Mallotoxin Orange solid. A cell-permeable protein kinase C inhibitor that exhibits greater selectivity for PKCd (IC50 = 3-6 µM) and PKCq. Inhibits the PKCa, PKCb, and PKCg isoforms, but with significantly reduced potency (IC50 = 30-42 µM). Has reduced inhibitory activity on PKCe, PKCh, and PKCz (IC50 = 80-100 µM). Also known to inhibit CaM kinase III (IC50 = 5.3 µM). Purity: ≥98% by HPLC. RTECS AM6913800, CAS 82-08-6. Merck Index: 14, 8272 Ref.: Villalba, M., et al. 1999. J. Immunol. 163, 5813. Gschwendt, M., et al. 1994. Biochem. Biophys. Res. Commun. 199, 93. Gschwendt, M., et al. 1994. FEBS Lett. 338, 85. Gschwendt, M., et al. 1984. Cancer Lett. 25, 177. |