Istituto Superiore di Sanità, Dipartimento del Farmaco, Rome, Italy.
J Chromatogr A. 2011 Nov 18;1218(46):8394-8. doi: 10.1016/j.chroma.2011.09.052. Epub 2011 Sep 24.
In this work, we report on the difference in performance of the two 3 μm particle-based Chiralpak IA-3 and Chiralpak AD-3 chiral stationary phases (CSPs) in the direct resolution of four racemic cinnamyl 2-aminoanilides, endowed with histone deacetylase inhibitory activity. The 3 μm CSPs were explored to determine if they could provide an effective resolution of enantiomers in presence of alcoholic eluents such as pure methanol, ethanol and 2-propanol. Temperature variable enantioselective HPLC and subsequent van't Hoff analysis were performed. In most of cases the van't Hoff plots were found to show a non-linear behaviour. The knowledge of the enantiomeric elution order associated with the data coming from enantioselective HPLC permitted to advance some hypothesis about the groups involved in chiral recognition mechanism.
在这项工作中,我们报告了两种基于 3μm 颗粒的手性固定相 Chiralpak IA-3 和 Chiralpak AD-3 在直接拆分具有组蛋白去乙酰化酶抑制活性的四种外消旋肉桂基 2-氨基苯甲酰胺中的性能差异。我们研究了 3μm CSP 是否可以在甲醇、乙醇和异丙醇等醇类洗脱剂存在的情况下提供对对映异构体的有效分离。进行了温度可变的对映选择性 HPLC 实验,并随后进行了范特霍夫分析。在大多数情况下,发现范特霍夫图呈非线性。与手性高效液相色谱数据相关的对映体洗脱顺序的知识使我们能够提出一些关于手性识别机制中涉及的基团的假设。