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Fig. 5 in Alkaloids isolated from Tropaeolum tuberosum with cytotoxic activity and apoptotic capacity in tumour cell lines
Fig. 5. Synthesis of compound 2.
Fig. 4. 1H–1H in Alkaloids isolated from Tropaeolum tuberosum with cytotoxic activity and apoptotic capacity in tumour cell lines
Fig. 4. 1H–1H COSY and HMBC type correlations of compound 2.
Fig. 2. 1H– 1H in Alkaloids isolated from Tropaeolum tuberosum with cytotoxic activity and apoptotic capacity in tumour cell lines
Fig. 2. 1H– 1H COSY and HMBC type correlations of compound 1.
Fig. 6 in Alkaloids isolated from Tropaeolum tuberosum with cytotoxic activity and apoptotic capacity in tumour cell lines
Fig. 6. Biosynthesis of compounds 1 and 2.
Fig. 2 in Isolation, structure elucidation and neuroprotective effects of caffeoylquinic acid derivatives from the roots of Arctium lappa L.
Fig. 2. The key HMBC (1H→13C) correlations of compounds 1–5.
Fig. 1 in Isolation, structure elucidation and neuroprotective effects of caffeoylquinic acid derivatives from the roots of Arctium lappa L.
Fig. 1. Chemical structures of compounds 1–5.
Fig. 1 in Gigantelline, gigantellinine and gigancrinine, cherylline- and crinine-type alkaloids isolated from Crinum jagus with anti-acetylcholinesterase activity
Fig. 1. Structures of the isolated compounds (1–9).
Fig. 1. Compounds 1–16, isolated from Glandularia x in Chemosystematically valuable triterpenoid saponins from Glandularia x hybrida
Fig. 1. Compounds 1–16, isolated from Glandularia x hybrida.
Fig. 2 in Gigantelline, gigantellinine and gigancrinine, cherylline- and crinine-type alkaloids isolated from Crinum jagus with anti-acetylcholinesterase activity
Fig. 2. The key correlations observed in the HMBC and NOESY spectra of alkaloids 1–3.
Fig. 4 in Study of two isoforms of lipoxygenase by kinetic assays, docking and molecular dynamics of a specialised metabolite isolated from the aerial portion of Lithrea caustica (Anacardiaceae) and its synthetic analogs
Fig. 4. (Z)-3-(pentadec-10′-enyl)-catechol (1) and 3-pentadecylcatechol (2) Lineweaver-Burk graphs.
Fig. 1 in Study of two isoforms of lipoxygenase by kinetic assays, docking and molecular dynamics of a specialised metabolite isolated from the aerial portion of Lithrea caustica (Anacardiaceae) and its synthetic analogs
Fig. 1. Basic structure of urushiol.
Fig. 7. Other compounds isolated from D in Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses
Fig. 7. Other compounds isolated from D. giraldii.
Fig. 6. Diterpenoids isolated from D in Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses
Fig. 6. Diterpenoids isolated from D. giraldii.
Fig. 5. Lignans isolated from D in Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses
Fig. 5. Lignans isolated from D. giraldii.
Fig. 2. Coumarins isolated from D in Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses
Fig. 2. Coumarins isolated from D. giraldii.
Fig. 4. Flavans isolated from D in Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses
Fig. 4. Flavans isolated from D. giraldii.
Fig. 5 in Collacyclumines A-D from the endophytic fungus Colletotrichum salsolae SCSIO 41021 isolated from the mangrove Kandelia candel
Fig. 5. Plausible biogenetic pathways of 1−5.
Fig. 4. X in Collacyclumines A-D from the endophytic fungus Colletotrichum salsolae SCSIO 41021 isolated from the mangrove Kandelia candel
Fig. 4. X-ray structure of 1.
Fig. 3. Flavonoids isolated from D in Daphne giraldii Nitsche (Thymelaeaceae): Phytochemistry, pharmacology and medicinal uses
Fig. 3. Flavonoids isolated from D. giraldii.
Fig. 1 in Collacyclumines A-D from the endophytic fungus Colletotrichum salsolae SCSIO 41021 isolated from the mangrove Kandelia candel
Fig. 1. The structures of the compounds 1–5.
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.