Fig. 8. The ability to inhibit LPS-induced NO production in BV-2 microglial cell of compounds 1–7.Published as part of Xu, Wei, Bai, Ming, Liu, De-Feng, Qin, Shu-Yan, Lv, Tian-Ming, Li, Qian, Lin, Bin, Song, Shao-Jiang & Huang, Xiao-Xiao, 2022, MS/MS-based molecular networking accelerated discovery of germacrane-type sesquiterpene lactones from Elephantopus scaber L, pp. 1-11 in Phytochemistry (113136) 198 on page 8, DOI: 10.1016/j.phytochem.2022.113136, http://zenodo.org/record/823552
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of 1.Published as part of Luo, Di, Xie, Ji-Zhao...
Fig. 5. The ORTEP drawing of compound 1.Published as part of Bai, Ming, Chen, Jing-Jie, Xu, Wei, Don...
Fig. 3. Selected HMBC (solid arrows) and NOESY (dashed arrows) correlations for compounds 1 and 3.Pu...
Fig. 4. Key NOESY correlations of compounds 1–6.Published as part of Xu, Wei, Bai, Ming, Liu, De-Fen...
Fig. 6. The ORTEP drawing of compounds 1, 2, 4 and 5.Published as part of Xu, Wei, Bai, Ming, Liu, D...
Xu, Wei, Bai, Ming, Liu, De-Feng, Qin, Shu-Yan, Lv, Tian-Ming, Li, Qian, Lin, Bin, Song, Shao-Jiang,...
Fig. 2. Molecular network of E. scaber crude extract obtained using GNPS platform and visualized wit...
Fig. 7. 13C NMR calculation results of compound 2, 2a, 2b. Linear correlation plots of calculated vs...
Fig. 3. Key HMBC correlations and 1 H- 1 H COSY correlations of compounds 1 6.Published as part of X...
Fig. 5. Experimental and calculated ECD spectra for compounds 1–6 in MeOH.Published as part of Xu, W...
Fig. 3. Key 1 H– 1 H COSY, HMBC, and NOESY correlations of compound 6.Published as part of Li, Hongl...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compound 1.Published as part of Li, Honglian...
Fig. 5. ORTEP diagrams of compounds 1, 4, 6 and 8.Published as part of Li, Hongliang, Liu, Liu, Liu,...
Fig. 5. Putative biosynthetic pathway of 1 and 2.Published as part of Luo, Di, Xie, Ji-Zhao, Zou, Lu...
Fig. 4. Experimental ECD spectra of compounds 1–9.Published as part of Li, Hongliang, Liu, Liu, Liu,...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of 1.Published as part of Luo, Di, Xie, Ji-Zhao...
Fig. 5. The ORTEP drawing of compound 1.Published as part of Bai, Ming, Chen, Jing-Jie, Xu, Wei, Don...
Fig. 3. Selected HMBC (solid arrows) and NOESY (dashed arrows) correlations for compounds 1 and 3.Pu...
Fig. 4. Key NOESY correlations of compounds 1–6.Published as part of Xu, Wei, Bai, Ming, Liu, De-Fen...
Fig. 6. The ORTEP drawing of compounds 1, 2, 4 and 5.Published as part of Xu, Wei, Bai, Ming, Liu, D...
Xu, Wei, Bai, Ming, Liu, De-Feng, Qin, Shu-Yan, Lv, Tian-Ming, Li, Qian, Lin, Bin, Song, Shao-Jiang,...
Fig. 2. Molecular network of E. scaber crude extract obtained using GNPS platform and visualized wit...
Fig. 7. 13C NMR calculation results of compound 2, 2a, 2b. Linear correlation plots of calculated vs...
Fig. 3. Key HMBC correlations and 1 H- 1 H COSY correlations of compounds 1 6.Published as part of X...
Fig. 5. Experimental and calculated ECD spectra for compounds 1–6 in MeOH.Published as part of Xu, W...
Fig. 3. Key 1 H– 1 H COSY, HMBC, and NOESY correlations of compound 6.Published as part of Li, Hongl...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compound 1.Published as part of Li, Honglian...
Fig. 5. ORTEP diagrams of compounds 1, 4, 6 and 8.Published as part of Li, Hongliang, Liu, Liu, Liu,...
Fig. 5. Putative biosynthetic pathway of 1 and 2.Published as part of Luo, Di, Xie, Ji-Zhao, Zou, Lu...
Fig. 4. Experimental ECD spectra of compounds 1–9.Published as part of Li, Hongliang, Liu, Liu, Liu,...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of 1.Published as part of Luo, Di, Xie, Ji-Zhao...
Fig. 5. The ORTEP drawing of compound 1.Published as part of Bai, Ming, Chen, Jing-Jie, Xu, Wei, Don...
Fig. 3. Selected HMBC (solid arrows) and NOESY (dashed arrows) correlations for compounds 1 and 3.Pu...