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Quassinoids from the Roots of Eurycoma longifolia and Their Anti-Proliferation Activities

A phytochemical investigation on the roots of medicinal plant Eurycoma longifolia resulted in the isolation of 10 new highly oxygenated C(20) quassinoids longifolactones G‒P (1–10), along with four known ones (11–14). Their chemical structures and absolute configurations were unambiguously elucidate...

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Detalles Bibliográficos
Autores principales: Yang, Wei-Qun, Tang, Wei, Huang, Xiao-Jun, Song, Jian-Guo, Li, Yue-Yue, Xiong, Yu, Fan, Chun-Lin, Wu, Zhen-Long, Wang, Ying, Ye, Wen-Cai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8512324/
https://www.ncbi.nlm.nih.gov/pubmed/34641483
http://dx.doi.org/10.3390/molecules26195939
Descripción
Sumario:A phytochemical investigation on the roots of medicinal plant Eurycoma longifolia resulted in the isolation of 10 new highly oxygenated C(20) quassinoids longifolactones G‒P (1–10), along with four known ones (11–14). Their chemical structures and absolute configurations were unambiguously elucidated on the basis of comprehensive spectroscopic analysis and X-ray crystallographic data. Notably, compound 1 is a rare pentacyclic C(20) quassinoid featuring a densely functionalized 2,5-dioxatricyclo[5.2.2.0(4,8)]undecane core. Compound 4 represents the first example of quassinoids containing a 14,15-epoxy functionality, and 7 features an unusual α-oriented hydroxyl group at C-14. All isolated compounds were evaluated for their anti-proliferation activities on human leukemia cells. Among the isolates, compounds 5, 12, 13, and 14 potently inhibited the in vitro proliferation of K562 and HL-60 cells with IC(50) values ranging from 2.90 to 8.20 μM.