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Fig. 2 in HRESIMS-guided isolation of aspidosperma-scandine type bisindole alkaloids from Melodinus cochinchinensis and their anti-inflammatory and cytotoxic activities
Fig. 2. Structures of compounds 1–3.
Fig. 4 in HRESIMS-guided isolation of aspidosperma-scandine type bisindole alkaloids from Melodinus cochinchinensis and their anti-inflammatory and cytotoxic activities
Fig. 4. Calculated and experimental ECD spectra of BIA 1.
Fig. 3 in Impairment of botrydial production in Botrytis cinerea allows the isolation of undescribed polyketides and reveals new insights into the botcinins biosynthetic pathway
Fig. 3. Biosynthetic route to botrylactone (6), botcinin A (4) and botcinin K (24).
Fig. 2. Key 1H–1H in Twelve undescribed derivatives of ganoderic acid isolated from Ganoderma luteomarginatum and their cytotoxicity against three human cancer cell lines
Fig. 2. Key 1H–1H COSY and HMBC correlations of 1–12.
Fig. 3 in Twelve undescribed derivatives of ganoderic acid isolated from Ganoderma luteomarginatum and their cytotoxicity against three human cancer cell lines
Fig. 3. Key NOESY correlations of 1–12.
Fig. 1. Some metabolites isolated from B in Impairment of botrydial production in Botrytis cinerea allows the isolation of undescribed polyketides and reveals new insights into the botcinins biosynthetic pathway
Fig. 1. Some metabolites isolated from B. cinerea.
Fig. 1 in Twelve undescribed derivatives of ganoderic acid isolated from Ganoderma luteomarginatum and their cytotoxicity against three human cancer cell lines
Fig. 1. Structures of compounds 1–12.
Fig. 3 in The racemic trimeric quinone and polycyclic quinones isolated from the aerial parts of Morinda umbellata L
Fig. 3. Key HMBC correlations of compounds 1–4.
Fig. 6. X in The racemic trimeric quinone and polycyclic quinones isolated from the aerial parts of Morinda umbellata L
Fig. 6. X-ray crystal structure of 4.
Fig. 1 in The racemic trimeric quinone and polycyclic quinones isolated from the aerial parts of Morinda umbellata L
Fig. 1. Structures of compounds 1–4.
Fig. 7 in Three phragmalin-type limonoids orthoesters and the structure of odoratone isolated from the bark of Entandrophragma candollei (Meliaceae)
Fig. 7. Acetonide formation of compound 5.
Fig. 8 in Three phragmalin-type limonoids orthoesters and the structure of odoratone isolated from the bark of Entandrophragma candollei (Meliaceae)
Fig. 8. Cytotoxicity activity of compound 4 against KB3-1 cell line.
Fig. 6 in Three phragmalin-type limonoids orthoesters and the structure of odoratone isolated from the bark of Entandrophragma candollei (Meliaceae)
Fig. 6. Structure and ORTEP-like view of scopoletin (6).
Fig. 3 in Three phragmalin-type limonoids orthoesters and the structure of odoratone isolated from the bark of Entandrophragma candollei (Meliaceae)
Fig. 3. ORTEP-like view of the asymmetric unit of the mixed crystal of compounds 1 + 3.
Fig. 1 in Three phragmalin-type limonoids orthoesters and the structure of odoratone isolated from the bark of Entandrophragma candollei (Meliaceae)
Fig. 1. Chemical structures of compounds 1–5 isolated from E. candollei.
Fig. 3 in The isolation, structure and fragmentation characteristics of natural truxillic and truxinic acid derivatives in Abrus mollis leaves
Fig. 3. Key COSY, HMBC and selected observed ROE correlations of compounds 1–5 and 8.
Fig. 1. Chemical structures for compounds 1–10 in The isolation, structure and fragmentation characteristics of natural truxillic and truxinic acid derivatives in Abrus mollis leaves
Fig. 1. Chemical structures for compounds 1–10.
Fig. 6 in The isolation, structure and fragmentation characteristics of natural truxillic and truxinic acid derivatives in Abrus mollis leaves
Fig. 6. The CD spectra of compounds 1–8.
Fig. 2 in Antimalarial and antimicrobial substances isolated from the endophytic actinomycete, Streptomyces aculeolatus MS1-6
Fig. 2. The COSY and selected HMBC correlations of compounds 1, 3, and 5–7.
Fig. 3 in Antimalarial and antimicrobial substances isolated from the endophytic actinomycete, Streptomyces aculeolatus MS1-6
Fig. 3. ΔδS-R Values of R- and S- MTPA derivatives of compound 14.
ScienceDex guides
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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.