Mesoridazine
A phenothiazine antipsychotic medication used to treat schizophrenia in patients who have not responded to other treatments. Due to its risk of serious heart rhythm abnormalities, its use is now very limited.
Peso molecular
386,6000 g/mol
LogP
4,50
TPSA
68,10 Ų
Regla de cinco de Lipinski
Cumple
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
CN1CCCCC1CCN1c2ccccc2Sc2ccc([S+](C)[O-])cc21
InChI
InChI=1S/C21H26N2OS2/c1-22-13-6-5-7-16(22)12-14-23-18-8-3-4-9-20(18)25-21-11-10-17(26(2)24)15-19(21)23/h3-4,8-11,15-16H,5-7,12-14H2,1-2H3
Molecular Formula
C21H26N2OS2
HBD / HBA
- / 5
Enlaces Rotables
4
Átomos Pesados
26
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
A phenothiazine antipsychotic medication used to treat schizophrenia in patients who have not responded to other treatments. Due to its risk of serious heart rhythm abnormalities, its use is now very limited.
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, Mesoridazine 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). CHEMBL1088. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 4078. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.
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