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Synonyms:
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | EMD-C02602 is a GCN2 inhibitor with IC50 values of 0.023 μM for GCN2, 4.52 μM for PERK, >10 μM for HRl, and 0.048 μM for PKR. |
| In vitro | EMD-C02602 exhibits a U-shaped activity response in MOLM-16 cells over a range of 0-10 μM for 72 hours, with the most significant reduction in cell viability at moderate concentrations (around 0.05 μM) and reduced inhibition at both lower and higher concentrations. Additionally, EMD-C02602 at concentrations between 0.05-0.12 μM for 8 hours increases ATF4 expression in these cells, and at concentrations of 0.5-1.1 μM for 8 hours, it enhances p-GCN2 expression without affecting GCN2 expression. |
| 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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