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Ertiprotafib

Cat. No. M29684
Ertiprotafib Structure
Synonym:

PTP 112

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Biological Activity

Ertiprotafib is an inhibitor of PTP1B, IkB kinase β (IKK-β), and a dual PPARα and PPARβ agonist, with an IC50 of 1.6 μM for PTP1B, 400 nM for IKK-β, an EC50 of ~1 μM for PPARα/PPARβ.

Chemical Information
Molecular Weight 559.51
Formula C31H27BrO3S
CAS Number 251303-04-5
Form Solid
Solubility (25°C) DMSO 100 mg/mL (ultrasonic)
Storage 4°C, protect from light, dry, sealed
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Ganesan Senthil Kumar, et al. PLoS One. The mode of action of the Protein tyrosine phosphatase 1B inhibitor Ertiprotafib

[2] Jun-Zheng Liu, et al. Bioorg Med Chem Lett. Discovery of novel PTP1B inhibitors via pharmacophore-oriented scaffold hopping from Ertiprotafib

[3] Suja Shrestha, et al. Bioorg Med Chem Lett. PTP1B inhibitor Ertiprotafib is also a potent inhibitor of IkappaB kinase beta (IKK-beta)

[4] Z Tong, et al. Xenobiotica. Effects of ertiprotafib on hepatic cytochrome P450 and peroxisomal enzymes in rats and dogs, and in rat and human primary hepatocytes

[5] David V Erbe, et al. Mol Pharmacol. Ertiprotafib improves glycemic control and lowers lipids via multiple mechanisms

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Keywords: Ertiprotafib, PTP 112 supplier, Phosphatase, inhibitors, activators


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