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MY05 selectively targets c-MYC within cells and disrupts the interaction between MYC and MAX. It binds to intracellular c-MYC, modulating its thermal stability, reducing the transcriptional targets of c-MYC, and exhibiting anticancer activity (TNBC, triple-negative breast cancer).

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | MY05 selectively targets c-MYC within cells and disrupts the interaction between MYC and MAX. It binds to intracellular c-MYC, modulating its thermal stability, reducing the transcriptional targets of c-MYC, and exhibiting anticancer activity (TNBC, triple-negative breast cancer). |
| In vitro | MY05 exhibits IC 50 values of 10.6 μM, 13.5 μM, and 39.4 μM against MDA-MB 231, MDA-MB 468, and MCF-7 cell lines, respectively. It induces apoptosis and inhibits the growth of MYC-driven breast tumor spheres. |
| In vivo | In a mouse model of triple-negative breast cancer (TNBC), MY05 (10 mg/kg) effectively inhibits the growth of MYC-driven solid tumors. |
| Molecular Weight | 346.77 |
| Formula | C19H11ClN4O |
| Cas No. | 667909-97-9 |
| Smiles | N#CC1=CC=2C(=NN(C=3C=CC=CC3)C2NC1=O)C=4C=CC(Cl)=CC4 |
| 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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