GFT505

Chemical Information
Elafibranor is a dual peroxisome proliferator-activated receptor (PPAR) α and β/δ agonist that works to inhibit bile acid synthesis. On June 10, 2024, elafibranor was granted accelerated approval by the FDA for the treatment of primary biliary cholangitis (PBC). The drug was also approved by the EMA on September 23, 2024.
| CAS Number | 824932-88-9 |
| PubChem CID | 9864881 |
| IUPAC Name | 2-[2,6-dimethyl-4-[(E)-3-(4-methylsulfanylphenyl)-3-oxoprop-1-enyl]phenoxy]-2-methylpropanoic acid |
| Molecular Formula | C22H24O4S |
| Molecular Weight | 384.5 |
| XLogP | 5.1 |
| Topological Polar Surface Area | 88.9 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 537 |
| Property | Value |
|---|---|
| Molecular Weight | 384.5 |
| XLogP3 | 5.1 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 7 |
| Exact Mass | 384.13953042 |
| Monoisotopic Mass | 384.13953042 |
| Topological Polar Surface Area | 88.9 Ų |
| Heavy Atom Count | 27 |
| Formal Charge | 0 |
| Complexity | 537 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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