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BMS309403 is a potent and selective inhibitor of adipocyte fatty acid binding protein aFABP. It improves endothelial function in apolipoprotein E-deficient mice and cultured human endothelial cells. It interacts with the fatty acid binding pocket inside the protein and competitively inhibits the binding of endogenous fatty acids.
Pack Size | Price | Availability | Quantity |
---|---|---|---|
2 mg | 28 € | In Stock | |
5 mg | 45 € | In Stock | |
10 mg | 80 € | In Stock | |
25 mg | 157 € | In Stock | |
50 mg | 205 € | In Stock | |
100 mg | 266 € | In Stock | |
1 mL x 10 mM (in DMSO) | 50 € | In Stock |
Description | BMS309403 is a potent and selective inhibitor of adipocyte fatty acid binding protein aFABP. It improves endothelial function in apolipoprotein E-deficient mice and cultured human endothelial cells. It interacts with the fatty acid binding pocket inside the protein and competitively inhibits the binding of endogenous fatty acids. |
Targets&IC50 | FABP3: 250 nM , FABP4:< 2 nM, FABP5: 350 nM |
In vitro | Treatment with BMS309403 significantly reduced MCP-1 production in THP-1 macrophages in a dose- and time-dependent manner.[1] |
In vivo | METHODS: 3 weeks after the onset of diabetes, mice were orally treated with BMS309403 (40 mg/kg, daily) for 3 weeks. During treatment, monitor blood sugar levels. RESULTS BMS309403 can significantly reduce the protein expression of FABP4 in mouse retinal tissue and partially reduce blood glucose levels in mice. [2] |
Molecular Weight | 474.55 |
Formula | C31H26N2O3 |
Cas No. | 300657-03-8 |
Smiles | CCc1c(c(nn1-c1ccccc1-c1cccc(OCC(O)=O)c1)-c1ccccc1)-c1ccccc1 |
Relative Density. | 1.17 g/cm3 |
Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||||||||||||
Solubility Information | Ethanol: 20 mM, Heating is recommended. DMSO: 50 mg/mL (105.36 mM) | ||||||||||||||||||||||||||||||||||||||||
Solution Preparation Table | |||||||||||||||||||||||||||||||||||||||||
Ethanol/DMSO
DMSO
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