Catalog classification, reference sizes, lab math links, and source-backed data. Educational use only — not medical advice.
Researched for: PepTools vendor-neutral scientific reference catalog
Also known as: MGL-3196, VIA-3196, Rezdiffra
Resmetirom is a synthetic small molecule that selectively activates thyroid hormone receptor-beta, the predominant thyroid hormone receptor isoform in the liver. Its molecular formula is C17H12Cl2N6O4 and its molecular weight is 435.22 g/mol. The compound is indicated in the United States, under the name Rezdiffra, for adults with noncirrhotic metabolic dysfunction-associated steatohepatitis with moderate to advanced liver fibrosis, in conjunction with diet and exercise.
Catalog descriptions reflect research context only. Not a medical claim or treatment recommendation.
Data source: Primary literature, regulator records, trial registries, and identity-specific evidence search
Reflects preclinical/research literature context only. Not a medical claim, dosing instruction, or treatment recommendation.
The current DailyMed label was updated in July 2026. U.S. approval was granted on March 14, 2024, under the accelerated-approval pathway for noncirrhotic MASH with moderate to advanced fibrosis. The cited sources describe tablet strengths of 60 mg, 80 mg, and 100 mg and oral administration; they do not establish a general research-material presentation or noncommercial reference size.
Supplementary research context only. Not medical advice or a treatment recommendation.
CAS RN 920509-32-6; PubChem CID 15981237; UNII RE0V0T1ES0; ChEMBL CHEMBL3261331; molecular formula C17H12Cl2N6O4; molecular weight 435.22 g/mol; InChIKey FDBYIYFVSAHJLY-UHFFFAOYSA-N; IUPAC name 2-[3,5-dichloro-4-[(6-oxo-5-propan-2-yl-1H-pyridazin-3-yl)oxy]phenyl]-3,5-dioxo-1,2,4-triazine-6-carbonitrile
Resmetirom is a partial agonist of thyroid hormone receptor-beta. In an in vitro functional assay, it produced 83.8% of the maximum response of triiodothyronine at THR-beta, with an EC50 of 0.21 micromolar. THR-beta activation in the liver is associated with reduced intrahepatic triglycerides. Resmetirom is metabolized by CYP2C8; its major metabolite is MGL-3623. It is greater than 99% protein-bound and is also an inhibitor of CYP2C8, OATP1B1, OATP1B3, and BCRP according to the current U.S. prescribing information.
Reflects published research. Educational reference — not a recommendation for use.
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Research Use Only. All content is for educational and research reference only. Not medical advice, a treatment recommendation, or guidance on human use. Compounds are not FDA-approved drugs unless specifically noted.