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刺桐茎皮中的具有抗诱变作用的异戊烯基黄酮类化合物。

Antigenotoxic prenylated flavonoids from stem bark of Erythrina latissima.

作者信息

Zarev Yancho, Foubert Kenn, Lucia de Almeida Vera, Anthonissen Roel, Elgorashi Esameldin, Apers Sandra, Ionkova Iliana, Verschaeve Luc, Pieters Luc

机构信息

Natural Products & Food Research and Analysis (NatuRA), Department of Pharmaceutical Sciences, University of Antwerp, Universiteitsplein 1, 2610, Antwerp, Belgium; Department of Pharmacognosy, Faculty of Pharmacy, Medical University - Sofia, Str. Dunav 2, 1000, Sofia, Bulgaria.

Natural Products & Food Research and Analysis (NatuRA), Department of Pharmaceutical Sciences, University of Antwerp, Universiteitsplein 1, 2610, Antwerp, Belgium.

出版信息

Phytochemistry. 2017 Sep;141:140-146. doi: 10.1016/j.phytochem.2017.06.003. Epub 2017 Jun 12.

Abstract

A series of prenylated flavonoids was obtained from antigenotoxic extracts and fractions of stem bark of Erythrina latissima E. Mey (Leguminosae). In addition to five constituents never reported before, i.e. (2S)-5,7-dihydroxy-2-(4-hydroxy-2-(prop-1-en-2-yl)-2,3-dihydrobenzofuran-6-yl)chroman-4-one (erylatissin D), (2S)-5,7-dihydroxy-2-(4-methoxy-2-(prop-1-en-2-yl)-2,3-dihydrobenzofuran-6-yl)chroman-4-one (erylatissin E), 5,7-dihydroxy-3-(4-methoxy-2-(prop-1-en-2-yl)-2,3-dihydrobenzofuran-6-yl)-4H-chromen-4-one (erylatissin F), (2S)-5,7,8'-trihydroxy-2',2'-dimethyl-[2,6'-bichroman]-4-one (erylatissin G) and (2S)-5,7-dihydroxy-8'-methoxy-2',2'-dimethyl-[2,6'-bichroman]-4-one (dihydroabyssinin I), 18 known flavonoids were identified. Evaluation of the antigenotoxic properties (against genotoxicity induced by aflatoxin B1, metabolically activated) in the Vitotox assay revealed that most flavonoids were active. Sigmoidin A and B showed the highest activity, with an IC value of 18.7 μg/mL, equivalent to that of curcumin (IC 18.4 μg/mL), used as a reference antigenotoxic compound.

摘要

从刺桐(豆科)茎皮的具有抗基因毒性的提取物和馏分中获得了一系列异戊烯基黄酮类化合物。除了之前从未报道过的5种成分,即(2S)-5,7-二羟基-2-(4-羟基-2-(丙-1-烯-2-基)-2,3-二氢苯并呋喃-6-基)苯并二氢吡喃-4-酮(刺桐素D)、(2S)-5,7-二羟基-2-(4-甲氧基-2-(丙-1-烯-2-基)-2,3-二氢苯并呋喃-6-基)苯并二氢吡喃-4-酮(刺桐素E)、5,7-二羟基-3-(4-甲氧基-2-(丙-1-烯-2-基)-2,3-二氢苯并呋喃-6-基)-4H-色原酮(刺桐素F)、(2S)-5,7,8'-三羟基-2',2'-二甲基-[2,6'-联苯并二氢吡喃]-4-酮(刺桐素G)和(2S)-5,7-二羟基-8'-甲氧基-2',2'-二甲基-[2,6'-联苯并二氢吡喃]-4-酮(二氢深渊菌素I)外,还鉴定出了18种已知的黄酮类化合物。在Votox试验中对抗黄曲霉毒素B1代谢活化诱导的基因毒性的抗基因毒性特性评估显示,大多数黄酮类化合物具有活性。西格莫定A和B表现出最高活性,IC值为18.7μg/mL,与用作参考抗基因毒性化合物的姜黄素(IC 18.4μg/mL)相当。

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