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BI 894999

Cat. No. M20727

All AbMole products are for research use only, cannot be used for human consumption.

BI 894999 Structure

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Quality Control & Documentation
Biological Activity

BI 894999 is a potent and selective BET inhibitor with IC50 of 5 nM and 41 nM for the binding of BRD4-BD1 and BRD4-BD2 to acetylated histones, respectively. BI 894999 is highly selective for BRD2/3/4 and BRDT (Kd of 0.49-1.6 nM), with at least a 200-fold selectivity vs. BRD4-BD1.

Chemical Information
Molecular Weight 429.51
Formula C25H27N5O2
CAS Number 1660117-38-3
Solubility (25°C) DMSO 86 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Ulrike Tontsch-Grunt, et al. Br J Cancer. Therapeutic impact of BET inhibitor BI 894999 treatment: backtranslation from the clinic

[2] Daniel Gerlach, et al. Oncogene. The novel BET bromodomain inhibitor BI 894999 represses super-enhancer-associated transcription and synergizes with CDK9 inhibition in AML

[3] Ulrike Tontsch-Grunt, et al. Cancer Lett. Synergistic activity of BET inhibitor BI 894999 with PLK inhibitor volasertib in AML in vitro and in vivo

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  Catalog
Abmole Inhibitor Catalog




Keywords: BI 894999 supplier, Epigenetic Reader Domain, inhibitors, activators

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