FIELD: pharmaceutics.
SUBSTANCE: present invention relates to benzotriazole derivatives, specifically to a compound of formula 1 or a pharmaceutically acceptable salt thereof, in which W1 is C; W2 is C; W3 is C; W4 is C; W5 is N; W6 is N; W7 is N; where each of R1, R2, R3 and R4 independently represents hydrogen, hydroxyl group, halogen group, -CF3, -(O)CF3, C1-C6 alkyl group, C1-C6 alkoxy group or an amino group -NR7R8; Z is present or absent, wherein, when Z is present, Z is -CH2 or -C2H4; R5 is -A-R6, where A is C3-C6 cycloalkyl, C5 bicycloalkyl, C4-C6 heterocyclic group, containing one N heteroatom, optionally fused with phenyl, phenyl group or C4-C5 heteroaryl group containing one heteroatom, selected from a group consisting of N and S, R6 is a carboxyl group (-C(O)OH), a nitrile group (-CN), -S(O)2NHR7, -CH2NHS(O)2NHR7, CH(CH3)NHS(O)2NHR7, -CH(CH3)NHS(O)2NH2, -CH2NHS(O)2NH2, CH2NR7S(O)2NH2, -S(O)2NH2, -C2H4NHS(O)2NH2, -CH2NHS(O)2R7, CH2NHSO(NH)R7, -CH2NHP(O)OR7OR8, or -CH2NHP(O)(OH)2, A can be further substituted with one or two substituents independently selected from the group consisting of a halogen group, a methyl group, a nitrile group (-CN) and a methoxy group, in addition to R6, and each of R7 and R8 independently represents hydrogen, C1-C6 alkyl group, phenyl group substituted or unsubstituted with C1-C6 alkyl, amino group (-NH2), -Boc, or -NHBoc. Invention also relates to a pharmaceutical composition, ENPP 1 inhibitor and a STING signaling pathway activator based on said compound.
EFFECT: design of alternative compounds for treating ENPP1-mediated diseases, as well as diseases mediated by the STING signaling pathway.
7 cl, 4 tbl, 124 ex
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Authors
Dates
2024-08-12—Published
2022-01-28—Filed