Fig. 5. Putative biosynthetic pathway of 1 and 2.Published as part of Luo, Di, Xie, Ji-Zhao, Zou, Lu-Hui, Qiu, Li, Huang, Dong-Ping, Xie, Yun-Feng, Xu, Huan-Ji & Wu, Xin-Duo, 2020, Lanostane-type triterpenoids from Ganoderma applanatum and their inhibitory activities on NO production in LPS-induced BV-2 cells, pp. 1-8 in Phytochemistry (112453) 177 on page 6, DOI: 10.1016/j.phytochem.2020.112453, http://zenodo.org/record/829607
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–8.Published as part of Su, Hai-Guo, Peng...
Fig. 4. Single-crystal X-ray structure of 5.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, ...
Fig. 5. Effects of compounds 1, 6, and 8–10 (15 μM) on ALT activity (A), AST activity (B), LDH activ...
Fig. 3. ORTEP drawings of 1 and 2.Published as part of Luo, Di, Xie, Ji-Zhao, Zou, Lu-Hui, Qiu, Li, ...
Fig. 1. Structures of the compounds from G. applanatum.Published as part of Luo, Di, Xie, Ji-Zhao, Z...
Luo, Di, Xie, Ji-Zhao, Zou, Lu-Hui, Qiu, Li, Huang, Dong-Ping, Xie, Yun-Feng, Xu, Huan-Ji, Wu, Xin-D...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of 1.Published as part of Luo, Di, Xie, Ji-Zhao...
Fig. 4. Experimental (black line) and calculated (red line) ECD spectra of 1–5 (A–E) and their enant...
Fig. 1. Structures of compounds 1–15.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, Qiang-Q...
Fig. 1. Structures of compounds 1–31.Published as part of Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing...
Fig. 3. Key NOESY correlations for compounds 1–10.Published as part of Zhang, Xueqing, Gao, Xiaoxu, ...
Fig. 3. Key NOESY correlations of compounds 1–5, 7 and 8.Published as part of Su, Hai-Guo, Peng, Xin...
Su, Hai-Guo, Peng, Xing-Rong, Shi, Qiang-Qiang, Huang, Yan-Jie, Zhou, Lin, Qiu, Ming-Hua (2020): Lan...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–10.Published as part of Zhang, Xueqing, ...
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. 4. Single-crystal X-ray structure of 5.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, ...
Fig. 5. Effects of compounds 1, 6, and 8–10 (15 μM) on ALT activity (A), AST activity (B), LDH activ...
Fig. 3. ORTEP drawings of 1 and 2.Published as part of Luo, Di, Xie, Ji-Zhao, Zou, Lu-Hui, Qiu, Li, ...
Fig. 1. Structures of the compounds from G. applanatum.Published as part of Luo, Di, Xie, Ji-Zhao, Z...
Luo, Di, Xie, Ji-Zhao, Zou, Lu-Hui, Qiu, Li, Huang, Dong-Ping, Xie, Yun-Feng, Xu, Huan-Ji, Wu, Xin-D...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of 1.Published as part of Luo, Di, Xie, Ji-Zhao...
Fig. 4. Experimental (black line) and calculated (red line) ECD spectra of 1–5 (A–E) and their enant...
Fig. 1. Structures of compounds 1–15.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, Qiang-Q...
Fig. 1. Structures of compounds 1–31.Published as part of Zhang, Xueqing, Gao, Xiaoxu, Long, Guoqing...
Fig. 3. Key NOESY correlations for compounds 1–10.Published as part of Zhang, Xueqing, Gao, Xiaoxu, ...
Fig. 3. Key NOESY correlations of compounds 1–5, 7 and 8.Published as part of Su, Hai-Guo, Peng, Xin...
Su, Hai-Guo, Peng, Xing-Rong, Shi, Qiang-Qiang, Huang, Yan-Jie, Zhou, Lin, Qiu, Ming-Hua (2020): Lan...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–10.Published as part of Zhang, Xueqing, ...
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. 4. Single-crystal X-ray structure of 5.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, ...
Fig. 5. Effects of compounds 1, 6, and 8–10 (15 μM) on ALT activity (A), AST activity (B), LDH activ...