Difenoxin

CHEMBL1201321 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
424.5 g/mol
LogP
2.7
Phase
4

An active metabolite of diphenoxylate and opioid-related antidiarrheal agent that reduces intestinal motility by acting on opioid receptors in the gut wall. It is combined with atropine in formulations to discourage abuse. It is used for the symptomatic treatment of diarrhea.

Molekularmasse

424,5000 g/mol

LogP

2,70

TPSA

64,30 Ų

Lipinski-Regel der Fünf

Bestanden

Wirkmechanismus

Binds to mu (μ), kappa (κ), and/or delta (δ) opioid receptors in the central and peripheral nervous system, mimicking endogenous endorphins. Activation of these G-protein-coupled receptors inhibits pain signal transmission and modulates the emotional response to pain.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanismus

Binds to mu (μ), kappa (κ), and/or delta (δ) opioid receptors in the central and peripheral nervous system, mimicking endogenous endorphins. Activation of these G-protein-coupled receptors inhibits pain signal transmission …

2D-Struktur

SVG PNG

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SMILES

N#CC(CCN1CCC(C(=O)O)(c2ccccc2)CC1)(c1ccccc1)c1ccccc1

InChI

InChI=1S/C28H28N2O2/c29-22-28(24-12-6-2-7-13-24,25-14-8-3-9-15-25)18-21-30-19-16-27(17-20-30,26(31)32)23-10-4-1-5-11-23/h1-15H,16-21H2,(H,31,32)

Molecular Formula

C28H28N2O2

HBD / HBA

1 / 4

Rotierbare Bindungen

7

Schwere Atome

32

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

An active metabolite of diphenoxylate and opioid-related antidiarrheal agent that reduces intestinal motility by acting on opioid receptors in the gut wall. It is combined with atropine in formulations to discourage abuse. It is used for the symptomatic treatment of diarrhea.

Binds to mu (μ), kappa (κ), and/or delta (δ) opioid receptors in the central and peripheral nervous system, mimicking endogenous endorphins. Activation of these G-protein-coupled receptors inhibits pain signal transmission and modulates the emotional response to pain.

Yes, Difenoxin 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). CHEMBL1201321. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 34328. 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.