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Abstract

The invention relates to a compound of formula (I), or a pharmaceutically acceptable salt or ester thereof, wherein: R¹ is —NR⁷(CO)R¹¹; R² is aryl, heteroaryl, fused aryl-C_3-6-heterocycloalkyl or fused heteroaryl-C_3-6-heterocycloalkyl, each of which is optionally substituted; each R⁷ is selected from hydrogen, C_1-6-alkyl and C_3-7-cycloalkyl, wherein said C1-6-alkyl is optionally substituted by one or more halogens; each R¹¹ is independently selected from C_1-6-alkyl, C_3-7-cycloalkyl, C_1-6alkyl-C_3-7-cycloalkyl, Ĉ-heterocycloalkyl, aryl and heteroaryl, each of which may be optionally substituted. Further aspects of the invention relate to pharmaceutical compositions comprising the same, and methods for treating or preventing a disorder selected from cancer, septic shock, Primary open Angle Glaucoma (POAG), hyperplasia, rheumatoid arthritis, psoriasis, artherosclerosis, retinopathy, osteoarthritis, endometriosis, chronic inflammation and Alzheimer's disease. Another aspect of the invention relates to the use of a compound as described above in the preparation of a medicament for the prevention or treatment of a disorder caused by, associated with or accompanied by any abnormal kinase activity, wherein the kinase is selected from TBK1, ERK8, CDK2, MARK3, YES1, VEG-FR, IKKepsilon and combinations thereof.

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First Claim