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Fig. 1 in Isolation and evaluation of virucidal activities of flavanone glycosides and rosmarinic acid derivatives from Dracocephalum spp. against feline calicivirus
Fig. 1. Structures of compounds 1–21.
Fig. 3 in Metabolites isolated from the human intestinal fungus Penicillium oxalicum SL2 and their agonistic effects on PXR and FXR
Fig. 3. Selected NOESY correlations of compounds 1 and 8.
Fig. 2. Selected HMBC and 1H–1H in Metabolites isolated from the human intestinal fungus Penicillium oxalicum SL2 and their agonistic effects on PXR and FXR
Fig. 2. Selected HMBC and 1H–1H COSY correlations of compounds 1, 2, 5, and 8.
Fig. 6. X in Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
Fig. 6. X-ray structure of compounds 1, 8, 9 and 24.
Fig. 5 in Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
Fig. 5. Key NOESY correlations of undescribed compounds 1-13.
Fig. 7. Experimental and calculated ECD spectra compounds 1-13 in Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
Fig. 7. Experimental and calculated ECD spectra compounds 1-13.
Fig. 3 in Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
Fig. 3. Chemical structure of compounds 1-32.
Fig. 1 in Guide isolation of guaiane-type sesquiterpenoids from Daphne tangutica maxim. And their anti-inflammatory activities
Fig. 1. Clusters from the molecular network of the all subfractions of D. tangutica.
Fig. 2. Compounds 1–15 isolated from E. tomentosus L in HSQC-based small molecule accurate recognition technology discovery of diverse cytotoxic sesquiterpenoids from Elephantopus tomentosus L. and structural revision of molephantins A and B
Fig. 2. Compounds 1–15 isolated from E. tomentosus L.
Fig. 1. Isolated Lycopodium alkaloids 1–12 in Phlegcarines A-C, three Lycopodium alkaloids from Phlegmariurus carinatus (Desv. ex Poir.) Ching
Fig. 1. Isolated Lycopodium alkaloids 1–12 from an ornamental species of club moss P. carinatus.
Fig. 4 in Targeted isolation of sesquiterpene lactone dimers from Aucklandia lappa guided by LC-HRMS/MS-based molecular networking
Fig. 4. Comparison of experimental and calculated ECD spectrum of compounds 1–4.
Fig. 1 in Targeted isolation of sesquiterpene lactone dimers from Aucklandia lappa guided by LC-HRMS/MS-based molecular networking
Fig. 1. The molecular networks of the n-hexane-soluble fraction of A. lappa.
Fig. 3. Key HMBC, 1H–1H in Targeted isolation of sesquiterpene lactone dimers from Aucklandia lappa guided by LC-HRMS/MS-based molecular networking
Fig. 3. Key HMBC, 1H–1H COSY, and ROESY correlations of compounds 1–4.
Fig. 2 in Targeted isolation of sesquiterpene lactone dimers from Aucklandia lappa guided by LC-HRMS/MS-based molecular networking
Fig. 2. Structure 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. 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.
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.