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Synonyms:
BTK-IN-48
| 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 | BTK-IN-48 is a BTK inhibitor with an IC50 of 1.14 μM. It suppresses recombinant BTK and c-Src, and exhibits moderate inhibitory effects on LCK, BMX/ETK, FLT3, and PIM1. BTK-IN-48 is applicable in the research of B-cell malignancies and autoimmune diseases. |
| In vitro | BTK-IN-48 (Compound 6b) is a potent inhibitor of recombinant BTK, with an IC50 value of 1.14 μM, achieving an inhibition rate of up to 88.6% at a concentration of 10 μM. At this concentration, BTK-IN-48 effectively suppresses recombinant BTK and c-Src, while exhibiting moderate inhibitory effects on LCK, BMX/ETK, FLT3, and PIM1. When used at concentrations ranging from 0-40 μM over four days, it induces slight growth inhibition in normal B cells RPMI-1788 and RPMI-7666 without causing significant cell death. |
| Molecular Weight | 333.34 |
| Formula | C19H15N3O3 |
| Cas No. | 3114078-55-3 |
| Smiles | OC=1C=CC(=C(O)C1)C2=NC3=CC=CN=C3N2C4=CC=C(OC)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.
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