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从. 中分离得到的抗破骨细胞环阿屯烷型皂苷

Anti-osteoclastogenic cycloartane saponins from .

机构信息

Vietnam Academy of Science and Technology (VAST), University of Science and Technology of Hanoi, Hanoi, Viet Nam.

Department of Biochemistry, Kangwon National University, Chuncheon, Gangwon-Do, Korea.

出版信息

Nat Prod Res. 2022 Sep;36(18):4597-4604. doi: 10.1080/14786419.2021.2012671. Epub 2021 Dec 13.

Abstract

The methanolic extract of Dryand leaves exhibited significant anti-osteoclastogenic activity. Chemical investigation of led to the isolation of one new cycloartane saponin, mussaendoside X () along with eight known compounds: heinsiagenin A 3--[-L-rhamnopyranosyl-(1→2)---D-glucopyranosyl-(1→2)]---D-glucopyranoside (), mussaendoside O (), heinsiagenin A 3--[-L-rhamnopyranosyl-(1→2)---D-glucopyranosyl-(1→2)]---D-glucopyranosyl-(1→4)---D-glucopyranoside (), mussaendoside G (), mussaendoside U (), shanzhiside methyl ester (), barlerin () and musaenoside (). Their structures were elucidated by extensive spectroscopic methods including 1D- and 2D-NMR as well as MS analysis and comparison with the literature. Cycloartane saponins - positively suppressed osteoclast formation in an anti-osteoclastogenic screening assay. Consequently, treatment of RANKL-stimulated RAW 264.7 cells with compounds - significantly decreased the number of osteoclasts in a concentration-dependent manner. Six compounds from , with the new cycloartane, mussaendoside X, were shown for the first time as potential effective inhibitors of osteoclastogenesis.

摘要

雷公藤叶的甲醇提取物表现出显著的抗破骨细胞生成活性。对雷公藤的化学研究导致分离得到一种新的环阿尔廷烷皂苷,木栓酮苷 X(),以及另外 8 种已知化合物:海斯苷元 A3-[-L-鼠李吡喃糖基-(1→2)--D-吡喃葡萄糖基-(1→2)]---D-吡喃葡萄糖苷()、木栓酮苷 O()、海斯苷元 A3-[-L-鼠李吡喃糖基-(1→2)--D-吡喃葡萄糖基-(1→2)]---D-吡喃葡萄糖基-(1→4)--D-吡喃葡萄糖苷()、木栓酮苷 G()、木栓酮苷 U()、山芝苷甲酯()、巴利林()和木萨诺苷()。它们的结构通过广泛的光谱方法阐明,包括 1D-和 2D-NMR 以及 MS 分析,并与文献进行了比较。环阿尔廷烷皂苷-在抗破骨细胞生成筛选试验中阳性抑制破骨细胞形成。因此,用化合物-处理 RANKL 刺激的 RAW 264.7 细胞,可浓度依赖性地显著减少破骨细胞的数量。首次表明雷公藤中的 6 种化合物,包括新的环阿尔廷烷,木栓酮苷 X,是潜在有效的破骨细胞生成抑制剂。

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