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1,046 results for “anti-inflammatories”

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Fig. 2. Key 1 H– 1 H in Polyacetylene glucosides from the florets of Carthamus tinctorius and their anti-inflammatory activity

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

opennotspecifiedJul 2021View details →
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Fig. 1A in Isoflavanquinones from Abrus precatorius roots with their antiproliferative and anti-inflammatory effects

Fig. 1A. Structures of compounds 1–6.

opennotspecifiedJul 2021View details →
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Fig. 1B in Isoflavanquinones from Abrus precatorius roots with their antiproliferative and anti-inflammatory effects

Fig. 1B. Structures of compounds 7–11.

opennotspecifiedJul 2021View details →
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Fig. 1 in Polyacetylene glucosides from the florets of Carthamus tinctorius and their anti-inflammatory activity

Fig. 1. Chemical structures of compounds 1–8 and 1a.

opennotspecifiedJul 2021View details →
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Fig. 4. Key HMBC and 1H-1H in Antifeedant, cytotoxic, and anti-inflammatory neo-clerodane diterpenoids in the peltate glandular trichomes and fresh leaves of Ajuga forrestii

Fig. 4. Key HMBC and 1H-1H COSY correlations of compounds 8a/b and 9a/b.

opennotspecifiedJun 2021View details →
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Fig. 3 in Antifeedant, cytotoxic, and anti-inflammatory neo-clerodane diterpenoids in the peltate glandular trichomes and fresh leaves of Ajuga forrestii

Fig. 3. Proposed biosynthetic pathway of the neo-clerodane diterpenoids in A. forrestii.

opennotspecifiedJun 2021View details →
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Fig. 3 in Alkaloids bearing rare skeletons from Forsythia suspensa with anti-inflammatory and anti-viral activities in vitro

Fig. 3. Key NOESY (↔) correlations of compound 1.

opennotspecifiedJun 2021View details →
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Fig. 6 in Alkaloids bearing rare skeletons from Forsythia suspensa with anti-inflammatory and anti-viral activities in vitro

Fig. 6. Cell viability of different concentrations of compounds 1–5 acting on MDCK cells.

opennotspecifiedJun 2021View details →
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Fig. 5. X in Alkaloids bearing rare skeletons from Forsythia suspensa with anti-inflammatory and anti-viral activities in vitro

Fig. 5. X-ray ORTEP drawing of 2.

opennotspecifiedJun 2021View details →
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Fig. 2. Key 1H–1H in Alkaloids bearing rare skeletons from Forsythia suspensa with anti-inflammatory and anti-viral activities in vitro

Fig. 2. Key 1H–1H COSY (▬) and HMBC (→) correlations of compounds 1–2.

opennotspecifiedJun 2021View details →
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Fig. 1 in Alkaloids bearing rare skeletons from Forsythia suspensa with anti-inflammatory and anti-viral activities in vitro

Fig. 1. Structures of compounds 1–5 isolated from Forsythia suspensa.

opennotspecifiedJun 2021View details →
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Fig. 4 in Benzofuran ε-caprolactam glucosides, amides and phenylpropanoid derivatives with anti-inflammatory activity from Oxybaphus himalaicus

Fig. 4. Experimental ECD spectrum of 3.

opennotspecifiedNov 2021View details →
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Fig. 5 in Benzofuran ε-caprolactam glucosides, amides and phenylpropanoid derivatives with anti-inflammatory activity from Oxybaphus himalaicus

Fig. 5. Proposed biosynthetic pathway of 1a and 1b.

opennotspecifiedNov 2021View details →
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Fig. 1 in Benzofuran ε-caprolactam glucosides, amides and phenylpropanoid derivatives with anti-inflammatory activity from Oxybaphus himalaicus

Fig. 1. Structures of 1

opennotspecifiedNov 2021View details →
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Fig. 1 in Determination of phenolic profiles of Herniaria polygama and Herniaria incana fractions and their in vitro antioxidant and anti-inflammatory effects

Fig. 1. The chemical structures of isolated compounds (21, 22, 31, and 35) from Herniaria polygama.

opennotspecifiedOct 2021View details →
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Fig. 6 in Glycosylated constituents isolated from the trunk of Abies holophylla and their anti-inflammatory and neurotrophic activity

Fig. 6. SAR study on the five cases of isolated compounds for antineuroinflammatory activity.

opennotspecifiedDec 2021View details →
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Fig. 7. 1H–1H in Guaiane-type sesquiterpenoids from Cinnamomum migao H. W. Li: And their anti-inflammatory activities

Fig. 7. 1H–1H COSY and key HMBC correlations of compounds 9, 10, and 11.

opennotspecifiedOct 2021View details →
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Fig. 4 in Guaiane-type sesquiterpenoids from Cinnamomum migao H. W. Li: And their anti-inflammatory activities

Fig. 4. CD spectrum of compounds 1 and 2.

opennotspecifiedOct 2021View details →
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Fig. 1 in Guaiane-type sesquiterpenoids from Cinnamomum migao H. W. Li: And their anti-inflammatory activities

Fig. 1. Chemical structures of compounds 1–11.

opennotspecifiedOct 2021View details →
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Fig. 1 in Glycosylated constituents isolated from the trunk of Abies holophylla and their anti-inflammatory and neurotrophic activity

Fig. 1. Chemical structures of 1–31.

opennotspecifiedDec 2021View details →

ScienceDex guides

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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.

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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.

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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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