Arbaclofen placarbil
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| Systematic (IUPAC) name | |
|---|---|
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(3R)-3-(4-chlorophenyl)-4-[[[(1S)-2-methyl-1-[(2-methylpropanoyl)oxy]propoxy]carbonyl]amino]butanoic acid | |
| Clinical data | |
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| Identifiers | |
| CAS Number | 847353-30-4 |
| ATC code | none |
| PubChem | CID 11281011 |
| ChemSpider | 9456008 |
| KEGG |
D08861 |
| ChEMBL |
CHEMBL2107312 |
| Chemical data | |
| Formula | C19H26ClNO6 |
| Molar mass | 399.86 g/mol |
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Arbaclofen placarbil (ar-BAC-loe-fen pla-KAR-bil, also known as XP19986) is a prodrug of R-baclofen. Arbaclofen placarbil possesses more favorable pharmacokinetic profile than baclofen, with less fluctuations in plasma drug levels. It was being developed as a potential treatment for patients with GERD and spasticity due to multiple sclerosis; however, in May 2013 XenoPort announced the termination of development because of unsuccessful results in phase III clinical trials.[1]
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