Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–10.Published as part of Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing, Yang, Yongcheng, Chen, Gang, Hou, Guoli, Huo, Xuting, Jia, Jingming, Wang, Anhua & Hu, Gaosheng, 2022, Lanostane-type triterpenoids from the mycelial mat of Ganoderma lucidum and their hepatoprotective activities, pp. 1-11 in Phytochemistry (113131) 198 on page 6, DOI: 10.1016/j.phytochem.2022.113131, http://zenodo.org/record/823570
Fig. 3. Key NOESY correlations for 1 and 4 in acetone-d6.Published as part of Yangchum, Arunrat, Fuj...
Fig. 4. (a) Key 1H–1H COSY () and selected HMBC correlations (H→C) of 7; (b) Key NOESY correlations ...
Fig. 3. Key NOESY correlations for 1, 2, and 4.Published as part of Isaka, Masahiko, Chinthanom, Pan...
Fig. 3. Key NOESY correlations for compounds 1–10.Published as part of Zhang, Xueqing, Gao, Xiaoxu, ...
Fig. 1. Structures of compounds 1–31.Published as part of Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–8.Published as part of Su, Hai-Guo, Peng...
Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing, Yang, Yongcheng, Chen, Gang, Hou, Guoli, Huo, Xuting, Ji...
Fig. 2. COSY and HMBC correlations for 1, 4, 5, and 9.Published as part of Yangchum, Arunrat, Fujii,...
Fig. 5. Effects of compounds 1, 6, and 8–10 (15 μM) on ALT activity (A), AST activity (B), LDH activ...
Fig. 3. Key NOESY correlations of compounds 1–5, 7 and 8.Published as part of Su, Hai-Guo, Peng, Xin...
Fig. 2. COSY and HMBC correlations for 1, 2, and 4.Published as part of Isaka, Masahiko, Chinthanom,...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of 1.Published as part of Luo, Di, Xie, Ji-Zhao...
Fig. 4. Hepatoprotective effects of the indicated compounds against H2O2-induced injury in HepG2 cel...
Fig. 2. (a) Key 1H–1H COSY () and selected HMBC correlations (H→C) of 1; (b) Key NOESY correlations ...
Fig. 1. Structures of compounds 1–15.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, Qiang-Q...
Fig. 3. Key NOESY correlations for 1 and 4 in acetone-d6.Published as part of Yangchum, Arunrat, Fuj...
Fig. 4. (a) Key 1H–1H COSY () and selected HMBC correlations (H→C) of 7; (b) Key NOESY correlations ...
Fig. 3. Key NOESY correlations for 1, 2, and 4.Published as part of Isaka, Masahiko, Chinthanom, Pan...
Fig. 3. Key NOESY correlations for compounds 1–10.Published as part of Zhang, Xueqing, Gao, Xiaoxu, ...
Fig. 1. Structures of compounds 1–31.Published as part of Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–8.Published as part of Su, Hai-Guo, Peng...
Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing, Yang, Yongcheng, Chen, Gang, Hou, Guoli, Huo, Xuting, Ji...
Fig. 2. COSY and HMBC correlations for 1, 4, 5, and 9.Published as part of Yangchum, Arunrat, Fujii,...
Fig. 5. Effects of compounds 1, 6, and 8–10 (15 μM) on ALT activity (A), AST activity (B), LDH activ...
Fig. 3. Key NOESY correlations of compounds 1–5, 7 and 8.Published as part of Su, Hai-Guo, Peng, Xin...
Fig. 2. COSY and HMBC correlations for 1, 2, and 4.Published as part of Isaka, Masahiko, Chinthanom,...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of 1.Published as part of Luo, Di, Xie, Ji-Zhao...
Fig. 4. Hepatoprotective effects of the indicated compounds against H2O2-induced injury in HepG2 cel...
Fig. 2. (a) Key 1H–1H COSY () and selected HMBC correlations (H→C) of 1; (b) Key NOESY correlations ...
Fig. 1. Structures of compounds 1–15.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, Qiang-Q...
Fig. 3. Key NOESY correlations for 1 and 4 in acetone-d6.Published as part of Yangchum, Arunrat, Fuj...
Fig. 4. (a) Key 1H–1H COSY () and selected HMBC correlations (H→C) of 7; (b) Key NOESY correlations ...
Fig. 3. Key NOESY correlations for 1, 2, and 4.Published as part of Isaka, Masahiko, Chinthanom, Pan...