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ZM600 is an effective and orally active anti-hepatic fibrosis agent that can reduce the protein expression of collagen I, α-SM, and p-p65. This compound shows promising potential for use in hepatic fibrosis research.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
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| 10 mg | Inquiry | Inquiry | Inquiry | |
| 50 mg | Inquiry | Inquiry | Inquiry |
| Description | ZM600 is an effective and orally active anti-hepatic fibrosis agent that can reduce the protein expression of collagen I, α-SM, and p-p65. This compound shows promising potential for use in hepatic fibrosis research. |
| In vitro | ZM600 exhibits cytotoxic effects on LX-2 cells with an IC50 value of 38.17 µM. ZM600 (0, 5, 10, 20 µM; 2+48 h) reduces the protein and mRNA expression of collagen I and α-SM induced by LPS and TGF-β1. Additionally, ZM600 (0, 5, 10, 20 µM; 2+2 h) diminishes the expression of p-p65, p-Smad2/3, and p-AKT proteins in LX-2 cells triggered by LPS and TGF-β1. |
| In vivo | ZM600, administered orally at doses of 15 and 30 mg/kg daily for a period of three weeks, was found to alleviate CCl4-induced experimental liver fibrosis. |
| 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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