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首页> 外文期刊>Molecules >Synthesis and Biological Evaluation of Benzochromenopyrimidinones as Cholinesterase Inhibitors and Potent Antioxidant, Non-Hepatotoxic Agents for Alzheimer’s Disease
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Synthesis and Biological Evaluation of Benzochromenopyrimidinones as Cholinesterase Inhibitors and Potent Antioxidant, Non-Hepatotoxic Agents for Alzheimer’s Disease

机译:苯并色素嘧啶酮类化合物作为胆碱酯酶抑制剂和有效的抗氧化剂,非肝毒性药物的合成和生物学评估

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摘要

We report herein the straightforward two-step synthesis and biological assessment of novel racemic benzochromenopyrimidinones as non-hepatotoxic, acetylcholinesterase inhibitors with antioxidative properties. Among them, compound 3Bb displayed a mixed-type inhibition of human acetylcholinesterase (IC 50 = 1.28 ± 0.03 μM), good antioxidant activity, and also proved to be non-hepatotoxic on human HepG2 cell line.
机译:我们在这里报告了简单的两步合成和新的外消旋苯并二甲氧基嘧啶酮作为具有抗氧化特性的非肝毒性,乙酰胆碱酯酶抑制剂的生物学评估。其中,化合物3Bb表现出对人乙酰胆碱酯酶的混合型抑制(IC 50 = 1.28±0.03μM),良好的抗氧化活性,并且还被证明对人HepG2细胞无肝毒性。

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