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Phenolic Constituents of the Roots of Rhamnoneuron balansae with Senolytic Activity.
Cho, Hyo-Moon; Lee, Yae-Rin; Lee, Ba-Wool; Zhang, Mi; Ryu, Byeol; Nghiem, Du-Trong; Pham, Ha-Thanh-Tung; Oh, Won-Keun.
Afiliación
  • Cho HM; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
  • Lee YR; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
  • Lee BW; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
  • Zhang M; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
  • Ryu B; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
  • Nghiem DT; Department of Botany, Hanoi University of Pharmacy, Hanoi, Vietnam.
  • Pham HT; Department of Botany, Hanoi University of Pharmacy, Hanoi, Vietnam.
  • Oh WK; Korea Bioactive Natural Material Bank, Research Institute of Pharmaceutical Sciences, College of Pharmacy, Seoul National University, Seoul 08826, Republic of Korea.
J Nat Prod ; 83(12): 3661-3670, 2020 12 24.
Article en En | MEDLINE | ID: mdl-33256407
ABSTRACT
With the advent of senolytic agents capable of selectively removing senescent cells in old tissues, the perception of age-associated diseases has been changing from being an inevitable to a preventable phenomenon of human life. In the search for materials with senolytic activity from natural products, six new flavonostilbenes (1-6), three new phenylethylchromanones (7-9), three new phenylethylchromones (10-12), and four known compounds (13-16) were isolated from the roots of Rhamnoneuron balansae. The chemical structures of these isolated compounds were determined based on the interpretation of spectroscopic data, including 1D and 2D NMR, ECD, and HRMS. The absolute configuration of compound 1 was also determined by a Mosher ester analysis and ECD calculations. Compounds 6-8 were shown to selectively destroy senescent cells, and the promoter activity of p16INK4A, a representative senescence marker, was reduced significantly by compound 6. The present results suggest the potential activity of flavonostilbene and phenylethylchromanone skeletons from R. balansae as new senolytics.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fenoles / Senescencia Celular / Raíces de Plantas / Malvales Idioma: En Revista: J Nat Prod Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fenoles / Senescencia Celular / Raíces de Plantas / Malvales Idioma: En Revista: J Nat Prod Año: 2020 Tipo del documento: Article