FIELD: organic chemistry, pharmaceuticals.
SUBSTANCE: invention relates to compounds of general formula I , wherein Z is -NH-; X is radical; E is phenyl optionally monosubstituted with halogen; T is -O(CH2)m-, -S(CH2)m-; L is phenyl etc.; G1, G2, G3, and G4 are independently hydrogen, C1-C6-alkoxy, R2NH; R7 is -J; M is >NR6; W is direct bond; Het is pyrrolidine optionally monosubstituted at R6, hydroxy; each R6 is independently hydrogen, C1-C6-alkyl, C2-C6-alkenyl; R2 is ; each R3 is , etc; J are independently hydrogen, chlorine, bromine or iodine; a = 0 or 1; n = 0 or 1; M = 1; p = 2-4; r = 1-4; u = 4 and pharmaceutically acceptable salts thereof. Also disclosed are methods for treatment, growth inhibiting or combating of neoplasm and other disorders and pharmaceutical composition having activity of EGF-R and HER2 kinase inhibitors, as well as method for production of abovementioned compounds.
EFFECT: new compounds with useful biological properties.
31 cl, 3 tbl, 10 ex
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Authors
Dates
2007-10-27—Published
2002-11-26—Filed