Mepazine Acetate
A salt form of mepazine, sharing the same therapeutic uses.
Khối lượng phân tử
370,5000 g/mol
TPSA
69,10 Ų
Cơ chế tác dụng
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 …
Cấu trúc 2D
Cite this structure
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SMILES
CC(=O)O.CN1CCCC(CN2c3ccccc3Sc3ccccc32)C1
InChI
InChI=1S/C19H22N2S.C2H4O2/c1-20-12-6-7-15(13-20)14-21-16-8-2-4-10-18(16)22-19-11-5-3-9-17(19)21;1-2(3)4/h2-5,8-11,15H,6-7,12-14H2,1H3;1H3,(H,3,4)
Molecular Formula
C21H26N2O2S
HBD / HBA
1 / 5
Liên kết có thể quay
2
Nguyên tử nặng
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.
Câu hỏi thường gặp
A salt form of mepazine, sharing the same therapeutic uses.
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, Mepazine Acetate 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). CHEMBL1712842. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 2834213. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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