Citalopram Hydrobromide
The hydrobromide salt is the standard oral formulation of citalopram used clinically for depression and anxiety disorders. It shares the same SSRI mechanism and dose-dependent QT prolongation risk as the parent compound. Gradual dose titration is recommended to minimize side effects including nausea and activation symptoms.
分子量
405.3000 g/mol
TPSA
36.30 Ų
治療領域
作用機序
Selectively inhibits the serotonin reuptake transporter (SERT) at presynaptic neurons, increasing serotonin concentration in the synaptic cleft. This enhanced serotonergic neurotransmission is associated with antidepressant and anxiolytic effects.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Selectively inhibits the serotonin reuptake transporter (SERT) at presynaptic neurons, increasing serotonin concentration in the synaptic cleft. This enhanced serotonergic neurotransmission is associated with antidepressant and anxiolytic effects.
2D構造
Cite this structure
Embed this structure
SMILES
Br.CN(C)CCCC1(c2ccc(F)cc2)OCc2cc(C#N)ccc21
InChI
InChI=1S/C20H21FN2O.BrH/c1-23(2)11-3-10-20(17-5-7-18(21)8-6-17)19-9-4-15(13-22)12-16(19)14-24-20;/h4-9,12H,3,10-11,14H2,1-2H3;1H
Molecular Formula
C20H22BrFN2O
HBD / HBA
1 / 4
回転可能結合数
5
重原子数
25
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.
よくある質問
The hydrobromide salt is the standard oral formulation of citalopram used clinically for depression and anxiety disorders. It shares the same SSRI mechanism and dose-dependent QT prolongation risk as the parent compound. Gradual dose titration is recommended to minimize side effects including nausea and activation symptoms.
Selectively inhibits the serotonin reuptake transporter (SERT) at presynaptic neurons, increasing serotonin concentration in the synaptic cleft. This enhanced serotonergic neurotransmission is associated with antidepressant and anxiolytic effects.
Yes, Citalopram Hydrobromide 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). CHEMBL1200781. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 77995. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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