A series of novel polymethoxyflavone Marmich base derivatives 1--8 was synthesized by Mannich reaction of 5-hydroxy-3,7,3＇,4＇-tetramethoxyflavone 9 with various secondary aliphatic amines and formaldehyde. Their ace...A series of novel polymethoxyflavone Marmich base derivatives 1--8 was synthesized by Mannich reaction of 5-hydroxy-3,7,3＇,4＇-tetramethoxyflavone 9 with various secondary aliphatic amines and formaldehyde. Their acetylcholmesterase（AChE） inhibitory activities were evaluated. The results showed that most of them exhibited AChE inhibitory activity and especially piperidin-l-yl methyl substituent derivative 5（IC50=0.238 μmol/L） demon- strated stronger activity comparable with the positive control, neoeserinemethyl sulfate（IC50=1.39 μmol/L）, which is worthy of further development as an agent for Alzheimer＇s disease treatment.展开更多
基金Supported by the National Natural Science Foundation of China（No.J1210040） and the Hunan Provincial Natural Science Foundation, China（No. 14JJ2048）.
文摘A series of novel polymethoxyflavone Marmich base derivatives 1--8 was synthesized by Mannich reaction of 5-hydroxy-3,7,3＇,4＇-tetramethoxyflavone 9 with various secondary aliphatic amines and formaldehyde. Their acetylcholmesterase（AChE） inhibitory activities were evaluated. The results showed that most of them exhibited AChE inhibitory activity and especially piperidin-l-yl methyl substituent derivative 5（IC50=0.238 μmol/L） demon- strated stronger activity comparable with the positive control, neoeserinemethyl sulfate（IC50=1.39 μmol/L）, which is worthy of further development as an agent for Alzheimer＇s disease treatment.
