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CathepsinL-IN-6 (Compound 6a) is a selective inhibitor of cathepsin L, with an IC50 of 0.021 μM. It inhibits cathepsin L by directly binding to it. Additionally, CathepsinL-IN-6 suppresses the expression of IL-6 and IL-8 and exhibits significant anti-inflammatory activity. This compound is applicable in research related to acute lung injury.
| 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 | CathepsinL-IN-6 (Compound 6a) is a selective inhibitor of cathepsin L, with an IC50 of 0.021 μM. It inhibits cathepsin L by directly binding to it. Additionally, CathepsinL-IN-6 suppresses the expression of IL-6 and IL-8 and exhibits significant anti-inflammatory activity. This compound is applicable in research related to acute lung injury. |
| Targets&IC50 | cathepsin L:0.021 μM |
| Molecular Weight | 418.47 |
| Formula | C24H23FN4O2 |
| Cas No. | 3077842-39-5 |
| Smiles | O=C(NCCCCCN1C=CC=2C(=NC=NC21)OC=3C=CC=CC3)C4=CC=C(F)C=C4 |
| 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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