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VCP/p97 inhibitor-1, a highly effective compound, inhibits VCP/p97 (also known as Cdc48, CDC-48, or Ter94) with an IC 50 of 54.7 nM. This inhibitor induces a disruption in protein homeostasis and interferes with the degradation process of misfolded polypeptides by the ubiquitin-proteasome system (UPS).

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,520 | Inquiry | Inquiry |
| Description | VCP/p97 inhibitor-1, a highly effective compound, inhibits VCP/p97 (also known as Cdc48, CDC-48, or Ter94) with an IC 50 of 54.7 nM. This inhibitor induces a disruption in protein homeostasis and interferes with the degradation process of misfolded polypeptides by the ubiquitin-proteasome system (UPS). |
| Targets&IC50 | VCP/p97:54.7 nM |
| In vitro | VCP/p97 inhibitor-1 (compound 17), administered at 3-fold serial dilutions with a maximum concentration of 10 μM for 72 hours, demonstrates an anti-proliferative effect on A549 and RPMI8226 cells, with IC50 values of 2.9 μM and 0.86 μM, respectively, as shown in the Cell Viability Assay[1]. |
| Synonyms | VCP/p97 inhibitor-1 |
| Molecular Weight | 491.37 |
| Formula | C24H26BN5O4S |
| Cas No. | 2630950-38-6 |
| Smiles | Cc1cc2c(NS(C)(=O)=O)cccc2n1-c1nc2CCCc2c(NCc2cccc(c2)B(O)O)n1 |
| Relative Density. | 1.43 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. |
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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