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570 results for “Euphorbia”
Fig. 4. X in Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
Fig. 4. X-ray crystallographic diagram and experimental CD/calculated ECD spectra of 1.
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 and 4–7 in Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 and 4–7.
Fig. 3 in Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
Fig. 3. Key NOE correlations of compounds 1, 3, 6, and 7.
Fig. 5. 1H in Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
Fig. 5. 1H NMR spectra and assignments of compounds 1–3.
Fig. 5. Selected 2D in Phorneroids A-M, diverse types of diterpenoids from Euphorbia neriifolia
Fig. 5. Selected 2D NMR correlations of compound 12.
Fig. 4. Selected 2D in Phorneroids A-M, diverse types of diterpenoids from Euphorbia neriifolia
Fig. 4. Selected 2D NMR correlations of compound 8.
Fig. 7 in Phorneroids A-M, diverse types of diterpenoids from Euphorbia neriifolia
Fig. 7. Experimental and calculated ECD spectra of compounds 2 (A), 3 (B), 8 (C), and 12 (D).
Fig. 3. Selected 2D in Phorneroids A-M, diverse types of diterpenoids from Euphorbia neriifolia
Fig. 3. Selected 2D NMR correlations of compound 5.
Fig. 2. Selected 2D in Phorneroids A-M, diverse types of diterpenoids from Euphorbia neriifolia
Fig. 2. Selected 2D NMR correlations of compound 1.
Fig. 2. 1H–1H in Ingenane and jatrophane-type diterpenoids from Euphorbia kansui with multidrug resistance reversal activity
Fig. 2. 1H–1H COSY and key HMBC (A) and ROESY (B) correlations of 1.
Fig. 1 in Ingenane and jatrophane-type diterpenoids from Euphorbia kansui with multidrug resistance reversal activity
Fig. 1. Structures of compounds 1–32 isolated from Euphorbia kansui.
Fig. 22 in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 22. The SAR studies of abietane diterpenoids 10–11, 14–20 and 32.
Fig. 19. Essential oil isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 19. Essential oil isolated from E. ebracteolata.
Fig. 18. Steroids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 18. Steroids isolated from E. ebracteolata.
Fig. 17. Tannins isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 17. Tannins isolated from E. ebracteolata.
Fig. 14. Triterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 14. Triterpenoids isolated from E. ebracteolata.
Fig. 16. Flavonoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 16. Flavonoids isolated from E. ebracteolata.
Fig. 12. Tigliane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 12. Tigliane diterpenoids isolated from E. ebracteolata.
Fig. 10. Lathyrane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 10. Lathyrane diterpenoids isolated from E. ebracteolata.
Fig. 8. Kaurane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 8. Kaurane diterpenoids isolated from E. ebracteolata.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.