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HDAC8-IN-4 is a selective HDAC8 inhibitor with IC50 values of 0.15 μM for HDAC8 and 12 μM for HDAC3 [1].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | Inquiry | 8-10 weeks | 8-10 weeks | |
| 50 mg | Inquiry | 8-10 weeks | 8-10 weeks |
| Description | HDAC8-IN-4 is a selective HDAC8 inhibitor with IC50 values of 0.15 μM for HDAC8 and 12 μM for HDAC3 [1]. |
| Targets&IC50 | HDAC8:0.15 μM, HDAC3:12 μM |
| In vitro | HDAC8-IN-4 (Compound 9) reduces HDAC8 protein levels in HeLa cells at concentrations of 1-100 μM over a period of 5-6 days [1]. Additionally, HDAC8-IN-4 inhibits the growth of T-cell lymphoma cells (Jurkat, HH, MT4, HUT78) at approximate concentrations of 0-50 μM for 72 hours [1]. |
| Molecular Weight | 342.44 |
| Formula | C17H14N2O2S2 |
| Cas No. | 1600528-05-9 |
| Smiles | C(SC1=CC=CC=C1)C2=NC(=CS2)C3=CC(C(NO)=O)=CC=C3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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