Fig. 1. Structures of the compounds 1–7.Published as part of Bai, Ming, Chen, Jing-Jie, Xu, Wei, Dong, Shu-Hui, Liu, Qing-Bo, Yao, Guo-Dong, Lin, Bin, Huang, Xiao-Xiao & Song, Shao-Jiang, 2020, Germacranolides from Elephantopus scaber L. and their cytotoxic activities, pp. 1-8 in Phytochemistry (112479) 178 on page 2, DOI: 10.1016/j.phytochem.2020.112479, http://zenodo.org/record/829305
Fig. 1. Structure of isolated compounds.Published as part of Nyamboki, Divinah Kwamboka, Bedane, Kib...
Fig. 4. Structures of compound 2 and daucovirgolide G (9).Published as part of Sirignano, Carmina, H...
Fig. 8. The ability to inhibit LPS-induced NO production in BV-2 microglial cell of compounds 1–7.Pu...
Fig. 5. The ORTEP drawing of compound 1.Published as part of Bai, Ming, Chen, Jing-Jie, Xu, Wei, Don...
Bai, Ming, Chen, Jing-Jie, Xu, Wei, Dong, Shu-Hui, Liu, Qing-Bo, Yao, Guo-Dong, Lin, Bin, Huang, Xia...
Fig. 3. Key NOESY correlations (blue line) of the compounds 1–7.Published as part of Bai, Ming, Chen...
Fig. 2. Key HMBC correlations (blue line) of the compounds 1–7 (H→C).Published as part of Bai, Ming,...
Fig. 4. Comparison of the experimental and calculated ECD spectra of 1–6 in MeOH. Spectra were calcu...
Fig. 6. Determination of the absolute configuration of 7. Comparison of the calculated ECD spectra o...
Fig. 7. Apoptosis induced by 7 in HepG2, Hep3B, and MCF-7 cells. Flow cytometry analysis of Annexin ...
Fig. 1. Chemical structures of 1–6.Published as part of Iguchi, Tomoki, Yokosuka, Akihito, Kawahata,...
Fig. 1. Structures of 1–10.Published as part of Iguchi, Tomoki, Yokosuka, Akihito, Tamura, Naoya, Ta...
Fig. 6. The ORTEP drawing of compounds 1, 2, 4 and 5.Published as part of Xu, Wei, Bai, Ming, Liu, D...
Fig. 4. Key NOESY correlations of compounds 1–6.Published as part of Xu, Wei, Bai, Ming, Liu, De-Fen...
Fig. 1. Chemical structures of compounds isolated from D. carota.Published as part of Sirignano, Car...
Fig. 1. Structure of isolated compounds.Published as part of Nyamboki, Divinah Kwamboka, Bedane, Kib...
Fig. 4. Structures of compound 2 and daucovirgolide G (9).Published as part of Sirignano, Carmina, H...
Fig. 8. The ability to inhibit LPS-induced NO production in BV-2 microglial cell of compounds 1–7.Pu...
Fig. 5. The ORTEP drawing of compound 1.Published as part of Bai, Ming, Chen, Jing-Jie, Xu, Wei, Don...
Bai, Ming, Chen, Jing-Jie, Xu, Wei, Dong, Shu-Hui, Liu, Qing-Bo, Yao, Guo-Dong, Lin, Bin, Huang, Xia...
Fig. 3. Key NOESY correlations (blue line) of the compounds 1–7.Published as part of Bai, Ming, Chen...
Fig. 2. Key HMBC correlations (blue line) of the compounds 1–7 (H→C).Published as part of Bai, Ming,...
Fig. 4. Comparison of the experimental and calculated ECD spectra of 1–6 in MeOH. Spectra were calcu...
Fig. 6. Determination of the absolute configuration of 7. Comparison of the calculated ECD spectra o...
Fig. 7. Apoptosis induced by 7 in HepG2, Hep3B, and MCF-7 cells. Flow cytometry analysis of Annexin ...
Fig. 1. Chemical structures of 1–6.Published as part of Iguchi, Tomoki, Yokosuka, Akihito, Kawahata,...
Fig. 1. Structures of 1–10.Published as part of Iguchi, Tomoki, Yokosuka, Akihito, Tamura, Naoya, Ta...
Fig. 6. The ORTEP drawing of compounds 1, 2, 4 and 5.Published as part of Xu, Wei, Bai, Ming, Liu, D...
Fig. 4. Key NOESY correlations of compounds 1–6.Published as part of Xu, Wei, Bai, Ming, Liu, De-Fen...
Fig. 1. Chemical structures of compounds isolated from D. carota.Published as part of Sirignano, Car...
Fig. 1. Structure of isolated compounds.Published as part of Nyamboki, Divinah Kwamboka, Bedane, Kib...
Fig. 4. Structures of compound 2 and daucovirgolide G (9).Published as part of Sirignano, Carmina, H...
Fig. 8. The ability to inhibit LPS-induced NO production in BV-2 microglial cell of compounds 1–7.Pu...