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Furostanol glycosides, stilbenoids and nucleosides from the roots of Smilax perfoliata, and evaluation of their cytotoxic and anticholinesterase activities.
Sidthinam, Kitipong; Singha, Suriphon; Yahuafai, Jantana; Siriwattanasathien, Yuttana; Suksamrarn, Apichart; Sutthivaiyakit, Somyote.
Afiliación
  • Sidthinam K; Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Ramkhamhaeng University, Hua Mark, Bangkapi, Bangkok, Thailand.
  • Singha S; Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Ramkhamhaeng University, Hua Mark, Bangkapi, Bangkok, Thailand.
  • Yahuafai J; Division of Research and Technology Assessment, National Cancer Institute, Bangkok, Thailand.
  • Siriwattanasathien Y; Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Ramkhamhaeng University, Hua Mark, Bangkapi, Bangkok, Thailand.
  • Suksamrarn A; Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Ramkhamhaeng University, Hua Mark, Bangkapi, Bangkok, Thailand.
  • Sutthivaiyakit S; Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Ramkhamhaeng University, Hua Mark, Bangkapi, Bangkok, Thailand.
Nat Prod Res ; : 1-11, 2024 Jun 04.
Article en En | MEDLINE | ID: mdl-38832521
ABSTRACT
Three undescribed compounds including two furosteroid glycosides (perfoloside and 22-O-methylperfoloside) and one stilbenedimer (perfolostilbene) together with 21 known compounds were isolated from the roots of Smilax perfoliata. The structural elucidation was established by extensive uses of HRMS, 1D and 2D spectroscopic techniques. The assignment of the stereocenters in perfolostilbene was based on NOESY data and ECD calculation. Among the isolates, two compounds showed marginal cytotoxic activity against KB and Hela cell lines while seven stilbenoids showed strong to weak antiacetylcholinesterase and antibutyrylcholinesterase activities with IC50 ranging between 2-197 µM.
Palabras clave

Texto completo: 1 Colección: 01-internacional 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: Tailandia

Texto completo: 1 Colección: 01-internacional 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: Tailandia