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卷柏黄酮A - F,从江南卷柏中分离得到的六种新型黄酮类化合物。

Seladoeflavones A-F, six novel flavonoids from Selaginella doederleinii.

作者信息

Zou ZhenXing, Xu KangPing, Xu PingSheng, Li XiaoMin, Cheng Fei, Li Jing, Yu Xia, Cao DongSheng, Li Dan, Zeng Wei, Zhang GuoGang, Tan GuiShan

机构信息

Xiangya Hospital of Central South University, Changsha 410008, PR China; School of Pharmaceutical Sciences, Central South University, Changsha 410013, PR China.

School of Pharmaceutical Sciences, Central South University, Changsha 410013, PR China.

出版信息

Fitoterapia. 2017 Jan;116:66-71. doi: 10.1016/j.fitote.2016.11.014. Epub 2016 Nov 24.

Abstract

Six new flavonoids, seladoeflavones A-F (1-6), were isolated from the whole herbs of Selaginella doederleinii, together with one known flavonoid (7). Their structures including absolute configuration were characterized on the basis of extensive spectroscopic methods including NMR, HRMS, and electronic circular dichroism (ECD). All compounds consist of an aryl substituent at the C-3' position of naringenin or apigenin skeletons, and compounds 1 and 6 were identified as R configurations, which are uncommonly encountered in nature. A possible biosynthetic pathway was postulated. In addition, bioassay of the isolates revealed that 5-7 exhibited moderate cytotoxicity against three human cancer cell lines NCI-H460, A549, and K562 in vitro with IC values ranging from 8.17 to 18.66μM.

摘要

从江南卷柏全草中分离得到6个新黄酮类化合物,即江南卷柏黄酮A-F(1-6),以及1个已知黄酮类化合物(7)。通过核磁共振(NMR)、高分辨质谱(HRMS)和电子圆二色光谱(ECD)等多种光谱方法对其结构包括绝对构型进行了表征。所有化合物在柚皮素或芹菜素骨架的C-3'位均有一个芳基取代基,化合物1和6被鉴定为R构型,这在自然界中并不常见。推测了一条可能的生物合成途径。此外,对分离物的生物活性测定表明,5-7对三种人癌细胞系NCI-H460、A549和K562在体外表现出中等细胞毒性,IC值范围为8.17至18.66μM。

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