Fig. 2. 1H–1H COSY, key HMBC, and key NOESY correlations of zephyranines A D (1–4).Published as part of Zhan, Guanqun, Gao, Biao, Zhou, Junfei, Liu, Tingting, Zheng, Guijuan, Jin, Zhong & Yao, Guangmin, 2023, Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities, pp. 1-15 in Phytochemistry (113564) 207 on page 4, DOI: 10.1016/j.phytochem.2022.113564, http://zenodo.org/record/829053
Fig. 6. Key HMBC (HC) and 1H–1H COSY () correlations for compound 3.Published as part of Ye, Xiao, W...
Fig. 4. Key 1H–1H COSY and HMBC correlations of 1 8.Published as part of Yu, Muyuan, Kang, Xin, Li, ...
Fig. 2. Key HMBC (HC) and 1H–1H COSY () correlations for compound 1.Published as part of Ye, Xiao, W...
Fig. 5. Proposed biosynthetic pathway of zephyranine A (1).Published as part of Zhan, Guanqun, Gao, ...
Fig. 1. Chemical structures of the isolated alkaloids 1–26.Published as part of Zhan, Guanqun, Gao, ...
Zhan, Guanqun, Gao, Biao, Zhou, Junfei, Liu, Tingting, Zheng, Guijuan, Jin, Zhong, Yao, Guangmin (20...
Fig. 8. Experimental ECD spectra of zephyranines G–I (7–9), 6-O-ethylnerinine (10) and the calculate...
Fig. 7. Experimental and calculated ECD spectra of zephyranines C F (3–6), isolated as mixtures of r...
Fig. 4. Experimental and calculated ECD spectra of zephyranines A (1) and B (2) and their enantiomer...
Fig. 6. Linear correlation plots between the experimental and calculated 13C NMR data for two isomer...
Fig. 3. Linear correlation plots between the experimental and calculated 13C NMR data for four isome...
Fig. 10. The binding modes of 1 (A), 7 (B), 8 (C), and galanthamine (D) with AChE (PDB ID: 4M0E). Th...
Fig. 9. ORTEP drawing of the X-ray structures of haemanthamine (18) and (+)-tazettine (24).Published...
Sixteen new alkaloids belonging to the galanthamine (<b>1</b>–<b>6</b>), plicamine (<b>7</b>–<b>14</...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–11.Published as part of Huang, Wei-ming,...
Fig. 6. Key HMBC (HC) and 1H–1H COSY () correlations for compound 3.Published as part of Ye, Xiao, W...
Fig. 4. Key 1H–1H COSY and HMBC correlations of 1 8.Published as part of Yu, Muyuan, Kang, Xin, Li, ...
Fig. 2. Key HMBC (HC) and 1H–1H COSY () correlations for compound 1.Published as part of Ye, Xiao, W...
Fig. 5. Proposed biosynthetic pathway of zephyranine A (1).Published as part of Zhan, Guanqun, Gao, ...
Fig. 1. Chemical structures of the isolated alkaloids 1–26.Published as part of Zhan, Guanqun, Gao, ...
Zhan, Guanqun, Gao, Biao, Zhou, Junfei, Liu, Tingting, Zheng, Guijuan, Jin, Zhong, Yao, Guangmin (20...
Fig. 8. Experimental ECD spectra of zephyranines G–I (7–9), 6-O-ethylnerinine (10) and the calculate...
Fig. 7. Experimental and calculated ECD spectra of zephyranines C F (3–6), isolated as mixtures of r...
Fig. 4. Experimental and calculated ECD spectra of zephyranines A (1) and B (2) and their enantiomer...
Fig. 6. Linear correlation plots between the experimental and calculated 13C NMR data for two isomer...
Fig. 3. Linear correlation plots between the experimental and calculated 13C NMR data for four isome...
Fig. 10. The binding modes of 1 (A), 7 (B), 8 (C), and galanthamine (D) with AChE (PDB ID: 4M0E). Th...
Fig. 9. ORTEP drawing of the X-ray structures of haemanthamine (18) and (+)-tazettine (24).Published...
Sixteen new alkaloids belonging to the galanthamine (<b>1</b>–<b>6</b>), plicamine (<b>7</b>–<b>14</...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–11.Published as part of Huang, Wei-ming,...
Fig. 6. Key HMBC (HC) and 1H–1H COSY () correlations for compound 3.Published as part of Ye, Xiao, W...
Fig. 4. Key 1H–1H COSY and HMBC correlations of 1 8.Published as part of Yu, Muyuan, Kang, Xin, Li, ...
Fig. 2. Key HMBC (HC) and 1H–1H COSY () correlations for compound 1.Published as part of Ye, Xiao, W...