Fig. 3. The key 1H–1H NOESY () correlations of compounds 1–8.Published as part of Li, Yahui, Liu, Jingwen, Wu, Yingchun, Li, Yiming & Guo, Fujiang, 2022, Guaiane-type sesquiterpenes from Curcuma wenyujin, pp. 1-10 in Phytochemistry (113164) 198 on page 4, DOI: 10.1016/j.phytochem.2022.113164, http://zenodo.org/record/823606
Fig. 3. The key NOESY correlations of compounds 1–6 and 8.Published as part of Cheng, Zhuo-Yang, Hou...
Fig. 3. Key NOESY correlations of compounds 1, 3, 6, and 9.Published as part of Chen, Keliang, Chen,...
Fig. 3. Key NOESY correlations of compounds 1–5.Published as part of Wang, Junchi, Wang, Huijuan, Zh...
Fig. 2. 1H–1H COSY () and key 1H–13C HMBC () correlations of compounds 1–8.Published as part of Li, ...
Fig. 5. (continued).Published as part of Li, Yahui, Liu, Jingwen, Wu, Yingchun, Li, Yiming & Guo, Fu...
Fig. 4. X-ray single crystal results of compounds 1, 3, 5, 7, and 8.Published as part of Li, Yahui, ...
Li, Yahui, Liu, Jingwen, Wu, Yingchun, Li, Yiming, Guo, Fujiang (2022): Guaiane-type sesquiterpenes ...
Fig. 6. Nrf2-luciferase activity in HEK 293 cells treated with 15 and 16 (2.5–200 μM, n = 4). *p <0....
Fig. 3. Key NOESY correlations of compounds 1, 2, 3 and 4.Published as part of Muhammad, Ishaq, Luo,...
Fig. 7. 1H–1H COSY and key HMBC correlations of compounds 9, 10, and 11.Published as part of Muhamma...
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1–8.Published as part of Zhao, Yan-...
Fig. 2. 1H–1H COSY, key HMBC and NOSEY correlations of compounds 1–7.Published as part of Li, Hongli...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
The sesquiterpenoids are one of major groups of antioxidants in Curcuma besides curcuminoids. Howeve...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–6.Published as part of Wang, Junchi, Wan...
Fig. 3. The key NOESY correlations of compounds 1–6 and 8.Published as part of Cheng, Zhuo-Yang, Hou...
Fig. 3. Key NOESY correlations of compounds 1, 3, 6, and 9.Published as part of Chen, Keliang, Chen,...
Fig. 3. Key NOESY correlations of compounds 1–5.Published as part of Wang, Junchi, Wang, Huijuan, Zh...
Fig. 2. 1H–1H COSY () and key 1H–13C HMBC () correlations of compounds 1–8.Published as part of Li, ...
Fig. 5. (continued).Published as part of Li, Yahui, Liu, Jingwen, Wu, Yingchun, Li, Yiming & Guo, Fu...
Fig. 4. X-ray single crystal results of compounds 1, 3, 5, 7, and 8.Published as part of Li, Yahui, ...
Li, Yahui, Liu, Jingwen, Wu, Yingchun, Li, Yiming, Guo, Fujiang (2022): Guaiane-type sesquiterpenes ...
Fig. 6. Nrf2-luciferase activity in HEK 293 cells treated with 15 and 16 (2.5–200 μM, n = 4). *p <0....
Fig. 3. Key NOESY correlations of compounds 1, 2, 3 and 4.Published as part of Muhammad, Ishaq, Luo,...
Fig. 7. 1H–1H COSY and key HMBC correlations of compounds 9, 10, and 11.Published as part of Muhamma...
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1–8.Published as part of Zhao, Yan-...
Fig. 2. 1H–1H COSY, key HMBC and NOSEY correlations of compounds 1–7.Published as part of Li, Hongli...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
The sesquiterpenoids are one of major groups of antioxidants in Curcuma besides curcuminoids. Howeve...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–6.Published as part of Wang, Junchi, Wan...
Fig. 3. The key NOESY correlations of compounds 1–6 and 8.Published as part of Cheng, Zhuo-Yang, Hou...
Fig. 3. Key NOESY correlations of compounds 1, 3, 6, and 9.Published as part of Chen, Keliang, Chen,...
Fig. 3. Key NOESY correlations of compounds 1–5.Published as part of Wang, Junchi, Wang, Huijuan, Zh...
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