Enantiomeric separation of thiourea derivatives of naringenin on amylose and cellulose polymeric chromatographic chiral columns

IF 2.8 4区 化学 Q2 CHEMISTRY, ANALYTICAL Chirality Pub Date : 2024-03-06 DOI:10.1002/chir.23659
Imran Ali, Rekia Nabti, Nasser Belboukhari, Khaled Sekkoum, Mohammed El Amin Zaid, Khairedine Kraim, Zeid A. ALOthman, Marcello Locatelli, Ersin Demir
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Abstract

Due to a great demand for amylose and cellulose polymeric chromatographic chiral columns, the enantiomeric separation of thiourea derivatives of naringenin was achieved on the different amylose (Chiralpak-IB) and cellulose chiral (Chiralcel-OJ and Chiralcel-OD-3R) columns with varied chromatographic conditions. The isocratic mobile phases used were ethanol and methanol, where ethanol/hexane and methanol/hexane were used as gradient mode and were prepared in volume/volume relation. The separation and resolution factors for all the enantiomers were in the range of 1.25 to 3.47 and 0.48 to 1.75, respectively. The enantiomeric resolution was obtained within 12 min making fast separation. The docking studies confirmed the chiral recognition mechanisms with binding affinities in the range of −4.7 to −5.7 kcal/mol. The reported compounds have good anticoagulant activities and may be used as anticoagulants in the future. Besides, chiral separation is fast and is useful for enantiomeric separation in any laboratory in the world.

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在淀粉和纤维素聚合物色谱手性柱上分离柚皮苷硫脲衍生物的对映体。
由于对直链淀粉和纤维素聚合物色谱手性色谱柱的需求量很大,本研究采用不同的直链淀粉色谱柱(Chiralpak-IB)和纤维素手性色谱柱(Chiralcel-OJ 和 Chiralcel-OD-3R),在不同的色谱条件下实现了柚皮苷硫脲衍生物对映体的分离。使用的等度流动相为乙醇和甲醇,其中乙醇/正己烷和甲醇/正己烷为梯度模式,以体积/容积关系制备。所有对映体的分离度和分辨度分别为 1.25 至 3.47 和 0.48 至 1.75。对映体在 12 分钟内就得到了快速分离。对接研究证实了手性识别机制,其结合亲和力在 -4.7 至 -5.7 kcal/mol 之间。所报告的化合物具有良好的抗凝活性,将来可用作抗凝剂。此外,手性分离速度快,可用于世界上任何实验室的对映体分离。
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来源期刊
Chirality
Chirality 医学-分析化学
CiteScore
4.40
自引率
5.00%
发文量
124
审稿时长
1 months
期刊介绍: The main aim of the journal is to publish original contributions of scientific work on the role of chirality in chemistry and biochemistry in respect to biological, chemical, materials, pharmacological, spectroscopic and physical properties. Papers on the chemistry (physiochemical, preparative synthetic, and analytical), physics, pharmacology, clinical pharmacology, toxicology, and other biological aspects of chiral molecules will be published.
期刊最新文献
Issue Information Chiral Differentiation of Chiral Lactides and Chiral Diketones on Native and Phenylcarbamoylated Cyclodextrin Chiral Stationary Phases Multiwavelength Optical Rotation Detection: An Effective Approach for the Recognition of Analytical and Semi-Preparative HPLC Enantioseparation of the Chiral Pheromone Olean and Its Stereochemical Characterization Emergence of Optical Activity and Surface Morphology Changes in Racemic Amino Acid Films Under Circularly Polarized Lyman-α Light Irradiation Proceedings From 33rd Symposium on Chirality 2023, Rome, Italy
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