Theoretical and Molecular Docking Study of Ketoconazole on Heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin as Chiral Selector.

Abstract:

:A molecular docking study, using molecular mechanics calculations with AutoDock and semi-empirical PM3 calculations, was used to predict the enantiodiscrimination of heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin (TMβCD) and ketoconazole (KTZ) enantiomers. A Density Functional Theory (DFT) single-point calculation at the level of B3LYP/6-311G (d,p) was performed for the PM3-optimized complexes to obtain more accurate binding energy and the electronic structures of the complexes. The difference in energies of the inclusion complexes between the KTZ enantiomers and TMβCD is probably a measure of chiral discrimination, which results in the separation of the enantiomers as observed in the experimental studies.

journal_name

Chirality

journal_title

Chirality

authors

Arsad SR,Maarof H,Wan Ibrahim WA,Aboul-Enein HY

doi

10.1002/chir.22554

subject

Has Abstract

pub_date

2016-03-01 00:00:00

pages

209-14

issue

3

eissn

0899-0042

issn

1520-636X

journal_volume

28

pub_type

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