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Phenolic constituents from the branches of Viburnum chinshanense as potential α-amylase and α-glucosidase inhibitory agents.
Zhou, Hong-Juan; Yang, Meng-Ya; Chen, Jia; Ji, Wei; Shao, Jian-Hua; Wang, Zi-Han; Zhao, Chun-Chao.
Afiliación
  • Zhou HJ; Joint International Research Laboratory of Agriculture & Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou, China.
  • Yang MY; Joint International Research Laboratory of Agriculture & Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou, China.
  • Chen J; Joint International Research Laboratory of Agriculture & Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou, China.
  • Ji W; Joint International Research Laboratory of Agriculture & Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou, China.
  • Shao JH; Joint International Research Laboratory of Agriculture & Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou, China.
  • Wang ZH; Joint International Research Laboratory of Agriculture & Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou, China.
  • Zhao CC; Joint International Research Laboratory of Agriculture & Agri-Product Safety of Ministry of Education of China, Yangzhou University, Yangzhou, China.
Nat Prod Res ; : 1-7, 2024 Apr 15.
Article en En | MEDLINE | ID: mdl-38619012
ABSTRACT
This paper reports the isolation of two undescribed phenolic glycosides (1 and 2), together with seven known compounds (3-9) from the branches of Viburnum chinshanense. The structures of undescribed compounds were elucidated by comprehensive spectroscopic methods (1D NMR, 2D NMR, and HRESIMS). The sugar units of compounds 1 and 2 were identified by acid hydrolysis and HPLC analysis of the chiral derivatives of the monosaccharides. Furthermore, the α­amylase and α-glucosidase inhibitory activities of all isolates were evaluated and compounds 1, 5, and 8 displayed potential α­amylase and α-glucosidase inhibitory activities. The molecular docking analyses of compounds 1 and 8 with the potent inhibition towards the target enzymes were also performed.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Nat Prod Res / Nat. prod. res. (Online) / Natural product research (Online) Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Nat Prod Res / Nat. prod. res. (Online) / Natural product research (Online) Año: 2024 Tipo del documento: Article País de afiliación: China