生药学
阿尔茨海默病
传统医学
生物
化学
立体化学
医学
疾病
生物化学
生物活性
内科学
体外
作者
Zhiwei Bian,Xiaoying Liu,Jiaxuan Li,Shian Hu,Yeun‐Mun Choo,Ze‐Yu Zhao,Jin‐Feng Hu,Kunmei Ji,Mark T. Hamann,Xin Wang,Xiaojuan Wang
标识
DOI:10.1021/acs.jnatprod.5c00486
摘要
Twelve new compounds, bletistrosides M-X (1-12), including five glucosyloxybenzyl 2-isobutylmalates (1-5), along with four neolignan glycosides (6-9), two phenanthrene derivatives (10-11), and one bibenzyl derivative (12), were isolated from the tubers of Bletilla striata (B. striata). The structures and absolute configurations of the undescribed compounds were elucidated on the basis of spectroscopic data analysis, experimental and calculated electronic circular dichroism data, chiroptical analysis, and chemical derivatizations. In silico, compounds 2, 3, and 12 bound well to Aβ1-42. Compounds 2, 3, and 12 significantly delayed the paralysis phenotype in CL4176 worms compared to controls. Higher nonparalysis rates were observed in these treatment groups (5 μM for compound 2; 25, 50 μM for compounds 2, 3 and 12), suggesting their potential role in anti-Alzheimer's disease.
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