FIELD: pharmacology.
SUBSTANCE: invention relates to a compound represented by the formula I, or its pharmacologically acceptable salt, where R1 is a substituted or unsubstituted group selected from a group consisting of a phenyl and a 5-membered heteroaryl containing 1 heteroatom selected from O; Y is O; R2 is -C (=O)R4, where R4 is a substituted or unsubstituted group selected from a group consisting of cyclohexyl, phenyl and a 5-membered heteroaryl containing 1 heteroatom selected from O; is a double bond or a single bond, and when it is a double bond, R3 represents O, when it is a single bond, R3 represents OR5 or F, while R5 represents H, Boc, CH2SCH3, -CH2OP(=O)(OH)2 or -CH2OP(=O)(OBn)2; each X represents H; each of the above terms “substituted” independently means that one hydrogen atom in the group is replaced by a substituent selected from a group consisting of a halogenated C1-C8 alkyl and an unsubstituted C1-C8 alkoxy. The invention also relates to methods for obtaining these compounds and to a pharmaceutical composition that has an immunosuppressive and antitumor effect, based on them.
EFFECT: obtaining new compounds and a pharmaceutical composition based on them, which can be used in medicine for the treatment of tumor diseases.
I
9 cl, 2 dwg, 4 tbl, 13 ex
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