Imipramine Pamoate

CHEMBL3989845 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
949.2 g/mol
LogP
Phase
4

This pamoate salt of imipramine provides extended-release characteristics suitable for once-daily dosing in the treatment of depression and anxiety. The pamoate salt reduces gastrointestinal side effects and provides sustained drug levels throughout the day. Like other imipramine formulations, it inhibits neurotransmitter reuptake and carries the same cautions regarding cardiac and anticholinergic effects.

Molekularmasse

949,2000 g/mol

TPSA

128,00 Ų

Therapeutische Bereiche

Wirkmechanismus

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

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

2D-Struktur

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SMILES

CN(C)CCCN1c2ccccc2CCc2ccccc21.CN(C)CCCN1c2ccccc2CCc2ccccc21.O=C(O)c1cc2ccccc2c(Cc2c(O)c(C(=O)O)cc3ccccc23)c1O

InChI

InChI=1S/C23H16O6.2C19H24N2/c24-20-16(14-7-3-1-5-12(14)9-18(20)22(26)27)11-17-15-8-4-2-6-13(15)10-19(21(17)25)23(28)29;2*1-20(2)14-7-15-21-18-10-5-3-8-16(18)12-13-17-9-4-6-11-19(17)21/h1-10,24-25H,11H2,(H,26,27)(H,28,29);2*3-6,8-11H,7,12-15H2,1-2H3

Molecular Formula

C61H64N4O6

HBD / HBA

4 / 10

Rotierbare Bindungen

12

Schwere Atome

71

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.

Häufig gestellte Fragen

This pamoate salt of imipramine provides extended-release characteristics suitable for once-daily dosing in the treatment of depression and anxiety. The pamoate salt reduces gastrointestinal side effects and provides sustained drug levels throughout the day. Like other imipramine formulations, it inhibits neurotransmitter reuptake and carries the same cautions regarding cardiac and anticholinergic effects.

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

Yes, Imipramine Pamoate 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). CHEMBL3989845. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 24904. Chemical information database.

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

Medizinischer Haftungsausschluss

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.