Loxapine Hydrochloride
The hydrochloride salt form of loxapine, used as an antipsychotic for schizophrenia and bipolar disorder. It shares the dopamine and serotonin receptor blocking properties of the parent compound.
分子量
364.3000 g/mol
TPSA
28.10 Ų
治療領域
作用機序
Blocks dopamine D2 receptors in the mesolimbic pathway, reducing excessive dopaminergic neurotransmission associated with psychotic symptoms. Many also antagonize serotonin 5-HT2A receptors, which may improve negative symptoms and reduce extrapyramidal side effects.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Blocks dopamine D2 receptors in the mesolimbic pathway, reducing excessive dopaminergic neurotransmission associated with psychotic symptoms. Many also antagonize serotonin 5-HT2A receptors, which may improve negative symptoms and reduce extrapyramidal …
2D構造
Cite this structure
Embed this structure
SMILES
CN1CCN(C2=Nc3ccccc3Oc3ccc(Cl)cc32)CC1.Cl
InChI
InChI=1S/C18H18ClN3O.ClH/c1-21-8-10-22(11-9-21)18-14-12-13(19)6-7-16(14)23-17-5-3-2-4-15(17)20-18;/h2-7,12H,8-11H2,1H3;1H
Molecular Formula
C18H19Cl2N3O
HBD / HBA
1 / 3
回転可能結合数
1
重原子数
24
No targets recorded
Target interaction data is not yet available for this drug.
No interactions recorded
Drug interaction data is not yet available for this compound.
No side effects recorded
Side effect data is not yet available for this drug.
よくある質問
The hydrochloride salt form of loxapine, used as an antipsychotic for schizophrenia and bipolar disorder. It shares the dopamine and serotonin receptor blocking properties of the parent compound.
Blocks dopamine D2 receptors in the mesolimbic pathway, reducing excessive dopaminergic neurotransmission associated with psychotic symptoms. Many also antagonize serotonin 5-HT2A receptors, which may improve negative symptoms and reduce extrapyramidal side effects.
Yes, Loxapine Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1201060. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 71400. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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