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首页> 外文期刊>Organic & biomolecular chemistry >Regioselective and enantiospecific synthesis of the HSP co-inducer arimoclomol from chiral glycidyl derivatives
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Regioselective and enantiospecific synthesis of the HSP co-inducer arimoclomol from chiral glycidyl derivatives

机译:从手性缩水甘油基衍生物合成HSP协同诱导剂阿莫洛莫的区域选择性和对映体特异性

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摘要

A new efficient chiral synthesis of enantiopure arimoclomol (2) is reported from (R)-(-)-glycidyl nosylate (11) with complete retention of chiral integrity. Off-target pharmacology of arimoclomol (2) was evaluated against a representative set of drug targets and showed modest binding to a few kinases. Pharmacokinetic data was generated in vivo in mouse and showed a low brain:plasma ratio. These studies will be helpful towards a better understanding of the PK-PD relationship of 2 in disease models.
机译:从(R)-(-)-羟基乙酸缩水甘油基酯(11)报道了对映体纯的阿莫氯酚(2)的一种新的有效手性合成方法,该方法完全保留了手性完整性。针对一组代表性的药物靶标评估了arimoclomol(2)的脱靶药理学,并显示了与几种激酶的适度结合。在小鼠体内产生了药代动力学数据,并且显示出较低的脑:血浆比例。这些研究将有助于更好地了解疾病模型中2的PK-PD关系。

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  • 来源
    《Organic & biomolecular chemistry》 |2017年第46期|9794-9799|共6页
  • 作者单位

    Alzheimer's Research UK UCL Drug Discovery Institute, Cruciform Building, University College London, Gower Street, London, United Kingdom;

    Alzheimer's Research UK UCL Drug Discovery Institute, Cruciform Building, University College London, Gower Street, London, United Kingdom;

    Alzheimer's Research UK UCL Drug Discovery Institute, Cruciform Building, University College London, Gower Street, London, United Kingdom;

    Alzheimer's Research UK UCL Drug Discovery Institute, Cruciform Building, University College London, Gower Street, London, United Kingdom;

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