EED226 |
EED226 : Allosteric inhibitor of EED
Probe Summary
Selectivity
Potency
In Vivo
Control Compounds
Chemical Information
References
Vendors
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Probe Summary
| Targets | Biochemical/Biophysical Potency | Cellular Potency |
|---|---|---|
| EED |
|
Allosteric
100 nM - 1 uM
Selectivity
In Vitro Selectivity Assessment
Potency Assay Off-Target:
EED226 had limited activity against 21 protein methyltransferases (IC50 >100 uM).
EED226 inhibited ...
Selectivity Assessment Description:
EED226 had limited activity against 23 kinases (IC50 >10 uM), and 22 GPCRs, ion channels, nucl ...
Potency Cellular
In Vitro
EED
Mode of Action: Allosteric
Structure-Activity-Relationship data available? Yes
DOI Reference: 10.1038/nchembio.2304
In Vivo Validations
Mouse
Dose: 4 and 40 mg/kg
Route of delivery:
Oral
Organ of interest (O):
Karpas422 xenograft
Target engagement assay:
EED226 led to dose-dependent decrease in global H3K27me3 levels.
DOI Reference: 10.1038/nchembio.2304
Chemical Information
| Molecular Formula | C17H15N5O3S |
| SMILEs | CS(=O)(=O)c1ccc(-c2cnc(NCc3ccco3)n3cnnc23)cc1 |
| InChI | InChI=1S/C17H15N5O3S/c1-26(23,24)14-6-4-12(5-7-14)15-10-19-17(22-11-20-21-16(15)22)18-9-13-3-2-8-25-13/h2-8,10-11H,9H2,1H3,(H,18,19) |
| Molecular weight | 369.09 Da |
| AlogP | 2.3999000000000006 |
| HBond acceptors | 8 |
| HBond donors | 1 |
| Atoms | 41 |
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