Ervogastat | DGAT2 inhibitor

Ervogastat chemical structure

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5 mg$100.00
25 mg$395.00

Ervogastat (2186700-33-2) is a potent (IC50 = 17.2 nM) and selective (against DGAT1 and MGATs 1-3) inhibitor of diacylglycerol transferase 2 (DGAT2). It reduced liver and plasma triglyceride levels in Sprague-Dawley rats feed a high fat high cholesterol diet by 49% and 70% respectively.1 Ervogastat displayed efficacy in combination with the ACC inhibitor clesacostat in resolving metabolic dysfunction-associated steatohepatitis (MASH) with liver fibrosis.2

References/Citations:

  1. Futatsugi et al. (2022), Discovery of Ervogastat (PF-06865571): A Potent and Selective Inhibitor of Diacylglycerol Acyltransferase 2 for the Treatment of Non-alcoholic Steatohepatitis; J. Med. Chem. 65 15000
  2. Wong et al. (2025), Efficacy and safety of ervogastat alone and in combination with clesacostat in patients with biopsy-confirmed metabolic dysfunction-associated steatohepatitis and F2-F3 fibrosis (MIRNA): results from a phase 2, randomized, double-blind, double-dummy study; Lancet Gastroenterol. Hepatol. 10 924
2186700-33-2, DGAT2 inhibitor, Ergvogastat supplier, Ervogastat, PF-06865571, PF-06865571 supplier, selective DGAT2 inhibitor
Alternate Name:
PF-06865571

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