FIELD: medicine, pharmaceutics.
SUBSTANCE: invention relates to novel azabicyclic compounds, represented by the given below general formula
,
or to their pharmaceutically acceptable salts. The said compounds demonstrate inhibition activity with respect to HSP90 and action inhibiting cellular proliferation. In formula (I) X1 represents CH or N; one of X2, X3 and X4 represents N, and the others represent CH; one or two of Y1, Y2, Y3 and Y4 represent C-R4, one of the remaining ones represents CH or N and the remaining one represents CH; R1 represents a monocyclic group optionally substituted 5- or 6-membered unsaturated heterocyclic group, which contains from 1 to 2 heteroatoms, selected from N, S and O, or an optionally substituted 9- or 10-membered bicyclic unsaturated heterocyclic group, which contains from 1 to 2 heteroatoms, selected from N, S and O, where the possible substituent is determined in the formula of the invention; R2 represents a hydrogen atom, an optionally substituted with halogen atoms alkyl group, containing from 1 to 6 carbon atoms, or an alkenyl group, containing from 2 to 6 carbon atoms; and R3 represents CO-R5; R4 are similar or different and represent a hydrogen atom, a halogen atom, a cyanogroup, an alkyl group, which contains from 1 to 6 carbon atoms, optionally substituted with a mono- or di(C1-C6-alkyl)aminogroup or a morpholine group, a cycloalkyl group, which contains from 3 to 7 carbon atoms, an alkenyl group, which contains from 2 to 6 carbon atoms, an alkoxygroup, which contains from 1 to 6 carbon atoms, a phenyl group, -N(R6)(R7), -S-R8 or -CO-R9; R5 represents an aminogroup or mono- or di(C1-C6alkyl)aminogroup; R6-R9 have values, given in the invention formula.
EFFECT: invention relates to the pharmaceutical product, pharmaceutical composition and method of treating a cancer disease.
11 cl, 3 tbl, 191 ex
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Authors
Dates
2015-10-20—Published
2010-07-09—Filed