Clomacran
An antipsychotic agent belonging to the phenothiazine class used to treat psychiatric conditions. It helps manage symptoms such as hallucinations and disordered thinking.
Molecular Weight
300.8000 g/mol
LogP
4.60
TPSA
15.30 Ų
Lipinski RO5
Pass
Mechanism of Action
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 Structure
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SMILES
CN(C)CCCC1c2ccccc2Nc2ccc(Cl)cc21
InChI
InChI=1S/C18H21ClN2/c1-21(2)11-5-7-14-15-6-3-4-8-17(15)20-18-10-9-13(19)12-16(14)18/h3-4,6,8-10,12,14,20H,5,7,11H2,1-2H3
Molecular Formula
C18H21ClN2
HBD / HBA
1 / 2
Rotatable Bonds
4
Heavy Atoms
21
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.
Frequently Asked Questions
An antipsychotic agent belonging to the phenothiazine class used to treat psychiatric conditions. It helps manage symptoms such as hallucinations and disordered thinking.
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, Clomacran 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). CHEMBL1615350. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 21382. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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