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Synonyms:
CHI3L1-IN-7
| 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 | CHI3L1-IN-7 is a selective inhibitor of CHI3L1, with a Kd of 7.40 μM and an IC50 of 15.4 μM. This compound disrupts the interaction between CHI3L1 and galectin-3, inhibits STAT3 phosphorylation, and reduces the viability of multicellular 3D glioblastoma spheroids. CHI3L1-IN-7 is useful for research involving glioblastoma and CHI3L1-mediated tumor immunoregulation. |
| In vitro | CHI3L1-IN-7 (100 μM) binds to the CHI3L1 protein with a dissociation constant (K_d) of 7.40 μM. In AlphaLISA assays, CHI3L1-IN-7 inhibits the interaction between CHI3L1 and galectin-3, with an IC_50 of 15.4 μM. Additionally, at concentrations of 10-50 μM over 72 hours, this compound reduces the viability of multicellular 3D glioblastoma (GBM) spheroids and inhibits the phosphorylation of STAT3. |
| Molecular Weight | 357.43 |
| Formula | C17H19N5O2S |
| Cas No. | 2248987-74-6 |
| Smiles | O=C1C=2C=CSC2N=CN1CC(=O)NC=3C=NN(C3C)C4CCCC4 |
| 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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