Fig. 1. Structures of compounds 1–10.Published as part of Li, Hang-Ying, Li, Ya, Wei, Wen-Jun, Ma, Kai-Liang, Chen, Jian-Jun & Gao, Kun, 2020, Halimane and labdane diterpenoids from Leonurus japonicus and their anti-inflammatory activity, pp. 1-6 in Phytochemistry (112280) 172 on page 2, DOI: 10.1016/j.phytochem.2020.112280, http://zenodo.org/record/829430
Leojaponin (2), a labdane diterpene, was isolated from the EtOH extract of the herb of Leonurus japo...
Fig. 1. Chemical structures of compounds 1–15.Published as part of Huang, Wei-ming, Bian, Yu-ting, C...
Fig. 1. The structures of compounds 1–13.Published as part of Liu, Yushuang, Liu, Wei, Li, Miaomiao ...
Li, Hang-Ying, Li, Ya, Wei, Wen-Jun, Ma, Kai-Liang, Chen, Jian-Jun, Gao, Kun (2020): Halimane and la...
Fig. 3. The key NOESY correlations of compounds 2, 5, 8, and 10.Published as part of Li, Hang-Ying, ...
Fig. 2. 1 H– 1 H COSY and selected HMBC correlations of compounds 2, 5, 8, and 10.Published as part ...
Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su, Zhenzhen, Zhong, Yan, Cao, Zeyu, Cao, Liang, Huang, Wenzhe...
Fig. 2. Selected HMBC correlations of compounds 2–7.Published as part of Yang, Biao, Hu, Yumei, Chen...
Fig. 1. Key HMBC and NOESY correlations of 1.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ning...
Fig. 3. Key NOESY correlations of 2–5.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su,...
Fig. 5. Comparison of experimental and calculated ECD spectra of 5–7 in MeOH.Published as part of Ya...
Fig. 4. Comparison of experimental and calculated ECD spectra of 1–4 in MeOH.Published as part of Ya...
<p>Two new labdane diterpenoids, Leojaponin E (<b>1</b>) and F (<b>2</b>), together with three known...
Fig. 1. Structures of compounds 1–15.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, Qiang-Q...
Fig. 1. Structures of compounds 1–10.Published as part of Yu, Zhang-Xin, Wang, Can-Hong, Nong, Xu-Hu...
Leojaponin (2), a labdane diterpene, was isolated from the EtOH extract of the herb of Leonurus japo...
Fig. 1. Chemical structures of compounds 1–15.Published as part of Huang, Wei-ming, Bian, Yu-ting, C...
Fig. 1. The structures of compounds 1–13.Published as part of Liu, Yushuang, Liu, Wei, Li, Miaomiao ...
Li, Hang-Ying, Li, Ya, Wei, Wen-Jun, Ma, Kai-Liang, Chen, Jian-Jun, Gao, Kun (2020): Halimane and la...
Fig. 3. The key NOESY correlations of compounds 2, 5, 8, and 10.Published as part of Li, Hang-Ying, ...
Fig. 2. 1 H– 1 H COSY and selected HMBC correlations of compounds 2, 5, 8, and 10.Published as part ...
Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su, Zhenzhen, Zhong, Yan, Cao, Zeyu, Cao, Liang, Huang, Wenzhe...
Fig. 2. Selected HMBC correlations of compounds 2–7.Published as part of Yang, Biao, Hu, Yumei, Chen...
Fig. 1. Key HMBC and NOESY correlations of 1.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ning...
Fig. 3. Key NOESY correlations of 2–5.Published as part of Yang, Biao, Hu, Yumei, Cheng, Ningbo, Su,...
Fig. 5. Comparison of experimental and calculated ECD spectra of 5–7 in MeOH.Published as part of Ya...
Fig. 4. Comparison of experimental and calculated ECD spectra of 1–4 in MeOH.Published as part of Ya...
<p>Two new labdane diterpenoids, Leojaponin E (<b>1</b>) and F (<b>2</b>), together with three known...
Fig. 1. Structures of compounds 1–15.Published as part of Su, Hai-Guo, Peng, Xing-Rong, Shi, Qiang-Q...
Fig. 1. Structures of compounds 1–10.Published as part of Yu, Zhang-Xin, Wang, Can-Hong, Nong, Xu-Hu...
Leojaponin (2), a labdane diterpene, was isolated from the EtOH extract of the herb of Leonurus japo...
Fig. 1. Chemical structures of compounds 1–15.Published as part of Huang, Wei-ming, Bian, Yu-ting, C...
Fig. 1. The structures of compounds 1–13.Published as part of Liu, Yushuang, Liu, Wei, Li, Miaomiao ...