Ervogastat (PF-06865571) | DGAT2 inhibitor

Chemical Structure : PF-06865571

CAS No.: 2186700-33-2

PF-06865571 (Ervogastat, PF 06865571)

Catalog No.: PC-72624Not For Human Use, Lab Use Only.

PF-06865571 (Ervogastat, PF 06865571) is a potent, selective diacylglycerol acyltransferase DGAT2 inhibitor with IC50 of 17.2 and 833 nM for human and rat DGAT2, respectively.

Packing	Price	Stock
5 mg	$228	In stock
10 mg	$358	In stock
25 mg	$558	In stock
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Biological Activity

PF-06865571 (Ervogastat, PF 06865571) is a potent, selective diacylglycerol acyltransferase DGAT2 inhibitor with IC50 of 17.2 and 833 nM for human and rat DGAT2, respectively.

PF-06865571 displays no significant inhibitions against MGAT1-3 and DGAT1 (IC50>50 uM).

PF-06865571 showspotent inhibitory activities in human, rat, and monkey hepatocytes with IC50 values of 2.79, 6.02, and 2.13 nM, respectively.

PF-06865571 is a non-time-dependent, reversible, rapid binding inhibitor of DGAT2.

shows no significant inhibitions in hERG, a kinase selectivity panel, and a PDE selectivity panel

PF-06865571 (0.3, 3, 10, 30, or 90 mg/kg, orally twice daily for 7 days) reduces plasma triglyceride levels in sucrose diet-fed Sprague-Dawley rats.

Physicochemical Properties

M.Wt	407.423
Formula	C21H21N5O4
Appearance	Solid
CAS No.
Storage	Solide Powder -20°C 12 Months; 4°C 6 Months	In Solvent -80°C 6 Months; -20°C 6 Months
Shipping
Solubility	10 mM in DMSO
Chemical Name/SMILES	5-Pyrimidinecarboxamide, 2-[5-[(3-ethoxy-2-pyridinyl)oxy]-3-pyridinyl]-N-[(3S)-tetrahydro-3-furanyl]-

References

1. Roberto A Calle, et al. Nat Med. 2021 Oct;27(10):1836-1848.
2. Futatsugi K, et al. J Med Chem. 2022 Nov 24;65(22):15000-15013.

PF-06865571 (Ervogastat, PF 06865571)

Biological Activity

Physicochemical Properties

References

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