Isopropamide

CHEMBL1201232 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
353.5 g/mol
LogP
4.3
Phase
4

This anticholinergic drug reduces secretions from glands and relaxes smooth muscle in the digestive tract, making it useful for treating peptic ulcers and irritable bowel syndrome. It works by blocking muscarinic receptors that stimulate secretions and gut motility.

分子量

353.5000 g/mol

LogP

4.30

TPSA

43.10 Ų

リピンスキーの五則

適合

作用機序

Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.

2D構造

SVG PNG

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SMILES

CC(C)[N+](C)(CCC(C(N)=O)(c1ccccc1)c1ccccc1)C(C)C

InChI

InChI=1S/C23H32N2O/c1-18(2)25(5,19(3)4)17-16-23(22(24)26,20-12-8-6-9-13-20)21-14-10-7-11-15-21/h6-15,18-19H,16-17H2,1-5H3,(H-,24,26)/p+1

Molecular Formula

C23H33N2O+

HBD / HBA

1 / 1

回転可能結合数

8

重原子数

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.

よくある質問

This anticholinergic drug reduces secretions from glands and relaxes smooth muscle in the digestive tract, making it useful for treating peptic ulcers and irritable bowel syndrome. It works by blocking muscarinic receptors that stimulate secretions and gut motility.

Increases water content in the intestinal lumen through osmotic or stimulant mechanisms, promoting bowel motility and facilitating defecation.

Yes, Isopropamide 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). CHEMBL1201232. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 3775. Chemical information database.

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

医学的免責事項

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.