Naloxol
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| Names | |||
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| IUPAC names
α-naloxol: (4R,4aS,7S,7aR,12bS)-3-allyl-2,3,4,4a,5,6,7,7a-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,7,9-triol
β-naloxol: (4R,4aS,7R,7aR,12bS)-3-allyl-2,3,4,4a,5,6,7,7a-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,7,9-triol |
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| Identifiers | |||
20410-95-1 (α)  53154-12-4 (β) 58691-01-3 (α/β) |
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| ChemSpider | 4590928 (α)  9177198 (β) |
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| Jmol 3D model | (α): Interactive image (β): Interactive image |
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| PubChem | 5492271 (α) 5492293 (β) |
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| Properties | |||
| C19H23NO4 | |||
| Molar mass | 329.40 g·mol−1 | ||
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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 verify (what is ?) |
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| Infobox references | |||
Naloxol is an opioid antagonist closely related to naloxone. It exists in two isomeric forms, α-naloxol and β-naloxol.
α-naloxol is a human metabolite of naloxone.[1] Synthetically, α-naloxol can be prepared from naloxone by reduction of the ketone group, and β-naloxol can be prepared from α-naloxol by a Mitsunobu reaction.[2]
Naloxol can be said to be the oxymorphol analogue of naloxone.
See also[edit]
References[edit]
- ^ Weinstein, S. H.; Pfeffer, M.; Schor, J. M.; Indindoli, L.; Mintz, M. (1971). "Metabolites of naloxone in human urine". Journal of Pharmaceutical Sciences. 60 (10): 1567–1568. doi:10.1002/jps.2600601030. PMID 5129377.
- ^ Simon, C (1994). "Stereoselective synthesis of β-naltrexol, β-naloxol β-naloxamine, β-naltrexamine and related compounds by the application of the mitsunobu reac". Tetrahedron. 50 (32): 9757. doi:10.1016/S0040-4020(01)85541-1.
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