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Fig. 2. Key 2D NMR correlations for compounds 1, 3, 12, 17, 18 in Iridoid glycosides and lignans from the fruits of Gardenia jasminoides Eills
Fig. 2. Key 2D NMR correlations for compounds 1, 3, 12, 17, 18, and 21.
Fig. 4. Key NOESY correlations for seneciojanine B-D in Pyrrolizidine alkaloids and unusual millingtojanine A-B from Jacobaea vulgaris (syn. Senecio jacobaea L.)
Fig. 4. Key NOESY correlations for seneciojanine B-D (2–4).
Fig. 2. Selected HMBC correlations for brevianthrones A1 in Brevianthrones, bianthrones from a Chinese isolate of the endophytic fungus Colletotrichum brevisporum
Fig. 2. Selected HMBC correlations for brevianthrones A1 (1), B1 (4) and B4 (7).
Fig. 6. Key NOE correlations for compounds 6 and 7 in Dimeric and esterified sesquiterpenes from the liverwort Chiastocaulon caledonicum
Fig. 6. Key NOE correlations for compounds 6 and 7.
Fig. 3. Primary NOESY correlations for 1–6 in Sesquiterpenes from Echinacea purpurea and their anti-inflammatory activities
Fig. 3. Primary NOESY correlations for 1–6.
Fig. 2. Important HMBC and 1H–1H COSY correlations for 1–6 in Sesquiterpenes from Echinacea purpurea and their anti-inflammatory activities
Fig. 2. Important HMBC and 1H–1H COSY correlations for 1–6.
Fig. 5. HMBC correlations observed for 3 in Ecdysteroids from the underground parts of Rhaponticum acaule (L.) DC
Fig. 5. HMBC correlations observed for 3.
Fig. 7. NOESY correlations observed for 4 and 5 in Ecdysteroids from the underground parts of Rhaponticum acaule (L.) DC
Fig. 7. NOESY correlations observed for 4 and 5.
Fig. 2. Key HMBC correlations for compound 1 in Semipapposides A-M, triterpenoid bidesmosides saponins from the roots of Scabiosa semipapposa
Fig. 2. Key HMBC correlations for compound 1.
Fig. 2. Significant 1 H– 1 H COSY and key HMBC correlations for russelliinosides A-C in Dammarane-type triterpenoid saponins from Salvia russellii Benth.
Fig. 2. Significant 1 H– 1 H COSY and key HMBC correlations for russelliinosides A-C; 1–3.
Fig. 2. Key HMBC and 1H–1H COSY correlations for 1–3 and 5 in Triterpene glycosides and phenylpropane derivatives from Staurogyne concinnula possessing anti-angiogenic activity
Fig. 2. Key HMBC and 1H–1H COSY correlations for 1–3 and 5.
Fig. 3. Key ROESY correlations for compounds 1–3 and 7 in Iridoids from Valeriana jatamansi with anti-inflammatory and antiproliferative properties
Fig. 3. Key ROESY correlations for compounds 1–3 and 7.
Fig. 2. COSY and key HMBC correlations for 1 and 2 in Limonoids from fruiting bodies of the wood-rot basidiomycete Fulvifomes xylocarpicola associated with the mangrove tree Xylocarpus granatum
Fig. 2. COSY and key HMBC correlations for 1 and 2.
Fig. 3. Key NOESY correlations for 1 in Limonoids from fruiting bodies of the wood-rot basidiomycete Fulvifomes xylocarpicola associated with the mangrove tree Xylocarpus granatum
Fig. 3. Key NOESY correlations for 1.
Fig. 7. Selected key NOESY correlations for compound 3 in Ten undescribed cembrane-type diterpenoids from the gum resin of Boswellia sacra and their biological activities
Fig. 7. Selected key NOESY correlations for compound 3.
Fig. 3. Selected key ROESY correlations for compound 1 in Ten undescribed cembrane-type diterpenoids from the gum resin of Boswellia sacra and their biological activities
Fig. 3. Selected key ROESY correlations for compound 1.
Fig. 3. Key ROESY correlations for compounds 6 and 9 in Iridoids and bis-iridoids from Valeriana jatamansi and their cytotoxicity against human glioma stem cells
Fig. 3. Key ROESY correlations for compounds 6 and 9.
Fig. 7. Key COSY and NOSEY correlations for compound 3 in New tricks for old dogs: Two new macrocyclic trichothecene epimers and absolute configuration of 16-hydroxyverrucarin B
Fig. 7. Key COSY and NOSEY correlations for compound 3.
Fig. 2. Key HMBC correlations and COSY couplings for compounds 1–7, Y in Norlignan glucosides from Hypoxis hemerocallidea and their potential in vitro anti-inflammatory activity via inhibition of iNOS and NF-ΚB
Fig. 2. Key HMBC correlations and COSY couplings for compounds 1–7, Y, and Z.
Fig. 2. Key COSY and NOSEY correlations for compound 1 in New tricks for old dogs: Two new macrocyclic trichothecene epimers and absolute configuration of 16-hydroxyverrucarin B
Fig. 2. Key COSY and NOSEY correlations for compound 1.
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.