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PLX7922, a RAF inhibitor, demonstrates binding affinity with BRAF V600E and exhibits inhibitory effects on pERK in BRAF V600E cell lines, while inducing pERK activation in mutant NRAS cell lines.


| Description | PLX7922, a RAF inhibitor, demonstrates binding affinity with BRAF V600E and exhibits inhibitory effects on pERK in BRAF V600E cell lines, while inducing pERK activation in mutant NRAS cell lines. |
| In vitro | PLX7922, at concentrations ranging from 1 to 1000 nanomoles (nM), effectively inhibits phosphorylated ERK (pERK) in cells expressing the BRAF V600E mutation while concurrently activating pERK in cell lines with mutated NRAS (specifically B9 and IPC-298)[1]. |
| Synonyms | PLX7922 |
| Molecular Weight | 464.58 |
| Formula | C20H25FN6O2S2 |
| Cas No. | 1638772-61-8 |
| Smiles | CCN(C)S(=O)(=O)Nc1cccc(-c2nc(sc2-c2ccnc(N)n2)C(C)(C)C)c1F |
| 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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