Fig. 2. Key HMBC (H C) and 1H–1H COSY (H▬H) correlations of 1, 3, 4, 5 and 6a.Published as part of Xu, Ke, Li, Gang, Zhu, Rongxiu, Xie, Fei, Li, Yuelan, Yang, Wenjing, Xu, Lintao, Shen, Tao, Zhao, Zuntian & Lou, Hongxiang, 2020, Polyketides from the endolichenic fungus Eupenicillium javanicum and their anti-inflammatory activities, pp. 1-7 in Phytochemistry (112191) 170 on page 3, DOI: 10.1016/j.phytochem.2019.112191, http://zenodo.org/record/829261
Fig. 5. Inhibitory activity of compounds 5, 9 and 10 against NO production in RAW 264.7 cells. Cells...
Fig. 3. Key NOESY correlations of compounds 2–7. (Asterisk (*) indicates the partial structures of c...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 3. Key NOESY correlations (H↔H) of compounds 1, 4, 5 and 6a.Published as part of Xu, Ke, Li, Ga...
Fig. 1. Structures of compounds 1–10.Published as part of Xu, Ke, Li, Gang, Zhu, Rongxiu, Xie, Fei, ...
Xu, Ke, Li, Gang, Zhu, Rongxiu, Xie, Fei, Li, Yuelan, Yang, Wenjing, Xu, Lintao, Shen, Tao, Zhao, Zu...
Fig. 4. Calculated ECD and experimental ECD curves of 1, 4 and 5.Published as part of Xu, Ke, Li, Ga...
Fig. 2. Key 1H–1H COSY, HMBC, NOESY, and 1H–15N HMBC correlations of compound 1.Published as part of...
Fig. 2. 1H – 1H COSY and key HMBC correlations of compounds 1–7.Published as part of Zhao, Min, Chen...
Fig. 5. Key 1H–1H COSY, HMBC, NOESY, and ROESY correlations of compounds 2–5.Published as part of Za...
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
Fig. 2. The key HMBC () and 1H–1H COSY () correlations of compounds 1 and 3.Published as part of Yan...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of 1–5.Published as part of Li, Xin-Rui, Liu, Juan, ...
Fig. 2. 1H–1H COSY and key HMBC correlations of compounds 1–7.Published as part of Xian, Peng-Jie, L...
Fig. 4. Key 1H–1H COSY (¡), HMBC (→), and NOESY (↔) correlations of compound 1.Published as part of ...
Fig. 5. Inhibitory activity of compounds 5, 9 and 10 against NO production in RAW 264.7 cells. Cells...
Fig. 3. Key NOESY correlations of compounds 2–7. (Asterisk (*) indicates the partial structures of c...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...
Fig. 3. Key NOESY correlations (H↔H) of compounds 1, 4, 5 and 6a.Published as part of Xu, Ke, Li, Ga...
Fig. 1. Structures of compounds 1–10.Published as part of Xu, Ke, Li, Gang, Zhu, Rongxiu, Xie, Fei, ...
Xu, Ke, Li, Gang, Zhu, Rongxiu, Xie, Fei, Li, Yuelan, Yang, Wenjing, Xu, Lintao, Shen, Tao, Zhao, Zu...
Fig. 4. Calculated ECD and experimental ECD curves of 1, 4 and 5.Published as part of Xu, Ke, Li, Ga...
Fig. 2. Key 1H–1H COSY, HMBC, NOESY, and 1H–15N HMBC correlations of compound 1.Published as part of...
Fig. 2. 1H – 1H COSY and key HMBC correlations of compounds 1–7.Published as part of Zhao, Min, Chen...
Fig. 5. Key 1H–1H COSY, HMBC, NOESY, and ROESY correlations of compounds 2–5.Published as part of Za...
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
Fig. 2. The key HMBC () and 1H–1H COSY () correlations of compounds 1 and 3.Published as part of Yan...
Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of 1–5.Published as part of Li, Xin-Rui, Liu, Juan, ...
Fig. 2. 1H–1H COSY and key HMBC correlations of compounds 1–7.Published as part of Xian, Peng-Jie, L...
Fig. 4. Key 1H–1H COSY (¡), HMBC (→), and NOESY (↔) correlations of compound 1.Published as part of ...
Fig. 5. Inhibitory activity of compounds 5, 9 and 10 against NO production in RAW 264.7 cells. Cells...
Fig. 3. Key NOESY correlations of compounds 2–7. (Asterisk (*) indicates the partial structures of c...
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–7.Published as part of Wang, Jia-Peng, Shu, Yan, L...