BI-78D3

BI-78D3

CAT N°: 21183
Price:

From 48.00 40.80

BI-78D3 is an inhibitor of JNK (IC50 = 280 nM in a TR-FRET assay) that is competitive for JNK1 binding with pepJIP1, a JNK-interacting protein, with an IC50 value of 500 nM.{38279} It is selective for JNK, being 100-fold less active for the structurally similar MAPK family protein p38? and inactive at mammalian target of rapamycin (mTOR) or phosphatidylinositol 3-kinase ? (PI3K?). In a cell-based kinase assay, BI-78D3 inhibits c-Jun phosphorylation induced by TNF-? (EC50 = 12.4 µM). In a mouse model of type 2 diabetes, BI-78D3 (25 mg/kg) restores insulin sensitivity, reducing blood glucose levels when administered 30 minutes prior to insulin. BI-78D3 (30 µM) reduces contractions in human prostate strips induced by phenylephrine (Item Nos. 17205 | 18619) or norepinephrine (Item No. 16673) and reduces phosphorylation of c-Jun, a JNK substrate.{38280}

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