Wilton D C, Akhtar M
Biochem J. 1975 Jul;149(1):233-5. doi: 10.1042/bj1490233.
The conversion of 4,4-dimethylcholest-7-enol into 4alpha-methylcholest-7-enol by rat liver microsomal preparations involves the decarboxylation of a sterol 3-oxo-4alpha-carboxylic acid. By using an (18)O-labelled substrate it was shown that this decarboxylation does not involve a Schiff-base intermediate.
大鼠肝脏微粒体制剂将4,4-二甲基胆甾-7-烯醇转化为4α-甲基胆甾-7-烯醇的过程涉及甾醇3-氧代-4α-羧酸的脱羧反应。通过使用(18)O标记的底物表明,这种脱羧反应不涉及席夫碱中间体。