Levallorphan
This opioid antagonist reverses the effects of opioid medications, particularly respiratory depression caused by opioid overdose. It was historically used to counteract narcotic-induced breathing problems but has largely been replaced by more selective agents.
분자량
283.4000 g/mol
LogP
3.50
TPSA
23.50 Ų
리핀스키 5의 법칙
통과
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
C=CCN1CC[C@]23CCCC[C@H]2[C@H]1Cc1ccc(O)cc13
InChI
InChI=1S/C19H25NO/c1-2-10-20-11-9-19-8-4-3-5-16(19)18(20)12-14-6-7-15(21)13-17(14)19/h2,6-7,13,16,18,21H,1,3-5,8-12H2/t16-,18+,19+/m0/s1
Molecular Formula
C19H25NO
HBD / HBA
1 / 2
회전 가능 결합
2
무거운 원자
21
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
This opioid antagonist reverses the effects of opioid medications, particularly respiratory depression caused by opioid overdose. It was historically used to counteract narcotic-induced breathing problems but has largely been replaced by more selective agents.
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, Levallorphan 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). CHEMBL1254682. Open-access bioactivity database.
- PubChem — National Center for Biotechnology Information (NCBI). CID 5359371. Chemical information database.
Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.
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