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Catalog: | HY-16107 |
Brand: | MCE |
CAS: | 943962-47-8 |
MDL | MFCD25976797 |
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Molecular Weight | 424.30 |
Molecular Formula | C19H15Cl2NO4S |
SMILES | O=S(C1=CC(Cl)=CC(Cl)=C1O)(NC2=CC(C3=CC=CC=C3)=CC=C2OC)=O |
BMS-303141 is a potent, cell-permeable ATP-citrate lyase ( ACL ) inhibitor with an IC 50 of 0.13 μM.
IC50: 0.13 uM (ACL) [1]
In HepG2 cells, BMS-303141 shows inhibition of total lipid syntheses with an IC 50 of 8 μM. BMS-303141 shows no cytotoxicity up to 50 lM under a cell based Alamar Blue cytotoxicity assay, indicating the observed inhibition of lipid synthesis is not a result of compound-induced cytotoxicity [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Chronic oral dosing of BMS-303141 in high-fat fed mice lowers approximate 20-30% plasma cholesterol and triglycerides, as well as 30-50% fasting plasma glucose. Chronic treatment with BMS-303141 shows a gradual inhibition of weight gain along with a reduction in adiposity without apparent changes in food intake. BMS-303141 shows an oral bioavailability of 55% but a relatively short half-life of 2.1 h [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : 25 mg/mL ( 58.92 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
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1 mM | 2.3568 mL | 11.7841 mL | 23.5682 mL |
5 mM | 0.4714 mL | 2.3568 mL | 4.7136 mL |
10 mM | 0.2357 mL | 1.1784 mL | 2.3568 mL |
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