FIELD: pharmaceutics.
SUBSTANCE: invention relates to a compound of formula I,
,
where ring A and ring B are condensed bicyclic group, R1 denotes a substitute selected from hydrogen, halogen or ORf7; each R2a, R2b, R2c, R3 are independently selected from hydrogen, halogen, -CN, -ORf7 or C1-6 alkyl, optionally substituted with one or more substitutes selected from =O and E1; X is a straight bond; Y denotes -arylene-, -heteroarylene-, where -arylene- and -heteroarylene- may be substituted with E3, where E3 denotes halogen, or -heterocycloalkylene-, optionally substituted with one or more substitutes selected from =O and E4, RN denotes hydrogen or C1-6 alkyl, optionally substituted with one or more substitutes selected from =O and E5; Z denotes -C(O)-[T1]- or -C(O)N(Rx3)-[T1]-, where T1 denotes -(CH2)0-4-T2- and T2 denotes a direct bond or -C(O)-N(H)-CH2-; or its pharmaceutically acceptable ester, amide.
EFFECT: compounds are suitable for use in treating the diseases in which it is desirable and/or require inhibition of protein-or lipid-kinase (PI3-K, for example, especially class I PI3K kinase family, PIM and/or mTOR), and especially in treating cancer.
9 cl, 1 dwg, 4 tbl
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Authors
Dates
2016-09-27—Published
2012-05-18—Filed