Lumateperone Tosylate
The tosylate salt form of lumateperone, used in treating schizophrenia and bipolar depression. It is the pharmaceutical form of this multi-receptor antipsychotic agent.
الوزن الجزيئي
565,7000 g/mol
TPSA
89,50 Ų
المجالات العلاجية
آلية العمل
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 …
البنية ثنائية الأبعاد
Cite this structure
Embed this structure
SMILES
CN1CCN2c3c(cccc31)[C@@H]1CN(CCCC(=O)c3ccc(F)cc3)CC[C@@H]12.Cc1ccc(S(=O)(=O)O)cc1
InChI
InChI=1S/C24H28FN3O.C7H8O3S/c1-26-14-15-28-21-11-13-27(16-20(21)19-4-2-5-22(26)24(19)28)12-3-6-23(29)17-7-9-18(25)10-8-17;1-6-2-4-7(5-3-6)11(8,9)10/h2,4-5,7-10,20-21H,3,6,11-16H2,1H3;2-5H,1H3,(H,8,9,10)/t20-,21-;/m0./s1
Molecular Formula
C31H36FN3O4S
HBD / HBA
1 / 8
الروابط القابلة للدوران
6
الذرات الثقيلة
40
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.
الأسئلة الشائعة
The tosylate salt form of lumateperone, used in treating schizophrenia and bipolar depression. It is the pharmaceutical form of this multi-receptor antipsychotic agent.
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, Lumateperone Tosylate 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). CHEMBL3233142. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 44241743. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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