Fig. 4. Antiproliferative activity of MAPs isolated from Hypericum hengshanense against five cancer cell lines (n = 3, ***p <0.001 and **p <0.01 compared with the control group, cisplatin (DDP) and taxol served as positive control).Published as part of Zhang, Ruifei, Cheng, Zhuo, Fang, Qiong, Kennelly, Edward J. & Long, Chunlin, 2023, Monoterpenoid acylphloroglucinols from Hypericum hengshanense W. T. Wang with antiproliferative activities, pp. 1-8 in Phytochemistry (113500) 205 on page 6, DOI: 10.1016/j.phytochem.2022.113500, http://zenodo.org/record/823037
AbstractNatural products are regarded as major and important sources of molecules used in chemothera...
Fig. 1. Structures of compounds 1–10.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi, Bu, Pengfe...
Fig. 1. Chemical structures of compounds 1–7.Published as part of Shi, Zhengyi, Tan, Xiaosheng, Hu, ...
Zhang, Ruifei, Cheng, Zhuo, Fang, Qiong, Kennelly, Edward J., Long, Chunlin (2023): Monoterpenoid ac...
Fig. 2. Key HMBC, COSY, and NOESY/ROESY correlations of hyphengshanols A–D (1–3 and 9).Published as ...
Fig. 8. Calculated and experimental ECD spectra of 5 (A) and experimental ECD curves of compounds 5,...
Fig. 4. Experimental and calculated ECD spectra of 1 (A) and experimental ECD curves of compounds 1 ...
Natural products are regarded as major and important sources of molecules used in chemotherapy. Hype...
Fig. 9. The anti-inflammatory activity of compound 1–13.Published as part of Sun, Haoran, Wang, Jiaj...
Fig. 6. Experimental and calculated ECD spectra of 3 (A) and experimental ECD curves of compounds 3 ...
Duan, Yulin, Hu, Ping, Guo, Yi, Bu, Pengfei, Shi, Zhengyi, Cao, Yunfang, Zhang, Yeting, Hu, Hong, To...
Fig. 10. Effects of compounds 1 and 10 to cancer cell lines. HL60 and SU-DHL-4 cells were exposed to...
Fig. 6. Key 2D correlations of compounds 4 and 5.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 2. Key 2D correlations of compounds 1 and 3.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
AbstractNatural products are regarded as major and important sources of molecules used in chemothera...
Fig. 1. Structures of compounds 1–10.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi, Bu, Pengfe...
Fig. 1. Chemical structures of compounds 1–7.Published as part of Shi, Zhengyi, Tan, Xiaosheng, Hu, ...
Zhang, Ruifei, Cheng, Zhuo, Fang, Qiong, Kennelly, Edward J., Long, Chunlin (2023): Monoterpenoid ac...
Fig. 2. Key HMBC, COSY, and NOESY/ROESY correlations of hyphengshanols A–D (1–3 and 9).Published as ...
Fig. 8. Calculated and experimental ECD spectra of 5 (A) and experimental ECD curves of compounds 5,...
Fig. 4. Experimental and calculated ECD spectra of 1 (A) and experimental ECD curves of compounds 1 ...
Natural products are regarded as major and important sources of molecules used in chemotherapy. Hype...
Fig. 9. The anti-inflammatory activity of compound 1–13.Published as part of Sun, Haoran, Wang, Jiaj...
Fig. 6. Experimental and calculated ECD spectra of 3 (A) and experimental ECD curves of compounds 3 ...
Duan, Yulin, Hu, Ping, Guo, Yi, Bu, Pengfei, Shi, Zhengyi, Cao, Yunfang, Zhang, Yeting, Hu, Hong, To...
Fig. 10. Effects of compounds 1 and 10 to cancer cell lines. HL60 and SU-DHL-4 cells were exposed to...
Fig. 6. Key 2D correlations of compounds 4 and 5.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1 and 3.Published as part of Shi, Z...
Fig. 2. Key 2D correlations of compounds 1 and 3.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi...
AbstractNatural products are regarded as major and important sources of molecules used in chemothera...
Fig. 1. Structures of compounds 1–10.Published as part of Duan, Yulin, Hu, Ping, Guo, Yi, Bu, Pengfe...
Fig. 1. Chemical structures of compounds 1–7.Published as part of Shi, Zhengyi, Tan, Xiaosheng, Hu, ...