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Synonyms:

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | 6-8 weeks | 6-8 weeks | |
| 50 mg | $1,980 | 6-8 weeks | 6-8 weeks | |
| 100 mg | $2,500 | 6-8 weeks | 6-8 weeks |
| Description | HDAC6-IN-10 is a potent and specific HDAC6 inhibitor, exhibiting an IC50 value of 0.73 nM. It demonstrates remarkable selectivity towards HDAC6, with a selectivity range of 144 to 10,941-fold over other HDAC isoforms. Furthermore, HDAC6-IN-10 exhibits notable anti-proliferative effects on multiple myeloma cells [1]. |
| Targets & IC50 | HDAC7:752 nM, HDAC5:4370 nM, HDAC1:8020 nM, HDAC9:2560 nM, HDAC8:513 nM, HDAC11:1800 nM, HDAC6:0.73 nM, HDAC10:105 nM, HDAC4:5620 nM |
| In vitro | HDAC6-IN-10 (Compound 21b) demonstrates high specificity for inhibiting HDAC6 when administered at 0.1 to 10 μM over 24 hours [1]. At 0 to 100 μM over 72 hours, it exerts anti-proliferative effects on multiple myeloma cell lines RPMI-8226 and U266 [1]. In HCT-116 Western Blot analyses with 0.1, 1, and 10 μM over 24 hours, a dose-dependent increase in Ac-tubulin levels was observed. Cell Proliferation Assays showed inhibition of RPMI-8226 and U266 cell growth, with IC 50 values of 33.183 μM and 43.233 μM, respectively [1]. |
| Molecular Weight | 392.41 |
| Formula | C21H20N4O4 |
| Cas No. | 2408286-73-5 |
| Smiles | C(C=1C=2C(NC1)=CC=CC2)[C@@H]3C(=O)N(CC4=CC=C(C(NO)=O)C=C4)CC(=O)N3 |
| 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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