Shopping Cart
Remove All
Your shopping cart is currently empty
QC6352 is a selective and effective KDM4C inhibitor (IC50: 35 nM).

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | 3-6 months | 3-6 months | |
| 50 mg | $1,980 | 3-6 months | 3-6 months | |
| 100 mg | $2,500 | 3-6 months | 3-6 months | |
| 1 mL x 10 mM (in DMSO) | $434 | 3-6 months | 3-6 months |
| Description | QC6352 is a selective and effective KDM4C inhibitor (IC50: 35 nM). |
| Targets&IC50 | KDM4C:35 nM, KDM4B:56 nM, KDM4D:104 nM, KDM5B:750 nM, KDM4A:104 nM |
| In vitro | QC6352 is an effective KDM4C inhibitor (IC50: 35±8 nM). QC6352 blocks the proliferation and self-renewal of BCSCs. In a concentration-dependent manner QC6352 dramatically decreases the anchorage-independent sphere-forming capacity of BCSC1 and BCSC2. The protein levels of (Epidermal growth factor receptor) EGFR are reduced in both BCSC1 and BCSC2 upon treatment with QC6352 [1][2]. |
| In vivo | QC6352 significantly inhibits tumor growth and final tumor weight in both BCSC1 and BCSC2 xenografts. The treatment is well tolerated, with no impact on mice body weight. Administration of the KDM4 inhibitor QC6352 effectively blocks BCSC xenograft tumor growth [2]. |
| Molecular Weight | 387.47 |
| Formula | C24H25N3O2 |
| Cas No. | 1851373-36-8 |
| Smiles | CN(c1ccccc1)c1ccc2[C@H](CNc3cnccc3C(O)=O)CCCc2c1 |
| Relative Density. | 1.243 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. | ||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 25 mg/mL (64.52 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+40% PEG300+5% Tween-80+45% Saline: 1.5 mg/mL (3.87 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | ||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||
DMSO
| |||||||||||||||||||||||||||||||
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 |
|---|

Copyright © 2015-2026 TargetMol Chemicals Inc. All Rights Reserved.