2-[1-3(Aminopropyl)indol-3-yl]-3(1-methyl-1H-indol-3-yl)maleimide, Acetate Bisindolylmaleimide VIII, Acetate Red to reddish-orange solid. PROTECT FROM LIGHT. A selective protein kinase C (PKC) inhibitor (IC50 = 158 nM for rat brain PKC) that acts at the ATP binding site of PKC. Does not inhibit the tyrosine phosphorylation or the activation of phospholipase Cg1. Exhibits some degree of PKC isozyme specificity (IC50 = 53 nM for PKCa, 195 nM for PKCbI, 163 nM for PKCbII, 213 nM for PKCg, and 175 nM for PKCe). Inhibits carbachol-evoked noradrenaline release (IC50 = 600 nM). Purity: ≥98% by TLC. CAS 125313-65-7. Ref.: Zhang, C., et al. 1997. J. Immunol. 158, 4968. Turner, N.A., et al. 1996. J. Neurochem. 66, 2381. Ozawa, K., et al. 1993. J. Biol. Chem. 268, 1749. Wilkinson, S.E., et al. 1993. Biochem. J. 294, 335. |