Zhao, Min, Chen, Xiao-Cong, Pan, Wen-Cong, Liu, Xia, Tan, Shao-Li, Cui, Hui, Zhao, Zhong-Xiang (2022): Meroterpenoids from the fungus Penicillium sclerotiorum GZU-XW03-2 and their anti-inflammatory activity. Phytochemistry (113307) 202: 1-8, DOI: 10.1016/j.phytochem.2022.113307, URL: http://dx.doi.org/10.1016/j.phytochem.2022.11330
Peniandranoids A–E (1–5), five new meroterpenoids, together with three known analogues (6–8), were i...
Fig. 3. Key NOESY correlations of 1, 2, and 4.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yon...
Isopenicins A–C (1–3), three novel meroterpenoids possessing two types of unprecedented terpenoid-po...
Fig. 1. Structures of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan, Wen-Cong, ...
Fig. 2. 1H – 1H COSY and key HMBC correlations of compounds 1–7.Published as part of Zhao, Min, Chen...
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
Fig. 4. The experimental and calculated ECD spectra of compounds 1–7.Published as part of Zhao, Min,...
Fig. 5. Effects of compound 4 on COX-2 (A), IL-6 (B) and IL-1β (C) release from LPS-stimulated RAW26...
Fig. 6. Effect of compound 4 on LPS-stimulated protein iNOS expression in RAW264.7 cells. Data are p...
Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun, Xin-Yu, Lei, Chun, Li, Jing-Ya, Hou, Ai-Jun (2020): Mer...
An unusual austinoid, 1,2-dehydro-terredehydroaustin (1), together with two known meroterpenoids (2 ...
Pang, Xiaoyan, Wang, Pei, Liao, Shengrong, Zhou, Xuefeng, Lin, Xiuping, Yang, Bin, Tian, Xinpeng, Wa...
To discover the new medical entity from edible marine algae, our continuously natural product invest...
Fig. 5. X-ray ORTEP drawing for 2a.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun,...
Five new meroterpenoids, purpurogenolides A–E (<b>1</b>–<b>5</b>), and four known metabolites (<b>6<...
Peniandranoids A–E (1–5), five new meroterpenoids, together with three known analogues (6–8), were i...
Fig. 3. Key NOESY correlations of 1, 2, and 4.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yon...
Isopenicins A–C (1–3), three novel meroterpenoids possessing two types of unprecedented terpenoid-po...
Fig. 1. Structures of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan, Wen-Cong, ...
Fig. 2. 1H – 1H COSY and key HMBC correlations of compounds 1–7.Published as part of Zhao, Min, Chen...
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
Fig. 4. The experimental and calculated ECD spectra of compounds 1–7.Published as part of Zhao, Min,...
Fig. 5. Effects of compound 4 on COX-2 (A), IL-6 (B) and IL-1β (C) release from LPS-stimulated RAW26...
Fig. 6. Effect of compound 4 on LPS-stimulated protein iNOS expression in RAW264.7 cells. Data are p...
Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun, Xin-Yu, Lei, Chun, Li, Jing-Ya, Hou, Ai-Jun (2020): Mer...
An unusual austinoid, 1,2-dehydro-terredehydroaustin (1), together with two known meroterpenoids (2 ...
Pang, Xiaoyan, Wang, Pei, Liao, Shengrong, Zhou, Xuefeng, Lin, Xiuping, Yang, Bin, Tian, Xinpeng, Wa...
To discover the new medical entity from edible marine algae, our continuously natural product invest...
Fig. 5. X-ray ORTEP drawing for 2a.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yong-Mei, Sun,...
Five new meroterpenoids, purpurogenolides A–E (<b>1</b>–<b>5</b>), and four known metabolites (<b>6<...
Peniandranoids A–E (1–5), five new meroterpenoids, together with three known analogues (6–8), were i...
Fig. 3. Key NOESY correlations of 1, 2, and 4.Published as part of Shi, Qing, Li, Teng-Teng, Wu, Yon...
Isopenicins A–C (1–3), three novel meroterpenoids possessing two types of unprecedented terpenoid-po...