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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Exploration of liquid and supercritical fluid chromatographic chiral separation and purification of Nutlin-3--a small molecule antagonist of MDM2.
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Exploration of liquid and supercritical fluid chromatographic chiral separation and purification of Nutlin-3--a small molecule antagonist of MDM2.

机译:Nutlin-3--MDM2的小分子拮抗剂的液相和超临界液相色谱手性分离与纯化研究。

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摘要

Inhibition of the MDM2-p53 interaction can stabilize the p53 protein and offer a novel strategy for cancer therapy. The imidazoline compound (Nutlin-3) is a promising small molecule antagonist of the MDM2-p53 interaction. This compound was synthesized as a racemic mixture, and one enantiomer is 100-200-fold more active than the other enantiomer. In this study, various enantiomeric separation approaches were explored to resolve the Nutlin-3 enantiomers using chiral supercritical fluid chromatography (SFC) as well as chiral liquid chromatography (LC) under normal phase mode, reversed phase mode and polar organic phase mode. The chiral SFC method based on Chiralcel OD column showed superior separation in terms of selectivity and efficiency. Optimization of the chiral separation method enabled high throughput preparative scale purification. Ultimately, 5 g of racemic mixture were purified on Prep-SFC in 75 min with the recovery rate above 92%.
机译:MDM2-p53相互作用的抑制可以稳定p53蛋白,并为癌症治疗提供了一种新的策略。咪唑啉化合物(Nutlin-3)是MDM2-p53相互作用的有希望的小分子拮抗剂。该化合物以外消旋混合物形式合成,一种对映异构体的活性比另一种对映异构体高100-200倍。在这项研究中,探索了各种对映体分离方法,以在正相模式,反相模式和极性有机相模式下使用手性超临界流体色谱(SFC)和手性液相色谱(LC)拆分Nutlin-3对映体。基于Chiralcel OD柱的手性SFC方法在选择性和效率方面显示出优异的分离效果。手性分离方法的优化实现了高通量制备规模的纯化。最终,在Prep-SFC上于75分钟内纯化了5 g外消旋混合物,回收率超过92%。

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