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PROTACPAPD5 degrader 1 (compound 12b) demonstrates the ability to inhibit hepatitis A virus (HAV) and hepatitis B virus (HBV) both in vitro and in vivo, with an IC50 of 10.59 μM and a CC50 greater than 50 μM in Huh7 cells.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | PROTACPAPD5 degrader 1 (compound 12b) demonstrates the ability to inhibit hepatitis A virus (HAV) and hepatitis B virus (HBV) both in vitro and in vivo, with an IC50 of 10.59 μM and a CC50 greater than 50 μM in Huh7 cells. |
| Formula | C49H63N5O16 |
| 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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