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BAY 299

Cat. No. M6487

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

BAY 299 Structure
Size Price Availability Quantity
5mg USD 55  USD55 In stock
10mg USD 85  USD85 In stock
25mg USD 180  USD180 In stock
50mg USD 300  USD300 In stock
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Quality Control & Documentation
Biological Activity

BAY 299 is a potent and selective BRD1 and TAF1 inhibitor (IC50 values are 6-67 and 8-13 nM, respectively). Displays selectivity over other bromodomains (>30-fold over other members of the BRPF family; BRD9 and ATAD2; >300-fold over BRD4). Displays BRD1 and TAF1 inhibition in a NanoBRET cell assay. Inhibits binding of BRD1 and TAF1 to histone H4 (IC50 values are 575 nM and 0.9 μM, respectively) and histone H3.3 (IC50 values are 825 nM and 1.4 μM, respectively).

Chemical Information
Molecular Weight 429.47
Formula C25H23N3O4
CAS Number 2080306-23-4
Form Solid
Solubility (25°C) DMSO 42.95 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Jewett, et al. Brain Res. The kappa-opioid antagonist GNTI reduces U50,488-, DAMGO-, and deprivation-induced feeding, but not butorphanol- and neuropeptide Y-induced feeding in rats.

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  Catalog
Abmole Inhibitor Catalog




Keywords: BAY 299 supplier, Epigenetic Reader Domain, inhibitors, activators

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