FIELD: chemistry.
SUBSTANCE: invention relates to substituted amides of benzoic acid of formula (I), their isomers and salts as inhibitors of KDR and FLT tyrosine kinase, as well as to medication based on them. Compounds can find application as medications for treating diseases caused by persisting angiogenesis. In general formula (I) (I), A represents group =NH, W represents oxygen, Z represents bond or branched or non-branched C1-C12alkyl, R1 represents branched or non-branched C1-C6alkyl or optionally single- or multi-substituted with C1-C6alkyl C3-C10cycloalkyl, or unsubstituted or optionally single- or multisubstituted with halogen, C1-C6alkyl, single- or multisubstituted with halogen C1-C6alkyl phenyl, naphtyl, quinolyl, isochinolyl, indenyl, R2 and R3represent hydrogen, OH-group or group XR11, X represents C2-C6alkyl, C2-C6alkenyl or C2-C6alkinyl, R11 represents unsubstituted or optionally single- or multisubstituted with halogen, C1-C6alkoxygroup or hydroxy group phenyl ot pyridyl, R4, R5, R6 and R7represent hydrogen, R2 and R3 simultaneously do not represent hydrogen, and if R7 represents OH-group, R3 does not represent hydrogen, and if R3 represents OH-group, R2 does not represent hydrogen.
EFFECT: obtaining compounds which can be applied as medications for treating diseases caused by persisting angiogenesis.
3 cl, 160 ex
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Authors
Dates
2009-04-27—Published
2001-04-24—Filed