三萜
立体化学
化学
萜烯
内酯
二维核磁共振波谱
二萜
医学
病理
替代医学
作者
Yuxun Zhu,Shang-Yi Wang,Cheng-Shuo Yang,Zhao-Xin Zhang,Huanping Zhang,Li-Sha Chai,Guo‐Zhu Su,Yong Li
标识
DOI:10.1080/10286020.2023.2286994
摘要
A 1,2:3,4:9,10:9,19-tetraseco-cycloartane triterpene spiroketal lactone, pseudoamaolide P (1), two new labdane-type diterpenoids, pseudoamains A and B (2-3), and four known cembrane-type diterpenoids (4–7) were isolated from the seeds of Pseudolarix amabilis. The structures of these compounds were elucidated by spectroscopic analyses, including HRESIMS, 1D-, and 2D-NMR. The anti-inflammatory activities of the compounds were evaluated by suppressing the transcription of the NF-κB-dependent reporter gene in LPS-induced 293 T/NF-κB-luc cells. All compounds do not show potent activity.
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