FIELD: medicine; pharmaceuticals.
SUBSTANCE: invention refers to 1,4-disubstituted imidazole derivatives used as a drug. Disclosed is compound of formula (1a'), where ring Q1 is a phenyl, pyridyl or cyclohexyl group; R1 and R2 represent independently a hydrogen atom, a halogen atom or a C1-6 alkyl group; W1a and W3a are an optionally substituted C1-4 alkylene group; W2 is a methylene group; W2a-Q2a is -NR3aC(O)-Q2a, -NR3aC(O)CH2O-Q2a, -C(O)NR3a-Q2a or -NR3aC(O)-CH=CH-Q2a, where R3a represents a hydrogen atom or a C1-6 alkyl group; ring Q2 is a pyridyl, pyrimidyl, pyridazinyl, pyrazyl, oxazolyl, thiazolyl, isoxazolyl or isothiazolyl group; m is 1, 2, 3, 4 or 5; R11 is independently a hydrogen atom, a halogen atom, an optionally substituted C1-6 alkyl group or C1-6 alkoxy group; R12 and R13 are independently a hydrogen atom, a halogen atom, C1-6 alkyl group, C1-6 alkoxy group, C3-10 cycloalkyl group, C2-6 alkenyl group, C2-6 alkynyl group, cyano or amino group; R14 is a hydroxyl group or C1-6 alkoxy group; and a pharmacologically acceptable salt thereof. Invention also discloses a medicinal preparation for treating cancer, an antitumour agent, a pharmaceutical composition containing said compound, method of treating cancer using said compound and versions of using the disclosed compound for preparing an agent for treating cancer.
EFFECT: technical result is disclosed compound has powerful inhibiting action on ability of cancer cells to spherogenesis and can be used as an orally administered antitumour agent.
29 cl, 85 ex
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Authors
Dates
2021-01-22—Published
2016-06-21—Filed