FIELD: medicine; pharmaceuticals.
SUBSTANCE: invention relates to a compound of formula I-b:
(Formula I-b),
where L is SO2, each R1 and R2 is independently selected from a group consisting of H and C1-4 alkyl; R3 is selected from a group consisting of C1-3 alkyl, optionally substituted with R21; ring is selected from a group consisting of
, , , , , , , , , , and $; each R4, R5, R7 and R8 is independently selected from a group consisting of H, F, Cl, Br, C1-4 alkyl, N3, NH2, CF3, OCHF2, OCF3, OC1-4 alkyl, benzoyl, -OCH2C≡CH, CN, and NO2; R6 is selected from a group consisting of H, Br and R17; R9 is H; R10 is H or Br; each R11, R12 and R13 independently represents H, F, Cl or Br; each R14, R15 and R16 independently represents H, methyl or ethyl; R17 is phenyl, optionally substituted with one or more substitutes selected from the group consisting of NO2 and -NR18CO-(C1-4alkyl); each R18 independently represents H; each R21 is independently selected from a group, consisting of H, CN and OR22; each R22 independently represents H; and to compounds of similar structure, presented by specific chemical formulas, as well as to a pharmaceutical composition for treating colon cancer, comprising a therapeutically effective amount of such compounds, and a method of treating colon cancer.
EFFECT: therapeutic agents aimed at truncated proteins of adenomatous polyposis coli (APC) are proposed.
9 cl, 62 dwg, 1 tbl, 3 ex
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Authors
Dates
2020-07-22—Published
2014-09-10—Filed