Diphenoxylate

CHEMBL1201294 Phase 4 Zugelassen Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
452.6 g/mol
LogP
5.7
Phase
4

An opioid-related antidiarrheal agent used to reduce intestinal motility and treat acute and chronic diarrhea. It is combined with a small amount of atropine in commercial preparations (e.g., Lomotil) to discourage abuse, as the atropine causes unpleasant effects if large doses are taken. At recommended doses, very little is absorbed systemically.

Molekularmasse

452,6000 g/mol

LogP

5,70

TPSA

53,30 Ų

Lipinski-Regel der Fünf

Bestanden

Therapeutische Bereiche

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

CCOC(=O)C1(c2ccccc2)CCN(CCC(C#N)(c2ccccc2)c2ccccc2)CC1

InChI

InChI=1S/C30H32N2O2/c1-2-34-28(33)29(25-12-6-3-7-13-25)18-21-32(22-19-29)23-20-30(24-31,26-14-8-4-9-15-26)27-16-10-5-11-17-27/h3-17H,2,18-23H2,1H3

Molecular Formula

C30H32N2O2

HBD / HBA

- / 4

Rotierbare Bindungen

9

Schwere Atome

34

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 opioid-related antidiarrheal agent used to reduce intestinal motility and treat acute and chronic diarrhea. It is combined with a small amount of atropine in commercial preparations (e.g., Lomotil) to discourage abuse, as the atropine causes unpleasant effects if large doses are taken. At recommended doses, very little is absorbed systemically.

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, Diphenoxylate 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). CHEMBL1201294. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 13505. 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.