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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 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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