Naloxol (original) (raw)
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. 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. Naloxol can be said to be the oxymorphol analogue of naloxone.
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dbo:abstract | 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. 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. Naloxol can be said to be the oxymorphol analogue of naloxone. (en) ナロキソール(英語:Naloxegol)はナロキソンに類似した、オピオイドに対するアンタゴニスト()である。α-ナロキソールとβ-ナロキソールの2つの異性体がある。α-ナロキソールはヒトがナロキソンを代謝したときに生成する物質である。α-ナロキソールはケトンを還元して合成し、β-ナロキソールはα-ナロキソールを光延反応によって変換する。 (ja) |
dbo:iupacName | 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 (en) 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 (en) |
dbo:thumbnail | wiki-commons:Special:FilePath/alpha-Naloxol.svg?width=300 |
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dbo:wikiPageLength | 4262 (xsd:nonNegativeInteger) |
dbo:wikiPageRevisionID | 1090162036 (xsd:integer) |
dbo:wikiPageWikiLink | dbr:Metabolite dbc:4,5-Epoxymorphinans dbc:Allyl_compounds dbc:Human_drug_metabolites dbr:Mitsunobu_reaction dbr:Naloxegol dbr:Naloxone dbr:Opioid_antagonist dbr:Organic_redox_reaction dbc:Mu-opioid_receptor_antagonists dbr:Ketone dbr:Oxymorphol dbr:Isomer |
dbp:imagealtl | α-naloxol (en) |
dbp:imagealtr | β-naloxol (en) |
dbp:imagecaptionl | α-naloxol (en) |
dbp:imagecaptionr | β-naloxol (en) |
dbp:imagefilel | alpha-Naloxol.svg (en) |
dbp:imagefiler | beta-Naloxol.svg (en) |
dbp:iupacname | α-naloxol: -3-allyl-2,3,4,4a,5,6,7,7a-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,7,9-triol (en) β-naloxol: -3-allyl-2,3,4,4a,5,6,7,7a-octahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinoline-4a,7,9-triol (en) |
dbp:verifiedfields | changed (en) |
dbp:verifiedrevid | 452697223 (xsd:integer) |
dbp:watchedfields | changed (en) |
dbp:wikiPageUsesTemplate | dbt:Analgesic-stub dbt:Chembox dbt:Chembox_Hazards dbt:Chembox_Identifiers dbt:Chembox_Properties dbt:Reflist dbt:Cascite dbt:Chemspidercite dbt:Fdacite dbt:Stdinchicite dbt:Opioid_receptor_modulators |
dcterms:subject | dbc:4,5-Epoxymorphinans dbc:Allyl_compounds dbc:Human_drug_metabolites dbc:Mu-opioid_receptor_antagonists |
gold:hypernym | dbr:Antagonist |
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rdfs:comment | 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. 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. Naloxol can be said to be the oxymorphol analogue of naloxone. (en) ナロキソール(英語:Naloxegol)はナロキソンに類似した、オピオイドに対するアンタゴニスト()である。α-ナロキソールとβ-ナロキソールの2つの異性体がある。α-ナロキソールはヒトがナロキソンを代謝したときに生成する物質である。α-ナロキソールはケトンを還元して合成し、β-ナロキソールはα-ナロキソールを光延反応によって変換する。 (ja) |
rdfs:label | ナロキソール (ja) Naloxol (en) |
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prov:wasDerivedFrom | wikipedia-en:Naloxol?oldid=1090162036&ns=0 |
foaf:depiction | wiki-commons:Special:FilePath/alpha-Naloxol.svg wiki-commons:Special:FilePath/beta-Naloxol.svg |
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