Fig. 1. Structures of compounds 1–20 isolated from A. alpina.Published as part of Xue, Gui-Min, Zhao, Chen-Guang, Xue, Jin-Feng, Du, Kun, Duan, Jiang-Jing, Pan, Hao, Li, Meng, Chen, Hui, Sun, Yan-Jun, Feng, Wei-Sheng, Ma, Ting & Zhang, Wen-Da, 2022, Germacranolide- and guaianolide-type sesquiterpenoids from Achillea alpina L. reduce insulin resistance in palmitic acid-treated HepG2 cells via inhibition of the NLRP3 inflammasome pathway, pp. 1-9 in Phytochemistry (113297) 202 on page 4, DOI: 10.1016/j.phytochem.2022.113297, http://zenodo.org/record/823610
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compound 1.Published as part of Li, Honglian...
Fig. 3. ORTEP drawing of compounds 1, 4 and 6.Published as part of Li, Hongliang, Li, Jun, Liu, Meng...
Further phytochemical investigation into the aerial parts of Achillea clavennae has resulted in the ...
Xue, Gui-Min, Zhao, Chen-Guang, Xue, Jin-Feng, Du, Kun, Duan, Jiang-Jing, Pan, Hao, Li, Meng, Chen, ...
Fig. 4. The glucose consumption assay of compounds 1–20. The concentrations of these compounds were ...
Fig. 2. 1H–1H COSY, key HMBC and ROESY correlations of compounds 1 and 6–8.Published as part of Xue,...
Fig. 3. Experimental and calculated ECD spectra of 1–8.Published as part of Xue, Gui-Min, Zhao, Chen...
Fig. 5. The glucose consumption assay of compounds 4–6, 10 and 11 in different concentrations. The c...
Fig. 6. The inhibitory effects of 4 on the production of IL-1β and ROS in HepG2-IR cells. The expres...
Fig. 7. Inhibitory effects of 4 on the expression of proteins related to NLRP3 inflammasome in PA-in...
Fig. 6. The anti-inflammatory activity of compounds 1, 3, 4 and 10.Published as part of Li, Honglian...
Fig. 1. Structures of Millefolactons B1–B9 (1–9) isolated from A. millefolium L.Published as part of...
Fig. 1. Structures of compounds 1–12.Published as part of Li, Hongliang, Li, Jun, Liu, Mengqi, Xie, ...
Fig. 3. Key 1 H– 1 H COSY, HMBC, and NOESY correlations of compound 6.Published as part of Li, Hongl...
Fig. 5. ORTEP diagrams of compounds 1, 4, 6 and 8.Published as part of Li, Hongliang, Liu, Liu, Liu,...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compound 1.Published as part of Li, Honglian...
Fig. 3. ORTEP drawing of compounds 1, 4 and 6.Published as part of Li, Hongliang, Li, Jun, Liu, Meng...
Further phytochemical investigation into the aerial parts of Achillea clavennae has resulted in the ...
Xue, Gui-Min, Zhao, Chen-Guang, Xue, Jin-Feng, Du, Kun, Duan, Jiang-Jing, Pan, Hao, Li, Meng, Chen, ...
Fig. 4. The glucose consumption assay of compounds 1–20. The concentrations of these compounds were ...
Fig. 2. 1H–1H COSY, key HMBC and ROESY correlations of compounds 1 and 6–8.Published as part of Xue,...
Fig. 3. Experimental and calculated ECD spectra of 1–8.Published as part of Xue, Gui-Min, Zhao, Chen...
Fig. 5. The glucose consumption assay of compounds 4–6, 10 and 11 in different concentrations. The c...
Fig. 6. The inhibitory effects of 4 on the production of IL-1β and ROS in HepG2-IR cells. The expres...
Fig. 7. Inhibitory effects of 4 on the expression of proteins related to NLRP3 inflammasome in PA-in...
Fig. 6. The anti-inflammatory activity of compounds 1, 3, 4 and 10.Published as part of Li, Honglian...
Fig. 1. Structures of Millefolactons B1–B9 (1–9) isolated from A. millefolium L.Published as part of...
Fig. 1. Structures of compounds 1–12.Published as part of Li, Hongliang, Li, Jun, Liu, Mengqi, Xie, ...
Fig. 3. Key 1 H– 1 H COSY, HMBC, and NOESY correlations of compound 6.Published as part of Li, Hongl...
Fig. 5. ORTEP diagrams of compounds 1, 4, 6 and 8.Published as part of Li, Hongliang, Liu, Liu, Liu,...
Fig. 2. Key 1H–1H COSY, HMBC, and NOESY correlations of compound 1.Published as part of Li, Honglian...
Fig. 3. ORTEP drawing of compounds 1, 4 and 6.Published as part of Li, Hongliang, Li, Jun, Liu, Meng...
Further phytochemical investigation into the aerial parts of Achillea clavennae has resulted in the ...