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6PGD-IN-2 is a non-competitive inhibitor of 6-phosphogluconate dehydrogenase (6PGD) with an IC50 value of 5.1 μM. It disrupts 6PGD oligomerization in a substrate-dependent manner and induces the production of NADPH and Ru-5-P while reducing DNA synthesis in A549 cells. 6PGD-IN-2 is applicable in research on non-small cell cancer and liver cancer.
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| Description | 6PGD-IN-2 is a non-competitive inhibitor of 6-phosphogluconate dehydrogenase (6PGD) with an IC50 value of 5.1 μM. It disrupts 6PGD oligomerization in a substrate-dependent manner and induces the production of NADPH and Ru-5-P while reducing DNA synthesis in A549 cells. 6PGD-IN-2 is applicable in research on non-small cell cancer and liver cancer. |
| In vitro | Enpp-1-IN-27 (Compound 19n) exhibits non-competitive inhibition towards both 6PG and NADP+, with inhibition constants (Ki) of 64 μM and 9.5 μM, respectively. At concentrations ranging from 0-10 μM over a period of 72 hours to 14 days, Enpp-1-IN-27 inhibits the proliferation and colony formation of A549 cells (with an anti-survival efficacy EC50 of 9.0 μM) and Huh7 cells. Meanwhile, 6PGD-IN-2 at 0-40 μM lowers the NADPH/NADP+ ratio and Ru-5-P levels in A549 cells, leading to a decrease in DNA synthesis. |
| 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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