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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >SYNTHESES AND ANTICHOLINESTERASE ACTIVITIES OF NOVEL 3-AMINOCARBONYLMETHYLENE-3-METHYL-2,3-DIHYDROBENZOFURAN-5-YL CARBAMATES
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SYNTHESES AND ANTICHOLINESTERASE ACTIVITIES OF NOVEL 3-AMINOCARBONYLMETHYLENE-3-METHYL-2,3-DIHYDROBENZOFURAN-5-YL CARBAMATES

机译:新型3-氨基羰基亚甲基-3-甲基-2,3-二羟基苯并呋喃-5-基氨基甲酸酯的合成及抗胆碱酯酶活性

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摘要

Novel carbamates 4 and 5 were synthesized from starting material 5-hydroxy-3-methyl-3H-benzofuran-2-one,17.The acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory activities of 4 and 5 were determined against fresh human enzyme,are in the realm of clinically valuable compounds and are discussed.In addition,the reductive properties of the 2-carbonyl group of 3H-benzofuran-2-one,possessing an unsaturated substituted group in its 3 position (9,11 and 14),were studied.
机译:由原料5-羟基-3-甲基-3H-苯并呋喃-2-酮17合成了新型氨基甲酸酯4和5。确定了4和5对新鲜人类酶的乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BChE)抑制活性。此外,还讨论了3H-苯并呋喃-2-酮的2-羰基的还原特性,在其3位上具有不饱和取代基(9,11和14)被研究。

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