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Xanthine oxidase inhibitory constituents from the roots of Ampelopsis japonica.
Li, Yu-Lin; Liu, Fen; Zhao, Li-Yun; Li, Han-Xiang; Jumai, Aikebaier; Xu, Zhi-Fang; Qiu, Sheng-Xiang.
Afiliação
  • Li YL; State Key Laboratory of Plant Diversity and Specialty Crops & Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China.
  • Liu F; South China National Botanical Garden, Guangzhou, China.
  • Zhao LY; State Key Laboratory of Plant Diversity and Specialty Crops & Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China.
  • Li HX; South China National Botanical Garden, Guangzhou, China.
  • Jumai A; University of Chinese Academy of Sciences, Beijing, China.
  • Xu ZF; State Key Laboratory of Plant Diversity and Specialty Crops & Guangdong Provincial Key Laboratory of Applied Botany, South China Botanical Garden, Chinese Academy of Sciences, Guangzhou, China.
  • Qiu SX; South China National Botanical Garden, Guangzhou, China.
Nat Prod Res ; : 1-10, 2024 Apr 18.
Article em En | MEDLINE | ID: mdl-38635344
ABSTRACT
Bioassay-guided purification of the xanthine oxidase (XOD) inhibitory extract of the roots of Ampelopsis japonica resulted in the isolation of two new triterpenoids (1-2), designated Ampejaponoside A and B, along with sixteen known compounds (3-18). The structures of Ampejaposide A and B were elucidated by comprehensive analysis of spectroscopic data with the structures of the known compounds 3-18 confirmed by comparison the spectral data with corresponding values reported in literatures. All the isolates were evaluated for their XOD inhibitory activity in vitro. As a result, compounds 2, 8, and 14-16 displayed significant XOD inhibitory effect, particularly 16 being the most potent with an IC50 value of 0.21 µM, superior to positive substance allopurinol (IC50 1.95 µM). Molecular docking uncovered a unique interaction mode of 16 with the active site of XOD. The current study showed that the triterpenoids and polyphenols from A. japonica could serve as new lead compounds with the potential to speed up the development of novel XOD inhibitors with clinical potential to treat hyperuricaemia and gout.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article