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Kanglexin is an orally active novel anthraquinone compound. It inhibits NLRP3 inflammasome activation and pyroptosis, offering cardioprotective benefits. By stimulating the FGFR1/ERK signaling pathway, Kanglexin promotes angiogenesis and accelerates wound healing in diabetes. Additionally, it has lipid-lowering effects and inhibits vascular smooth muscle cell dedifferentiation, making it a potential compound for studying hyperlipidemia, fatty liver, and atherosclerosis.

| 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 | Kanglexin is an orally active novel anthraquinone compound. It inhibits NLRP3 inflammasome activation and pyroptosis, offering cardioprotective benefits. By stimulating the FGFR1/ERK signaling pathway, Kanglexin promotes angiogenesis and accelerates wound healing in diabetes. Additionally, it has lipid-lowering effects and inhibits vascular smooth muscle cell dedifferentiation, making it a potential compound for studying hyperlipidemia, fatty liver, and atherosclerosis. |
| In vitro | Kanglexin (10-20 μM; 24 hours) inhibits pyroptosis in cardiomyocytes treated with hypoxia or LPS. Additionally, Kanglexin (5-20 μM; 24 hours) reduces lipid levels in oleic acid-treated HepG2 cells via the AMPK/SREBP-2/PCSK9/LDLR signaling pathway. |
| In vivo | Kanglexin (20-40 mg/kg; gavage; 7 days) demonstrates beneficial effects in a mouse model of myocardial infarction. Additionally, Kanglexin (20-80 mg/kg; oral; 2 weeks) shows improvements in a rat model of hyperlipidemia. |
| Molecular Weight | 398.36 |
| Formula | C21H18O8 |
| Cas No. | 2228847-12-7 |
| Smiles | O=C1C=2C=C(OC(=O)CCC(=O)OCC)C=C(O)C2C(=O)C3=C(O)C=C(C=C13)C |
| 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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