FIELD: pharmaceutics.
SUBSTANCE: present invention relates to compounds of formula (I) and based on it composition used in medicine at abnormal cell growth
,
where Y is N or CR6; L1 and L2 are independently selected from a linking of -R6NR7-, -R6OR7-, -R6SR7-, alkyl, C5-6-carbocycle and 5-6-member heterocycle containing 1-2 heteroatoms selected from nitrogen; where L1 and L2 can be connected to any position; W1 is selected from C6-12-aryl, optionally substituted by 1-3 halogens, in case when C6-12-aryl is substituted with only two substitutes, these two substitutes are not placed in para positions; W2 is selected from C6-12-aryl and 5-6-member heteroaryl containing 1-2 heteroatoms selected from nitrogen, optionally substituted by halogen, -OR6, -SR6, -N(R6)R7, alkyl or alkyl substituted by halogen; R1 is selected from a group consisting of hydrogen and halogen; R2 and R3 are selected from hydrogen, halogen and alkyl; and R4 and R5 are independently selected from -OR6 and alkyl; where R6 and R7 are selected from hydrogen, halogen and C1-12-alkyl.
EFFECT: new substances modulating protein kinase activity and applicable for treating oncological diseases, ALK or cMet mediated disorders are suggested, including by EML4-ALK mediated fused protein having at least one mutation selected from L1196M, R1275Q and F1174L.
33 cl, 29 ex
Title | Year | Author | Number |
---|---|---|---|
SUBSTITUTED 2-AMINOPYRIDINE PROTEIN KINASE INHIBITOR | 2014 |
|
RU2671212C2 |
EPIDERMAL GROWTH FACTOR RECEPTOR INHIBITORS | 2022 |
|
RU2821531C2 |
SUBSTITUTED PIRIDAZINE-CARBOXAMIDE COMPOUNDS AS KINASE-INHIBITING COMPOUNDS | 2009 |
|
RU2526618C2 |
HETEROCYCLIC SUBSTITUTED PHENYLMETHANONES AS GLYCINE TRANSPORTER 1 INHIBITORS | 2006 |
|
RU2405771C2 |
COMBINATION OF mGluR2 RECEPTOR ANTAGONIST AND AChE ENZYME INHIBITOR FOR ACUTE ANDN/OR CHRONIC NEURALGIC DISEASES | 2004 |
|
RU2357734C2 |
SACCHARIN DERIVATIVES OR THEIR PHARMACEUTICALLY ACCEPTABLE ACID OR BASE ADDITIVE SALT, PHARMACEUTICAL COMPOSITION EXHIBITING ACTIVITY OF ELASTASE INHIBITOR | 1992 |
|
RU2114835C1 |
ACIDIFIED INDANYLAMINES AND THEIR USE AS PHARMACEUTICAL PREPARATIONS | 2002 |
|
RU2339614C2 |
2,4-DI(PHENYLAMINO)PYRIMIDINES, APPLIED IN TREATMENT OF NEOPLASTIC DISEASES, INFLAMMATORY DISORDERS AND IMMUNE SYSTEM DISORDERS | 2004 |
|
RU2400477C2 |
SUBSTITUTED N2-(4-AMINO-2-METHOXYPHENYL)-N4-[2-(DIMETHYLPHOSPHORYL)-PHENYL]-5-CHLORO-PYRIMIDINE-2,4-DIAMINES AS MODULATORS OF ALK AND EGFR, APPLICABLE FOR TREATING CANCER | 2015 |
|
RU2607371C1 |
PURINYL DERIVATIVES AND USE THEREOF AS POTASSIUM CHANNEL MODULATORS | 2008 |
|
RU2468026C2 |
Authors
Dates
2016-09-27—Published
2012-02-22—Filed