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GSK-J4, MedChemExpress
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Quantity:
10 mg
50 mg
Unit Size:
10mg
50mg
Description
GSK-J4 is a potent dual inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A with IC50s of 8.6 and 6.6 μM, respectively. GSK-J4 inhibits LPS-induced TNF-α production in human primary macrophages with an IC50 of 9 μM. GSK J4 is a cell permeable prodrug of GSK-J1. GSK-J4 induces endoplasmic reticulum stress-related apoptosis.
Specifications
Specifications
| Chemical Name or Material | GSK-J4 |
| Physical Form | Oil |
| CAS | 1373423-53-0 |
| Color | Yellow |
| Quantity | 50 mg |
| Purity Grade Notes | Research |
| Molecular Formula | C24H27N5O2 |
| For Use With (Application) | Cancer-programmed cell death |
| Solubility Information | DMSO : ≥ 36 mg/mL (86.23 mM) |
| SMILES | O=C(OCC)CCNC1=NC(C2=CC=CC=N2)=NC(N3CCC(C=CC=C4)=C4CC3)=C1 |
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Research purposes only
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