FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound having the general formula I, where X1 is independently in each case selected from CR3 and N; X2 is independently selected from CR4 and N in each case; n is independently selected from 0 and 1 in each case; and independently in each case selected from any structure given in the following group W; R1 is independently in each case selected from the group consisting of hydrogen, C1-C6 alkyl, -(C=O)R5; R2 represents -OR8; R3 and R4 are independently in each case selected from the group consisting of hydrogen, halogen, C1-C3 alkyl, C1-C4 haloalkyl; R5 and R6 are independently in each case selected from the group consisting of hydrogen, C1-C6 alkyl, C3-C10 cycloalkyl; R8 is independently in each case a C1-C4 haloalkyl; Z1 in each case is independently selected from the group consisting of hydrogen, C1-C6 alkyl, C1-C6 alkyl substituted with one of OR5 and NR5R6, C3-C10 cycloalkyl, C3-C10 heterocycloalkyl containing 1 heteroatom, selected from O and N; R11 and R12 are independently in each case selected from the group consisting of C1-C6 alkyl, C1-C4 haloalkyl, and pharmacologically acceptable salts thereof. The invention also relates to a pharmaceutical composition based on the said compound.
EFFECT: obtaining of a new compound and a pharmaceutical composition based on it to be used in medicine for the treatment of disorders mediated by the receptor tyrosine kinase Axl/Mer and CSF1R, namely for the treatment of myeloid leukemia, breast cancer and non-small cell lung cancer.
19 cl, 8 tbl, 8 ex, 2 dwg
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Authors
Dates
2024-01-30—Published
2019-05-31—Filed