Bioassay-Guided Isolation and Identification of Xanthine Oxidase Inhibitory Constituents from the Fruits of Chaenomeles speciosa (Sweet) Nakai

<i>Chaenomeles speciosa</i> (Sweet) Nakai (<i>C. speciosa</i>) is a traditional Chinese herbal medicine that possesses not only abundant nutritional value but also significant medicinal properties. The extracts of <i>C. speciosa</i> fruits effectively reduce urate levels, but the specific chemical constituents responsible for this effect in <i>C. speciosa</i> fruits are still unknown. Therefore, this study aims to investigate and analyze the structure-activity relationships of these constituents to better understand their ability to lower uric acid. Activity-guided fractionation and purification processes were used to isolate compounds with xanthine oxidase (XO) inhibitory activity from <i>C. speciosa</i> fruits, resulting in three extracts: petroleum ether, ethyl acetate, and <i>n</i>-butanol. The ethyl acetate and <i>n</i>-butanol fractions showed strong activity and underwent further separation and purification using chromatographic techniques. Twenty-four compounds were isolated and identified, with nine showing potent activity, including chlorogenic acid, methyl chlorogenate, butyl chlorogenate, ethyl chlorogenate, cryptochlorogenic acid methyl ester, caffeic acid, <i>p</i>-coumaric acid, benzoic acid and protocatechuic acid. The docking analysis showed that these compounds interacted with amino acid residues in the active site of XO through hydrogen bonding and hydrophobic interactions. These findings suggest that these compounds help reduce uric acid in <i>C. speciosa</i>, supporting further investigation into their mechanism of action.

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Publication Details

Journal
Molecules
Published
2024-09-20
DOI
https://doi.org/10.3390/molecules29184468
Citations
4
Primary Topic
Gout, Hyperuricemia, Uric Acid
Type
article
Field-Weighted Citation Impact
1.36
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article

Bioassay-Guided Isolation and Identification of Xanthine Oxidase Inhibitory Constituents from the Fruits of Chaenomeles speciosa (Sweet) Nakai

Ruoling Xu, Meng‐Ting Kuang, Ning Li, Kui Li et al.
4 citations
Molecules
Gout, Hyperuricemia, Uric Acid
1.36
article

Bioassay-Guided Isolation and Identification of Xanthine Oxidase Inhibitory Constituents from the Fruits of Chaenomeles speciosa (Sweet) Nakai

Ruoling Xu, Meng‐Ting Kuang, Ning Li, Kui Li, Wei Ma
article en
4 citations

Abstract

<i>Chaenomeles speciosa</i> (Sweet) Nakai (<i>C. speciosa</i>) is a traditional Chinese herbal medicine that possesses not only abundant nutritional value but also significant medicinal properties. The extracts of <i>C. speciosa</i> fruits effectively reduce urate levels, but the specific chemical constituents responsible for this effect in <i>C. speciosa</i> fruits are still unknown. Therefore, this study aims to investigate and analyze the structure-activity relationships of these constituents to better understand their ability to lower uric acid. Activity-guided fractionation and purification processes were used to isolate compounds with xanthine oxidase (XO) inhibitory activity from <i>C. speciosa</i> fruits, resulting in three extracts: petroleum ether, ethyl acetate, and <i>n</i>-butanol. The ethyl acetate and <i>n</i>-butanol fractions showed strong activity and underwent further separation and purification using chromatographic techniques. Twenty-four compounds were isolated and identified, with nine showing potent activity, including chlorogenic acid, methyl chlorogenate, butyl chlorogenate, ethyl chlorogenate, cryptochlorogenic acid methyl ester, caffeic acid, <i>p</i>-coumaric acid, benzoic acid and protocatechuic acid. The docking analysis showed that these compounds interacted with amino acid residues in the active site of XO through hydrogen bonding and hydrophobic interactions. These findings suggest that these compounds help reduce uric acid in <i>C. speciosa</i>, supporting further investigation into their mechanism of action.

MoleculesVol. 29(18)
Anhui Medical University (CN)
Zero hunger
Openalex Percentile: Top 17%
Gout, Hyperuricemia, Uric Acid
1.36
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