Powder: -20°C for 3 years | In solvent: -80°C for 1 year
BJE6-106 (B106) is a potent, selective PKCδ inhibitor (IC50: 0.05 μM) and targets selectivity over classical PKCα (IC50: 50 μM). BJE6-106 induces caspase-dependent apoptosis with tumor-specific effect.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
25 mg | 6-8 weeks | $ 1,140.00 | |
50 mg | 6-8 weeks | $ 1,490.00 | |
100 mg | 6-8 weeks | $ 2,320.00 | |
1 mL * 10 mM (in DMSO) | 6-8 weeks | $ 365.00 |
Description | BJE6-106 (B106) is a potent, selective PKCδ inhibitor (IC50: 0.05 μM) and targets selectivity over classical PKCα (IC50: 50 μM). BJE6-106 induces caspase-dependent apoptosis with tumor-specific effect. |
Targets&IC50 | PKCα:50 μM, PKCδ:0.05 μM |
In vitro | BJE6-106 (0.2 μM, 0.5 μM; 6-24 hours) triggers caspase-dependent apoptosis, increases the activity of caspase 3/7, the effect of B106 is greater than rottlerin (10-fold) in SBcl2 cells. BJE6-106 (0.2 μM, 0.5 μM; 24-72 hours) suppresses cell survival in melanoma cell lines with NRAS mutations. BJE6-106 (0.5 μM; 2-10 hours) activates the MKK4-JNK-H2AX Pathway by inducing JNK, MKK4, and H2AX activation at different times in SBcl2 cells. |
Synonyms | B106 |
Molecular Weight | 381.47 |
Formula | C26H23NO2 |
CAS No. | 1564249-38-2 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
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BJE6-106 1564249-38-2 Chromatin/Epigenetic Cytoskeletal Signaling PKC BJE6106 BJE-6-106 BJE6 106 B 106 B106 B-106 inhibitor inhibit