Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
1,183
datasets available to search
ShareScore release 0.9.0
Dataset results
1,183 results for “Skeleton”
Fig. 2. Selected 1H–1H COSY and HMBC correlations for 3 in Bond reactivity indices approach analysis of the [2+2] cycloaddition of jatrophane skeleton diterpenoids from Euphorbia gaditana Coss to tetracyclic gaditanone
Fig. 2. Selected 1H–1H COSY and HMBC correlations for 3.
Fig. 4 in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 4. Experimental and calculated ECD spectra of compounds 1–4 and 6–11.
Fig. 2. Key 1H–1H in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–11.
Fig. 4 in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 4. (continued).
Fig. 7 in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 7. (continued).
Fig. 1 in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 1. Structures of compounds 1–18.
Fig. 5. Single-crystal X in Bioactive diterpenoids and sesquiterpenoids with different skeletons from Salvia digitaloides Diels
Fig. 5. Single-crystal X-ray structure of compound 5.
Fig. 2 in (+)- and ()-trichodermatrione A: a pair of enantiomers with a cyclobutane-containing skeleton from the endophytic fungus Trichoderma sp. EFT2
Fig. 2. Key COSY, HMBC and NOESY correlations of 1.
Fig. 1 in (+)- and ()-trichodermatrione A: a pair of enantiomers with a cyclobutane-containing skeleton from the endophytic fungus Trichoderma sp. EFT2
Fig. 1. (A) Chemical structure and (B) X-ray crystallographic structure of trichodermatrione A (1).
Fig. 4 in (+)- and ()-trichodermatrione A: a pair of enantiomers with a cyclobutane-containing skeleton from the endophytic fungus Trichoderma sp. EFT2
Fig. 4. Proposed mechanism of formation of 1.
Fig. 3 in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134
Fig. 3. ECD and NMR of 1 and 2.
Fig. 2. Key 2D in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134
Fig. 2. Key 2D NMR correlations of compounds 1–9.
Fig. 1 in Sesquiterpenes with diverse skeletons from histone deacetylase inhibitor modified cultures of the basidiomycete Cyathus stercoreus (Schwein.) De Toni HFG134
Fig. 1. The chemical structures of compounds 1–13.
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.
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.
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.
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.
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.
Fig. 1 in Asporychalasin, a bioactive cytochalasan with an unprecedented 6/6/11 skeleton from the Red Sea sediment Aspergillus oryzae
Fig. 1. Chemical structure of asporychalasin (1).
Fig. 5 in Asporychalasin, a bioactive cytochalasan with an unprecedented 6/6/11 skeleton from the Red Sea sediment Aspergillus oryzae
Fig. 5. Proposed biosynthetic pathway for asporychalasin.
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.