Imipramine Hydrochloride
This hydrochloride salt of imipramine is the most commonly used formulation of this tricyclic antidepressant for treating depression, panic disorder, and nocturnal enuresis. It inhibits the reuptake of norepinephrine and serotonin, elevating mood over several weeks of treatment. Anticholinergic side effects including dry mouth, constipation, and urinary retention are common.
分子量
316.9000 g/mol
TPSA
6.50 Ų
治療領域
作用機序
Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.
Pharmacokinetics (PK)
Pharmacodynamics (PD)
Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.
2D構造
Cite this structure
Embed this structure
SMILES
CN(C)CCCN1c2ccccc2CCc2ccccc21.Cl
InChI
InChI=1S/C19H24N2.ClH/c1-20(2)14-7-15-21-18-10-5-3-8-16(18)12-13-17-9-4-6-11-19(17)21;/h3-6,8-11H,7,12-15H2,1-2H3;1H
Molecular Formula
C19H25ClN2
HBD / HBA
1 / 2
回転可能結合数
4
重原子数
22
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
This hydrochloride salt of imipramine is the most commonly used formulation of this tricyclic antidepressant for treating depression, panic disorder, and nocturnal enuresis. It inhibits the reuptake of norepinephrine and serotonin, elevating mood over several weeks of treatment. Anticholinergic side effects including dry mouth, constipation, and urinary retention are common.
Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.
Yes, Imipramine Hydrochloride 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). CHEMBL1692. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 8228. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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