Loxapine

TargetMol
Product Code: TAR-T21629
Supplier: TargetMol
CodeSizePrice
TAR-T21629-50mg50mg£111.00
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Quantity:
TAR-T21629-1mL1 mL * 10 mM (in DMSO)£132.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
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Overview

Regulatory Status: RUO
Shipping:
cool pack
Storage:
-20℃

Images

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Further Information

Bioactivity:
Loxapine is a D2DR and D4DR inhibitor, serotonergic receptor antagonist and also a dibenzoxazepine anti-psychotic agent,used primarily in the treatment of schizophrenia. The drug is a member of the dibenzoxazepine class and structurally related to clozapine (which belongs to the chemically akin class of dibenzodiazepines).
CAS:
1977-10-2
Formula:
C18H18ClN3O
Molecular Weight:
327.81
Pathway:
Neuroscience; GPCR/G Protein
Purity:
0.9998
SMILES:
CN1CCN(CC1)C1=Nc2ccccc2Oc2ccc(Cl)cc12
Target:
Dopamine Receptor; 5-HT Receptor

References

1. Berardis D D , Fornaro M , Orsolini L , et al. The Role of Inhaled Loxapine in the Treatment of Acute Agitation in Patients with Psychiatric Disorders: A Clinical Review[J]. International Journal of Molecular ences, 2017, 18(2):349. 1. Labuzek K, et al. Chlorpromazine and loxapine reduce interleukin-1beta and interleukin-2 release by rat mixed glial and microglial cell cultures. Eur Neuropsychopharmacol. 2005 Jan;15(1):23-30. 2. Labuzek K, et al. Eur Neuropsychopharmacol, 2005, 15(1), 23-30. 2. Kalkman HO, et al. Clozapine inhibits catalepsy induced by olanzapine and loxapine, but prolongs catalepsy induced by SCH 23390 in rats. Naunyn Schmiedebergs Arch Pharmacol. 1997 Mar;355(3):361-4. 3. Lee T, et al. Psychiatry Res, 1984, 12(4), 277-285. 3. Singh AN, et al. A neurochemical basis for the antipsychotic activity of loxapine: interactions with dopamine D1, D2, D4 and serotonin 5-HT2 receptor subtypes. J Psychiatry Neurosci. 1996 Jan;21(1):29-35.