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4,563 results for “correlations”
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. Selected NOE correlations for 1–9 in Cirrhosinones A-H, 24-hydroxy cevanine-type alkaloids from Fritillaria cirrhosa
Fig. 4. Selected NOE correlations for 1–9.
Fig. 2. 1H–1H COSY and selective HMBC correlations for 1, 3 in Chemical constituents of Entandrophragma angolense and their anti-inflammatory activity
Fig. 2. 1H–1H COSY and selective HMBC correlations for 1, 3/4, 10, and 13.
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. 3. Key NOESY correlations for 1 and 4 in Lanostane triterpenoids from cultivated fruiting bodies of basidiomycete Ganoderma mbrekobenum
Fig. 3. Key NOESY correlations for 1 and 4 in acetone-d6.
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. 2. COSY and HMBC correlations for 1, 4, 5 in Lanostane triterpenoids from cultivated fruiting bodies of basidiomycete Ganoderma mbrekobenum
Fig. 2. COSY and HMBC correlations for 1, 4, 5, and 9.
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.
Fig. 3. 1H–1H COSY and selected HMBC correlations for 1–5 in Molecular networking-based discovery of anti-inflammatory chromene dimers from Melicope pteleifolia
Fig. 3. 1H–1H COSY and selected HMBC correlations for 1–5.
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 and 4–7 in Neritriterpenols A-G, euphane and tirucallane triterpenes from Euphorbia neriifolia L. and their bioactivity
Fig. 2. 1H–1H COSY and key HMBC correlations for compounds 1 and 4–7.
Fig. 3. Key HMBC correlations and 1 H- 1 H in MS/MS-based molecular networking accelerated discovery of germacrane-type sesquiterpene lactones from Elephantopus scaber L
Fig. 3. Key HMBC correlations and 1 H- 1 H COSY correlations of compounds 1 6.
Fig. 5. Keys NOE correlations for compounds 3, 4, 5 in Prenylated cyclohexene-type meroterpenoids and sulfur-containing xanthones produced by Pseudopestalotiopsis theae
Fig. 5. Keys NOE correlations for compounds 3, 4, 5.
Fig. 2. Key 2D NMR correlations for 1–6 in Undescribed ecdysteroids and phenolic glycosides from the roots of Cyathula officinalis Kuan and their anti-inflammatory activity in LPS-induced RAW 264.7 macrophages in vitro
Fig. 2. Key 2D NMR correlations for 1–6.
Supplementary materials for "Entropy is a good approximation to the electronic (static) correlation energy"
<p>Jupyter notebooks and data needed to reproduce the figures in the manuscript.</p>
Fig. 3. Key NOSEY correlations for metabolites 1–4 in Biotransformation of artemisinic acid to bioactive derivatives by endophytic Penicillium oxalicum B4 from Artemisia annua L.
Fig. 3. Key NOSEY correlations for metabolites 1–4.
Fig. 2. Key HMBC and 1H-1H COSY correlations for metabolites 1–5 in Biotransformation of artemisinic acid to bioactive derivatives by endophytic Penicillium oxalicum B4 from Artemisia annua L.
Fig. 2. Key HMBC and 1H-1H COSY correlations for metabolites 1–5.
Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10 in Sesquiterpene coumarins from Ferula samarkandica Korovin and their bioactivity
Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10.
Fig. 2. NOESY correlations for compound 1 and HMBC correlations for compound 2 in Indole alkaloids from the leaves of Ravenia spectabilis engl. with activity against pancreatic cancer cell line
Fig. 2. NOESY correlations for compound 1 and HMBC correlations for compound 2.
Fig. 2. Key COSY and HMBC correlations observed for lepidiline E in Alkaloids from Lepidium meyenii (Maca), structural revision of macaridine and UPLC-MS/MS feature-based molecular networking
Fig. 2. Key COSY and HMBC correlations observed for lepidiline E (1) F (2) and G (3).
Fig. 2. Key HMBC correlations observed for 1 and 3–6 in Calyhedins I-VI: Resin glycosides from the rhizomes of Calystegia hederacea
Fig. 2. Key HMBC correlations observed for 1 and 3–6 (600 MHz, in pyridine-d5).
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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.