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12,346 results for “derivatives”
Fig. 3. X in Punicesterones A-G, polyhydroxylated mycoecdysteroids from the deep-sea-derived fungus Aspergillus puniceus SCSIO z021
Fig. 3. X-ray crystal structures of compounds 1–6 and 9.
Fig. 1 in Punicesterones A-G, polyhydroxylated mycoecdysteroids from the deep-sea-derived fungus Aspergillus puniceus SCSIO z021
Fig. 1. Structures of compounds 1–9 isolated from A. puniceus SCSIO z021.
Fig. 2 in Punicesterones A-G, polyhydroxylated mycoecdysteroids from the deep-sea-derived fungus Aspergillus puniceus SCSIO z021
Fig. 2. Key COSY, HMBC, and NOESY correlations of compounds 1–3.
Fig. 1 in Puerol and pueroside derivatives from Pueraria lobata and their anti-inflammatory activity
Fig. 1. Structures of compounds 1–8.
Fig. 3 in Puerol and pueroside derivatives from Pueraria lobata and their anti-inflammatory activity
Fig. 3. The calculated and experimental ECD curves of compounds 1a and 1b.
Fig. 2 in Puerol and pueroside derivatives from Pueraria lobata and their anti-inflammatory activity
Fig. 2. Key HMBC correlations of compounds 1 and 2.
Fig. 5 in The anti-TMV potency of the tobacco-derived fungus Aspergillus versicolor and its active alkaloids, as anti-TMV activity inhibitors
Fig. 5. The experimental and calculated ECD spectra of compounds 1–5.
Fig. 1 in The anti-TMV potency of the tobacco-derived fungus Aspergillus versicolor and its active alkaloids, as anti-TMV activity inhibitors
Fig. 1. The structures of compounds 1–13 from the tobacco-derived fungus A. versicolor.
Fig. 3 in 30-norlanostane triterpenoids and steroid derivatives from the endophytic fungus Aspergillus nidulans
Fig. 3. The key NOESY correlations of compounds 1–4.
Fig. 2. Key 1H–1H in 30-norlanostane triterpenoids and steroid derivatives from the endophytic fungus Aspergillus nidulans
Fig. 2. Key 1H–1H COSY and HMBC correlations of compounds 1–4.
Fig. 5 in 30-norlanostane triterpenoids and steroid derivatives from the endophytic fungus Aspergillus nidulans
Fig. 5. The experimental and calculated ECD spectra of compound 4.
Fig. 1 in 30-norlanostane triterpenoids and steroid derivatives from the endophytic fungus Aspergillus nidulans
Fig. 1. Chemical structures of compounds 1–10.
Fig. 8 in Benzobicyclic ketones, cycloheptenone oxide derivatives, guaiane-type sesquiterpenes, and alkaloids isolated from Taraxacum mongolicum Hand.-Mazz.
Fig. 8. The proposed biosynthetic pathway of 7.
Fig. 7. X in Benzobicyclic ketones, cycloheptenone oxide derivatives, guaiane-type sesquiterpenes, and alkaloids isolated from Taraxacum mongolicum Hand.-Mazz.
Fig. 7. X-ray crystal structures of compounds 4 and 6–8.
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. 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.
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.