Lorcaserin
| Clinical data | |
|---|---|
| Trade names | Belviq | 
| Other names | APD-356 | 
| AHFS/Drugs.com | Monograph | 
| MedlinePlus | a613014 | 
| License data | 
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| Routes of administration | Oral | 
| ATC code | |
| Legal status | |
| Legal status | 
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| Pharmacokinetic data | |
| Protein binding | 70% | 
| Metabolism | Hepatic (extensive) | 
| Elimination half-life | 11 hours | 
| Excretion | Renal (92.3%), Faecal (2.2%) | 
| Identifiers | |
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| CAS Number | |
| PubChem CID | |
| IUPHAR/BPS | |
| DrugBank | |
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| ChEMBL | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.237.138 | 
| Chemical and physical data | |
| Formula | C11H14ClN | 
| Molar mass | 195.69 g·mol−1 | 
| 3D model (JSmol) | |
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Lorcaserin, marketed under the brand name Belviq, was a weight-loss drug developed by Arena Pharmaceuticals. It reduces appetite by activating serotonin receptor the 5-HT2C receptor in the hypothalamus, a region of the brain which is known to control appetite. It was approved in 2012, and in 2020, it was removed from the market in the United States due to an increased risk of cancer detected in users of Belviq.