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XD14 

Cat. No. M28271

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

XD14  Structure

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Quality Control & Documentation
Biological Activity

XD14 is a potent BET inhibitor with antitumor effect. It binds to BRD2, BRD3, and BRD4 with Kds of 170, 380, and 160 nM, respectively.

Chemical Information
Molecular Weight 421.51
Formula C20H27N3O5S
CAS Number 1370888-71-3
Form Solid
Solubility (25°C) DMSO 125 mg/mL (ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Linda Schäker-Hübner, et al. J Med Chem. 4-Acyl Pyrrole Capped HDAC Inhibitors: A New Scaffold for Hybrid Inhibitors of BET Proteins and Histone Deacetylases as Antileukemia Drug Leads

[2] Jennifer M Sahni, et al. Pharmacol Res. Targeting bromodomain and extraterminal proteins in breast cancer

[3] Daqiang Pan, et al. Int J Mol Sci. Metabolic Response to XD14 Treatment in Human Breast Cancer Cell Line MCF-7

[4] Martin Hügle, et al. J Med Chem. 4-Acyl Pyrrole Derivatives Yield Novel Vectors for Designing Inhibitors of the Acetyl-Lysine Recognition Site of BRD4(1)

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BBC0403 

BBC0403 is a selective BRD2 inhibitor with Kds of 7.64 μM and 41.37 μM for BRD2 (BD2) and BRD2 (BD1), respectively.

BAY-155 

BAY-155 is a potent and selective menin-MLL tool inhibitor, with an IC50 of 8 nM.

FHT-1015 

FHT-1015 is a potent SMARCA4/SMARCA2 ATPase (BRG1 and BRM) inhibitor with IC50s of ≤10 nM.

ISOX-DUAL 

ISOX-DUAL is a dual CBP/BRD4 inhibitor with IC50 values of 0.65 μM and 1.5 μM for CBP and BRD4, respectively.

  Catalog
Abmole Inhibitor Catalog




Keywords: XD14  supplier, Epigenetic Reader Domain, inhibitors, activators

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