FIELD: chemistry.
SUBSTANCE: invention relates to new derivatives of formula 1 dispiro-indolinones or pharmaceutically acceptable salts thereof, or optical isomers, where R1 is selected from the group including phenyl optionally substituted with 1-2 substituents selected from halogen atom, lower alkoxy group; R2 is selected from the group consisting of hydrogen, unsubstituted pyridyl or phenyl optionally substituted with a substituent selected from halogen, lower alkoxy, C1-C6alkyl or -O-C5cycloalkyl; R3 is selected from the group incuding a hydrogen or halogen atom; R4 represents C1-C5alkyl; R5 is selected from the group consisting of hydrogen, methyl or propargyl HC≡C-CH2-. The invention also relates to the active ingredient, based on formula 1 compounda, pharmaceutical composition based of the said active ingredient, a drug based on this active ingredient or pharmaceutical composition, method for MDM2/p53 protein-protein interaction inhibition.
EFFECT: new dispiro-indolinone derivatives are obtained, that are useful for cancer treatment.
10 cl, 1 tbl, 15 ex
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Authors
Dates
2017-09-01—Published
2015-04-09—Filed