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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.
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. 2 in In silico and in vitro studies of isolated constituents from Callistemon citrinus leaves: Anti-microbial potential and inhibition of iNOS activity
Fig. 2. Key HMBC, COSY and NOESY correlations for compounds 1-5.
Fig. 1 in In silico and in vitro studies of isolated constituents from Callistemon citrinus leaves: Anti-microbial potential and inhibition of iNOS activity
Fig. 1. Structures of isolated compounds 1-34.
Fig. 6 in Glycosylated constituents isolated from the trunk of Abies holophylla and their anti-inflammatory and neurotrophic activity
Fig. 6. SAR study on the five cases of isolated compounds for antineuroinflammatory activity.
Fig. 1 in Glycosylated constituents isolated from the trunk of Abies holophylla and their anti-inflammatory and neurotrophic activity
Fig. 1. Chemical structures of 1–31.
Fig. 4 in Molecular networking-driven isolation of 8 -Glycosylated biscoumarins from Cruciata articulata
Fig. 4. Proposed fragmentation pathway of compounds 1 and 4; positive mode.
Fig. 1 in Isolation, identification, and activity evaluation of diterpenoid alkaloids from Aconitum sinomontanum
Fig. 1. Structures of compounds 1–25.
Fig. 3 in Molecular networking-driven isolation of 8 -Glycosylated biscoumarins from Cruciata articulata
Fig. 3. Selected HMBC (solid arrows) and NOESY (dashed arrows) correlations for compounds 1 and 3.
Fig. 3 in Isolation, identification, and activity evaluation of diterpenoid alkaloids from Aconitum sinomontanum
Fig. 3. ORTEP drawing of compounds 4 and 8.
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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.