FIELD: chemistry.
SUBSTANCE: invention refers to a new at least one compound chosen from the compounds of formula where each X1 and X2 independently represents -OR3, R1 is chosen from the group including C1-C8alkyl, C1-C4alkyl, attached to (C4-C8)cycloalkyl, and C4-C8 cycloalkyl, R2 stands for hydrogen or -C=OR9, R3 is chosen from the group including (lower) alkyl and (lower) alkyl substitutted with group R8, R8 represents halogen, R9 represents saturated 6-merous cycle containing at least one heteroatom N, and optionally substituted with the group chosen from (lower) alkyl, -C=O-R11, (lower) alkyl substituted with hydroxygroup, =O, and 5 and 6-merous saturated cycles containing at least one heteroatom N, R11 represents (lower) alkyl, or to its pharmaceutically acceptable salt or to its ester. Besides, the invention concerns a pharmaceutical composition.
EFFECT: production of the new biologically active compounds inhibiting to interaction of protein MDM2 and r-53 with a similar peptide.
14 cl, 60 ex, 1 tbl
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Authors
Dates
2009-05-10—Published
2004-06-09—Filed