Lurasidone Hydrochloride
A hydrochloride salt form of lurasidone, an atypical antipsychotic used to treat schizophrenia and bipolar depression by balancing dopamine and serotonin signaling in the brain.
分子量
529.1000 g/mol
TPSA
85.00 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
Cl.O=C1[C@@H]2[C@H]3CC[C@H](C3)[C@@H]2C(=O)N1C[C@@H]1CCCC[C@H]1CN1CCN(c2nsc3ccccc23)CC1
InChI
InChI=1S/C28H36N4O2S.ClH/c33-27-24-18-9-10-19(15-18)25(24)28(34)32(27)17-21-6-2-1-5-20(21)16-30-11-13-31(14-12-30)26-22-7-3-4-8-23(22)35-29-26;/h3-4,7-8,18-21,24-25H,1-2,5-6,9-17H2;1H/t18-,19+,20-,21-,24+,25-;/m0./s1
Molecular Formula
C28H37ClN4O2S
HBD / HBA
1 / 6
回転可能結合数
5
重原子数
36
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
A hydrochloride salt form of lurasidone, an atypical antipsychotic used to treat schizophrenia and bipolar depression by balancing dopamine and serotonin signaling in the brain.
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, Lurasidone 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). CHEMBL1615372. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 11237860. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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