC(O)OR6; R5 is -H, -OH or -Cl; R6 and R7 are -(C1-C8) alkyl; n is equal to integer 1, 2, 3 or 4; each alkyl, cycloalkyl, alkenyl, alkynyl, haloalkyl and aryl are independently optionally substituted with CN, halogen atom, (C1-C3)haloalkyl, aryl, OH, O-(C1-C3)alkyl, C(O)R8, S(C1-C8)alkyl, C(O)NOR8, C(O)NR8R8, C(O)NR8SO2 alkyl, NR8R8, and R8 independently represents -H, -OH or -(C1-C8)alkyl. Invention also relates to compounds having a structure presented in the claim and pharmaceutically acceptable salts thereof, to a pharmaceutical composition and a method of treating diseases caused by TLR7 agonism.
EFFECT: providing TLR7 agonist compounds.
23 cl, 4 tbl, 370 ex
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Authors
Dates
2024-04-09—Published
2019-05-24—Filed