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GSK-J1

Cat. No. M2730

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

GSK-J1 Structure
Size Price Availability Quantity
10mM*1mL in DMSO USD 65  USD65 In stock
5mg USD 40  USD40 In stock
10mg USD 63  USD63 In stock
25mg USD 98  USD98 In stock
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Quality Control & Documentation
Biological Activity

GSK-J1 is a potent inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A, with IC50 of 60 nM towards KDM6B. GSK J1 is selective for the H3K27 demethylases JMJD3 and UTX.

Chemical Information
Molecular Weight 389.45
Formula C22H23N5O2
CAS Number 1373422-53-7
Solubility (25°C) DMSO 40 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Wei Zhang, et al. Therapeutically targeting head and neck squamous cell carcinoma through synergistic inhibition of LSD1 and JMJD3 by TCP and GSK-J1

[2] Eric Murillo-Rodrguez, et al. Sleep and Neurochemical Modulation by DZNep and GSK-J1: Potential Link With Histone Methylation Status

[3] Sarder Arifuzzaman, et al. Research update and opportunity of non-hormonal male contraception: Histone demethylase KDM5B-based targeting

[4] Reza Raeisossadati, et al. Small Molecule GSK-J1 Affects Differentiation of Specific Neuronal Subtypes in Developing Rat Retina

[5] Bo Heinemann, et al. Inhibition of demethylases by GSK-J1/J4

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Keywords: GSK-J1 supplier, Histone demethylase, inhibitors, activators

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