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Synonyms:
HDAC6-IN-74
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | HDAC6-IN-74 is a selective oral inhibitor of histone deacetylase 6 (HDAC6) with an IC50 of 0.036 μM. It induces tumor cell apoptosis (apoptosis), arrests cells in the S phase of the cell cycle, and reduces cell migration, invasion, and colony-forming abilities. HDAC6-IN-74 exhibits anticancer activity without significant toxicity and can be utilized in research on cancers such as liver cancer. |
| Targets & IC50 | HDAC6:0.036 μM |
| 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.
| Size | Quantity | Unit Price | Amount | Operation |
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