Fig. 2. Key HMBC and 1H–1H COSY correlations of glycyuralins Q-X (1–8).Published as part of Hasan, Aobulikasimu, Zhang, Meng, Shang, Zhan-Peng, Yi, Yang, Kuang, Yi, Yu, Rong, Fan, Jing-Jing, Huang, Yu-Xi, Nijat, Dilaram, Qiao, Xue & Ye, Min, 2022, Bioactive prenylated phenolic compounds from the aerial parts of Glycyrrhiza uralensis, pp. 1-9 in Phytochemistry (113284) 201 on page 3, DOI: 10.1016/j.phytochem.2022.113284, http://zenodo.org/record/823685
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1–8.Published as part of Zhao, Yan-...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1, 3, 6, 9, 10 and 11.Published as part of...
Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10.Published as part of K...
Fig. 1. Structures of compounds 1–26 from the aerial parts of G. uralensis.Published as part of Hasa...
Hasan, Aobulikasimu, Zhang, Meng, Shang, Zhan-Peng, Yi, Yang, Kuang, Yi, Yu, Rong, Fan, Jing-Jing, H...
Fig. 3. The comparison of experimental and calculated ECD spectra of (1′′R, 2′′S)-1, (1′′S, 2′′R)-1,...
Fig. 4. The docking model and IC50 values of (1''R, 2''S)-1 and (1''S, 2''R)-1 against 3CLpro and PL...
Fig. 5. Bioactivity screening of compounds 1-26 [1a, (1''R, 2''S)-1; 1b, (1''S, 2''R)-1]. Each data ...
Fig. 2. Key 1H-1H COSY and HMBC correlations of 1–6.Published as part of Shu, Yan, Wang, Jia-Peng, L...
Fig. 2. Selected HMBC and 1H– 1H COSY correlations of compounds 1–4, 6, 8, 12, and 16.Published as p...
Fig. 2. Key HMBC, 1 H– 1 H COSY and NOESY correlations of compounds (1 3) and X-ray ORTEP drawing of...
Fig. 2. Key 1H-1H COSY and HMBC correlations of 1-7.Published as part of Huang, Ya-Ping, Zhao, Yuan-...
Fig. 2. Key HMBC correlations observed for 1 and 3–6 (600 MHz, in pyridine-d5).Published as part of ...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–5.Published as part of Mo, Shuyuan, Yin,...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1–8.Published as part of Zhao, Yan-...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1, 3, 6, 9, 10 and 11.Published as part of...
Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10.Published as part of K...
Fig. 1. Structures of compounds 1–26 from the aerial parts of G. uralensis.Published as part of Hasa...
Hasan, Aobulikasimu, Zhang, Meng, Shang, Zhan-Peng, Yi, Yang, Kuang, Yi, Yu, Rong, Fan, Jing-Jing, H...
Fig. 3. The comparison of experimental and calculated ECD spectra of (1′′R, 2′′S)-1, (1′′S, 2′′R)-1,...
Fig. 4. The docking model and IC50 values of (1''R, 2''S)-1 and (1''S, 2''R)-1 against 3CLpro and PL...
Fig. 5. Bioactivity screening of compounds 1-26 [1a, (1''R, 2''S)-1; 1b, (1''S, 2''R)-1]. Each data ...
Fig. 2. Key 1H-1H COSY and HMBC correlations of 1–6.Published as part of Shu, Yan, Wang, Jia-Peng, L...
Fig. 2. Selected HMBC and 1H– 1H COSY correlations of compounds 1–4, 6, 8, 12, and 16.Published as p...
Fig. 2. Key HMBC, 1 H– 1 H COSY and NOESY correlations of compounds (1 3) and X-ray ORTEP drawing of...
Fig. 2. Key 1H-1H COSY and HMBC correlations of 1-7.Published as part of Huang, Ya-Ping, Zhao, Yuan-...
Fig. 2. Key HMBC correlations observed for 1 and 3–6 (600 MHz, in pyridine-d5).Published as part of ...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–5.Published as part of Mo, Shuyuan, Yin,...
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1, 3, 6, and 9.Published as part of Chen, ...
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1–8.Published as part of Zhao, Yan-...
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1, 3, 6, 9, 10 and 11.Published as part of...
Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10.Published as part of K...