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GSK J1

Cat. No. M2730
GSK J1 Structure
Size Price Availability Quantity
5mg USD 50  USD50 In stock
10mg USD 68  USD68 In stock
25mg USD 110  USD110 In stock
50mg USD 195  USD195 In stock
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Quality Control & Documentation
Biological Activity

GSK J1 is selective for the H3K27 demethylases JMJD3 (IC50=60 nM) and UTX.

Chemical Information
Molecular Weight 389.45
Formula C22H23N5O2
CAS Number 1373422-53-7
Solubility (25°C) DMSO 30 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

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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