Fenclozic acid
From Wikipedia, the free encyclopedia
| Clinical data | |
|---|---|
| Trade names | Myalex |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C11H8ClNO2S |
| Molar mass | 253.70 g·mol−1 |
| 3D model (JSmol) | |
| |
| |
| | |
Fenclozic acid (proposed brand name Myalex) is a nonsteroidal anti-inflammatory drug (NSAID) with analgesic, antipyretic, and anti-inflammatory properties developed in 1960s by ICI Pharmaceuticals.[1][2] It failed to pass Phase III clinical trial and was withdrawn from clinical development in 1971 due to severe dose-related hepatotoxicity and jaundice in human, despite showing excellent preclinical safety profile and promising clinical efficacy in animal testings.[3][4] It is considered a classic example of human-specific drug induced liver injury linked to unique metabolic activation in humans.[4][5]