This specific epoxide structure provides the crucial stereochemistry needed for Seladelpar’s therapeutic activity as a selective PPAR-delta agonist, helping form its complex structure and influencing its interaction with biological targets, ultimately reducing liver inflammation and itching in PBC patients. (S)-2-((4-(Trifluoromethyl)phenoxy)methyl)oxirane serves as a key chiral building block or intermediate in the synthesis of Seladelpar (Livdelzi), the drug used for Primary Biliary Cholangitis (PBC).
(S)-2-((4-(Trifluoromethyl)phenoxy)methyl)oxirane
| API Name | Seladelpar |
|---|---|
| CAS No | 256372-58-4 |
| Molecular Formula | C10H9F3O2 |
| Molecular Weight | 218.17 g/mol |
| Synonyms | (2S)-2-[[4-(trifluoromethyl)phenoxy]methyl]oxirane |
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