FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula I and its pharmaceutically acceptable salts, where L1 is selected from -NR6 CON(R7)-, in which NR6 is connected to a nitrogen-containing heteroaryl substituted with R1, R2, R3; L2 is selected from C1-C4alkylene, where the alkylene may be optionally substituted with one or more G1; L3 is -O-; each R1, R2, R3 is independently selected from hydrogen; R4 is selected from hydrogen and halogen; R 5 is selected from hydrogen and halogen; each R6, R7 is independently selected from hydrogen, C1-C4alkyl; G1 is selected from C1-C4alkyl. The invention also relates to a pharmaceutical composition for the treatment or prevention of TRK-mediated diseases, comprising a therapeutically effective amount of a compound of the invention, or pharmaceutically acceptable salts thereof, and pharmaceutically acceptable carriers, diluents, and auxiliaries. The compounds of the invention, or pharmaceutically acceptable salts thereof, or a pharmaceutical composition based on them are used in the preparation of a medicament for the treatment or prevention of TRK-mediated diseases such as cancer, especially hematological malignancies, lung cancer, breast cancer, ovarian cancer, prostate cancer, cancer pancreas and glioma.
EFFECT: using compounds as TRK inhibitors.
4 cl, 1 tbl, 4 ex
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Authors
Dates
2023-09-20—Published
2019-06-25—Filed