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595 results for “Aspergillus”
Fig. 1 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
Fig. 1. Structures of monoterpenoids 1 and 2.
Fig. 6 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
Fig. 6. Structures of protoilludane-type sesquiterpenoids 101–103.
Fig. 3 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
Fig. 3. Structures of bisabliane-type sesquiterpenoids 31–82.
Fig. 2 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
Fig. 2. Structures of drimane-type sesquiterpenoids 3–30.
Fig. 4 in Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
Fig. 4. Structures of cadinane-type sesquiterpenoids (83–91).
Fig. 4 in Pyrazinopyrimidine alkaloids from a mangrove-derived fungus Aspergillus versicolor HDN11-84
Fig. 4. Plausible biosynthetic pathway of 1, 2, 4 and 5, and the conversion from 2 to 3.
Fig. 1 in Pyrazinopyrimidine alkaloids from a mangrove-derived fungus Aspergillus versicolor HDN11-84
Fig. 1. Structures of compounds 1–5 (3 is artifact converted from 2).
Fig. 2 in Pyrazinopyrimidine alkaloids from a mangrove-derived fungus Aspergillus versicolor HDN11-84
Fig. 2. Key COSY, HMBC and NOESY correlations of 1 5.
Fig. 2. Key 1H–1H in Transformation of 15-ene steviol by Aspergillus niger, Cunninghamella bainieri, and Mortierella isabellina
Fig. 2. Key 1H–1H COSY and HMBC correlations of 4, 7, 9 and 11.
Fig. 4 in Transformation of 15-ene steviol by Aspergillus niger, Cunninghamella bainieri, and Mortierella isabellina
Fig. 4. ORTEP drawing of the X-ray structure of 4•H2O, 7 and 11.
Fig. 1 in Transformation of 15-ene steviol by Aspergillus niger, Cunninghamella bainieri, and Mortierella isabellina
Fig. 1. Structures of stevioside and compounds 1–12.
Fig. 3. Key 1H–1H in Antifungal peptides from the marine gorgonian-associated fungus Aspergillus sp. SCSIO41501
Fig. 3. Key 1H–1H COSY, HMBC correlations of 4–7.
Fig. 2. Key 1 H– 1 H in Antifungal peptides from the marine gorgonian-associated fungus Aspergillus sp. SCSIO41501
Fig. 2. Key 1 H– 1 H COSY, HMBC, and NOESY correlations of 1.
Fig. 1 in Antifungal peptides from the marine gorgonian-associated fungus Aspergillus sp. SCSIO41501
Fig. 1. The structure of compounds 1–10.
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. 4. X in Asperanstinoids A-E: Undescribed 3,5-dimethylorsellinic acid-based meroterpenoids from Aspergillus calidoustus
Fig. 4. X-ray crystallographic structures of 1, 2, 4, 6, 8, and 9.
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.
Fig. 3 in Asperanstinoids A-E: Undescribed 3,5-dimethylorsellinic acid-based meroterpenoids from Aspergillus calidoustus
Fig. 3. Key NOESY correlations (dashed arrows) of compounds 1–5.
Fig. 2. Key HMBC and 1H–1H in Asperanstinoids A-E: Undescribed 3,5-dimethylorsellinic acid-based meroterpenoids from Aspergillus calidoustus
Fig. 2. Key HMBC and 1H–1H COSY correlations of compounds 1–5.
Fig. 1 in Asperanstinoids A-E: Undescribed 3,5-dimethylorsellinic acid-based meroterpenoids from Aspergillus calidoustus
Fig. 1. Chemical structures of compounds 1–12.
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.