FIELD: chemistry.
SUBSTANCE: present invention relates to a compound of formula I
or its pharmaceutically acceptable salt. According to formula I, is pyrrolidinone, oxazolidinone, imidazolidinone, dihydrotriazolone, piperidinone, tetrahydropyrimidinone, morpholinone, oxazinanone, piperazinone, thiomorpholinone, thiazinane dioxide, pyridinone, pyridazinone, oxazepanone, diazepanone, diazabicyclo[3.1.1]heptanone, diazabicyclo[3.2.1]octanone, diazabicyclo[3.2.2]nonanone or oxaazabicyclo[3.2.1]octanone where each ring represented by contains an alpha carbonyl with respect to the nitrogen atom that connects the ring to the backbone to form a cyclic amide; ring X is phenyl, a 5-6 membered monocyclic heteroaryl ring containing 1-4 heteroatoms independently selected from nitrogen and oxygen, fused with a 9-10 membered heterocyclic ring containing 1-3 heteroatoms independently selected from nitrogen and oxygen, or a condensed 9-10 membered heteroaryl ring containing 1-3 heteroatoms independently selected from nitrogen and sulfur; Z is N or CH; the values of Ra, R1, R2, R3, R4 and p are as defined in the claims. Also provided are a pharmaceutical composition, a method for inhibiting IRAK and a method for treating an IRAK-mediated disorder.
EFFECT: proposed compounds display inhibitory activity against IRAK and can be used for the treatment of IRAK-mediated disorders.
11 cl, 2 tbl, 234 ex
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Authors
Dates
2021-02-24—Published
2016-09-16—Filed