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Fig. 3. Key NOESY correlations observed for compounds 1 and 2 in Isoavenaciol and 7-hydroxy-isoavenaciol: Zn-chelating metallophores produced by root-endophytic Pezicula ericae in a Zn-accumulating plant, Aucuba japonica
Fig. 3. Key NOESY correlations observed for compounds 1 and 2.
Fig. 2. Key HMBC correlations observed for compound 1 in Isoavenaciol and 7-hydroxy-isoavenaciol: Zn-chelating metallophores produced by root-endophytic Pezicula ericae in a Zn-accumulating plant, Aucuba japonica
Fig. 2. Key HMBC correlations observed for compound 1.
Fig. 3. Key NOESY correlations for compounds 1–4 in Secondary metabolites from the underground parts of Valeriana sisymbriifolia Vahl. and their in vitro cytotoxic activities
Fig. 3. Key NOESY correlations for compounds 1–4.
Fig. 5. 2D NMR correlations for compound 6 in Bioactive pentacyclic triterpenoids from the whole plants of Pterocephalus hookeri
Fig. 5. 2D NMR correlations for compound 6.
Fig. 2. 2D NMR correlations for compound 1 in Bioactive pentacyclic triterpenoids from the whole plants of Pterocephalus hookeri
Fig. 2. 2D NMR correlations for compound 1.
Fig. 2. Key HMBC and 1H–1H in Bioactive prenylated phenolic compounds from the aerial parts of Glycyrrhiza uralensis
Fig. 2. Key HMBC and 1H–1H COSY correlations of glycyuralins Q-X (1–8).
Fig. 1 in Bioactive prenylated phenolic compounds from the aerial parts of Glycyrrhiza uralensis
Fig. 1. Structures of compounds 1–26 from the aerial parts of G. uralensis.
Fig. 3. Key ROESY correlations for compounds 1–7 in Cadinane sesquiterpenoids from the fungus Antrodiella albocinnamomea and their inhibitory activity against nitric oxide production
Fig. 3. Key ROESY correlations for compounds 1–7.
Fig. 4. ORTEP drawings for compounds 1, 3, 5 and 9 in Bridged cassane derivatives from the seeds of Caesalpinia sappan L. and their cytotoxic activities
Fig. 4. ORTEP drawings for compounds 1, 3, 5 and 9.
Fig. 2 in Chemical constituents of Antidesma bunius aerial parts and the anti-AGEs activity of selected compounds
Fig. 2. Key HMBC (H→C) and 1H–1H COSY correlations of compounds 1–5, 8, 16, 17, and 20.
Fig. 1 in Chemical constituents of Antidesma bunius aerial parts and the anti-AGEs activity of selected compounds
Fig. 1. (continued).
Fig. 1 in Chemical constituents of Antidesma bunius aerial parts and the anti-AGEs activity of selected compounds
Fig. 1. Chemical structures of isolated compounds from A. bunius aerial parts.
Fig. 1 in Cytotoxic compounds from the leaf of Bersama abyssinica subspecies abyssinica
Fig. 1. Structure of isolated compounds.
Fig. 1. Isolated compounds from D in Derrisrobustones A-D, isoflavones from the twig extract of Derris robusta (DC.) Benth. and their α-glucosidase inhibitory activity
Fig. 1. Isolated compounds from D. robusta twigs.
Fig. 2. Key HMBC and COSY correlations for compound 1a in Ingadosides A-C, acacic acid-type saponins from Inga sapindoides with potent inhibitory activity against downy mildew
Fig. 2. Key HMBC and COSY correlations for compound 1a.
Fig. 6. Experimental and calculated ECD spectra for compounds 2–7 in Jellynolide A, pokepola esters, and sponalisolides from the aquaculture sponge Spongia officinalis L
Fig. 6. Experimental and calculated ECD spectra for compounds 2–7 in MeOH.
Fig. 5. Experimental ECD spectra for compounds 1–6 and 9 in Kiiacylphnols A H, eight undescribed polycyclic polyprenylated acylphloroglucinols with anticancer activities from Hypericum przewalskii Maxim
Fig. 5. Experimental ECD spectra for compounds 1–6 and 9.
Fig. 3. Key NOESY correlations for compounds 1–10 in Lanostane-type triterpenoids from the mycelial mat of Ganoderma lucidum and their hepatoprotective activities
Fig. 3. Key NOESY correlations for compounds 1–10.
Fig. 4. Experimental and calculated ECD spectra for compounds 1 and 4 in Kiiacylphnols A H, eight undescribed polycyclic polyprenylated acylphloroglucinols with anticancer activities from Hypericum przewalskii Maxim
Fig. 4. Experimental and calculated ECD spectra for compounds 1 and 4.
Fig. 4. Key correlations for compounds 6–14 in Microbial transformation of capsaicin by several human intestinal fungi and their inhibitory effects against lysine-specific demethylase 1
Fig. 4. Key correlations for compounds 6–14 observed in HMBC and 1H–1H COSY spectra.
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.