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570 results for “Euphorbia”
Fig. 5. Rosane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 5. Rosane diterpenoids isolated from E. ebracteolata.
Fig. 6. Pimarane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 6. Pimarane diterpenoids isolated from E. ebracteolata.
Fig. 7. Atisane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 7. Atisane diterpenoids isolated from E. ebracteolata.
Fig. 4. Abietane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 4. Abietane diterpenoids isolated from E. ebracteolata.
Fig. 2. Monoterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 2. Monoterpenoids isolated from E. ebracteolata.
Fig. 3. Sesquiterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 3. Sesquiterpenoids isolated from E. ebracteolata.
Fig. 11. Ingenane diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 11. Ingenane diterpenoids isolated from E. ebracteolata.
Fig. 15. Acetophenones isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 15. Acetophenones isolated from E. ebracteolata.
Fig. 13. Dimeric diterpenoids isolated from E in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 13. Dimeric diterpenoids isolated from E. ebracteolata.
Fig. 23 in Euphorbia ebracteolata Hayata (Euphorbiaceae): A systematic review of its traditional uses, botany, phytochemistry, pharmacology, toxicology, and quality control
Fig. 23. The SAR studies of rosane diterpenoids 42–48, and 50.
Fig. 5. Proposed biosynthetic pathway for 1 in Euphorfinoids E-L: Diterpenoids from the roots of Euphorbia fischeriana with acetylcholinesterase inhibitory activity
Fig. 5. Proposed biosynthetic pathway for 1.
Fig. 1 in Euphorfinoids E-L: Diterpenoids from the roots of Euphorbia fischeriana with acetylcholinesterase inhibitory activity
Fig. 1. Structures of compounds 1–20 isolated from E. fischeriana Steud.
Fig. 4 in Euphorfinoids E-L: Diterpenoids from the roots of Euphorbia fischeriana with acetylcholinesterase inhibitory activity
Fig. 4. The ORTEP drawing of 1.
Fig. 2. Key 1H–1H in Euphorfinoids E-L: Diterpenoids from the roots of Euphorbia fischeriana with acetylcholinesterase inhibitory activity
Fig. 2. Key 1H–1H COSY, and HMBC correlations of compounds 1–8.
Fig. 6 in Diterpenoids from the aerial parts of Euphorbia antiquorum and their efficacy on nitric oxide inhibition
Fig. 6. Effect of 1 on the expression of iNOS protein.
Fig. 1 in Diterpenoids from the aerial parts of Euphorbia antiquorum and their efficacy on nitric oxide inhibition
Fig. 1. Structures of isolated compounds from the aerial parts of E. antiquorum.
Fig. 5 in Diterpenoids from the aerial parts of Euphorbia antiquorum and their efficacy on nitric oxide inhibition
Fig. 5. ORTEP drawing of 7.
Fig. 3 in Diterpenoids from the aerial parts of Euphorbia antiquorum and their efficacy on nitric oxide inhibition
Fig. 3. Key NOESY correlations of 1, 3, 5, and 8.
Fig. 4 in Diterpenoids from the aerial parts of Euphorbia antiquorum and their efficacy on nitric oxide inhibition
Fig. 4. ECD spectra of (a) 1 and 9 (b) 4 and 21, and (c) 7 and 22.
Fig. 2 in Diterpenoids from the aerial parts of Euphorbia antiquorum and their efficacy on nitric oxide inhibition
Fig. 2. Key COSY and HMBC correlations of 1, 3, and 5–8.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.