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CP-640186

Cat. No. M3149

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

CP-640186 Structure
Size Price Availability Quantity
10mM*1mL in DMSO USD 110  USD110 In stock
1mg USD 40  USD40 In stock
5mg USD 90  USD90 In stock
10mg USD 150  USD150 In stock
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Quality Control & Documentation
Biological Activity

CP-640186 is an isozyme-nonselective acetyl-CoA carboxylase (ACC) inhibitor with IC50s of 53 nM and 61 nM for rat liver ACC1 and rat skeletal muscle ACC2 respectively. CP-640186 inhibites fatty acid synthesis in rats, CD1 mice, and ob/ob mice with ED50s of 13, 11, and 4 mg/kg, and stimulated rat whole body fatty acid oxidation with an ED50 of ~30 mg/kg.

Product Citations
Customer Product Validations & Biological Datas
Source Am J Cancer Res 2020 Feb. Figure 4. CP-640186 (Abmole Bioscience, USA)
Method Western blot
Cell Lines ANGPTL4-/- mice
Concentrations -
Incubation Time -
Results Another reagent (CP-640186), an ACC1 inhibitor, also decreased the TNF-α and CD86 levels of ANGTPL4-/- macrophages to normal levels.
Chemical Information
Molecular Weight 485.62
Formula C30H35N3O3
CAS Number 591778-68-6
Solubility (25°C) DMSO 70 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Harwood HJ Jr, et al. J Biol Chem. Isozyme-nonselective N-substituted bipiperidylcarboxamide acetyl-CoA carboxylase inhibitors reduce tissue malonyl-CoA concentrations, inhibit fatty acid synthesis, and increase fatty acid oxidation in cultured cells and in experimental animals.

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Keywords: CP-640186 supplier, Acetyl-CoA Carboxylase, inhibitors, activators

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