Pseudoamaolide P, a 1,2:3,4:9,10:9,19-tetraseco-cycloartane triterpene spiroketal lactone from seeds of Pseudolarix amabilis .
Yu-Xun ZhuShang-Yi WangCheng-Shuo YangZhao-Xin ZhangHuan-Ping ZhangLi-Sha ChaiGuo-Zhu SuYong LiPublished in: Journal of Asian natural products research (2024)
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.
Keyphrases
- lps induced
- inflammatory response
- anti inflammatory
- induced apoptosis
- high resolution
- signaling pathway
- magnetic resonance
- cell cycle arrest
- molecular docking
- transcription factor
- pi k akt
- copy number
- genome wide
- oxidative stress
- gene expression
- cell death
- toll like receptor
- mass spectrometry
- dna methylation
- endoplasmic reticulum stress
- cell proliferation
- genome wide identification