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ELQ-453 is an inhibitor that targets the Qo site of the cytochrome bc1 complex (CytB) in the malignant Plasmodium falciparum, with an IC50 value of 0.57 μM. ELQ-453 disrupts mitochondrial function in parasites and prevents Plasmodium infection in mosquitoes, showing promise for malaria research.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | ELQ-453 is an inhibitor that targets the Qo site of the cytochrome bc1 complex (CytB) in the malignant Plasmodium falciparum, with an IC50 value of 0.57 μM. ELQ-453 disrupts mitochondrial function in parasites and prevents Plasmodium infection in mosquitoes, showing promise for malaria research. |
| 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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