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1,046 results for “anti-inflammatories”

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Fig. 6 in Guaiane-type sesquiterpenoids from Cinnamomum migao H. W. Li: And their anti-inflammatory activities

Fig. 6. CD spectrum of compounds 5 and 6

opennotspecifiedOct 2021View details →
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Fig. 5 in Guaiane-type sesquiterpenoids from Cinnamomum migao H. W. Li: And their anti-inflammatory activities

Fig. 5. CD spectrum of compounds 3 and 4.

opennotspecifiedOct 2021View details →
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Fig. 3 in Guaiane-type sesquiterpenoids from Cinnamomum migao H. W. Li: And their anti-inflammatory activities

Fig. 3. Key NOESY correlations of compounds 1, 2, 3 and 4.

opennotspecifiedOct 2021View details →
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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.

opennotspecifiedNov 2020View details →
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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.

opennotspecifiedNov 2020View details →
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Fig. 1 in Sesquiterpenes from Echinacea purpurea and their anti-inflammatory activities

Fig. 1. The structures of compounds 1–12.

opennotspecifiedNov 2020View details →
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Fig. 6 in Meroterpenoids with diverse structures and anti-inflammatory activities from Rhododendron anthopogonoides

Fig. 6. ΔδH(S R) values (in ppm) for (S)-/(R)-MTPA esters of 8a and 8b′.

opennotspecifiedDec 2020View details →
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Fig. 5. X-ray ORTEP drawing for 2a in Meroterpenoids with diverse structures and anti-inflammatory activities from Rhododendron anthopogonoides

Fig. 5. X-ray ORTEP drawing for 2a.

opennotspecifiedDec 2020View details →
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Fig. 2. Key 1 H– 1 H in Meroterpenoids with diverse structures and anti-inflammatory activities from Rhododendron anthopogonoides

Fig. 2. Key 1 H– 1 H COSY and HMBC correlations of 1, 2, 4, 5, and 9.

opennotspecifiedDec 2020View details →
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Fig. 3 in Meroterpenoids with diverse structures and anti-inflammatory activities from Rhododendron anthopogonoides

Fig. 3. Key NOESY correlations of 1, 2, and 4.

opennotspecifiedDec 2020View details →
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Fig. 4 in Polyketides from the endolichenic fungus Eupenicillium javanicum and their anti-inflammatory activities

Fig. 4. Calculated ECD and experimental ECD curves of 1, 4 and 5.

opennotspecifiedFeb 2020View details →
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Fig. 1 in Polyketides from the endolichenic fungus Eupenicillium javanicum and their anti-inflammatory activities

Fig. 1. Structures of compounds 1–10.

opennotspecifiedFeb 2020View details →
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Fig. 2 in Polyketides from the endolichenic fungus Eupenicillium javanicum and their anti-inflammatory activities

Fig. 2. Key HMBC (H C) and 1H–1H COSY (H▬H) correlations of 1, 3, 4, 5 and 6a.

opennotspecifiedFeb 2020View details →
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Fig. 3 in Polyketides from the endolichenic fungus Eupenicillium javanicum and their anti-inflammatory activities

Fig. 3. Key NOESY correlations (H↔H) of compounds 1, 4, 5 and 6a.

opennotspecifiedFeb 2020View details →
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Fig. 4 in Abietane diterpenoids from Dracocephalum moldavica L. and their anti-inflammatory activities in vitro

Fig. 4. Calculated and experimental ECD spectra of compound 1 (A) and compound 5 (B) in MeCN.

opennotspecifiedApr 2021View details →
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Fig. 1 in Abietane diterpenoids from Dracocephalum moldavica L. and their anti-inflammatory activities in vitro

Fig. 1. Structures of 1–11 isolated from D. moldavica L.

opennotspecifiedApr 2021View details →
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Fig. 10 in Lignanamides from the roots of Limonium gmelinii (Willd.) Kuntze and their anti-diabetic, cytotoxic and anti-inflammatory activities

Fig. 10. Cytotoxicities of compounds 1–19 against the HeLa and MCF-7 cell lines.

opennotspecifiedApr 2021View details →
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Fig. 5. Selected 1H–1H in Lignanamides from the roots of Limonium gmelinii (Willd.) Kuntze and their anti-diabetic, cytotoxic and anti-inflammatory activities

Fig. 5. Selected 1H–1H COSY and HMBC correlations of compound 6.

opennotspecifiedApr 2021View details →
zenodo28/100

Fig. 1 in Lignanamides from the roots of Limonium gmelinii (Willd.) Kuntze and their anti-diabetic, cytotoxic and anti-inflammatory activities

Fig. 1. Structures of compounds 1–21.

opennotspecifiedApr 2021View details →
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Fig. 4. Selected 1H–1H in Lignanamides from the roots of Limonium gmelinii (Willd.) Kuntze and their anti-diabetic, cytotoxic and anti-inflammatory activities

Fig. 4. Selected 1H–1H COSY and HMBC correlations of compound 5.

opennotspecifiedApr 2021View details →

ScienceDex guides

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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.

Compare curated 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.

allen-brain-atlas
neuroscienceopenDocumentation, web resources, and API references are available online.
Last verified 2026-04-30Open record

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.

abode-home-cage
behavioral-neuroscienceopenThe DataShare record exposes download links for annotations, documentation, license text, and the zipped per-snippet data directory.
Last verified 2026-04-30Open record

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.

dandi-nwb
electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

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.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record

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