1. Synthesis, crystal structure and biological evaluation of novel 2-phenylthiazole derivatives as butyrylcholinesterase inhibitors.
- Author
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Da-Hua Shi, Xiao-Dong Ma, Yu-Wei Liu, Wei Min, Fu-Jun Yin, Zong-Ming Tang, Meng-Qiu Song, Chen Lu, Xiao-Kai Song, Wei-Wei Liu, and Tong Dong
- Subjects
PHENYL compounds ,THIAZOLE derivatives ,CRYSTAL structure ,BUTYRYLCHOLINESTERASE ,NUCLEAR magnetic resonance ,CHOLINESTERASE inhibitors - Abstract
To find novel butyrylcholinesterase inhibitors, three novel 2-phenylthiazole derivatives were synthesised. The synthesised compounds were characterised by NMR and single-crystal X-ray diffraction analysis. Hirshfeld surface analysis and two-dimensional fingerprint plots of the compounds were used as a theoretical approach to assess the driving force for crystal structure formation via the intermolecular interactions in the crystal lattices of the synthesised compounds. Among the three compounds, N-(1,5-dimethyl-3-oxo-2-phenyl-2,3- dihydro- 1H-pyrazol-4-yl)-2-(4-methoxyphenyl)thiazole-4-carboxamide showed the best butyrylcholinesterase-inhibition activity with an IC
50 value of 75.12 µM. A docking study demonstrated that this compound interacts with the peripheral anionic site of butyrylcholinesterase. [ABSTRACT FROM AUTHOR]- Published
- 2018
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