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NXT629

Cat. No. M11286

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

NXT629  Structure

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Quality Control & Documentation
Biological Activity

NXT629 is an effective, selective and competitive PPAR-α antagonist. The IC50 value of HUMAN PPARα is 77 nM, which is higher than that of other nuclear hormone receptors, such as PPARδ, PPARγ, Erβ, GR and TRβ, with IC50 value of 6.0, 15, respectively. 15.2, 32.5 and >100 μM.

Product Citations
Chemical Information
Molecular Weight 609.78
Formula C35H39N5O3S
CAS Number 1454925-59-7
Solubility (25°C) DMSO ≥ 100 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Zakiah N Almohawes, et al. Arch Physiol Biochem. Salidroside inhibits insulin resistance and hepatic steatosis by downregulating miR-21 and subsequent activation of AMPK and upregulation of PPARα in the liver and muscles of high fat diet-fed rats

[2] Karin J Stebbins, et al. Eur J Pharmacol. In vitro and in vivo pharmacology of NXT629, a novel and selective PPARα antagonist

[3] Davorka Messmer, et al. Mol Med. A Selective Novel Peroxisome Proliferator-Activated Receptor (PPAR)-α Antagonist Induces Apoptosis and Inhibits Proliferation of CLL Cells In Vitro and In Vivo

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Keywords: NXT629 supplier, PPAR, inhibitors, activators

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