Resmetirom
Overview
Resmetirom is a small molecule active pharmaceutical ingredient (ChEMBL CHEMBL3261331).
API suppliers (12)
Suppliers of Resmetirom evidenced by a US FDA Type II Drug Master File or an EU Certificate of Suitability (CEP). Sources: FDA DMF list, EDQM certification database.
Country recorded for 10 of 12 suppliers.
5 of 12 hold a GMP certificate on record in the EU or UK registers
- LEE PHARMA LTDIndia1 active DMF GMP on record
- LEWENS LABS PRIVATE LTDIndia1 active DMF
- SICHUAN ELIXIR PHARMACEUTICAL CO LTD1 active DMF
- Cipla USA, Inc.USA1 active DMF
- Zhejiang Hisun Pharmaceutical Co., Ltd.China1 active DMF GMP on record
- CHANGZHOU PHARMACEUTICAL FACTORYChina1 active DMF GMP on record
- METROCHEM API PRIVATE LTDIndia1 active DMF
- APICHEM Laboratories Private LimitedIndia1 active DMF
- BIOPHORE INDIA PHARMACEUTICALS PVT LTD1 active DMF
- Shandong Loncom Pharmaceutical Co.,ltd.China1 active DMF
- AMI LIFESCIENCES PRIVATE LTDIndia1 active DMF GMP on record
- Zydus Lifesciences LimitedIndia1 active DMF GMP on record
Patent & exclusivity (US)
Per the FDA Orange Book (3 approved US products), the latest listed US patent on Resmetirom expires 4 Feb 2045 and exclusivity 14 Mar 2029. Generic API sourcing typically opens up once these lapse.
Chemical identity
- 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
- Canonical SMILES
- CC(C)C1=CC(=NNC1=O)OC2=C(C=C(C=C2Cl)N3C(=O)NC(=O)C(=N3)C#N)Cl
- InChIKey
- FDBYIYFVSAHJLY-UHFFFAOYSA-N
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