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一种用于甾体硫酸盐小规模合成及固相萃取纯化的简单方法。

A simple method for the small scale synthesis and solid-phase extraction purification of steroid sulfates.

作者信息

Waller Christopher C, McLeod Malcolm D

机构信息

Research School of Chemistry, Australian National University, Canberra, ACT 2601, Australia.

Research School of Chemistry, Australian National University, Canberra, ACT 2601, Australia.

出版信息

Steroids. 2014 Dec;92:74-80. doi: 10.1016/j.steroids.2014.09.006. Epub 2014 Oct 5.

Abstract

Steroid sulfates are a major class of steroid metabolite that are of growing importance in fields such as anti-doping analysis, the detection of residues in agricultural produce or medicine. Despite this, many steroid sulfate reference materials may have limited or no availability hampering the development of analytical methods. We report simple protocols for the rapid synthesis and purification of steroid sulfates that are suitable for adoption by analytical laboratories. Central to this approach is the use of solid-phase extraction (SPE) for purification, a technique routinely used for sample preparation in analytical laboratories around the world. The sulfate conjugates of sixteen steroid compounds encompassing a wide range of steroid substitution patterns and configurations are prepared, including the previously unreported sulfate conjugates of the designer steroids furazadrol (17β-hydroxyandrostan[2,3-d]isoxazole), isofurazadrol (17β-hydroxyandrostan[3,2-c]isoxazole) and trenazone (17β-hydroxyestra-4,9-dien-3-one). Structural characterization data, together with NMR and mass spectra are reported for all steroid sulfates, often for the first time. The scope of this approach for small scale synthesis is highlighted by the sulfation of 1μg of testosterone (17β-hydroxyandrost-4-en-3-one) as monitored by liquid chromatography-mass spectrometry (LCMS).

摘要

硫酸酯类固醇是一类主要的类固醇代谢物,在反兴奋剂分析、农产品或药物残留检测等领域的重要性日益凸显。尽管如此,许多硫酸酯类固醇参考物质的可得性可能有限或根本无法获得,这阻碍了分析方法的发展。我们报告了适用于分析实验室的硫酸酯类固醇快速合成和纯化的简单方案。这种方法的核心是使用固相萃取(SPE)进行纯化,这是一种在世界各地分析实验室中常规用于样品制备的技术。制备了包含广泛类固醇取代模式和构型的16种类固醇化合物的硫酸酯共轭物,包括设计类固醇呋咱雄醇(17β-羟基雄甾烷[2,3-d]异恶唑)、异呋咱雄醇(17β-羟基雄甾烷[3,2-c]异恶唑)和群勃龙(17β-羟基雌甾-4,9-二烯-3-酮)以前未报道的硫酸酯共轭物。报告了所有硫酸酯类固醇的结构表征数据,以及核磁共振和质谱数据,其中许多数据往往是首次报道。通过液相色谱-质谱联用(LCMS)监测1μg睾酮(17β-羟基雄甾-4-烯-3-酮)的硫酸化反应,突出了这种小规模合成方法的适用范围。

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