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Fig. 2. Selected HMBC correlations for brevianthrones A1 in Brevianthrones, bianthrones from a Chinese isolate of the endophytic fungus Colletotrichum brevisporum
Fig. 2. Selected HMBC correlations for brevianthrones A1 (1), B1 (4) and B4 (7).
Fig. 1. Isolated compounds from C in Dimeric and esterified sesquiterpenes from the liverwort Chiastocaulon caledonicum
Fig. 1. Isolated compounds from C. caledonicum.
Fig. 6 in Isolation and structure characterization of cytotoxic alkaloids from Micromelum integerrimum
Fig. 6. The calculated and experimental ECD spectra of compounds 9 and 10 in MeOH.
Fig. 2 in Isolation and structure characterization of cytotoxic alkaloids from Micromelum integerrimum
Fig. 2. Key HMBC correlations of compounds 1, 8, and 10.
Fig. 1. Previously undescribed alkaloids from M in Isolation and structure characterization of cytotoxic alkaloids from Micromelum integerrimum
Fig. 1. Previously undescribed alkaloids from M. integerrimum.
Fig. 3 in Antibacterial harziane diterpenoids from a fungal symbiont Trichoderma atroviride isolated from Colquhounia coccinea var. mollis
Fig. 3. Key ROESY correlations of compounds 1–5.
Fig. 4. X in Antibacterial harziane diterpenoids from a fungal symbiont Trichoderma atroviride isolated from Colquhounia coccinea var. mollis
Fig. 4. X-ray crystallographic structure of compound 1.
Fig. 2. 1H–1H in Antibacterial harziane diterpenoids from a fungal symbiont Trichoderma atroviride isolated from Colquhounia coccinea var. mollis
Fig. 2. 1H–1H COSY and key HMBC correlations of compounds 1–5.
Fig. 1 in Antibacterial harziane diterpenoids from a fungal symbiont Trichoderma atroviride isolated from Colquhounia coccinea var. mollis
Fig. 1. Chemical structures of compounds 1–8 isolated from Trichoderma atroviride B7.
Fig. 3. 1H–1H in Antitumoral potential of carbamidocyclophanes and carbamidocylindrofridin A isolated from the cyanobacterium Cylindrospermum stagnale BEA 0605B
Fig. 3. 1H–1H COSY and HMBC key correlations of carbamidocyclophane V (3).
Fig. 4. 1H–1H in Antitumoral potential of carbamidocyclophanes and carbamidocylindrofridin A isolated from the cyanobacterium Cylindrospermum stagnale BEA 0605B
Fig. 4. 1H–1H COSY and HMBC key correlations of carbamidocylindrofridin A (4).
Fig. 1. Isolated compounds 1–33 from A in Atalantiaphyllines A-G, prenylated acridones from Atalantia monophylla DC. and their aromatase inhibition and cytotoxic activities
Fig. 1. Isolated compounds 1–33 from A. monophylla.
Fig. 2 in Azaphilones with protein tyrosine phosphatase inhibitory activity isolated from the fungus Aspergillus deflectus
Fig. 2. Key HMBC and NOESY correlations of 1.
Fig. 1 in Azaphilones with protein tyrosine phosphatase inhibitory activity isolated from the fungus Aspergillus deflectus
Fig. 1. The structures of azaphilones 1–11.
Fig. 5 in Aromatin D-J: Seven previously undescribed labdane diterpenoids isolated from Blumea aromatica
Fig. 5. Calculated (Cal.) and experimental (Exp.) ECD spectra of compounds 1, 2, and 3.
Fig. 2. Key 1H–1H in Aromatin D-J: Seven previously undescribed labdane diterpenoids isolated from Blumea aromatica
Fig. 2. Key 1H–1H COSY and key HMBC correlations of 1–7.
Fig. 1 in Aromatin D-J: Seven previously undescribed labdane diterpenoids isolated from Blumea aromatica
Fig. 1. Chemical structures of the compounds isolated from Blumea aromatica (1–7).
Fig. 6 in Aromatin D-J: Seven previously undescribed labdane diterpenoids isolated from Blumea aromatica
Fig. 6. Experimental electronic circular dichroism (ECD) spectra of 1 and 3–6.
Fig. 4. X in Aromatin D-J: Seven previously undescribed labdane diterpenoids isolated from Blumea aromatica
Fig. 4. X-ray Ortep diagram of aromatin D (1), aromatin G (4), aromatin H (5) and aromatin J (7).
Fig. 3 in Aromatin D-J: Seven previously undescribed labdane diterpenoids isolated from Blumea aromatica
Fig. 3. Key NOESY correlations of compounds 1–7.
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.