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SuFEx 点击化学实现药物后期功能化。

SuFEx Click Chemistry Enabled Late-Stage Drug Functionalization.

机构信息

Department of Molecular Medicine, The Scripps Research Institute , La Jolla, California 92037, United States.

Department of Chemistry, The Scripps Research Institute , La Jolla, California 92037, United States.

出版信息

J Am Chem Soc. 2018 Feb 28;140(8):2919-2925. doi: 10.1021/jacs.7b12788. Epub 2018 Feb 16.

Abstract

Sulfur(VI) Fluoride Exchange (SuFEx) is a new family of click chemistry transformations which relies on readily available materials to produce compounds bearing the S-F motif. The potential of SuFEx in drug discovery has just started to be explored. We report the first method of SuFEx chemistry for the conversion of phenolic compounds to their respective arylfluorosulfate derivatives in situ in 96-well plates. This method is compatible with automated synthesis and screening to quickly assess the biological activities of the in situ generated, crude products. Using this method, we perform late-stage functionalization of a panel of known anticancer drugs to generate the corresponding arylfluorosulfates. These in situ generated arylfluorosulfates are directly tested in a cancer-cell growth inhibition assay in parallel with their phenolic precursors. We discover three arylfluorosulfates that exhibit improved anticancer cell proliferation activities compared to their phenol precursors. Among these three compounds, the fluorosulfate derivative of Fulvestrant possesses significantly enhanced activity to down-regulate estrogen receptor (ER) expression in ER breast cancer cell line MCF-7 and the fluorosulfate derivative of Combretastatin A4-a general anticancer drug currently being evaluated under clinical trials-exhibits a 70-fold increase in potency in the drug resistant colon cancer cell line HT-29.

摘要

硫(VI)氟交换(SuFEx)是一类新型点击化学转化反应,它依赖于易得的材料来生成含有 S-F 键的化合物。SuFEx 在药物研发中的应用潜力才刚刚开始被探索。我们报道了首例 SuFEx 化学方法,可在 96 孔板中就地将酚类化合物转化为其相应的芳基氟硫酸酯衍生物。该方法与自动化合成和筛选兼容,可快速评估原位生成的粗产物的生物学活性。使用该方法,我们对一组已知的抗癌药物进行了晚期的功能化,生成了相应的芳基氟硫酸酯。这些原位生成的芳基氟硫酸酯与它们的酚前体一起在癌细胞生长抑制测定中进行平行测试。我们发现三种芳基氟硫酸酯与它们的酚前体相比,具有改善的抗癌细胞增殖活性。在这三种化合物中,氟硫酸酯衍生物 Fulvestrant 在 ER 阳性乳腺癌细胞系 MCF-7 中对雌激素受体(ER)表达的下调作用显著增强,而 Combretastatin A4 的氟硫酸酯衍生物(一种正在临床试验中评估的广谱抗癌药物)在耐药性结肠癌细胞系 HT-29 中的效力提高了 70 倍。

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