FIELD: biotechnology.
SUBSTANCE: invention relates to a compound of the formula (I) or its pharmaceutically acceptable salt, which have inhibitory activity relatively to indolamine-2,3-dioxygenase (hereinafter – IDO). In the specified formula, n is 1; p is 1; in each case, A is -CH=; M is -O-; R1 is pyridinyl, where pyridinyl is optionally substituted with 1-3 substitutes independently selected from: (a) halogen, (b) -C3-8-cycloalkyl optionally substituted with -OH, (e) -O-C1-8-alkyl optionally substituted with 1-5 halogen atoms, (f) -O-C3-8-cycloalkyl, (g) -C1-8-alkyl optionally substituted with 1-4 substitutes independently selected from halogen, -OH, -NH2, (i) -C(O)-Rf, where Rf is selected from -OH, -NH2, and -NH-C1-8-alkyl; R2 is phenyl, where phenyl is optionally substituted with 1-3 substitutes independently selected from: (a) halogen, (c) -CN, (d) -O-C1-8-alkyl optionally substituted with 1-3 halogen atoms, and (e) -C1-8-alkyl optionally substituted with 1-3 substitutes independently selected from halogen; and R3 is selected from H and halogen. The invention also relates to a pharmaceutical composition inhibiting IDO and containing a pharmaceutically acceptable carrier and effective amount of the compound of the formula (I) or its pharmaceutically acceptable salt and to a separate compound of N-(4-fluorphenyl)-3-(4-(4-(2-hydroxypropane-2-yl)-6-(trifluoromethyl)pyridine-3-yl)phenyl)oxetane-3-carboxamide or its pharmaceutically acceptable salt.
EFFECT: obtainment of compounds for inhibition of indolamine-2,3-dioxygenase.
(I)
16 cl, 16 tbl, 152 ex
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Authors
Dates
2022-12-22—Published
2018-11-12—Filed