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Protein Kinase C (PKC) Pathway and Related Products

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  Rottlerin
Cat. No. 557370  
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Protein Kinase C (PKC)

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.

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10 mgY€96


SolubilityMolecular FormulaMol. Wt.
DMSO or EtOH C30H28O8 516.5 


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All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Protein Kinase C (PKC)

Selected Citations:
  1. Phuong Thi Nguyen Sarkis, et al. (2006) STAT1-independent cell type-specific regulation of antiviral APOBEC3G by IFN-α. Journal of Immunology 177, 4530-4540.
  2. Ying Zhang, Mingjuan Liao and Maria L. Dufau. (2006) Phosphatidylinositol 3-kinase/protein kinase Cγ-induced phosphorylation of Sp1 and p107 repressor release have a critical role in histone deacetylase inhibitor-mediated depression of transcription of the luteinizing hormone receptor gene. Molecular and Cellular Biology 26, 6748-6761.
  3. Yoon-Jin Lee, et al. (2005) HSP25 inhibits protein kinase Cγ-mediated cell death through direct interaction. Journal of Biological Chemistry 280, 18108-18119.