H. Xu, Jin Zhe, Si-Jie Liu
Jul 1, 2012
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Influential Citations
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Quality indicators
Journal
Chinese Chemical Letters
Abstract
Abstract Bromination is used as a strategy to improve biological activity in medicinal chemistry. In order to study on the structure–activity relationships of the novel acetylcholinesterase inhibitors with 7 H -thiazolo[3,2- b ]-1, 2, 4-triazin-7-one scaffold, based on our previous work and molecular modeling, a series of novel 3-aryl-6-(bromoarylmethyl)-7 H -thiazolo[3,2- b ]-1, 2, 4-triazin-7-one derivatives were designed by molecular docking, synthesized and characterized by mass spectra, infrared spectra, proton NMR and elemental analyses. The study of AChE inhibitory activity was carried out using the Ellman colorimetric assay with huperzine-A as the positive control. Most of all target compounds exhibited more than 45% inhibition at 10 μmol/L. The preliminary structure–activity relationship was the bromine atoms and the hydroxyl group at the phenyl ring at the C6 position of the parent nucleus played significant roles in the AChE inhibitory activity of the target compounds.