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440 results for “neuroprotection”
Fig. 1 in Chemical constituents from the fruits of Illicium simonsii and their antiviral activity and neuroprotective effect
Fig. 1. The structures of compounds 1–11.
Fig. 3 in Four undescribed ergostane-type steroids from Lasiodiplodia pseudotheobromae and their neuroprotective activity
Fig. 3. The key NOESY correlations of 1–4.
Fig. 2. The key 1H–1H in Four undescribed ergostane-type steroids from Lasiodiplodia pseudotheobromae and their neuroprotective activity
Fig. 2. The key 1H–1H COSY and HMBC correlations of 1–4.
Fig. 6 in Four undescribed ergostane-type steroids from Lasiodiplodia pseudotheobromae and their neuroprotective activity
Fig. 6. Experimental and calculated ECD spectra (200–400 nm) of 3 and 4.
Fig. 1 in Four undescribed ergostane-type steroids from Lasiodiplodia pseudotheobromae and their neuroprotective activity
Fig. 1. Structures of compounds 1–5.
Fig. 5. X in Four undescribed ergostane-type steroids from Lasiodiplodia pseudotheobromae and their neuroprotective activity
Fig. 5. X-ray crystal structures of 1 and 2.
Fig. 4 in Four undescribed ergostane-type steroids from Lasiodiplodia pseudotheobromae and their neuroprotective activity
Fig. 4. Candidate structures of compounds 1 and 2.
Fig. 1 in HPLC-PDA-Guided isolation of glucosyloxybenzyl 2-isobutylmalates from the pseudobulbs of Bletilla striata with neuroprotective and antimicrobial activities
Fig. 1. Structures of compounds 1–12 isolated from the pseudobulbs of Bletilla striata.
Fig. 3. Key 2D in HPLC-PDA-Guided isolation of glucosyloxybenzyl 2-isobutylmalates from the pseudobulbs of Bletilla striata with neuroprotective and antimicrobial activities
Fig. 3. Key 2D NMR correlations of compound 12.
Fig. 2. Key 2D in HPLC-PDA-Guided isolation of glucosyloxybenzyl 2-isobutylmalates from the pseudobulbs of Bletilla striata with neuroprotective and antimicrobial activities
Fig. 2. Key 2D NMR correlations of compounds 1, 3, 6, and 8.
Fig. 3 in Structures and neuroprotective activities of triterpenoids from Cynomorium coccineum subsp. songaricum (Rupr.) J. Leonard
Fig. 3. Key ROESY correlations of compounds 1‒4.
Fig. 5. Proposed biosynthetic pathways for 1 in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 5. Proposed biosynthetic pathways for 1.
Fig. 4 in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 4. Experimental and calculated ECD spectra of compounds 4–5.
Fig. 3 in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 3. Experimental and calculated ECD spectra of compounds 1–3.
Fig. 1 in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 1. Structures of compounds 1–5.
Fig. 2. Key 2D in Xylarinaps A-E, five pairs of naphthalenone derivatives with neuroprotective activities from Xylaria nigripes
Fig. 2. Key 2D NMR correlations of compounds 1–5.
Fig. 2. Key HMBC and 1H–1H in Lignans and neolignans with isovaleroyloxy moiety from Solanum lyratum Thunb.: Chiral resolution, configurational assignment and neuroprotective effects
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1, 4, 6, 8 and 9.
Fig. 3 in Lignans and neolignans with isovaleroyloxy moiety from Solanum lyratum Thunb.: Chiral resolution, configurational assignment and neuroprotective effects
Fig. 3. Key NOESY correlations of compounds 1–3, 8 and 9.
Fig. 6 in Guaiane-type sesquiterpenoids from the roots of Stellera chamaejasme L. and their neuroprotective activities
Fig. 6. The ORTEP drawing of 5 and 10.
Fig. 1 in Guaiane-type sesquiterpenoids from the roots of Stellera chamaejasme L. and their neuroprotective activities
Fig. 1. The structures of compounds 1–16 isolated from Stellera chamaejasme L.
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.