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1,046 results for “anti-inflammatories”
Fig. 3 in Abietane diterpenoids from Dracocephalum moldavica L. and their anti-inflammatory activities in vitro
Fig. 3. Selected NOESY (↔) correlations of compound 1.
Fig. 9. PTP1B in Lignanamides from the roots of Limonium gmelinii (Willd.) Kuntze and their anti-diabetic, cytotoxic and anti-inflammatory activities
Fig. 9. PTP1B and α-glucosidase inhibitory activity of compounds 1–6, 8–19.
Fig. 6. Selected 1H–1H in Lignanamides from the roots of Limonium gmelinii (Willd.) Kuntze and their anti-diabetic, cytotoxic and anti-inflammatory activities
Fig. 6. Selected 1H–1H COSY and HMBC correlations of compound 7.
Fig. 2. Selected 1H–1H in Lignanamides from the roots of Limonium gmelinii (Willd.) Kuntze and their anti-diabetic, cytotoxic and anti-inflammatory activities
Fig. 2. Selected 1H–1H COSY and HMBC correlations of compound 1.
Fig. 3. Selected 1H–1H in Lignanamides from the roots of Limonium gmelinii (Willd.) Kuntze and their anti-diabetic, cytotoxic and anti-inflammatory activities
Fig. 3. Selected 1H–1H COSY and HMBC correlations of compound 2.
Fig. 2 in HRESIMS-guided isolation of aspidosperma-scandine type bisindole alkaloids from Melodinus cochinchinensis and their anti-inflammatory and cytotoxic activities
Fig. 2. Structures of compounds 1–3.
Fig. 4 in HRESIMS-guided isolation of aspidosperma-scandine type bisindole alkaloids from Melodinus cochinchinensis and their anti-inflammatory and cytotoxic activities
Fig. 4. Calculated and experimental ECD spectra of BIA 1.
Fig. 1 in Glycoglycerolipids from the leaves of Perilla frutescens (L.) Britton (Labiatae) and their anti-inflammatory activities in lipopolysaccharide-stimulated RAW264.7 cells
Fig. 1. The separation procedures of glycoglycerolipids from Perilla frutescens leaves.
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. 1 in Iridoids from Valeriana jatamansi with anti-inflammatory and antiproliferative properties
Fig. 1. Structures of compounds 1–7 isolated from Valeriana jatamansi.
Fig. 3 in Sesquiterpene derivatives from the agarwood of Aquilaria malaccensis and their anti-inflammatory effects on NO production of macrophage RAW 264.7 cells
Fig. 3. Selected NOESY correlations of compounds 1–9.
Fig. 4. X in Sesquiterpene derivatives from the agarwood of Aquilaria malaccensis and their anti-inflammatory effects on NO production of macrophage RAW 264.7 cells
Fig. 4. X-ray crystallographic structure of compounds 1 and 4.
Fig. 1 in Sesquiterpene derivatives from the agarwood of Aquilaria malaccensis and their anti-inflammatory effects on NO production of macrophage RAW 264.7 cells
Fig. 1. Chemical structure of compounds 1–9.
Fig. 2. Key HMBC, 1 H–1 H in Sesquiterpene derivatives from the agarwood of Aquilaria malaccensis and their anti-inflammatory effects on NO production of macrophage RAW 264.7 cells
Fig. 2. Key HMBC, 1 H–1 H COSY correlations of compounds 1–9.
Fig. 3. Single-crystal X in Tirucallane triterpenoids from the mastic (Pistacia lentiscus) and their anti-inflammatory and cytotoxic activities
Fig. 3. Single-crystal X-ray structure of compound 1.
Fig. 3. Key 1H-1H in Terpenoid and phenolic derivatives from the aerial parts of Elsholtzia rugulosa and their anti-inflammatory activity
Fig. 3. Key 1H-1H COSY () and HMBC () correlations of compounds 1–4.
Fig. 4 in Terpenoid and phenolic derivatives from the aerial parts of Elsholtzia rugulosa and their anti-inflammatory activity
Fig. 4. Experimental and calculated ECD spectra of compounds 1–4.
Fig. 2. X in Terpenoid and phenolic derivatives from the aerial parts of Elsholtzia rugulosa and their anti-inflammatory activity
Fig. 2. X-ray crystallographic structure of 1.
Fig. 1 in Catecholic alkaloid sulfonates and aromatic nitro compounds from Portulaca oleracea and screening of their anti-inflammatory and anti-microbial activities
Fig. 1. Chemical structures of compounds 1–22 isolated from P. oleracea.
Fig. 3 in Catecholic alkaloid sulfonates and aromatic nitro compounds from Portulaca oleracea and screening of their anti-inflammatory and anti-microbial activities
Fig. 3. Crystal structure of compound 2 monohydrate.
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.