Matches in SemOpenAlex for { <https://semopenalex.org/work/W2061681391> ?p ?o ?g. }
- W2061681391 endingPage "1284" @default.
- W2061681391 startingPage "1267" @default.
- W2061681391 abstract "Abstract A total spectrum of glucuronide-conjugated metabolites of cortisol has been isolated from human urine and characterized: 22 steroid monoglucuronides and 7 steroid diglucuronides. Following i.v. administration of a tracer dose of [4-14C]-cortisol to 10 normal subjects, urine was collected for 2 consecutive 24-h periods. Free steroids were removed with ethyl acetate. All conjugated metabolites were extracted by means of an Amberlite XAD-2 column, and were further purified by chromatography on a polyethyleneimine-impregnated cellulose column. Groups of mono- and di-glucuronide conjugated steroids were then separated from each other, and from other groups of steroid conjugates by means of high voltage paper electrophoresis. Individual monoglucuronide-conjugated metabolites were then separated from each other by means of 15 consecutive paper chromatographies, and their homogeneity was ascertained. Each steroid conjugate was then subjected to the following characterization: (1) identification by RID of the steroid moiety released by β-glucuronidase hydrolysis; (2) identification of the glucuronide moiety; (3) determination of the steroid/glucuronide molar ratio; (4) determination of the site of conjugation. The following monoglucuronide-conjugated (-G) metabolites of cortisol were isolated: cortisol-21-G, cortisone-21-G, 20β-dihydrocortisol-21-G, tetrahydrocortisol-3-G, tetrahydrocortisol-21-G, 5α-tetrahydrocortisol-3-G,tetrahydrocortisone-3-G,5α-tetrahydrocortisone-3-G,cortol-20α-3-G, 5α-cortol-20α-3-G, cortol-20β-3-G, 5α-cortol-20β-3-G, cortolone-20α-3-G, 5α-cortolone-20α-3-G, cortolone-20β-3-G, 5α-cortolone-20β-3-G, ll-hydroxyaetiocholanolone-3-G,11-hydroxyandrosterone-3-G, 11-oxoaetiocholanolone-3-G, 11-oxoandrosterone-3-G. In addition, 6β-hydroxy-20β-dihydrocortisol and 6β-hydroxy-20β-cortol were also isolated as monoglucuronides, but their site of conjugation was not determined. The steroids identified as diglucuronide conjugates were: cortol-20α and −20β, cortolone-20α and −20β, tetrahydrocortisol, 5α-tetrahydrocortisol and tetrahydrocortisone. Most of these steroid metabolites have not been heretofore isolated and characterized as conjugates. Three of the isolated metabolites were not known to exist as glucuronide conjugates. The quantitation of individual steroid conjugates revealed interesting relationships between various metabolites, which are discussed." @default.
- W2061681391 created "2016-06-24" @default.
- W2061681391 creator A5021751851 @default.
- W2061681391 creator A5031294226 @default.
- W2061681391 date "1975-08-01" @default.
- W2061681391 modified "2023-09-24" @default.
- W2061681391 title "Studies on steroid conjugates—VIII: Isolation and characterization of glucuronide-conjugated metabolites of cortisol in human urine" @default.
- W2061681391 cites W101502894 @default.
- W2061681391 cites W118003988 @default.
- W2061681391 cites W13260450 @default.
- W2061681391 cites W176040915 @default.
- W2061681391 cites W1970838195 @default.
- W2061681391 cites W1974570973 @default.
- W2061681391 cites W1975230340 @default.
- W2061681391 cites W1979724308 @default.
- W2061681391 cites W1993543533 @default.
- W2061681391 cites W2001443899 @default.
- W2061681391 cites W2003470013 @default.
- W2061681391 cites W2007552540 @default.
- W2061681391 cites W2014526919 @default.
- W2061681391 cites W2025237065 @default.
- W2061681391 cites W2033736039 @default.
- W2061681391 cites W2035679428 @default.
- W2061681391 cites W2067392602 @default.
- W2061681391 cites W2067904853 @default.
- W2061681391 cites W2069262060 @default.
- W2061681391 cites W2074738884 @default.
- W2061681391 cites W2075966180 @default.
- W2061681391 cites W2079040149 @default.
- W2061681391 cites W208083473 @default.
- W2061681391 cites W2086226285 @default.
- W2061681391 cites W2107177527 @default.
- W2061681391 cites W2119645046 @default.
- W2061681391 cites W2133696313 @default.
- W2061681391 cites W2151104800 @default.
- W2061681391 cites W2162461225 @default.
- W2061681391 cites W2315868486 @default.
- W2061681391 cites W2341860536 @default.
- W2061681391 cites W2467485966 @default.
- W2061681391 cites W313621319 @default.
- W2061681391 doi "https://doi.org/10.1016/0022-4731(75)90118-1" @default.
- W2061681391 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/1177450" @default.
- W2061681391 hasPublicationYear "1975" @default.
- W2061681391 type Work @default.
- W2061681391 sameAs 2061681391 @default.
- W2061681391 citedByCount "34" @default.
- W2061681391 countsByYear W20616813912013 @default.
- W2061681391 countsByYear W20616813912014 @default.
- W2061681391 countsByYear W20616813912015 @default.
- W2061681391 countsByYear W20616813912017 @default.
- W2061681391 countsByYear W20616813912018 @default.
- W2061681391 countsByYear W20616813912019 @default.
- W2061681391 countsByYear W20616813912020 @default.
- W2061681391 countsByYear W20616813912021 @default.
- W2061681391 countsByYear W20616813912022 @default.
- W2061681391 crossrefType "journal-article" @default.
- W2061681391 hasAuthorship W2061681391A5021751851 @default.
- W2061681391 hasAuthorship W2061681391A5031294226 @default.
- W2061681391 hasConcept C112613896 @default.
- W2061681391 hasConcept C134306372 @default.
- W2061681391 hasConcept C178790620 @default.
- W2061681391 hasConcept C185592680 @default.
- W2061681391 hasConcept C197336794 @default.
- W2061681391 hasConcept C2775941552 @default.
- W2061681391 hasConcept C2779186261 @default.
- W2061681391 hasConcept C2780026642 @default.
- W2061681391 hasConcept C2780902042 @default.
- W2061681391 hasConcept C33923547 @default.
- W2061681391 hasConcept C43617362 @default.
- W2061681391 hasConcept C521977710 @default.
- W2061681391 hasConcept C55493867 @default.
- W2061681391 hasConcept C71315377 @default.
- W2061681391 hasConcept C86803240 @default.
- W2061681391 hasConcept C89423630 @default.
- W2061681391 hasConceptScore W2061681391C112613896 @default.
- W2061681391 hasConceptScore W2061681391C134306372 @default.
- W2061681391 hasConceptScore W2061681391C178790620 @default.
- W2061681391 hasConceptScore W2061681391C185592680 @default.
- W2061681391 hasConceptScore W2061681391C197336794 @default.
- W2061681391 hasConceptScore W2061681391C2775941552 @default.
- W2061681391 hasConceptScore W2061681391C2779186261 @default.
- W2061681391 hasConceptScore W2061681391C2780026642 @default.
- W2061681391 hasConceptScore W2061681391C2780902042 @default.
- W2061681391 hasConceptScore W2061681391C33923547 @default.
- W2061681391 hasConceptScore W2061681391C43617362 @default.
- W2061681391 hasConceptScore W2061681391C521977710 @default.
- W2061681391 hasConceptScore W2061681391C55493867 @default.
- W2061681391 hasConceptScore W2061681391C71315377 @default.
- W2061681391 hasConceptScore W2061681391C86803240 @default.
- W2061681391 hasConceptScore W2061681391C89423630 @default.
- W2061681391 hasIssue "8" @default.
- W2061681391 hasLocation W20616813911 @default.
- W2061681391 hasLocation W20616813912 @default.
- W2061681391 hasOpenAccess W2061681391 @default.
- W2061681391 hasPrimaryLocation W20616813911 @default.
- W2061681391 hasRelatedWork W1021316407 @default.
- W2061681391 hasRelatedWork W152889708 @default.
- W2061681391 hasRelatedWork W1541629431 @default.