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.
Peso molecular
565,7000 g/mol
TPSA
89,50 Ų
Áreas terapéuticas
Mecanismo de acción
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 …
Estructura 2D
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
Enlaces Rotables
6
Átomos Pesados
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.
Preguntas frecuentes
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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