Structure via PubChem · Public domain (PubChem)
dekstrorfan
Sign in to saveAlso known as d-3-hydroxy-N-methylmorphinan, (+)-3-hydroxy-N-methylmorphinan, DXO, D-morphan
związek chemiczny
Key facts
- Drug.Verifiedfields
- changed
- Drug.Watchedfields
- changed
- Drug.verifiedrevid
- 408496712
- Drug.IUPAC_name
- (+)-17-methyl-9a,13a,14a-morphinan-3-ol
- Drug.image
- Dextrorphan.svg
- Drug.image_class
- skin-invert-image
- Drug.legal_US
- Unscheduled
- Drug.CAS_number
- 125-73-5
- Drug.ATC_prefix
- None
- Drug.PubChem
- 5360697
- Drug.UNII
- 04B7QNO9WS
- Drug.ChEMBL
- 1254766
- Drug.ChemSpiderID
- 10489895
- Drug.synonyms
- DXO, Dextrorphanol
- Drug.C
- 17
- Drug.H
- 23
- Drug.N
- 1
- Drug.O
- 1
via Wikipedia infobox
Chemical data
- Formula
- C17H23NO
- Molecular weight
- 257.37 g/mol
- IUPAC name
- (1S,9S,10S)-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2(7),3,5-trien-4-ol
- SMILES
- CN1CC[C@@]23CCCC[C@@H]2[C@@H]1CC4=C3C=C(C=C4)O
- InChIKey
- JAQUASYNZVUNQP-PVAVHDDUSA-N
- XLogP
- 3.1
- Polar surface area
- 23.5 Ų
- H-bond donors
- 1
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
914 papers- Neurotoxicity of dextrorphan.Archives of medical research · 1999
- Dextrorphan and dextromethorphan attenuate glutamate neurotoxicity.Brain research · 1987
- Infant Dextromethorphan and Dextrorphan Exposure via Breast Milk From Mothers Who Are CYP2D6 Extensive Metabolizers.Journal of clinical pharmacology · 2022
- Evaluating dextrorphan as a wastewater biomarker for cough suppressant use: A longitudinal study in China.Water research · 2025
- Dopamine enhancement of dextrorphan-induced skin antinociception in response to needle pinpricks in rats.Pharmacological reports : PR · 2019
via PubMed
Wikidata facts
- Mass
- 257.177964
Show 6 more facts
via Wikidata · CC0
Article · Polski
Dekstrorfan (łac. dextrorphanum) – organiczny związek chemiczny, enancjomer leworfanolu (silnego opioidu), metabolit dekstrometorfanu. Powstaje w wyniku O-demetylacji w wątrobie. Działa na te same receptory co dekstrometorfan, głównie jednak antagonistycznie na receptor NMDA.
Abstract from DBpedia / Wikipedia · CC BY-SA