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Ertugliflozin

Cat. No. M6272

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

Ertugliflozin Structure
Synonym:

MK-8835, PF-04971729

Size Price Availability Quantity
5mg USD 55  USD55 In stock
10mg USD 75  USD75 In stock
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Quality Control & Documentation
Biological Activity

Inhibitory effects against the organic cation transporter 2-mediated uptake of [14C]metformin by PF-04971729 also were very weak (IC50 900μM).The disposition of PF-04971729, an orally active selective inhibitor of the sodium-dependent glucose cotransporter 2, was studied after a single 25-mg oral dose of [14C]-PF-04971729 to healthy human subjects. The absorption of PF-04971729 in humans was rapid with a Tmax at ~ 1.0 h. Of the total radioactivity excreted in feces and urine, unchanged PF-04971729 collectively accounted for ~ 35.3% of the dose, suggestive of moderate metabolic elimination in humans.

Chemical Information
Molecular Weight 436.88
Formula C22H25ClO7
CAS Number 1210344-57-2
Solubility (25°C) DMSO ≥ 80 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Baker WL, et al. J Am Heart Assoc. Effects of Sodium-Glucose Cotransporter 2 Inhibitors on 24-Hour Ambulatory Blood Pressure: A Systematic Review and Meta-Analysis.

[2] Kalgutkar AS, et al. Drug Metab Dispos. Preclinical species and human disposition of PF-04971729, a selective inhibitor of the sodium-dependent glucose cotransporter 2 and clinical candidate for the treatment of type 2 diabetes mellitus.

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Keywords: Ertugliflozin, MK-8835, PF-04971729 supplier, SGLT, inhibitors, activators

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