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

Author:

Ali Imran1ORCID,Nabti Rekia2,Belboukhari Nasser2,Sekkoum Khaled2ORCID,Zaid Mohammed El Amin2,Kraim Khairedine3,ALOthman Zeid A.4ORCID,Locatelli Marcello5,Demir Ersin6ORCID

Affiliation:

1. Department of Chemistry Jamia Millia Islamia (Central University) New Delhi India

2. Bioactive Molecules and Chiral Separation Laboratory, Faculty of Exact Sciences Tahri Mohammed's University Béchar Algeria

3. Higher Normal School of Technological Education of Skikda (ENSET) Skikda Algeria

4. Department of Chemistry, College of Science King Saud University Riyadh Saudi Arabia

5. Department of Pharmacy University “G. d'Annunzio” of Chieti‐Pescara Chieti Italy

6. Faculty of Pharmacy, Department of Analytical Chemistry Afyonkarahisar Health Sciences University Afyonkarahisar Turkey

Abstract

AbstractDue 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.

Funder

King Saud University

Publisher

Wiley

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