Fig. 6. Diterpenoids isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & Song, Shao-jiang, 2020, Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses, pp. 1-21 in Phytochemistry (112231) 171 on page 10, DOI: 10.1016/j.phytochem.2019.112231, http://zenodo.org/record/829401
Fig. 14. Concerted summary of SAR studies of flavans.Published as part of Han, Shuang, Li, Ling-zhi ...
Fig. 4. Key 1H–1H COSY, HMBC correlations of compounds 1, 2, 4, and 5.Published as part of Mi, Si-Hu...
Fig. 5. Key NOESY correlations of compounds 1, 2, 4, and 5.Published as part of Mi, Si-Hui, Zhao, Pe...
Fig. 7. Other compounds isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & S...
Fig. 3. Flavonoids isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & Song, ...
Fig. 5. Lignans isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & Song, Sha...
Fig. 2. Coumarins isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & Song, S...
Fig. 1. Leaves (A), flowers (B) and preparation (Zushima tablet) (C) of D. giraldii.Published as par...
Fig. 4. Flavans isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & Song, Sha...
Han, Shuang, Li, Ling-zhi, Song, Shao-jiang (2020): Daphne giraldii Nitsche (Thymelaeaceae): Phytoch...
Fig. 8. The mechanism of anti-inflammatory action of daphnetin (1) (Shen et al., 2017; Tu et al., 20...
Fig. 9. SAR studies of flavones with different substituted groups.Published as part of Han, Shuang, ...
Fig. 11. SAR studies of flavans 76–78, 81.Published as part of Han, Shuang, Li, Ling-zhi & Song, Sha...
Fig. 10. SAR studies of flavans 57–68.Published as part of Han, Shuang, Li, Ling-zhi & Song, Shao-ji...
Fig. 2. The structures of compounds 1–12.Published as part of Mi, Si-Hui, Zhao, Peng, Li, Qian, Zhan...
Fig. 14. Concerted summary of SAR studies of flavans.Published as part of Han, Shuang, Li, Ling-zhi ...
Fig. 4. Key 1H–1H COSY, HMBC correlations of compounds 1, 2, 4, and 5.Published as part of Mi, Si-Hu...
Fig. 5. Key NOESY correlations of compounds 1, 2, 4, and 5.Published as part of Mi, Si-Hui, Zhao, Pe...
Fig. 7. Other compounds isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & S...
Fig. 3. Flavonoids isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & Song, ...
Fig. 5. Lignans isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & Song, Sha...
Fig. 2. Coumarins isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & Song, S...
Fig. 1. Leaves (A), flowers (B) and preparation (Zushima tablet) (C) of D. giraldii.Published as par...
Fig. 4. Flavans isolated from D. giraldii.Published as part of Han, Shuang, Li, Ling-zhi & Song, Sha...
Han, Shuang, Li, Ling-zhi, Song, Shao-jiang (2020): Daphne giraldii Nitsche (Thymelaeaceae): Phytoch...
Fig. 8. The mechanism of anti-inflammatory action of daphnetin (1) (Shen et al., 2017; Tu et al., 20...
Fig. 9. SAR studies of flavones with different substituted groups.Published as part of Han, Shuang, ...
Fig. 11. SAR studies of flavans 76–78, 81.Published as part of Han, Shuang, Li, Ling-zhi & Song, Sha...
Fig. 10. SAR studies of flavans 57–68.Published as part of Han, Shuang, Li, Ling-zhi & Song, Shao-ji...
Fig. 2. The structures of compounds 1–12.Published as part of Mi, Si-Hui, Zhao, Peng, Li, Qian, Zhan...
Fig. 14. Concerted summary of SAR studies of flavans.Published as part of Han, Shuang, Li, Ling-zhi ...
Fig. 4. Key 1H–1H COSY, HMBC correlations of compounds 1, 2, 4, and 5.Published as part of Mi, Si-Hu...
Fig. 5. Key NOESY correlations of compounds 1, 2, 4, and 5.Published as part of Mi, Si-Hui, Zhao, Pe...