FIELD: pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula (II), where ring A represents isoxazolyl; R1 represents -C(Ra1)(Ra2)(Ra3), where Ra1, Ra2 and Ra3 independently represent H, C1-6 alkyl or C1-6 haloalkyl; alternatively Ra1, Ra2 and Ra3 are independently C1-4 alkyl or C1-4 haloalkyl; alternatively Ra1, Ra2 and Ra3 are independently methyl or halomethyl; R2 represents H; m is selected from 0, 1, 2 and 3; L1 represents CH2; RY is H or halogen, alternatively fluorine; Y4 represents CH or N; Z2 represents N or CRZ2 where RZ2 represents H; Z3 represents N or C; Z5 represents N, NRZ5 or CRZ5, where RZ5 represents H; Z6 represents NRZ6 or CRZ6, where RZ6 represents C1-6 alkyl; alternatively RZ6 is C1-4 alkyl; each of Rn1 and Rn2 is independently selected from H; or a pharmaceutically acceptable salt thereof; alternatively, wherein at most one of Z5 and Z6 represents a substituted or unsubstituted carbon atom. The invention relates to specific compounds (shown in the claims). The invention relates to a pharmaceutical composition used for inhibiting wild-type and mutant RET, KIF5B-RET, FLT3 and FLT3-ITD kinases, containing a therapeutically effective amount of a compound or a pharmaceutically acceptable salt thereof according to the invention and a pharmaceutically acceptable excipient.
(II)
EFFECT: aromatic derivative used in the production of a medicinal product for the treatment and/or prevention of a disease wherein the disease is mediated by protein kinases selected from wild type and mutant RET, KIF5B-RET, FLT3 and FLT3-ITD kinases.
28 cl, 6 dwg, 10 tbl, 13 ex
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Authors
Dates
2024-01-12—Published
2020-09-25—Filed