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Catalog: | HY-17540 |
Brand: | MCE |
CAS: | 1426944-49-1 |
MDL | MFCD28167744 |
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Molecular Weight | 421.96 |
Molecular Formula | C25H28ClN3O |
SMILES | CN(CCCNC(C1=CC=C(N=C(CCCC2)C2=C3Cl)C3=C1)=O)CC4=CC=CC=C4 |
HBX 19818 is a specific inhibitor of ubiquitin-specific protease 7 (USP7) , with an IC 50 of 28.1 μM.
IC50: 28.1 μM (USP7) [1]
HBX 19818 is an inhibitor of USP7, with an IC 50 of 28.1 μM. HBX 19818 shows no effects on USP8, USP5, USP10, CYLD, UCH-L1, UCH-L3 or on SENP1, a SUMO protease, with IC 50 s of > 200 μM. HBX 19818 selectively inhibits USP7 with IC 50 of ∼6 μM in in human cancer cells. In addition, HBX 19818 (1.5, 4, 12, 36, or 100 μM) inhibits USP7 deubiquitination of polyubiquitinated p53. HBX 19818 (30 μM) also causes significantly higher levels of Mdm2 polyubiquitinated forms in USP7-overproducing HEK293 cells than those in DMSO-treated control cells. HBX 19818 inhibits HCT116 proliferation in a dose-dependent manner, with an IC 50 of ∼2 μM [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
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4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
1M HCl : 100 mg/mL ( 236.99 mM ; ultrasonic and adjust pH to 1 with HCl)
DMSO : 20 mg/mL ( 47.40 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
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1 mM | 2.3699 mL | 11.8495 mL | 23.6989 mL |
5 mM | 0.4740 mL | 2.3699 mL | 4.7398 mL |
10 mM | 0.2370 mL | 1.1849 mL | 2.3699 mL |
Add each solvent one by one: 10% DMSO >> 90% corn oil
Solubility: ≥ 2 mg/mL (4.74 mM); Clear solution
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