Preparation and Stability in Solution of Androstenedione 3-Enol Glucosiduronate
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4-^<14>C-Androstenedione 3-enol glucosiduronate (^<14>C-AEG) was synthesized and its stability was studied by analyzing liberated steroids. Incubation of ^<14>C-AEG with human urine at 37° for 48 hr resulted in 49% hydrolysis. ^<14>C-AEG was fairly stable in neutral and basic media, but rapidly hy rolyzed at acidic pH. ^<14>C-AEG was solvolyzed almost quantitatively with acidic ethyl acetate in the same way as steroid sulfates. By incubation with β-glucuronidase (Ketodase, Helix pomatia, and bacterial β-glucuronidase) at pH 6.2 for 3 hr, 64-71% of ^<14>C-AEG was hydrolyzed. Hydrolysis with Helix pomatia β-glucuronidase was inhibited by D-glucaro-(1→4)-lactone. Analyses of liberated steroids by TLC revealed the formation of artifacts (polar steroids) in all cases so far examined. One of them was identified as 6β-hydroxyandrostenedione.
- 公益社団法人日本薬学会の論文
- 1974-11-25
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