Shopping Cart
- Remove All
- Your shopping cart is currently empty
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 | Availability | Quantity |
---|---|---|---|
10 mg | Inquiry | 10-14 weeks | |
50 mg | Inquiry | 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. |
Copyright © 2015-2025 TargetMol Chemicals Inc. All Rights Reserved.