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HDAC-IN-4, a selective HDAC6 and HDAC10 inhibitor (pIC50s: 7.2 and 6.8 in the BRET assay), exhibits antitumoral activity.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 2 mg | $68 | 5 days | 5 days | |
| 1 mL x 10 mM (in DMSO) | $161 | 5 days | 5 days |
| Description | HDAC-IN-4, a selective HDAC6 and HDAC10 inhibitor (pIC50s: 7.2 and 6.8 in the BRET assay), exhibits antitumoral activity. |
| Targets&IC50 | HDAC6:7.2(pIC50) |
| In vitro | HDAC-IN-4 demonstrates superior potency over Tubastatin A in targeting HDAC6, indicating its potential as a more effective HDAC6 probe. Additionally, it exhibits inhibitory effects on HDAC1, HDAC2, HDAC3, HDAC8, and HDAC10, with respective pIC50 values of 5.5, 4.6, 5.4, 5.4, and 6.7 in FRET assays. |
| Molecular Weight | 335.4 |
| Formula | C20H21N3O2 |
| Cas No. | 1252003-13-6 |
| Smiles | Cl.CN1CCc2c(C1)n(Cc1ccc(cc1)C(=O)NO)c1ccccc21 |
| Relative Density. | 1.28 g/cm3 (Predicted) |
| 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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