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349 results for “anti-inflammatory activity”
Fig. 9 in Diterpenoids from Sigesbeckia glabrescens with anti-inflammatory and AChE inhibitory activities
Fig. 9. AChE inhibitory rate of compounds 1–19 and rivastigmine at 20 μM.
Fig. 6 in Diterpenoids from Sigesbeckia glabrescens with anti-inflammatory and AChE inhibitory activities
Fig. 6. ECD curve of Rh2(OCOCF3)4 complex of compounds 8 and 12–14.
Fig. 5. Linear correlation between experimental and calculated 13C in Diterpenoids from Sigesbeckia glabrescens with anti-inflammatory and AChE inhibitory activities
Fig. 5. Linear correlation between experimental and calculated 13C NMR chemical shifts of 5.
Fig. 3 in Diterpenoids from Sigesbeckia glabrescens with anti-inflammatory and AChE inhibitory activities
Fig. 3. Calculated or experimental ECD spectra of 1–7 in MeOH.
Fig. 1 in Diterpenoids from Sigesbeckia glabrescens with anti-inflammatory and AChE inhibitory activities
Fig. 1. Structures of compounds 1–19.
Fig. 2. The key 1H–1H in Diterpenoids from Sigesbeckia glabrescens with anti-inflammatory and AChE inhibitory activities
Fig. 2. The key 1H–1H COSY, HMBC, and NOESY correlations of 1 and 8.
Fig. 4 in Bis(4-glycosyloxybenzyl) 2-isobutyltartrate and dihydrophenanthrene derivatives from the pseudobulbs of Pholidota chinensis and their anti-inflammatory activity
Fig. 4. Significant HMBC correlations of compound 6.
Fig. 3 in Bis(4-glycosyloxybenzyl) 2-isobutyltartrate and dihydrophenanthrene derivatives from the pseudobulbs of Pholidota chinensis and their anti-inflammatory activity
Fig. 3. Significant HMBC correlations of compounds 3–5.
Fig. 4 in Diterpenoids from Sigesbeckia glabrescens with anti-inflammatory and AChE inhibitory activities
Fig. 4. ECD curves of Mo2(OAc)4 complexes of compounds 3 and 4.
Fig. 5. X in Diverse undescribed compounds from the rhizome of Zingiber officinale Rosc. And their anti-inflammatory activity
Fig. 5. X-ray crystallographic analysis of 3.
Fig. 3 in Diverse undescribed compounds from the rhizome of Zingiber officinale Rosc. And their anti-inflammatory activity
Fig. 3. Experimental and calculated ECD curves of compound 1.
Fig. 1 in Diverse undescribed compounds from the rhizome of Zingiber officinale Rosc. And their anti-inflammatory activity
Fig. 1. Structures of compounds 1–7.
Fig. 2 in Diterpenoids with anti-inflammatory activity from Euphorbia wallichii
Fig. 2. Key HMBC correlations of compounds 1, 2, 5–9, and 13.
Fig. 5 in Eremophilane-type and xanthanolide-type sesquiterpenes from the aerial parts of Xanthium sibiricum and their anti-inflammatory activities
Fig. 5. ECD spectra of compound 1 and 2.
Fig. 4. X in Eremophilane-type and xanthanolide-type sesquiterpenes from the aerial parts of Xanthium sibiricum and their anti-inflammatory activities
Fig. 4. X-ray crystallographic structures of compound 1 and 2.
Fig. 3 in Eremophilane-type and xanthanolide-type sesquiterpenes from the aerial parts of Xanthium sibiricum and their anti-inflammatory activities
Fig. 3. Key ROESY correlations of compounds 1–5.
Fig. 2. Key 1H–1H in Eremophilane-type and xanthanolide-type sesquiterpenes from the aerial parts of Xanthium sibiricum and their anti-inflammatory activities
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–5.
Fig. 1 in Eremophilane-type and xanthanolide-type sesquiterpenes from the aerial parts of Xanthium sibiricum and their anti-inflammatory activities
Fig. 1. Structures of compounds 1–13 identified from X. sibiricum.
Fig. 1 in Diterpenoids with anti-inflammatory activity from Euphorbia wallichii
Fig. 1. Structures of compounds 1–23 from E. wallichii.
Fig. 2. Key 1H–1H in Diverse undescribed compounds from the rhizome of Zingiber officinale Rosc. And their anti-inflammatory activity
Fig. 2. Key 1H–1H COSY, HMBC and NOESY correlations of compounds 1–7.
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.