Phytochemicals, Two New Sulphur Glycosides and Two New Natural Products, from Shepherd’s Purse Seed and Their Activities

Two new sulfur glycosides, bursapastoris A-B (<b>3</b>-<b>4</b>), were extracted and isolated from shepherd's purse seed, along with two new natural products, 11-(methylsulfinyl)undecanoic acid (<b>2</b>) and 10-(methylsulfinyl)decanoic acid (<b>1</b>). Their structures were determined though infrared spectroscopy, one-dimensional nuclear magnetic resonance (<sup>1</sup>H and <sup>13</sup>C), and electrospray ionization mass spectrometry. Additionally, the structures of <b>3</b>-<b>4</b> were further identified by two-dimensional nuclear magnetic resonance (HMBC, HSQC, <sup>1</sup>H-<sup>1</sup>H COSY, and NOESY). Compounds <b>1</b>-<b>4</b> showed relatively favorable docking to NF-<i>κ</i>B. Unfortunately, we only discovered that compound <b>1</b>-<b>4</b> had weak anti-radiation activity at present. Therefore, further research regarding the biological activity of these organosulfur compounds is required at a later stage.

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Publication Details

Journal
Molecules
Published
2024-08-31
DOI
https://doi.org/10.3390/molecules29174145
Citations
1
Primary Topic
Phytochemicals and Antioxidant Activities
Type
article
Field-Weighted Citation Impact
0.22

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article

Phytochemicals, Two New Sulphur Glycosides and Two New Natural Products, from Shepherd’s Purse Seed and Their Activities

Zhen-Zhen Wei, Ti-Qiang Zhou, Shu‐Chen Liu, Bin Li et al.
1 citations
Molecules
Phytochemicals and Antioxidant Activities
0.22
article

Phytochemicals, Two New Sulphur Glycosides and Two New Natural Products, from Shepherd’s Purse Seed and Their Activities

Zhen-Zhen Wei, Ti-Qiang Zhou, Shu‐Chen Liu, Bin Li, Ying Tian, Chunbo Ge, Jianfeng Yi, Yujie Wang
article en
1 citations

Abstract

Two new sulfur glycosides, bursapastoris A-B (<b>3</b>-<b>4</b>), were extracted and isolated from shepherd's purse seed, along with two new natural products, 11-(methylsulfinyl)undecanoic acid (<b>2</b>) and 10-(methylsulfinyl)decanoic acid (<b>1</b>). Their structures were determined though infrared spectroscopy, one-dimensional nuclear magnetic resonance (<sup>1</sup>H and <sup>13</sup>C), and electrospray ionization mass spectrometry. Additionally, the structures of <b>3</b>-<b>4</b> were further identified by two-dimensional nuclear magnetic resonance (HMBC, HSQC, <sup>1</sup>H-<sup>1</sup>H COSY, and NOESY). Compounds <b>1</b>-<b>4</b> showed relatively favorable docking to NF-<i>κ</i>B. Unfortunately, we only discovered that compound <b>1</b>-<b>4</b> had weak anti-radiation activity at present. Therefore, further research regarding the biological activity of these organosulfur compounds is required at a later stage.

MoleculesVol. 29(17)
Jiangxi University of Traditional Chinese Medicine (CN), Beijing Institute of Technology (CN), Hebei University (CN)
China Postdoctoral Science Foundation, Jiangxi University of Traditional Chinese Medicine
Openalex Percentile: Top 54%
Phytochemicals and Antioxidant Activities
0.22
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