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HDAC6-IN-68 is an HDAC6 inhibitor (IC50 = 118 nM) and serves as a ligand for the PROTAC target protein (HDAC6). It is utilized in the synthesis of PROTAC HDAC6 degrader 7.
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | HDAC6-IN-68 is an HDAC6 inhibitor (IC50 = 118 nM) and serves as a ligand for the PROTAC target protein (HDAC6). It is utilized in the synthesis of PROTAC HDAC6 degrader 7. |
| Targets&IC50 | HDAC6:118 nM |
| In vitro | HDAC6 PROTAC consists of two ligands linked by a linker: one is an E3 ligase ligand (Thalidomide 5-fluoride), and the other is a target protein ligand (HDAC6-IN-68). The PROTAC system employs the intracellular ubiquitin-proteasome pathway to selectively degrade target proteins. |
| 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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