Fig. 4. Key HMBC and COSY correlations of compounds 7–9, 11, and 12.Published as part of Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horng-Huey, Wu, Ho-Cheng, Hsieh, Sung-Yuan, Wu, Ming-Der, Cheng, Ming-Jen & Chang, Hsun-Shuo, 2022, Undescribed alkyne-geranylcyclohexenetriols from the endophyte Diaporthe caulivora 09F0132 and their anti-melanogenic activity, pp. 1-12 in Phytochemistry (113312) 202 on page 6, DOI: 10.1016/j.phytochem.2022.113312, http://zenodo.org/record/823433
Fig. 2. The key HMBC () and 1H–1H COSY () correlations of compounds 1 and 3.Published as part of Yan...
Fig. 4. Key 1H–1H COSY and HMBC correlations of 1 8.Published as part of Yu, Muyuan, Kang, Xin, Li, ...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of neuropyrones A–E (1–5).Published as part of Li, X...
Fig. 2. Key HMBC and COSY correlations of compounds 1–6.Published as part of Yang, Shuen-Shin, Chen,...
Fig. 3. Key NOESY correlations of compounds 1–6.Published as part of Yang, Shuen-Shin, Chen, Yih-Fun...
Fig. 5. Key NOESY correlations of compounds 8 and 9.Published as part of Yang, Shuen-Shin, Chen, Yih...
Fig. 1. Structures of compounds 1–18.Published as part of Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horn...
Fig. 6. X-ray single crystallographic analysis of compound 8.Published as part of Yang, Shuen-Shin, ...
Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horng-Huey, Wu, Ho-Cheng, Hsieh, Sung-Yuan, Wu, Ming-Der, Chen...
Fig. 8. Anti-melanogenic activities of caulivotrioloxin A (1) in mouse melanoma B16–F10 cells. Cells...
Fig. 7. Effects of different compounds derived from D. caulivora 09F0132 on the cell viability of hu...
Fig. 9. The inhibitory effects of caulivotrioloxin A (1) on the protein expression of melanogenic pr...
Fig. 2. 1H–1H COSY and key HMBC correlations of compounds 1–7.Published as part of Xian, Peng-Jie, L...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
Fig. 3. Key NOESY correlations of compounds 2–7. (Asterisk (*) indicates the partial structures of c...
Fig. 2. The key HMBC () and 1H–1H COSY () correlations of compounds 1 and 3.Published as part of Yan...
Fig. 4. Key 1H–1H COSY and HMBC correlations of 1 8.Published as part of Yu, Muyuan, Kang, Xin, Li, ...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of neuropyrones A–E (1–5).Published as part of Li, X...
Fig. 2. Key HMBC and COSY correlations of compounds 1–6.Published as part of Yang, Shuen-Shin, Chen,...
Fig. 3. Key NOESY correlations of compounds 1–6.Published as part of Yang, Shuen-Shin, Chen, Yih-Fun...
Fig. 5. Key NOESY correlations of compounds 8 and 9.Published as part of Yang, Shuen-Shin, Chen, Yih...
Fig. 1. Structures of compounds 1–18.Published as part of Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horn...
Fig. 6. X-ray single crystallographic analysis of compound 8.Published as part of Yang, Shuen-Shin, ...
Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horng-Huey, Wu, Ho-Cheng, Hsieh, Sung-Yuan, Wu, Ming-Der, Chen...
Fig. 8. Anti-melanogenic activities of caulivotrioloxin A (1) in mouse melanoma B16–F10 cells. Cells...
Fig. 7. Effects of different compounds derived from D. caulivora 09F0132 on the cell viability of hu...
Fig. 9. The inhibitory effects of caulivotrioloxin A (1) on the protein expression of melanogenic pr...
Fig. 2. 1H–1H COSY and key HMBC correlations of compounds 1–7.Published as part of Xian, Peng-Jie, L...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
Fig. 3. Key NOESY correlations of compounds 2–7. (Asterisk (*) indicates the partial structures of c...
Fig. 2. The key HMBC () and 1H–1H COSY () correlations of compounds 1 and 3.Published as part of Yan...
Fig. 4. Key 1H–1H COSY and HMBC correlations of 1 8.Published as part of Yu, Muyuan, Kang, Xin, Li, ...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of neuropyrones A–E (1–5).Published as part of Li, X...