Fig. 6. X-ray single crystallographic analysis of compound 8.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. 4. X-ray crystallographic structure of 1.Published as part of Wang, Xue, Jin, Xue-Yang, Zhou, J...
Fig. 4. X-ray structure of compounds 1–3.Published as part of Xian, Peng-Jie, Liu, Shu-Zhi, Wang, We...
Fig. 1. The chemical structures of compounds 1–14.Published as part of Gao, Suying, Wu, Ping, Xue, J...
Fig. 1. Structures of compounds 1–18.Published as part of Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horn...
Fig. 4. Key HMBC and COSY correlations of compounds 7–9, 11, and 12.Published as part of Yang, Shuen...
Fig. 5. Key NOESY correlations of compounds 8 and 9.Published as part of Yang, Shuen-Shin, Chen, Yih...
Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horng-Huey, Wu, Ho-Cheng, Hsieh, Sung-Yuan, Wu, Ming-Der, Chen...
Fig. 3. Key NOESY correlations of compounds 1–6.Published as part of Yang, Shuen-Shin, Chen, Yih-Fun...
Fig. 2. Key HMBC and COSY correlations of compounds 1–6.Published as part of Yang, Shuen-Shin, 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. 7. Single-crystal X-ray structure of 10.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi, Bu...
Fig. 3. Key NOESY correlations of compounds 2–7. (Asterisk (*) indicates the partial structures of c...
Fig. 1. Structures of compounds 1–15.Published as part of Xian, Peng-Jie, Liu, Shu-Zhi, Wang, Wen-Ji...
Fig. 4. X-ray crystallographic structure of 1.Published as part of Wang, Xue, Jin, Xue-Yang, Zhou, J...
Fig. 4. X-ray structure of compounds 1–3.Published as part of Xian, Peng-Jie, Liu, Shu-Zhi, Wang, We...
Fig. 1. The chemical structures of compounds 1–14.Published as part of Gao, Suying, Wu, Ping, Xue, J...
Fig. 1. Structures of compounds 1–18.Published as part of Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horn...
Fig. 4. Key HMBC and COSY correlations of compounds 7–9, 11, and 12.Published as part of Yang, Shuen...
Fig. 5. Key NOESY correlations of compounds 8 and 9.Published as part of Yang, Shuen-Shin, Chen, Yih...
Yang, Shuen-Shin, Chen, Yih-Fung, Ko, Horng-Huey, Wu, Ho-Cheng, Hsieh, Sung-Yuan, Wu, Ming-Der, Chen...
Fig. 3. Key NOESY correlations of compounds 1–6.Published as part of Yang, Shuen-Shin, Chen, Yih-Fun...
Fig. 2. Key HMBC and COSY correlations of compounds 1–6.Published as part of Yang, Shuen-Shin, 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. 7. Single-crystal X-ray structure of 10.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi, Bu...
Fig. 3. Key NOESY correlations of compounds 2–7. (Asterisk (*) indicates the partial structures of c...
Fig. 1. Structures of compounds 1–15.Published as part of Xian, Peng-Jie, Liu, Shu-Zhi, Wang, Wen-Ji...
Fig. 4. X-ray crystallographic structure of 1.Published as part of Wang, Xue, Jin, Xue-Yang, Zhou, J...
Fig. 4. X-ray structure of compounds 1–3.Published as part of Xian, Peng-Jie, Liu, Shu-Zhi, Wang, We...
Fig. 1. The chemical structures of compounds 1–14.Published as part of Gao, Suying, Wu, Ping, Xue, J...