| Literature DB >> 23141055 |
Peng-Yu Zhuang1, Gui-Jie Zhang, Xiao-Jing Wang, Yan Zhang, Shi-Shan Yu, Shuang-Gang Ma, Yun-Bao Liu, Jing Qu, Yong Li, Song Xu, Hai-Ning Lü, Xia Chen, Li Li, Yi-Kang Si, Dan Zhang.
Abstract
Eleven prenylated C(6)-C(3) compounds, illihenryifunones A, B (1, 2), illihenryifunol A (3), illihenryipyranol A (4), illihenryiones A-G (5-11), and three known prenylated C(6)-C(3) compounds (12-14), were isolated from the roots of Illicium henryi. Structures of 1-11 were elucidated by spectroscopic methods including NMR, HRESIMS, and CD. The absolute configuration of the 11,12-diol moiety in 5 was determined by observing its induced circular dichroism after addition of Mo(2)(OAc)(4) in DMSO. The absolute configuration of C-11 in 4 was determined as S based on the Rh(2)(OCOCF(3))(4)-induced CD data; the absolute configuration of 3 was determined as R by comparison of its experimental and calculated electronic circular dichroism (ECD). The antioxidant activities of compounds 1-14 were also evaluated. Compound 4 exhibited strong antioxidant activity with an IC(50) value of 2.97±1.30 μM, whereas compounds 3 and 8 showed antioxidant activities with IC(50) values of 44.36±0.30 and 48.00±2.01 μM, respectively.Entities:
Mesh:
Substances:
Year: 2012 PMID: 23141055 DOI: 10.1016/j.phytochem.2012.10.002
Source DB: PubMed Journal: Phytochemistry ISSN: 0031-9422 Impact factor: 4.072