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江南卷柏中抑制黄嘌呤氧化酶的生物活性化合物。

Bioactive compounds of inhibiting xanthine oxidase from Selaginella labordei.

作者信息

Tan Wen-Jie, Xu Jia-Cheng, Li Li, Chen Ke-Li

机构信息

Hubei College of Traditional Chinese Medicine, Wuhan, P.R. China.

出版信息

Nat Prod Res. 2009;23(4):393-8. doi: 10.1080/14786410802228736.

Abstract

Four flavone compounds were isolated from the effective fractions inhibiting xanthine oxidase (XOD) of the medicinal plant Selaginella labordei with anti-virus activity, and the structures were elucidated as 4'-methylether robustaflavone (1), robustaflavone (2), eriodictyol (3) and amentoflavone (4). The 50% inhibitory concentration (IC(50)) of the three compounds of inhibiting XOD were 61.0, 0.199, 16.0 and 32.0 mg L(-1), respectively. All of these compounds were isolated from the species for the first time, and eriodictyol was found from Selaginellaceae for the first time. Among these compounds, robustaflavone has been reported as an effective compound against the hepatitis B virus.

摘要

从具有抗病毒活性的药用植物江南卷柏中分离出了四种黄酮化合物,这些化合物能抑制黄嘌呤氧化酶(XOD),其结构被鉴定为4'-甲基醚粗壮黄酮(1)、粗壮黄酮(2)、圣草酚(3)和穗花杉双黄酮(4)。这三种化合物抑制XOD的半数抑制浓度(IC50)分别为61.0、0.199、16.0和32.0 mg L(-1)。所有这些化合物均为首次从该物种中分离得到,圣草酚也是首次在卷柏科植物中发现。在这些化合物中,粗壮黄酮已被报道为一种抗乙型肝炎病毒的有效化合物。

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