Difenoxin Hydrochloride
The hydrochloride salt of difenoxin, used in combination with atropine in oral tablets to treat diarrhea by slowing intestinal movement. As an opioid-related compound, its combination with atropine is intended to prevent abuse. It is a controlled substance.
분자량
461.0000 g/mol
TPSA
64.30 Ų
작용 기전
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)
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 구조
Cite this structure
Embed this structure
SMILES
Cl.N#CC(CCN1CCC(C(=O)O)(c2ccccc2)CC1)(c1ccccc1)c1ccccc1
InChI
InChI=1S/C28H28N2O2.ClH/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);1H
Molecular Formula
C28H29ClN2O2
HBD / HBA
2 / 4
회전 가능 결합
7
무거운 원자
33
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.
자주 묻는 질문
The hydrochloride salt of difenoxin, used in combination with atropine in oral tablets to treat diarrhea by slowing intestinal movement. As an opioid-related compound, its combination with atropine is intended to prevent abuse. It is a controlled substance.
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 Hydrochloride is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.
References & Data Sources
- ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1200599. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 53447387. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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