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Hosimosines A-E, structurally diverse cytisine derivatives from the seeds of Ormosia hosiei Hemsl. et Wils.
Zhou, Qing-Qing; Xie, Xiao-Yan; Zhu, Jia-Wen; Pan, Wei-Wei; Xie, Bao-Gang; Zhou, Wu; Xu, Jin-Biao.
Afiliación
  • Zhou QQ; Department of Pharmacy, College of Medicine, Jiaxing University, Jiaxing 314001, China.
  • Xie XY; Department of Pharmacy, College of Medicine, Jiaxing University, Jiaxing 314001, China.
  • Zhu JW; Department of Pharmacy, College of Medicine, Jiaxing University, Jiaxing 314001, China.
  • Pan WW; Department of Pharmacy, College of Medicine, Jiaxing University, Jiaxing 314001, China.
  • Xie BG; Department of Pharmacy, College of Medicine, Jiaxing University, Jiaxing 314001, China.
  • Zhou W; Department of Pharmacy, College of Medicine, Jiaxing University, Jiaxing 314001, China.
  • Xu JB; Department of Pharmacy, College of Medicine, Jiaxing University, Jiaxing 314001, China. Electronic address: xujinbiao2015@126.com.
Fitoterapia ; 170: 105661, 2023 Oct.
Article en En | MEDLINE | ID: mdl-37648030
ABSTRACT
Ormosia hosiei Hemsl. et Wils (Fabaceae family) is an arbor species endemic to China. The seeds of O. hosiei have been used as traditional Chinese medicine to treat hernia, abdominal pain, blood stasis and amenorrhea. Cytisine-like and angustifoline type alkaloids were main components identified from this plant. In our research on the bioactive alkaloids from the promising Chinese medicinal plants, four new angustifoline type alkaloids (1-4) and a new cytisine-like alkaloid (5), named hosimosine A-E, together with 13 known analogues (6-18) were isolated from the seeds of O. hosiei. Their structures were elucidated by the extensive spectroscopic methods, especially the interpretation of NMR spectra and specific rotations, along with the methods of NMR and ECD calculation. Compounds 1-4 were identified as two pairs of epimers, whose relative configurations were deduced from density functional theory (DFT) calculations of NMR chemical shifts and DP4+ analysis, and absolute configurations were determined by comparison of their experimental and theoretical ECD spectra. Compound 5 displayed two sets of NMR data caused by the existence of tautomeric forms. Compounds 14, 17 and 18 were determined to be enantiomers of literature compounds. Some of the isolates exhibited moderate cytotoxic effects against HepG2, A2780 and MCF-7 cells.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Alcaloides / Fabaceae Límite: Female / Humans Idioma: En Revista: Fitoterapia Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Alcaloides / Fabaceae Límite: Female / Humans Idioma: En Revista: Fitoterapia Año: 2023 Tipo del documento: Article País de afiliación: China