Fig. 3. Key NOESY correlations for 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 7, DOI: 10.1016/j.phytochem.2022.113131, http://zenodo.org/record/823570
Fig. 2. COSY and HMBC correlations for 1, 2, and 4.Published as part of Isaka, Masahiko, Chinthanom,...
Fig. 7. Comparison of the chemical shifts (δН, ppm) of Hα-16, Hβ-16, and H3-18.Published as part of ...
Fig. 1. Structures of compounds 1–11.Published as part of Yangchum, Arunrat, Fujii, Ryoma, Choowong,...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–10.Published as part of Zhang, Xueqing, ...
Fig. 1. Structures of compounds 1–31.Published as part of Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing...
Fig. 3. Key NOESY correlations of compounds 1–5, 7 and 8.Published as part of Su, Hai-Guo, Peng, Xin...
Fig. 3. Key NOESY correlations for 1 and 4 in acetone-d6.Published as part of Yangchum, Arunrat, Fuj...
Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing, Yang, Yongcheng, Chen, Gang, Hou, Guoli, Huo, Xuting, Ji...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–8.Published as part of Su, Hai-Guo, Peng...
Fig. 3. Key NOESY correlations for 1, 2, and 4.Published as part of Isaka, Masahiko, Chinthanom, Pan...
Fig. 5. Effects of compounds 1, 6, and 8–10 (15 μM) on ALT activity (A), AST activity (B), LDH activ...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of 1.Published as part of Luo, Di, Xie, Ji-Zhao...
Fig. 2. COSY and HMBC correlations for 1, 4, 5, and 9.Published as part of Yangchum, Arunrat, Fujii,...
Fig. 1. Structures of compounds 1–15.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, Qiang-Q...
Fig. 4. Hepatoprotective effects of the indicated compounds against H2O2-induced injury in HepG2 cel...
Fig. 2. COSY and HMBC correlations for 1, 2, and 4.Published as part of Isaka, Masahiko, Chinthanom,...
Fig. 7. Comparison of the chemical shifts (δН, ppm) of Hα-16, Hβ-16, and H3-18.Published as part of ...
Fig. 1. Structures of compounds 1–11.Published as part of Yangchum, Arunrat, Fujii, Ryoma, Choowong,...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–10.Published as part of Zhang, Xueqing, ...
Fig. 1. Structures of compounds 1–31.Published as part of Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing...
Fig. 3. Key NOESY correlations of compounds 1–5, 7 and 8.Published as part of Su, Hai-Guo, Peng, Xin...
Fig. 3. Key NOESY correlations for 1 and 4 in acetone-d6.Published as part of Yangchum, Arunrat, Fuj...
Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing, Yang, Yongcheng, Chen, Gang, Hou, Guoli, Huo, Xuting, Ji...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–8.Published as part of Su, Hai-Guo, Peng...
Fig. 3. Key NOESY correlations for 1, 2, and 4.Published as part of Isaka, Masahiko, Chinthanom, Pan...
Fig. 5. Effects of compounds 1, 6, and 8–10 (15 μM) on ALT activity (A), AST activity (B), LDH activ...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of 1.Published as part of Luo, Di, Xie, Ji-Zhao...
Fig. 2. COSY and HMBC correlations for 1, 4, 5, and 9.Published as part of Yangchum, Arunrat, Fujii,...
Fig. 1. Structures of compounds 1–15.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, Qiang-Q...
Fig. 4. Hepatoprotective effects of the indicated compounds against H2O2-induced injury in HepG2 cel...
Fig. 2. COSY and HMBC correlations for 1, 2, and 4.Published as part of Isaka, Masahiko, Chinthanom,...
Fig. 7. Comparison of the chemical shifts (δН, ppm) of Hα-16, Hβ-16, and H3-18.Published as part of ...
Fig. 1. Structures of compounds 1–11.Published as part of Yangchum, Arunrat, Fujii, Ryoma, Choowong,...