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Enantiomeric separation of thiourea derivatives of naringenin on amylose and cellulose polymeric chromatographic chiral columns.
Ali, Imran; Nabti, Rekia; Belboukhari, Nasser; Sekkoum, Khaled; Zaid, Mohammed El Amin; Kraim, Khairedine; ALOthman, Zeid A; Locatelli, Marcello; Demir, Ersin.
Afiliação
  • Ali I; Department of Chemistry, Jamia Millia Islamia (Central University), New Delhi, India.
  • Nabti R; Bioactive Molecules and Chiral Separation Laboratory, Faculty of Exact Sciences, Tahri Mohammed's University, Béchar, Algeria.
  • Belboukhari N; Bioactive Molecules and Chiral Separation Laboratory, Faculty of Exact Sciences, Tahri Mohammed's University, Béchar, Algeria.
  • Sekkoum K; Bioactive Molecules and Chiral Separation Laboratory, Faculty of Exact Sciences, Tahri Mohammed's University, Béchar, Algeria.
  • Zaid MEA; Bioactive Molecules and Chiral Separation Laboratory, Faculty of Exact Sciences, Tahri Mohammed's University, Béchar, Algeria.
  • Kraim K; Higher Normal School of Technological Education of Skikda (ENSET), Skikda, Algeria.
  • ALOthman ZA; Department of Chemistry, College of Science, King Saud University, Riyadh, Saudi Arabia.
  • Locatelli M; Department of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Chieti, Italy.
  • Demir E; Faculty of Pharmacy, Department of Analytical Chemistry, Afyonkarahisar Health Sciences University, Afyonkarahisar, Turkey.
Chirality ; 36(3): e23659, 2024 Mar.
Article em En | MEDLINE | ID: mdl-38445305
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Flavanonas / Hexanos / Amilose Idioma: En Revista: Chirality Assunto da revista: BIOLOGIA MOLECULAR / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Flavanonas / Hexanos / Amilose Idioma: En Revista: Chirality Assunto da revista: BIOLOGIA MOLECULAR / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Índia País de publicação: Estados Unidos