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1,923 results for “compounds”
Fig. 10 in Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds
Fig. 10. NSEs extracted from Echium angustifolium and Quillaja Saponaria.
Fig. 7. NSEs extracted from N. tabacum, E. hiemale L and V in Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds
Fig. 7. NSEs extracted from N. tabacum, E. hiemale L and V. guineensis.
Fig. 4 in Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds
Fig. 4. NSEs extracted from Physalis solanaceus and Physalis peruviana.
Fig. 6 in Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds
Fig. 6. NSEs with aliphatic substituted extracted from Physalis plants.
Fig. 1 in Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds
Fig. 1. Chemical structure of sucrose.
Fig. 7. Selected key NOESY correlations for compound 3 in Ten undescribed cembrane-type diterpenoids from the gum resin of Boswellia sacra and their biological activities
Fig. 7. Selected key NOESY correlations for compound 3.
Fig. 3. Selected key ROESY correlations for compound 1 in Ten undescribed cembrane-type diterpenoids from the gum resin of Boswellia sacra and their biological activities
Fig. 3. Selected key ROESY correlations for compound 1.
Fig. 5 in A H NMR-based metabolomic approach to study the production of antimalarial compounds from Psiadia arguta leaves (pers.) voigt
Fig. 5. Compounds identified in P. arguta attacked plants.
Fig. 1 in A H NMR-based metabolomic approach to study the production of antimalarial compounds from Psiadia arguta leaves (pers.) voigt
Fig. 1. Process for obtaining all experimental plants in the present study.
Fig. 3. Key ROESY correlations for compounds 6 and 9 in Iridoids and bis-iridoids from Valeriana jatamansi and their cytotoxicity against human glioma stem cells
Fig. 3. Key ROESY correlations for compounds 6 and 9.
Fig. 6. Compound 11 inhibited the influenza A in Bioactive ent-isopimarane diterpenoids from Euphorbia neriifolia
Fig. 6. Compound 11 inhibited the influenza A virus in MDCK cells.
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. 5 in Bioactive sulfur-containing compounds from Xanthium sibiricum, including a revision of the structure of xanthiazinone
Fig. 5. Experimental and calculated ECD spectra of 1–4.
Fig. 4. Key 2D in Bioactive sulfur-containing compounds from Xanthium sibiricum, including a revision of the structure of xanthiazinone
Fig. 4. Key 2D NMR correlations of 1a, 2a and 4.
Fig. 1 in Bioactive sulfur-containing compounds from Xanthium sibiricum, including a revision of the structure of xanthiazinone
Fig. 1. Structures of compounds 1–11.
Fig. 5. Plausible biosynthetic pathway for compounds 1–6 in Unusual glycosidic labdane diterpenoids with cytotoxicity from the root of Phlomoides betonicoides
Fig. 5. Plausible biosynthetic pathway for compounds 1–6.
Fig. 2 in Bioactive sulfur-containing compounds from Xanthium sibiricum, including a revision of the structure of xanthiazinone
Fig. 2. Structure revision of xanthiazinone.
Fig. 7. Key COSY and NOSEY correlations for compound 3 in New tricks for old dogs: Two new macrocyclic trichothecene epimers and absolute configuration of 16-hydroxyverrucarin B
Fig. 7. Key COSY and NOSEY correlations for compound 3.
Fig. 2. Key HMBC correlations and COSY couplings for compounds 1–7, Y in Norlignan glucosides from Hypoxis hemerocallidea and their potential in vitro anti-inflammatory activity via inhibition of iNOS and NF-ΚB
Fig. 2. Key HMBC correlations and COSY couplings for compounds 1–7, Y, and Z.
Fig. 2. Key COSY and NOSEY correlations for compound 1 in New tricks for old dogs: Two new macrocyclic trichothecene epimers and absolute configuration of 16-hydroxyverrucarin B
Fig. 2. Key COSY and NOSEY correlations for compound 1.
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.