Fig. 6. Cytotoxicity assay of compounds 4, 6, and 9.Published as part of Mo, Shuyuan, Yin, Jie, Ye, Zi, Li, Fengli, Lin, Shuang, Zhang, Sitian, Yang, Beiye, Yao, Jun, Wang, Jianping, Hu, Zhengxi & Zhang, Yonghui, 2021, Asperanstinoids A-E: Undescribed 3,5-dimethylorsellinic acid-based meroterpenoids from Aspergillus calidoustus, pp. 1-9 in Phytochemistry (112892) 190 on page 7, DOI: 10.1016/j.phytochem.2021.112892, http://zenodo.org/record/825829
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
Fig. 6. Structures of protoilludane-type sesquiterpenoids 101–103.Published as part of Zhao, Wen-Yu,...
Fig. 31. Biological activities of the terpenoids from the genus Aspergillus.Published as part of Zha...
Mo, Shuyuan, Yin, Jie, Ye, Zi, Li, Fengli, Lin, Shuang, Zhang, Sitian, Yang, Beiye, Yao, Jun, Wang, ...
Fig. 1. Chemical structures of compounds 1–12.Published as part of Mo, Shuyuan, Yin, Jie, Ye, Zi, Li...
Fig. 4. X-ray crystallographic structures of 1, 2, 4, 6, 8, and 9.Published as part of Mo, Shuyuan, ...
Fig. 5. Experimental ECD curves of compounds 3 and 5 in MeOH and their calculated ECD spectra at the...
Fig. 3. Key NOESY correlations (dashed arrows) of compounds 1–5.Published as part of Mo, Shuyuan, Yi...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–5.Published as part of Mo, Shuyuan, Yin,...
Fig. 19. Structures of meroterpenoids 223–243.Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi...
Fig. 25. Structures of meroterpenoids 269–288.Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi...
Fig. 23. Structures of meroterpenoids 244–268.Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi...
Fig. 7. Compounds 3 and 6 induce apoptosis of human B lymphoma cells.Published as part of Wei, Mengs...
Fig. 9. Structures of isopimaric-type diterpenoids 119–144.Published as part of Zhao, Wen-Yu, Yi, Ji...
Fig. 7. Structures of other-type sesquiterpenoids 104–110.Published as part of Zhao, Wen-Yu, Yi, Jin...
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
Fig. 6. Structures of protoilludane-type sesquiterpenoids 101–103.Published as part of Zhao, Wen-Yu,...
Fig. 31. Biological activities of the terpenoids from the genus Aspergillus.Published as part of Zha...
Mo, Shuyuan, Yin, Jie, Ye, Zi, Li, Fengli, Lin, Shuang, Zhang, Sitian, Yang, Beiye, Yao, Jun, Wang, ...
Fig. 1. Chemical structures of compounds 1–12.Published as part of Mo, Shuyuan, Yin, Jie, Ye, Zi, Li...
Fig. 4. X-ray crystallographic structures of 1, 2, 4, 6, 8, and 9.Published as part of Mo, Shuyuan, ...
Fig. 5. Experimental ECD curves of compounds 3 and 5 in MeOH and their calculated ECD spectra at the...
Fig. 3. Key NOESY correlations (dashed arrows) of compounds 1–5.Published as part of Mo, Shuyuan, Yi...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–5.Published as part of Mo, Shuyuan, Yin,...
Fig. 19. Structures of meroterpenoids 223–243.Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi...
Fig. 25. Structures of meroterpenoids 269–288.Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi...
Fig. 23. Structures of meroterpenoids 244–268.Published as part of Zhao, Wen-Yu, Yi, Jing, Chang, Yi...
Fig. 7. Compounds 3 and 6 induce apoptosis of human B lymphoma cells.Published as part of Wei, Mengs...
Fig. 9. Structures of isopimaric-type diterpenoids 119–144.Published as part of Zhao, Wen-Yu, Yi, Ji...
Fig. 7. Structures of other-type sesquiterpenoids 104–110.Published as part of Zhao, Wen-Yu, Yi, Jin...
Fig. 3. Key NOESY correlations of compounds 1–7.Published as part of Zhao, Min, Chen, Xiao-Cong, Pan...
Fig. 6. Structures of protoilludane-type sesquiterpenoids 101–103.Published as part of Zhao, Wen-Yu,...
Fig. 31. Biological activities of the terpenoids from the genus Aspergillus.Published as part of Zha...