Department of Chemistry, The University of Texas at San Antonio, San Antonio, TX 78249-0698, United States.
Department of Chemistry, The University of Texas at San Antonio, San Antonio, TX 78249-0698, United States.
Steroids. 2019 Nov;151:108449. doi: 10.1016/j.steroids.2019.108449. Epub 2019 Jul 11.
7α-Hydroxy-cholest-4-en-3-one is a biomarker for bile acid loss, irritable bowel syndrome, and other diseases associated with defective bile acid biosynthesis. Furthermore, 7α-hydroxy-cholest-4-en-3-one is the physiological substrate for cytochrome P450 8B1 (P450 8B1 or CYP8B1), the oxysterol 12α-hydroxylase enzyme implicated in obesity and cardiovascular health. We report the chemical synthesis of this physiologically important oxysterol beginning with cholesterol. The key feature of this synthesis involves a regioselective C3-allylic oxidation of a 3-desoxy-Δ-7α-formate steroid precursor to form 7α-formyloxy-cholest-4-en-3-one, which was saponified to yield 7α-hydroxy-cholest-4-en-3-one.
7α-羟基胆甾-4-烯-3-酮是胆汁酸丢失、肠易激综合征和其他与胆汁酸生物合成缺陷相关疾病的生物标志物。此外,7α-羟基胆甾-4-烯-3-酮是细胞色素 P450 8B1(P450 8B1 或 CYP8B1)的生理底物,CYP8B1 是一种涉及肥胖和心血管健康的氧化固醇 12α-羟化酶。我们报告了这种生理上重要的氧化固醇的化学合成,从胆固醇开始。该合成的关键特征涉及 3-去氧-Δ-7α-甲酸盐甾体前体的区域选择性 C3-烯丙基氧化,形成 7α-甲酰氧基-胆甾-4-烯-3-酮,然后将其皂化得到 7α-羟基胆甾-4-烯-3-酮。