Description
Loxapine is an inhibitor of dopamine receptors D2 and D4. It is a serotonin receptor antagonist and displays antipsychotic properties. It is used to treat acute agitation in patients with bipolar disorder or schizophrenia.
| Product Unit Size | Cost | Quantity | Stock |
|---|
Loxapine is an inhibitor of dopamine receptors D2 and D4. It is a serotonin receptor antagonist and displays antipsychotic properties. It is used to treat acute agitation in patients with bipolar disorder or schizophrenia.
| Cas No. | 27833-64-3 |
|---|---|
| Purity | ≥99% |
| Formula | C18H18ClN3O • C4H6O4 |
| Formula Wt. | 445.90 |
| Chemical Name | 2-chloro-11-(4-methyl-1-piperazinyl)dibenzo[b,f][1,4]oxazepine succinate |
| IUPAC Name | butanedioic acid;8-chloro-6-(4-methylpiperazin-1-yl)benzo[b][1,4]benzoxazepine |
| Synonym | Loxapine succinate salt, Cloxazepine, Daxolin, Loxapac |
| Solubility | Insoluble in water. Ethanol 2 mg/mL DMSO 80 mg/mL |
| Store Temp | -20°C |
|---|---|
| Ship Temp | Ambient |
| MSDS | |
|---|---|
| Info Sheet |
de Berardis D., Fornaro M., et al. The Role of Inhaled Loxapine in the Treatment of Acute Agitation in Patients with Psychiatric Disorders: A Clinical Review. Int J Mol Sci. 18(2) (2017). PMID: 28208695.
Pollack C. Inhaled loxapine for the urgent treatment of acute agitation associated with schizophrenia or bipolar disorder. Curr Med Res Opin. 32(7):1253-60 (2016). PMID: 27121764.
Triterpenoid
1,8-Diaza-anthracene-tetrone; JNK and ERK5 inhi...
Derivative of methyl caffeate, hydroxycinnamic ...
β2-adrenergic agonist.
HPGDS inhibitor.
Fibrate; PPARα agonist.
Commercial food additive, antioxidant.
Proton pump inhibitor
Prodrug
AT1 inhibitor.
Bisphosphonate.
AMPK activator.
α1-adrenergic antagonist.
Impurity of diclofenac
Triterpene saponin found in species of Panax.
Synthesis impurity
Non-steroid; AR antagonist.
Prenylated flavonoid found in Humulus lupulus.<...
Polyene macrolide; ergosterol inhibitor.
Fluorouracil impurity