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SML-8-73-1 is a nucleotide-based inhibitor targeting KRASG12C. It is applicable for research in non-small cell lung cancer (NSCLC).
| 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 | SML-8-73-1 is a nucleotide-based inhibitor targeting KRASG12C. It is applicable for research in non-small cell lung cancer (NSCLC). |
| In vitro | SML-8-73-1, at a concentration of 2.5 μM over 2 hours, specifically covalently modifies KRAS G12C, without affecting KRAS WT. It effectively binds to KRAS G12C in environments with high intracellular nucleotide concentrations, thereby overcoming competitive inhibition. |
| Molecular Weight | 562.75 |
| Formula | C14H21ClN6O12P2 |
| Cas No. | 1536470-92-4 |
| Smiles | O=C1C2=C(N(C=N2)[C@@H]3O[C@H](COP(OP(OCCNC(CCl)=O)(=O)O)(=O)O)[C@@H](O)[C@H]3O)NC(N)=N1 |
| 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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