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533 results for “Aerial”
Fig. 2 in Guaianolide sesquiterpenes and benzoate esters from the aerial parts of Siegesbeckia orientalis L. and their xanthine oxidase inhibitory activity
Fig. 2. Key HMBC (H → C) and COSY (H
Fig. 1 in Guaianolide sesquiterpenes and benzoate esters from the aerial parts of Siegesbeckia orientalis L. and their xanthine oxidase inhibitory activity
Fig. 1. Structures of compounds 1–12 isolated from S. orientalis.
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.
Fig. 3 in The racemic trimeric quinone and polycyclic quinones isolated from the aerial parts of Morinda umbellata L
Fig. 3. Key HMBC correlations of compounds 1–4.
Fig. 6. X in The racemic trimeric quinone and polycyclic quinones isolated from the aerial parts of Morinda umbellata L
Fig. 6. X-ray crystal structure of 4.
Fig. 1 in The racemic trimeric quinone and polycyclic quinones isolated from the aerial parts of Morinda umbellata L
Fig. 1. Structures of compounds 1–4.
Fig. 3. Key 1H-1H in Terpenoid and phenolic derivatives from the aerial parts of Elsholtzia rugulosa and their anti-inflammatory activity
Fig. 3. Key 1H-1H COSY () and HMBC () correlations of compounds 1–4.
Fig. 4 in Terpenoid and phenolic derivatives from the aerial parts of Elsholtzia rugulosa and their anti-inflammatory activity
Fig. 4. Experimental and calculated ECD spectra of compounds 1–4.
Fig. 2. X in Terpenoid and phenolic derivatives from the aerial parts of Elsholtzia rugulosa and their anti-inflammatory activity
Fig. 2. X-ray crystallographic structure of 1.
Fig. 3. Hypothetical biosynthetic pathways for 1, 6 in Diverse alkaloids from the aerial parts of Aconitum carmichaelii and antiproliferative activity of costemline via inhibiting SIRT1/ROCK1/ P-STAT3 pathways
Fig. 3. Hypothetical biosynthetic pathways for 1, 6, and 21.
Fig. 2. Key 1H–1H in Diverse alkaloids from the aerial parts of Aconitum carmichaelii and antiproliferative activity of costemline via inhibiting SIRT1/ROCK1/ P-STAT3 pathways
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–6.
Fig. 4 in Study of two isoforms of lipoxygenase by kinetic assays, docking and molecular dynamics of a specialised metabolite isolated from the aerial portion of Lithrea caustica (Anacardiaceae) and its synthetic analogs
Fig. 4. (Z)-3-(pentadec-10′-enyl)-catechol (1) and 3-pentadecylcatechol (2) Lineweaver-Burk graphs.
Fig. 1 in Study of two isoforms of lipoxygenase by kinetic assays, docking and molecular dynamics of a specialised metabolite isolated from the aerial portion of Lithrea caustica (Anacardiaceae) and its synthetic analogs
Fig. 1. Basic structure of urushiol.
Fig. 3 in Phytotoxic neo-clerodane diterpenoids from the aerial parts of Scutellaria barbata
Fig. 3. ORTEP drawing of 1, 3, and 27.
Fig. 4 in Phytotoxic neo-clerodane diterpenoids from the aerial parts of Scutellaria barbata
Fig. 4. (a) HMBC and 1H–1H COSY (b) NOESY correlations of compound 25.
ScienceDex guides
Understand access before you commit
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.