SX 011 is a p38α inhibitor.

JNK3 inhibitor, potent and selective

n-Butyl α-D-fructofuranoside，分离自Ulmus davidiana var. japonica的根皮，通过激活JNK促进Nrf2活性，并表现出抗炎效应。

2-PyriMidinaMine, 4-[3-fluoro-5-(4-Morpholinyl)phenyl (Compound 9l) 是一种ATP竞争型的JNK(c-jun-N-terminal kinase)抑制剂，对JNK1和JNK3的IC50为0.099μM和0.148μM，具有可穿透血脑屏障的优点。2-PyriMidinaMine, 4-[3-fluoro-5-(4-Morpholinyl)phenyl能够抑制c-jun磷酸化和ROS生成，可用于研究神经退行性疾病。

Iso-AS601245 trifluoroacetate是AS601245的异构体，AS601245是一种ATP竞争性和选择性的JNK抑制剂，对hJNK1/2/3的IC50=150/220/70 nM，具有神经保护作用。

Lappaol C has antioxidant and antiaging properties, it may promote the C. elegans longevity and stress resistance through a JNK-1-DAF-16 cascade. Lappaol C also has potential chemosensitizing activity, it may be candidates for developing novel adjuvant an

8-hydroxy Efavirenz is a major oxidative metabolite of the non-nucleoside reverse transcriptase inhibitor efavirenz . 8-hydroxy Efavirenz is formed when efavirenz is metabolized by the cytochrome P450 (CYP) isoform CYP2B6. It induces apoptosis in rat primary hippocampal neurons and loss of dendritic spines in rat primary hippocampal neuronal cultures when used at a concentration of 0.01 μM.

JD118是一种JNK抑制剂，能够抑制JNK1的活性以及cJun (1 - 135) 的表达。

JNK-IN-22 (Compound 58) 被用作JNK-1抑制剂。