FIELD: heteroaromatic compounds.
SUBSTANCE: following is proposed: a compound of formula (I) or its stereoisomer, where: each X1 and X3 independently represents CRa; X2 is N or CRa; each Y1 and Y3 is independently N or CRb; Y2 is CRb; Z1 is O or NRc; Z2 is a bond or NRf; m is 0, 1 or 2; n is 1, 2 or 3; R1 is C1-C6 alkyl or C1-C6 alkyl substituted with -NRhRi; R2 is selected from the group consisting of hydrogen, halogen, CN, NO2 and CF3; R3 is C1-C6 alkyl; C1-C6 alkyl substituted with halogen; C1-C6 alkyl substituted with OH; heterocyclyl containing from 1 to 10 ring carbon atoms and from 1 to 4 ring heteroatoms selected from the group consisting of nitrogen, sulfur and oxygen; heterocylyl substituted with halogen, wherein the heterocyclyl contains from 1 to 10 ring carbon atoms and from 1 to 4 ring heteroatoms selected from the group consisting of nitrogen, sulfur and oxygen; aryl substituted with halogen, where aryl contains from 6 to 14 ring carbon atoms; and heteroaryl containing from 1 to 10 ring carbon atoms and at least one ring heteroatom selected from the group consisting of nitrogen, sulfur and oxygen; R4 is hydrogen or C1-C6 alkyl; Ra is H; Rb is H, halogen, -NH2 or -NO2; Rc represents H or C1-C6 alkyl; and each of Rf, Rh and Ri independently represents C1-C6 alkyl. Also specific compounds and the use of a compound of formula (I) for the treatment of diseases susceptible to inhibition of B-Raf V600E kinase and inhibition of B-Raf V600E kinase activity in a cell are provided.
EFFECT: obtaining heterocyclic compounds with inhibitory activity against B-Raf V600E kinase.
48 cl, 7 tbl, 53 ex
Title | Year | Author | Number |
---|---|---|---|
NITROIMIDAZOLE DERIVATIVE AGAINST PULMONARY TUBERCULOSIS | 2016 |
|
RU2675622C1 |
SUBSTITUTED PYRAZOLES, PHARMACEUTICAL COMPOSITION BASED ON THEREOF, USING PHARMACEUTICAL COMPOSITION AND METHOD FOR INHIBITION OF CATHEPSIN S ACTIVITY | 2001 |
|
RU2317988C2 |
HETEROARYL DERIVATIVE OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, A METHOD FOR PRODUCTION THEREOF AND A PHARMACEUTICAL COMPOSITION FOR PREVENTING OR TREATING DISEASES ASSOCIATED WITH PI3 KINASES, CONTAINING SAID ACTIVE SUBSTANCE | 2016 |
|
RU2719367C2 |
BROMODOMAIN INHIBITORS | 2017 |
|
RU2741808C2 |
MKK4 PROTEIN KINASE INHIBITORS FOR STIMULATION OF LIVER REGENERATION OR REDUCTION OR PREVENTION OF HEPATOCYTE DEATH | 2019 |
|
RU2788000C2 |
BICYCLIC LACTAMS AND METHODS FOR USE THEREOF | 2016 |
|
RU2716136C2 |
1,2,3,4-TETRAHYDROQUINOXALINE DERIVATIVE, METHOD FOR ITS OBTAINING AND ITS APPLICATION | 2019 |
|
RU2804127C2 |
2,3-DIHYDRO-6-NITROAMIDAZO [2,1-b] OXAZOLE DERIVATIVES | 2003 |
|
RU2326121C2 |
METHOD FOR TREATMENT OF ALLERGY BY USING SUBSTITUTED PYRAZOLES | 2001 |
|
RU2290179C2 |
NOVEL HETEROCYCLIC COMPOUNDS AND USE THEREOF IN MEDICINE AND COSMETICS | 2015 |
|
RU2712971C2 |
Authors
Dates
2023-08-07—Published
2018-09-20—Filed