Naloxol
From Infogalactic: the planetary knowledge core
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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 | ||
Vapor pressure | {{{value}}} | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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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
References
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