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Synonyms:
DKFZ-633
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | DKFZ-633 is a potent inhibitor of KLK6 and a KLK6-specific probe, exhibiting an IC50 of 250 nM against human KLK6. It selectively covalently labels the active state of KLK6, allowing for the successful pull-down and capture of endogenous active KLK6 from conditioned cell media. DKFZ-633 serves as an important tool for studying the function and regulatory mechanisms of KLK6 in head and neck cancer. |
| In vitro | DKFZ-633 (compound 44) inhibits recombinant triple-mutant human KLK6 at a concentration of 0.25 μM following a 30-minute pre-incubation at room temperature, achieving an IC50 of 0.25 μM. At concentrations of 12-25 μM for 1 hour at room temperature, DKFZ-633 dose-dependently pulls down active endogenous human KLK6 from FaDu cell conditioned medium. When used at 50 μM for 1 hour at room temperature, DKFZ-633 can also pull down active endogenous human KLK6 from conditioned media of various human cancer cell lines, including two glycoform-dependent cell types. |
| Molecular Weight | 440.49 |
| Formula | C26H24N4O3 |
| Cas No. | 2244425-14-5 |
| Smiles | O=C(OCC(=O)NC=1C(=NN(C=2C=CC=CC2)C1C)C)CC=3C=4C=C(C#C)C=CC4NC3C |
| 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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