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Cat.No.ABP000359 Chemical NamePF-04971729/PF04971729/ MDL: MFCD21609259 MolFormulaC22H25ClO7 MolWeight436.885 Purity >98%

Chemical Name : PF-04971729/PF04971729/

CAS : 1210344-57-2

Synonyms: PF-04971729

Storage:at  4 ℃ 2 years


PF-04971729), a potent and selective inhibitor of the sodium-dependent glucose cotransporter 2, is currently in phase 2 trials for the treatment of diabetes mellitus.Plasma clearance was low in rats (4.04 ml · min−1 · kg−1) and dogs (1.64 ml · min−1 · kg−1), resulting in half-lives of 4.10 and 7.63 h, respectively. Moderate to good bioavailability in rats (69%) and dogs (94%) was observed after oral dosing. The in vitro biotransformation profile of PF-04971729 in liver microsomes and cryopreserved hepatocytes from rat, dog, and human was qualitatively similar; prominent metabolic pathways included monohydroxylation, O-deethylation, and glucuronidation. No human-specific metabolites of PF-04971729 were detected in in vitro studies. Reaction phenotyping studies using recombinant enzymes indicated a role of CYP3A4/3A5, CYP2D6, and UGT1A9/2B7 in the metabolism of PF-04971729


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