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1,923 results for “compounds”
Fig. 1 in Structural characterization of prenylated compounds from Broussonetia kazinoki and their antiosteoclastogenic activity
Fig. 1. Chemical structures of compounds 1–19.
Fig. 4. Experimental and calculated ECD spectra for compounds 1, 4 in Brevianthrones, bianthrones from a Chinese isolate of the endophytic fungus Colletotrichum brevisporum
Fig. 4. Experimental and calculated ECD spectra for compounds 1, 4, and 7.
Fig. 3. Diagnostic NOESY interactions for compounds 1, 2, 4 in Sesquiterpene coumarins from Ferula samarkandica Korovin and their bioactivity
Fig. 3. Diagnostic NOESY interactions for compounds 1, 2, 4, and 5.
Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10 in Sesquiterpene coumarins from Ferula samarkandica Korovin and their bioactivity
Fig. 2. Selected 1H–1H COSY and HMBC correlations for compounds 1–3, 6 and 10.
Fig. 1 in Screening of in vitro and in silico α-amylase, α-glucosidase, and lipase inhibitory activity of oxyprenylated natural compounds and semisynthetic derivatives
Fig. 1. Chemical structures of the 23 analysed pure natural and semisynthetic compounds.
Fig. 5. Proposed biosynthetic pathway for compounds 1–12 in Immunosuppressive gentianellane-type sesterterpenoids from the traditional Uighur medicine Gentianella turkestanorum
Fig. 5. Proposed biosynthetic pathway for compounds 1–12.
Fig. 2. NOESY correlations for compound 1 and HMBC correlations for compound 2 in Indole alkaloids from the leaves of Ravenia spectabilis engl. with activity against pancreatic cancer cell line
Fig. 2. NOESY correlations for compound 1 and HMBC correlations for compound 2.
Fig. 6. Perspective ORTEP drawing for compound 4 in Chemical constituents of Psidium guajava leaves and their antibacterial activity
Fig. 6. Perspective ORTEP drawing for compound 4.
Fig. 7. Compounds 3 and 6 in Spectanoids A H: Eight undescribed sesterterpenoids from Aspergillus spectabilis
Fig. 7. Compounds 3 and 6 induce apoptosis of human B lymphoma cells.
Fig. 2. Key 2D NMR correlations for compounds 1, 3, 12, 17, 18 in Iridoid glycosides and lignans from the fruits of Gardenia jasminoides Eills
Fig. 2. Key 2D NMR correlations for compounds 1, 3, 12, 17, 18, and 21.
Fig. 10. Proposed biogenetic pathway for compounds 1–13 in Prenylated C -C derivatives from the stems and branches of Illicium ternstroemioides A. C. Smith with antiviral activity
Fig. 10. Proposed biogenetic pathway for compounds 1–13.
Fig. 1. Compounds 1–13 in Phenyl glycosides from the leaves of Flacourtia indica (Burm. f.) Merr (Salicaceae)
Fig. 1. Compounds 1–13 isolated from Flacourtia indica; for 13: tentative absolute configuration.
Fig. 7. Relative ATPase activity treated with 21 in Seasonal variation of phenolic compounds in Zostera marina (Zosteraceae) from the Baltic Sea
Fig. 7. Relative ATPase activity treated with 21 in micromolar range.
Fig. 3 in Seasonal variation of phenolic compounds in Zostera marina (Zosteraceae) from the Baltic Sea
Fig. 3. Chemical structure and HMBC key correlations of 7′′,8′′ -didehydrosalvianolic acid B.
Fig. 7. Compound 6 in Bioactive metabolites from the desert plant-associated endophytic fungus Chaetomium globosum (Chaetomiaceae)
Fig. 7. Compound 6 retarded seedling growth of A. thaliana.
Fig. 6. Key NOE correlations for compounds 6 and 7 in Dimeric and esterified sesquiterpenes from the liverwort Chiastocaulon caledonicum
Fig. 6. Key NOE correlations for compounds 6 and 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. 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. Key HMBC correlations for compound 1 in Semipapposides A-M, triterpenoid bidesmosides saponins from the roots of Scabiosa semipapposa
Fig. 2. Key HMBC correlations for compound 1.
Fig. 3. Key ROESY correlations for compounds 1–3 and 7 in Iridoids from Valeriana jatamansi with anti-inflammatory and antiproliferative properties
Fig. 3. Key ROESY correlations for compounds 1–3 and 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.