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COQ7-IN-1 is a powerful inhibitor of human coenzyme Q (COQ7), effectively disrupting the synthesis of ubiquinone (UQ) in the body. Notably, COQ7-IN-1 does not disrupt the natural growth of human normal culture cells. This compound proves valuable for investigating the equilibrium between two pathways of UQ supplementation: de novo UQ synthesis and extracellular UQ uptake[1].

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 2 mg | $58 | 5 days | 5 days | |
| 1 mL x 10 mM (in DMSO) | $98 | 5 days | 5 days |
| Description | COQ7-IN-1 is a powerful inhibitor of human coenzyme Q (COQ7), effectively disrupting the synthesis of ubiquinone (UQ) in the body. Notably, COQ7-IN-1 does not disrupt the natural growth of human normal culture cells. This compound proves valuable for investigating the equilibrium between two pathways of UQ supplementation: de novo UQ synthesis and extracellular UQ uptake[1]. |
| In vitro | COQ7-IN-1 (Compound 8; 0-30 μM; for 4 days) inhibits WI-38 cell growth with a GI50 of 19.0 μM and weakly inhibits C3A cell growth with a GI50 of 9.0±1.1 μM, without affecting C3A cell survival via inhibition of aerobic respiration or increased oxidative stress[1]. COQ7 converts demethoxy-UQ (DMQ) to demethyl-UQ (DMeQ), which is then converted to UQ by COQ3. Cells deficient in COQ7 cannot produce UQ, leading to DMQ accumulation. DMQ10 and UQ10 contents in COQ7-IN-1 (10 μM; for 2 days) cultured HeLa cells are 13.2 and 12.2 ng/well, respectively, with a DMQ10 content of 52.0%[1]. |
| Synonyms | COQ7-IN-1 |
| Molecular Weight | 271.7 |
| Formula | C14H10ClN3O |
| Cas No. | 2579696-72-1 |
| Smiles | Oc1cc(nn1-c1ccc(Cl)cn1)-c1ccccc1 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 100 mg/mL (368.05 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
| In Vivo Formulation | 10% DMSO+90% Corn Oil: 3.3 mg/mL (12.15 mM), Sonication is recommended. Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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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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