Anti-inflammatory labdane diterpenoids from Leonurus japonicus Houtt

Seven undescribed labdane diterpenoids, japonicones A-G, were isolated from the aerial parts of Leonurus japonicus Houtt. Japonicones C-G contained two keto carbonyl groups in their structures attached to C-3 and C-7, which are rare for labdane diterpenoids. The structures and absolute configuration...

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Veröffentlicht in:Phytochemistry (Oxford) 2020-05, Vol.173, p.112223-112223, Article 112223
Hauptverfasser: Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su, Zhenzhen, Zhong, Yan, Cao, Zeyu, Cao, Liang, Huang, Wenzhe, Wang, Zhenzhong, Xiao, Wei
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Sprache:eng
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Zusammenfassung:Seven undescribed labdane diterpenoids, japonicones A-G, were isolated from the aerial parts of Leonurus japonicus Houtt. Japonicones C-G contained two keto carbonyl groups in their structures attached to C-3 and C-7, which are rare for labdane diterpenoids. The structures and absolute configurations of japonicones A-G were established by means of spectroscopic analyses (HRESIMS, 1D and 2D NMR, and ECD). Their anti-inflammatory activities were evaluated by measuring their inhibitory effects on PGE2 production in LPS-stimulated RAW264.7 macrophages. Japonicones A-D and G showed inhibition of PGE2 production with IC50 values in the range of 8.62–30.71 μM (the positive control paracetamol showed an IC50 = 5.79 μM). [Display omitted] •Seven undescribed labdane diterpenoids were isolated from the aerial parts of Leonurus japonicus Houtt.•Their structures and absolute configurations were established by means of spectroscopic analyses.•Compounds 1−4, and 7 showed inhibition of PGE2 production with IC50 values in the range of 8.62−30.71 μM.
ISSN:0031-9422
1873-3700
DOI:10.1016/j.phytochem.2019.112223