This article may be too technical for most readers to understand.(August 2022) |
Clinical data | |
---|---|
Other names | threo-Hydrobupropion; Threohydroxybupropion; BW 494; BW A494U; threo-3-Chloro-N-tert-butyl-β-hydroxy-α-methylphenethylamine; threo-3-Chloro-N-tert-butyl-β-hydroxyamphetamine |
Pharmacokinetic data | |
Protein binding | 42%[1] |
Metabolism | Hydroxylation (CYP2B6, CYP2C19), glucuronidation (UGTs)[1] |
Elimination half-life | 37 hours[1][2] |
Identifiers | |
| |
CAS Number |
|
PubChem CID | |
ChemSpider | |
UNII | |
ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.216.731 |
Chemical and physical data | |
Formula | C13H20ClNO |
Molar mass | 241.76 g·mol−1 |
3D model (JSmol) | |
| |
|
Threohydrobupropion (developmental code names BW 494, BW A494U) is a substituted amphetamine derivative—specifically a β-hydroxyamphetamine—and a major active metabolite of the antidepressant drug bupropion (Wellbutrin).[1][2] Bupropion is a norepinephrine–dopamine reuptake inhibitor and nicotinic acetylcholine receptor negative allosteric modulator, with its metabolites contributing substantially to its activities.[1]