Lumateperone
An atypical antipsychotic used to treat schizophrenia and depressive episodes associated with bipolar disorder. It has a unique pharmacological profile acting simultaneously on dopamine, serotonin, and glutamate receptors.
Moleküler Ağırlık
393,5000 g/mol
LogP
3,80
TPSA
26,80 Ų
Lipinski RO5
Geçer
Terapötik Alanlar
Etki Mekanizması
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 Yapı
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Embed this structure
SMILES
CN1CCN2c3c(cccc31)[C@@H]1CN(CCCC(=O)c3ccc(F)cc3)CC[C@@H]12
InChI
InChI=1S/C24H28FN3O/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/h2,4-5,7-10,20-21H,3,6,11-16H2,1H3/t20-,21-/m0/s1
Molecular Formula
C24H28FN3O
HBD / HBA
- / 5
Döndürülebilir Bağlar
5
Ağır Atomlar
29
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.
Sıkça Sorulan Sorular
An atypical antipsychotic used to treat schizophrenia and depressive episodes associated with bipolar disorder. It has a unique pharmacological profile acting simultaneously on dopamine, serotonin, and glutamate receptors.
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 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). CHEMBL3306803. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 21302490. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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