Tetrasaccharide Resin Glycosides with Nitric Oxide Production Inhibitory Activity from <i>Cuscuta campestris</i>

LC-HRMS/MS-based molecular-network-guided chemical investigation of <i>Cuscuta campestris</i> led to the isolation of seven undescribed tetrasaccharide-type resin glycosides (<b>1</b>-<b>7</b>). Their structures were elucidated using 1D and 2D NMR and HRESIMS analysis. Isolated resin glycosides were comprised of d-glucose, d-fucose, d-quinovose, and l-rhamnose, and these monosaccharides were partially acylated with acetyl, isobutyryl, <i>n</i>-hexanoyl, and niloyl organic acids. The absolute configuration of aglycones were determined as <i>S</i>-configuration using Mosher's method after acid hydrolysis of resin glycoside fraction. All compounds were evaluated for their inhibitory activity against the production of nitric oxide in RAW 264.7 cells. Compounds <b>2</b> and <b>3</b> exhibited inhibitory activity, with IC<sub>50</sub> values of 14.3 and 10.4 μM, respectively.

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Publication Details

Journal
Journal of Natural Products
Published
2025-09-09
DOI
https://doi.org/10.1021/acs.jnatprod.5c00713
Primary Topic
Natural product bioactivities and synthesis
Type
article
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article

Tetrasaccharide Resin Glycosides with Nitric Oxide Production Inhibitory Activity from Cuscuta campestris

Jae Sang Han, Bang Yeon Hwang, Jin‐Young Jang, Jin Woo Lee et al.
Journal of Natural Products
Natural product bioactivities and synthesis
article

Tetrasaccharide Resin Glycosides with Nitric Oxide Production Inhibitory Activity from Cuscuta campestris

Jae Sang Han, Bang Yeon Hwang, Jin‐Young Jang, Jin Woo Lee, Dongho Lee, Mi Kyeong Lee, Yong Beom Cho, Jun Gu Kim, Vu Quan Dang
article en

Abstract

LC-HRMS/MS-based molecular-network-guided chemical investigation of <i>Cuscuta campestris</i> led to the isolation of seven undescribed tetrasaccharide-type resin glycosides (<b>1</b>-<b>7</b>). Their structures were elucidated using 1D and 2D NMR and HRESIMS analysis. Isolated resin glycosides were comprised of d-glucose, d-fucose, d-quinovose, and l-rhamnose, and these monosaccharides were partially acylated with acetyl, isobutyryl, <i>n</i>-hexanoyl, and niloyl organic acids. The absolute configuration of aglycones were determined as <i>S</i>-configuration using Mosher's method after acid hydrolysis of resin glycoside fraction. All compounds were evaluated for their inhibitory activity against the production of nitric oxide in RAW 264.7 cells. Compounds <b>2</b> and <b>3</b> exhibited inhibitory activity, with IC<sub>50</sub> values of 14.3 and 10.4 μM, respectively.

Journal of Natural ProductsVol. 88(9)
Chungbuk National University (KR), Korea University (KR), Department of Biotechnology (IN), Institute of Plant Biology and Biotechnology (KZ), Drug Discovery Laboratory (Norway) (NO), Duksung Women's University (KR)
Openalex Percentile: Top 79%
Natural product bioactivities and synthesis
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