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BMS303141

Cat. No. M3762

All AbMole products are for research use only, cannot be used for human consumption.

BMS303141 Structure
Size Price Availability Quantity
Free Sample (0.5-1 mg)  USD 0 In stock
2mg USD 39 In stock
5mg USD 56 In stock
10mg USD 80 In stock
50mg USD 260 In stock
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Quality Control & Documentation
Biological Activity

BMS303141 blocks lipid synthesis (IC50 = 8 μM in HepG2 cells). Under identical incubation conditions, BMS-303141 showed no cytotoxicity up to 50 μM, indicating the observed inhibition of lipid synthesis was not a result of compound-induced cytotoxicity. BMS303141 Lowers plasma glucose and triglycerides in a mouse model of hyperlipidemia. BMS303141 is Orally bioavailable.

Product Citations
Protocol (for reference only)
Cell Experiment
Cell lines
Preparation method
Concentrations
Incubation time
Animal Experiment
Animal models BALB/c nude mice (4‐5 weeks old) injected HepG2 cells
Formulation saline
Dosages 5 mg/kg/d for 8 days
Administration gavage
Chemical Information
Molecular Weight 424.3
Formula C19H15Cl2NO4S
CAS Number 943962-47-8
Solubility (25°C) DMSO ≥ 20 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Yihu Zheng, et al. J Cell Mol Med. ATP citrate lyase inhibitor triggers endoplasmic reticulum stress to induce hepatocellular carcinoma cell apoptosis via p-eIF2α/ATF4/CHOP axis

[2] Ma Z, et al. J Lipid Res. A novel direct homogeneous assay for ATP citrate lyase.

[3] Li JJ, et al. Bioorg Med Chem Lett. 2-hydroxy-N-arylbenzenesulfonamides as ATP-citrate lyase inhibitors.

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Keywords: BMS303141 supplier, inhibitors, activators

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