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595 results for “Aspergillus”
Fig. 4 in Punicesterones A-G, polyhydroxylated mycoecdysteroids from the deep-sea-derived fungus Aspergillus puniceus SCSIO z021
Fig. 4. Evaluation of the lipid-lowering effect of compounds 1–9 in 3T3- L1 adipocytes.
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. 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. 6 in Aureoterrolides B-M: Eremophilane-type sesquiterpenoids isolated from Aspergillus aureoterreus and their cytotoxicity
Fig. 6. Apoptosis induced by compound 13 in HL-60 cells.
Fig. 3 in Aureoterrolides B-M: Eremophilane-type sesquiterpenoids isolated from Aspergillus aureoterreus and their cytotoxicity
Fig. 3. Key ROESY correlations of compounds 1–12.
Fig. 2. 1H–1H in Aureoterrolides B-M: Eremophilane-type sesquiterpenoids isolated from Aspergillus aureoterreus and their cytotoxicity
Fig. 2. 1H–1H COSY and HMBC correlations of compounds 1–12.
Fig. 5 in Aureoterrolides B-M: Eremophilane-type sesquiterpenoids isolated from Aspergillus aureoterreus and their cytotoxicity
Fig. 5. Comparisons of calculated and experimental ECD spectra of 7‒12.
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. 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 in Cyclopiazonic acid type indole alkaloids from Nicotiana tabacum-derived fungus Aspergillus versicolor and their anti-tobacco mosaic virus activities
Fig. 1. The structures of compounds 1–8 from A. versicolor.
Fig. 2 in Cyclopiazonic acid type indole alkaloids from Nicotiana tabacum-derived fungus Aspergillus versicolor and their anti-tobacco mosaic virus activities
Fig. 2. The key HMBC () and 1H–1H COSY () correlations of compounds 1 and 3.
Fig. 31 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
Fig. 31. Biological activities of the terpenoids from the genus Aspergillus.
Fig. 28 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
Fig. 28. Biogenetic pathway for helvolic acid.
ScienceDex guides
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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.