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BJE6-106

Chemical Structure : BJE6-106

CAS No.: 1564249-38-2

BJE6-106 (B106)

Catalog No.: PC-62375Not For Human Use, Lab Use Only.

BJE6-106 (B106) is a potent, selective PKCδ inhibitor with IC50 of 50 nM, displays excellent selectivity over classical PKC isozymes (a 1,000-fold PKCδ selectivity over PKCα).

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

BJE6-106 (B106) is a potent, selective PKCδ inhibitor with IC50 of 50 nM, displays excellent selectivity over classical PKC isozymes (a 1,000-fold PKCδ selectivity over PKCα).
BJE6-106 induces cell growth inhibition in melanoma cell lines with NRAS mutations at nanomolar concentrations.
BJE6-106 induces phosphorylation (activation) of JNK1/2 (T183/Y185) most strongly after two hr of exposure in SBcl2 cells, induces phosphorylation of MKK4, JNK and H2AX in NRAS mutant melanoma WM1366 cells.

Physicochemical Properties

M.Wt 381.475
Formula C26H23NO2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

6-(2-(9H-carbazol-9-yl)ethyl)-2,2-dimethyl-2H-chromene-8-carbaldehyde

References

1. Takashima A, et al. ACS Chem Biol. 2014 Apr 18;9(4):1003-14.

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