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Synonyms:
KRAS-IN-55
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | KRAS-IN-55 is a broad-spectrum KRAS inhibitor with IC50 values of 4.3 nM for KRASG12C, 9.6 nM for KRASG12D, and 1.6 nM for KRASG12V. It induces the formation of a new binding pocket on KRAS, allowing for the creation of a high-affinity ternary complex with cyclophilin A (CYPA), thereby inhibiting the interaction between KRAS and downstream effectors RAF and PI3K, as well as blocking oncogenic MAPK and PI3K signaling pathways. KRAS-IN-55 is applicable in research concerning cancers such as colorectal cancer and non-small cell lung cancer. |
| 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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