Design,synthesis characterization and in vitro biological activity of a series of 3-aryl-6-(bromoarylmethyl)-7H-thiazolo[3,2-b]-1,2,4-triazin-7-one derivatives as the novel acetylcholinesterase inhibitors |
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Authors: | He Nan Xua b Zhe Jinb Si Jie Liub Hong Min Liua Shuo Lic Huang Quan Linc David Chicheong Wanc Chun Hua b a New Drug Research & Development Center Zhengzhou University Zhengzhou China b |
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Affiliation: | New Drug Research & Development Center, Zhengzhou University, Zhengzhou 450052, China ; Key Laboratory of Structure-Based Drug Design & Discovery, Ministry of Education; Shenyang Pharmaceutical University, Shenyang 110016, China ; Department of Biochemistry, The Chinese University of Hong Kong, Hong Kong SAR, China |
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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 7H-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-(bromoarylrnethyl)-7H-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 10μmol/L.The preliminary structureactivity 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. |
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Keywords: | Acetylcholinesterase inhibitor Bromination Heterocycle Synthesis 7H-Thiazolo[3,2-b]-1,2,4-triazin-7-one derivatives |
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