Loxapine
| Clinical data | |
|---|---|
| Trade names | Loxitane, Adasuve |
| AHFS/Drugs.com | Monograph |
| MedlinePlus | a682311 |
| License data | |
| Routes of administration | By mouth, inhalation, intramuscular |
| Drug class | Antipsychotic |
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| Pharmacokinetic data | |
| Protein binding | 96.8% |
| Metabolism | Extensive Liver; active metabolites include amoxapine and 8-hydroxyloxapine. Inhibits P-gp and is a substrate of CYP1A2, CYP3A4 and CYP2D6 |
| Elimination half-life | 4 hours (oral); 7.61 hours (inhalation) |
| Excretion | Majority are excreted within 24 hours, main route through urine (conjugated metabolites), small amounts through the feces (unconjugated metabolites) |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.016.215 |
| Chemical and physical data | |
| Formula | C18H18ClN3O |
| Molar mass | 327.81 g·mol−1 |
| 3D model (JSmol) | |
| Melting point | 109 to 110 °C (228 to 230 °F) |
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| (what is this?) (verify) | |
Loxapine, sold under the brand names Loxitane and Adasuve (inhalation only) among others, is a tricyclic antipsychotic medication used primarily in the treatment of schizophrenia. The medicine is a member of the dibenzoxazepine class and structurally very similar to clozapine. Several researchers have argued that loxapine, initially classified as a typical antipsychotic, behaves as an atypical antipsychotic.
Loxapine may be metabolized by N-demethylation to amoxapine, a tricyclic antidepressant.