JNK-IN-17 (Compound 9J) is a selective and potent JNK inhibitor with IC 50 values of 0.039, 0.079 μM for JNK1 and JNK3 . JNK-IN-17 can inhibit c-Jun phosphorylation with an IC 50 of 0.082 μM in Streptozotocin ( HY-13753 )-infuced INS-1 pancreatic islet β cells. JNK-IN-17 shows inhibition rate ≤ 33% on the four main P450 subtypes (2C9, 2D6, 3A4, 1A2) in human liver microsomes, indicating a relatively low risk of drug interactions. JNK-IN-17 can be used for researches of neurological and metabolic disease , such as Parkinson's disease.
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