Enantiomeric separation and molecular docking study of seven imidazole antifungal drugs on a cellulose tris-(3, 5-dimethylphenylcarbamate) chiral stationary phase. (20th October 2020)
- Record Type:
- Journal Article
- Title:
- Enantiomeric separation and molecular docking study of seven imidazole antifungal drugs on a cellulose tris-(3, 5-dimethylphenylcarbamate) chiral stationary phase. (20th October 2020)
- Main Title:
- Enantiomeric separation and molecular docking study of seven imidazole antifungal drugs on a cellulose tris-(3, 5-dimethylphenylcarbamate) chiral stationary phase
- Authors:
- Liu, Yanru
Cai, Liangzhao
Lun, Jia
Zhao, Min
Guo, Xingjie - Abstract:
- Abstract : Chiral separation and molecular docking study of seven imidazole antifungal drugs were performed on a cellulose tris-(3, 5-dimethylphenylcarbamate) chiral stationary phase (Chiralcel OD-RH). Abstract : The enantiomeric separation of seven imidazole antifungals was first systematically examined on a derivative polysaccharide chiral stationary phase (CSP), i.e. Chiralcel OD-RH in the reversed phase mode. The influence of the type and content of the organic modifier, the pH of buffer solution, type and concentration of buffer salt, and column temperature on enantiomeric separation were evaluated and optimized. The maximum resolution values for flutrimazole, econazole, miconazole, butoconazole, isoconazole, sulconazole, and climbazole were 2.36, 1.55, 0.89, 1.51, 0.96, 1.13, and 2.30. For a better understanding of the chiral recognition mechanism, detailed computational simulations of Chiralcel OD-RH interaction with seven pairs of enantiomers were carried out using the molecular docking software AutoDock. The various interactions affecting enantiomeric separation were confirmed in detail from the the molecular level. The modeling data were in agreement with the chromatographic results concerning enantioselectivity. It was found that the enantiomeric separation of imidazole analytes on Chiralcel OD-RH was the result of a mixture of hydrogen bonds, π–π, hydrophobic, dipole–dipole, and some special interactions. The docking results showed good agreement with ourAbstract : Chiral separation and molecular docking study of seven imidazole antifungal drugs were performed on a cellulose tris-(3, 5-dimethylphenylcarbamate) chiral stationary phase (Chiralcel OD-RH). Abstract : The enantiomeric separation of seven imidazole antifungals was first systematically examined on a derivative polysaccharide chiral stationary phase (CSP), i.e. Chiralcel OD-RH in the reversed phase mode. The influence of the type and content of the organic modifier, the pH of buffer solution, type and concentration of buffer salt, and column temperature on enantiomeric separation were evaluated and optimized. The maximum resolution values for flutrimazole, econazole, miconazole, butoconazole, isoconazole, sulconazole, and climbazole were 2.36, 1.55, 0.89, 1.51, 0.96, 1.13, and 2.30. For a better understanding of the chiral recognition mechanism, detailed computational simulations of Chiralcel OD-RH interaction with seven pairs of enantiomers were carried out using the molecular docking software AutoDock. The various interactions affecting enantiomeric separation were confirmed in detail from the the molecular level. The modeling data were in agreement with the chromatographic results concerning enantioselectivity. It was found that the enantiomeric separation of imidazole analytes on Chiralcel OD-RH was the result of a mixture of hydrogen bonds, π–π, hydrophobic, dipole–dipole, and some special interactions. The docking results showed good agreement with our experimental results. … (more)
- Is Part Of:
- New journal of chemistry. Volume 44:Number 42(2020)
- Journal:
- New journal of chemistry
- Issue:
- Volume 44:Number 42(2020)
- Issue Display:
- Volume 44, Issue 42 (2020)
- Year:
- 2020
- Volume:
- 44
- Issue:
- 42
- Issue Sort Value:
- 2020-0044-0042-0000
- Page Start:
- 18337
- Page End:
- 18346
- Publication Date:
- 2020-10-20
- Subjects:
- Chemistry -- Periodicals
Chimie -- Périodiques
540 - Journal URLs:
- http://www.rsc.org/ ↗
http://www.rsc.org/is/journals/current/newjchem/njc.htm ↗ - DOI:
- 10.1039/d0nj03657a ↗
- Languages:
- English
- ISSNs:
- 1144-0546
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6084.319900
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 14805.xml