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Inhibitor Libraries

Inhibitor Resource

VEGF Signaling Pathway
  Gö 6983
Cat. No. 365251  
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Protein Kinase C (PKC)

2-[1-(3-Dimethylaminopropyl)-5-methoxyindol-3-yl]-3-(1H-indol-3-yl) maleimide
Go 6983

Orange red solid. PROTECT FROM LIGHT. A potent, cell permeable inhibitor of protein kinase C (PKC) that inhibits several PKC isozymes (IC50 = 7 nM for PKCa and PKCb; 6 nM for PKCg; 10 nM for PKCd; and 60 nM for PKCz). Gö 6983 does not effectively inhibit PKCµ (IC50 = 20 µM) and can thus be used to differentiate PKCµ from other PKC isozymes. Purity: ≥95% by HPLC.

Ref.: Wang, D., et al. 1998. J. Biol. Chem. 273, 33027. Stempka, L., et al. 1997. J. Biol. Chem. 272, 6805. Gschwendt, M., et al. 1996. FEBS Lett. 392, 77.

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500 µgYN/A

SolubilityMolecular FormulaMol. Wt.
DMSO C26H26N4O3 442.5 


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365251: Gö 6983 - English
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Related Categories:
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. Rick B. Vega, et al. (2004) Protein Kinases C and D Mediate Agonist-Dependent Cardiac Hypertrophy through Nuclear Export of Histone Deacetylase 5. Molecular and Cellular Biology 24, 8374-8385.
  4. Bai Luo, Stephen M. Prescott and Matthew K. Topham. (2003) Association of Diacylglycerol Kinase ζ with Protein Kinase C α: Spatial Regulation of Diacylglycerol Signaling. Journal of Cell Biology 160, 929-937.