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来自……地上部分的化学成分。 你提供的原文似乎不完整,“.”处应该有具体植物名称等信息。

Chemical constituents from aerial parts of .

作者信息

Yang Yingbo, Han Zhuzhen, Tian Tong, Liao Qi, Geng Jiaran, Xiao Ying

机构信息

The SATCM Key Laboratory for New Resources & Quality Evaluation of Chinese Medicine, Institute of Chinese Materia Medica, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China.

Jiangsu Kanion Pharmaceutical Co., Ltd., Lianyungang 222000, China.

出版信息

Chin Herb Med. 2022 Oct 14;15(1):151-154. doi: 10.1016/j.chmed.2021.12.007. eCollection 2023 Jan.

Abstract

OBJECTIVE

To study the chemical constituents from the aerial parts of .

METHODS

Various chromatographic techniques were used to separate the constituents and their structures were elucidated using spectroscopic methods and by comparing their data to those reported in the literatures. The -glucosidase inhibitory activity assay was used to identify potential -glucosidase inhibitors.

RESULTS

Nine compounds were isolated from the aerial parts of . Their structures were identified as Scoparic zolone (), (2)-2,7-dihydroxy-2-1,4-benzoxazin-3(4)-one (), (2)-7-hydroxy-2-1,4-benzoxazin-3(4)-one-2----glucopyranoside (), (2)-7-methoxy-2-1,4-benzoxazin-3(4)-one-2----glucopyranoside (), (2)-7-hydroxy-2-1,4-benzoxazin-3(4)-one-2----glucopyranoside (), 6-methoxy-benzoxazolin-2(3)-one (), 4-acetonyl-3,5-dimethoxy--quinol (), zizyvoside I (), and 3,4-dihydroxy benzeneacetic acid (). Compound showed the potent α-glucosidase inhibitory activity with an IC value of (132.8 ± 11.5) μmol/L, which is 28-fold higher than the positive control acarbose.

CONCLUSION

Compound is a new natural product. Compounds and have not been reported in Scoparia before. Compounds , , , are isolated from Scrophulariaceae for the first time.

摘要

目的

研究[植物名称]地上部分的化学成分。

方法

采用多种色谱技术分离成分,并通过光谱方法以及与文献报道数据对比来阐明其结构。采用α - 葡萄糖苷酶抑制活性测定法来鉴定潜在的α - 葡萄糖苷酶抑制剂。

结果

从[植物名称]地上部分分离得到9种化合物。其结构分别鉴定为异泽兰酮()、(2)-2,7 - 二羟基 - 2H - 1,4 - 苯并恶嗪 - 3(4H)- 酮()、(2)-7 - 羟基 - 2H - 1,4 - 苯并恶嗪 - 3(4H)- 酮 - 2 - O - β - D - 吡喃葡萄糖苷()、(2)-7 - 甲氧基 - 2H - 1,4 - 苯并恶嗪 - 3(4H)- 酮 - 2 - O - β - D - 吡喃葡萄糖苷()、(2)-7 - 羟基 - 2H - 1,4 - 苯并恶嗪 - 3(4H)- 酮 - 2 - O - β - D - 吡喃葡萄糖苷()、6 - 甲氧基 - 苯并恶唑啉 - 2(3H)- 酮()、4 - 丙酮基 - 3,5 - 二甲氧基 - β - 喹啉()、紫堇苷I()和3,4 - 二羟基苯乙酸()。化合物[具体化合物编号]表现出较强的α - 葡萄糖苷酶抑制活性,IC50值为(132.8 ± 11.5) μmol/L,比阳性对照阿卡波糖高28倍。

结论

化合物[具体化合物编号]是一种新的天然产物。化合物[具体化合物编号]和[具体化合物编号]在之前的母草属植物中未见报道。化合物[具体化合物编号]、[具体化合物编号]、[具体化合物编号]、[具体化合物编号]首次从玄参科植物中分离得到。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6cde/9975620/8dbef12864b3/gr1.jpg

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