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.
6,383
datasets available to search
ShareScore release 0.9.0
Dataset results
6,383 results for “isolates”
Fig. 9 in Benzobicyclic ketones, cycloheptenone oxide derivatives, guaiane-type sesquiterpenes, and alkaloids isolated from Taraxacum mongolicum Hand.-Mazz.
Fig. 9. The proposed biosynthetic pathway of 8.
Fig. 4 in Benzobicyclic ketones, cycloheptenone oxide derivatives, guaiane-type sesquiterpenes, and alkaloids isolated from Taraxacum mongolicum Hand.-Mazz.
Fig. 4. Experimental ECD spectrum obtained in MeOH and calculated ECD spectra for 1.
Fig. 1 in Aureoterrolides B-M: Eremophilane-type sesquiterpenoids isolated from Aspergillus aureoterreus and their cytotoxicity
Fig. 1. Chemical structures of compounds 1–14.
Fig. 3 in Benzobicyclic ketones, cycloheptenone oxide derivatives, guaiane-type sesquiterpenes, and alkaloids isolated from Taraxacum mongolicum Hand.-Mazz.
Fig. 3. Key NOEs of compounds 1–3, 11.
Fig. 2 in Benzobicyclic ketones, cycloheptenone oxide derivatives, guaiane-type sesquiterpenes, and alkaloids isolated from Taraxacum mongolicum Hand.-Mazz.
Fig. 2. Key HMBC correlations of compounds 1–10.
Fig. 6 in Benzobicyclic ketones, cycloheptenone oxide derivatives, guaiane-type sesquiterpenes, and alkaloids isolated from Taraxacum mongolicum Hand.-Mazz.
Fig. 6. Experimental ECD spectrum obtained in MeOH and calculated ECD spectra for 3.
Fig. 1 in Benzobicyclic ketones, cycloheptenone oxide derivatives, guaiane-type sesquiterpenes, and alkaloids isolated from Taraxacum mongolicum Hand.-Mazz.
Fig. 1. Structures of compounds 1–11.
Fig. 4 in Aureoterrolides B-M: Eremophilane-type sesquiterpenoids isolated from Aspergillus aureoterreus and their cytotoxicity
Fig. 4. Comparisons of calculated and experimental ECD spectra of 1‒6.
Fig. 1. Isolated compounds from D in Derrisrobustones A-D, isoflavones from the twig extract of Derris robusta (DC.) Benth. and their α-glucosidase inhibitory activity
Fig. 1. Isolated compounds from D. robusta twigs.
Fig. 2 in Guided isolation of daphnane-type diterpenes from Daphne genkwa by molecular network strategies
Fig. 2. The structures of compounds 1–12.
Fig. 1 in HPLC-PDA-Guided isolation of glucosyloxybenzyl 2-isobutylmalates from the pseudobulbs of Bletilla striata with neuroprotective and antimicrobial activities
Fig. 1. Structures of compounds 1–12 isolated from the pseudobulbs of Bletilla striata.
Fig. 5 in Guided isolation of daphnane-type diterpenes from Daphne genkwa by molecular network strategies
Fig. 5. Key NOESY correlations of compounds 1, 2, 4, and 5.
Fig. 4. Key 1H–1H in Guided isolation of daphnane-type diterpenes from Daphne genkwa by molecular network strategies
Fig. 4. Key 1H–1H COSY, HMBC correlations of compounds 1, 2, 4, and 5.
Fig. 3. Key 2D in HPLC-PDA-Guided isolation of glucosyloxybenzyl 2-isobutylmalates from the pseudobulbs of Bletilla striata with neuroprotective and antimicrobial activities
Fig. 3. Key 2D NMR correlations of compound 12.
Fig. 2. Key 2D in HPLC-PDA-Guided isolation of glucosyloxybenzyl 2-isobutylmalates from the pseudobulbs of Bletilla striata with neuroprotective and antimicrobial activities
Fig. 2. Key 2D NMR correlations of compounds 1, 3, 6, and 8.
Fig. 4 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 4. Rh2(OCOCF3)4-induced ECD spectrum of compounds 1–3.
Fig. 5 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 5. Experimental and calculated ECD spectra of compounds 1–9.
Fig. 2 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 2. Selective oxidation reaction of the double bond (Δ11,12) in compound 1.
Fig. 3 in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 3. Stereochemical determination by acetonide formation of azaphilones.
Fig. 6. X in Isolation, absolute configurations and bioactivities of pestaphilones A-I: Undescribed methylated side chain containing-azaphilones from Pestalotiopsis oxyanthi
Fig. 6. X-ray ORTEP drawing of compounds 1–3.
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.