Desipramine Hydrochloride

CHEMBL1696 Phase 4 Đã phê duyệt Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
302.8 g/mol
LogP
Phase
4

The hydrochloride salt form of desipramine, a norepinephrine-selective tricyclic antidepressant used for depression and chronic pain conditions. It requires ECG monitoring in some patients due to potential cardiac conduction effects.

Khối lượng phân tử

302,8000 g/mol

TPSA

15,30 Ų

Lĩnh vực điều trị

Cơ chế tác dụng

Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Cơ chế

Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.

Cấu trúc 2D

SVG PNG

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SMILES

CNCCCN1c2ccccc2CCc2ccccc21.Cl

InChI

InChI=1S/C18H22N2.ClH/c1-19-13-6-14-20-17-9-4-2-7-15(17)11-12-16-8-3-5-10-18(16)20;/h2-5,7-10,19H,6,11-14H2,1H3;1H

Molecular Formula

C18H23ClN2

HBD / HBA

2 / 2

Liên kết có thể quay

4

Nguyên tử nặng

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.

Câu hỏi thường gặp

The hydrochloride salt form of desipramine, a norepinephrine-selective tricyclic antidepressant used for depression and chronic pain conditions. It requires ECG monitoring in some patients due to potential cardiac conduction effects.

Competitively blocks muscarinic acetylcholine receptors, reducing parasympathetic nervous system activity. Effects include decreased secretions, bronchodilation, and relaxation of smooth muscle.

Yes, Desipramine Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1696. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 65327. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Tuyên bố miễn trách y tế

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.