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Figure 4 from: Dadayan AS, Stepanyan LA, Sargsyan TH, Hovhannisyan AM, Dadayan SA (2021) Quantitative analysis of biologically active substances and the investigation of antioxidant and antimicrobial activities of some extracts of Osage orange fruits. Pharmacia 68(4): 731-739. https://doi.org/10.3897/pharmacia.68.e70180
Figure 4 Results of quantification and identification of flavonoids in aqueous extract of Osage Orange.
Figure 10 from: Dadayan AS, Stepanyan LA, Sargsyan TH, Hovhannisyan AM, Dadayan SA (2021) Quantitative analysis of biologically active substances and the investigation of antioxidant and antimicrobial activities of some extracts of Osage orange fruits. Pharmacia 68(4): 731-739. https://doi.org/10.3897/pharmacia.68.e70180
Figure 10 Evaluation of the antimicrobial activity of Osage Orange extracts on strains of Bacillus subtilis 1820, E. Coli 5002, Serratia marcescens 5251 and Staphylococcus aureus ATCC-6538.
Figure 6 from: Dadayan AS, Stepanyan LA, Sargsyan TH, Hovhannisyan AM, Dadayan SA (2021) Quantitative analysis of biologically active substances and the investigation of antioxidant and antimicrobial activities of some extracts of Osage orange fruits. Pharmacia 68(4): 731-739. https://doi.org/10.3897/pharmacia.68.e70180
Figure 6 Results of quantification and identification of flavonoids in ethyl acetate extract of Osage Orange.
Fig. 1 in Determination of phenolic profiles of Herniaria polygama and Herniaria incana fractions and their in vitro antioxidant and anti-inflammatory effects
Fig. 1. The chemical structures of isolated compounds (21, 22, 31, and 35) from Herniaria polygama.
Fig. 2 in Role of C-H bond in the antioxidant activities of rooperol and its derivatives: A DFT study
Fig. 2. The most stable geometries of ROP and its derivatives.
Fig. 1 in Role of C-H bond in the antioxidant activities of rooperol and its derivatives: A DFT study
Fig. 1. The structures of ROP and its derivatives.
Fig. 9 in Antioxidative potential of ferulic acid phenoxyl radical
Fig. 9. The Gibbs free energy change for studied mechanisms of FAPR.
Fig. 7 in Antioxidative potential of ferulic acid phenoxyl radical
Fig. 7. Formation of C-5−C-5 dimer and stabilization by keto-enol tautomerism.
Fig. 6 in Antioxidative potential of ferulic acid phenoxyl radical
Fig. 6. Non-cyclic dimers of FAPR.
Fig. 3 in Antioxidative potential of ferulic acid phenoxyl radical
Fig. 3. Studied reactions of FAPR.
Fig. 5 in Antioxidative potential of ferulic acid phenoxyl radical
Fig. 5. Keto-enol tautomerism.
Fig. 1 in Antioxidative potential of ferulic acid phenoxyl radical
Fig. 1. Formation of FAPR.
Fig. 1 in Antioxidant activity and mechanism of dihydrochalcone C-glycosides: Effects of C-glycosylation and hydroxyl groups
Fig. 1. Molecular structures and atomic numbering of the studied dihydrochalcones (DHCs).
Fig. 2 in Antioxidant activity and mechanism of dihydrochalcone C-glycosides: Effects of C-glycosylation and hydroxyl groups
Fig. 2. Double HAT mechanism in ethanol for ASP.
Fig. 3 in Arundinosides I-IX and graminifolosides A-B: 2R-benzylmalate and 2R-isobutylmalates derivatives from Arundina graminifolia (D.Don) Hochr. with antioxidant, cytocompatibility and cytoprotective properties
Fig. 3. Key HSQC-TOCSY, COSY, HMBC and NOESY correlations of arundinosides VI-IX (6–9).
Fig. 2 in Arundinosides I-IX and graminifolosides A-B: 2R-benzylmalate and 2R-isobutylmalates derivatives from Arundina graminifolia (D.Don) Hochr. with antioxidant, cytocompatibility and cytoprotective properties
Fig. 2. Key HSQC-TOCSY, COSY, HMBC and NOESY correlations of arundinosides I–V (1–5).
Fig. 1 in Arundinosides I-IX and graminifolosides A-B: 2R-benzylmalate and 2R-isobutylmalates derivatives from Arundina graminifolia (D.Don) Hochr. with antioxidant, cytocompatibility and cytoprotective properties
Fig. 1. Structures of the eleven isolated compounds.
Fig. 4 in Arundinosides I-IX and graminifolosides A-B: 2R-benzylmalate and 2R-isobutylmalates derivatives from Arundina graminifolia (D.Don) Hochr. with antioxidant, cytocompatibility and cytoprotective properties
Fig. 4. Key HSQC-TOCSY, COSY, HMBC and NOESY correlations of graminifoloside A-B (10–11).
Natural Antioxidant Intake After Exercise Can Oxidative Stress in the Third Trimester of Pragnancy
ClinicalTrials.gov study NCT04226183. IPD Sharing: NO. Countries: 0. Publications: 2.
Clinical Trial for Valuation of the Effectiveness of Lactoferrine in the Prevention of Sepsis in New Premature Born. Bimonitorization of the Antinflammatory Mechanisms, Antioxidants and the Intestinal
ClinicalTrials.gov study NCT03472170. IPD Sharing: YES. Countries: 1. Publications: 0.
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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)
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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.