奎宁酸二咖啡酯和二烯丙酯抗hsv -1及抗氧化活性

Celso O. Rezende Jr. , Caroline Rigotto , Wiliam Caneschi , Carlos A.M. Rezende , Mireille Le Hyaric , Mara R.C. Couri , Cláudia M.O. Simões , Mauro V. de Almeida
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引用次数: 9

摘要

合成了9种咖啡酸和没食子酸衍生物,并利用DPPH自由基清除活性测定法评估了它们的抗氧化活性和对HSV-1的抗疱疹活性。所有化合物的抗氧化活性均高于α-生育酚。化合物8的抗氧化活性最高(IC50 = 177 μM)。5个化合物(7、10、11、12和14)具有抗hsv -1活性,选择性指数在7.0 ~ 27.1之间。活性最高的是化合物10 (IC50 = 15.2 μM;si = 27.1)。
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Anti-HSV-1 and antioxidant activities of dicaffeoyl and digalloyl esters of quinic acid

Nine caffeic and gallic acids derivatives were synthesized and evaluated for their antioxidant activity using the DPPH radical scavenging activity assay and for their antiherpes activity against HSV-1. All compounds displayed higher antioxidant activities than α-tocopherol. The most active antioxidant was compound 8 (IC50 = 177 μM). Five compounds (7, 10, 11, 12 and 14) were found to possess anti-HSV-1 activity with selectivity indices values ranging from 7.0 to 27.1. The most active was compound 10 (IC50 = 15.2 μM; SI = 27.1).

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