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1,046 results for “anti-inflammatories”
Fig. 2 in Catecholic alkaloid sulfonates and aromatic nitro compounds from Portulaca oleracea and screening of their anti-inflammatory and anti-microbial activities
Fig. 2. Key HMBC (H→C) correlations of compounds 1, 3–6, 10, 16, and 17.
Fig. 9 in Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
Fig. 9. ORTEP drawing of the X-ray structures of haemanthamine (18) and (+)-tazettine (24).
Fig. 1 in Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
Fig. 1. Chemical structures of the isolated alkaloids 1–26.
Fig. 5 in Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
Fig. 5. Proposed biosynthetic pathway of zephyranine A (1).
Fig. 2. 1H–1H in Structurally diverse alkaloids with nine frameworks from Zephyranthes candida and their acetylcholinesterase inhibitory and anti-inflammatory activities
Fig. 2. 1H–1H COSY, key HMBC, and key NOESY correlations of zephyranines A D (1–4).
Fig. 3 in Sarcoelegans A-H, eight undescribed cembranes with anti-inflammatory and anti-thrombotic activities from the South China Sea soft coral Sarcophyton elegans
Fig. 3. Key NOESY correlations of compounds 1–8.
Fig. 5 in Sarcoelegans A-H, eight undescribed cembranes with anti-inflammatory and anti-thrombotic activities from the South China Sea soft coral Sarcophyton elegans
Fig. 5. Experimental and calculated ECD spectra of compounds 2–8.
Fig. 1 in Sarcoelegans A-H, eight undescribed cembranes with anti-inflammatory and anti-thrombotic activities from the South China Sea soft coral Sarcophyton elegans
Fig. 1. Structures of compounds 1–8.
Fig. 2. Key 1H–1H in Sarcoelegans A-H, eight undescribed cembranes with anti-inflammatory and anti-thrombotic activities from the South China Sea soft coral Sarcophyton elegans
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–8.
Fig. 8 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities
Fig. 8. The docked view of interactions between compound 5 with iNOS protein.
Fig. 1 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities
Fig. 1. Structures of compounds 1–19.
Fig. 4 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities
Fig. 4. The NOE correlations (A), CD spectrum, UV spectrum, and the exciton chirality (B) of 5.
Fig. 7 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities
Fig. 7. The Rh2(OCOCF3)4 induced CD spectrum of 11.
Fig. 6 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities
Fig. 6. The dihedral angles of four preferred conformations of 8 and 9.
Fig. 3 in Coumarin derivatives from the leaves and twigs of Murraya exotica L. and their anti-inflammatory activities
Fig. 3. The calculated and experimental ECD spectra of compounds 1a and 1b.
Fig. 3 in Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity
Fig. 3. Key NOESY correlations of compounds 1–3.
Fig. 5 in Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity
Fig. 5. Experimental and calculated ECD spectra of compounds 5 and 6.
Fig. 1 in Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity
Fig. 1. Chemical structures of 1–9.
Fig. 7 in Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity
Fig. 7. Inhibition against LPS-induced NO production in RAW264.7 macrophages.
Fig. 4 in Sesquiterpenoids from the roots of Daphne genkwa Siebold et Zucc. With potential anti-inflammatory activity
Fig. 4. Experimental and calculated ECD spectra of compounds 1–4.
ScienceDex guides
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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.