Fig. 2. Key HMBC and COSY correlations of compounds 1–6.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 4, DOI: 10.1016/j.phytochem.2022.113312, http://zenodo.org/record/823433
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–5.Published as part of Mo, Shuyuan, Yin,...
Fig. 2. The key HMBC () and 1H–1H COSY () correlations of compounds 1 and 3.Published as part of Yan...
Fig. 4. Key HMBC and COSY correlations of compounds 7–9, 11, and 12.Published as part of Yang, Shuen...
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...
Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horng-Huey, Wu, Ho-Cheng, Hsieh, Sung-Yuan, Wu, Ming-Der, Chen...
Fig. 6. X-ray single crystallographic analysis of compound 8.Published as part of Yang, Shuen-Shin, ...
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. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–5.Published as part of Mo, Shuyuan, Yin,...
Fig. 2. The key HMBC () and 1H–1H COSY () correlations of compounds 1 and 3.Published as part of Yan...
Fig. 4. Key HMBC and COSY correlations of compounds 7–9, 11, and 12.Published as part of Yang, Shuen...
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...
Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horng-Huey, Wu, Ho-Cheng, Hsieh, Sung-Yuan, Wu, Ming-Der, Chen...
Fig. 6. X-ray single crystallographic analysis of compound 8.Published as part of Yang, Shuen-Shin, ...
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. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–5.Published as part of Mo, Shuyuan, Yin,...
Fig. 2. The key HMBC () and 1H–1H COSY () correlations of compounds 1 and 3.Published as part of Yan...