FIELD: chemistry.
SUBSTANCE: invention relates to compounds of formula 1, where R1 is selected from group comprising 4-ethoxyphenyl, 4-chlorophenyl, 4-bromophenyl; R2 is selected from a group comprising phenyl, 4-ethoxyphenyl, 2-chlorophenyl, 3-chlorophenyl, 4-chlorophenyl, 4-ethylphenyl, 3,4-dimethoxyphenyl, 4-methoxyphenyl, 4-fluorophenyl, 2-methylphenyl; R3 is selected from a group comprising a chlorine, bromine or hydrogen atom; R4 represents a hydrogen atom or propargyl HC≡C-CH2-. Invention also relates to a method of producing compounds of formula 1, use as protein-protein interaction inhibitor MDM2/p53, pharmaceutical composition and a medicinal agent for treating oncological disease associated with protein-protein interaction MDM2/p53 and inhibition method.
EFFECT: technical result is compounds of formula 1 as inhibitors of protein-protein interaction MDM2/p53.
7 cl, 1 tbl, 33 ex
Title | Year | Author | Number |
---|---|---|---|
NEW DISPIRO-INDOLINONES, MDM2/p53 INTERACTION INHIBITORS, METHOD FOR PRODUCTION AND APPLICATION | 2015 |
|
RU2629750C2 |
METHOD OF OBTAINING DISPIROINDOLINONES | 2018 |
|
RU2682678C1 |
METHOD FOR OBTAINING DISPYROINDOLINONES BASED ON 5-INDOLIDENE-2-THIOHIDANTOINES | 2020 |
|
RU2756463C1 |
NOVEL 2',5'-DIARYLSPIRO[INDOLE-3,3'-PYRROLIDINE]-2(1H)-ONES AND A METHOD FOR PRODUCTION THEREOF | 2019 |
|
RU2730287C1 |
ISOINDOLINONE INHIBITORS OF MDM2-P53 INTERACTION WITH ANTI-CANCER ACTIVITY | 2016 |
|
RU2794333C1 |
2-R-6-R-5-ARYL-PYRROLE[3,4-c]CARBAZOLE-1,3(2H,6H)-DIONE SYNTHESIS METHOD | 2009 |
|
RU2404983C1 |
COMPOUNDS TARGETING TAU PROTEIN AND RELATED USE THEREOF | 2017 |
|
RU2805523C2 |
SUBSTITUTED N-(INDOLE-2-CARBONYL)-GLYCINEAMIDES AND THEIR DERIVATIVES, METHODS OF TREATMENT OF PATIENTS AND PHARMACEUTICAL COMPOSITION | 1996 |
|
RU2143424C1 |
SUBSTITUTED 1,3-DIETHYL-8-VINYL-7-METHYL-3,7-DIHYDROPURINE-2,6-DIONES - ANTAGONISTS OF ADENOSINE A RECEPTOR AND USE THEREOF | 2012 |
|
RU2480469C1 |
METHOD OF PRODUCING Α-DIAZOCARBONYL COMPOUNDS IN AQUEOUS MEDIUM | 2018 |
|
RU2686489C1 |
Authors
Dates
2020-08-21—Published
2019-05-31—Filed