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535 results for “scavengers”
Fig. 6 in Free radical scavenging potency of ellagic acid and its derivatives in multiple H /e processes
Fig. 6. The mechanisms proposed for the radical scavenge reaction of compound 5 in different phases. The values for BDE, PA and ETE are in red, blue, and orange for the gas, benzene and water phases respectively. The data in the form of underline and bold represent the lowest value in the same phase. For example, in the gas phase, the 3 OH BDE of ellagic acid is lower than the BDE of the other groups, ETE and all of the PA. Thus, it is in the form of underline and bold. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 5 in Free radical scavenging potency of ellagic acid and its derivatives in multiple H /e processes
Fig. 5. The mechanisms proposed for the radical scavenge reaction of compound 4 in different phases. The values for BDE, PA and ETE are in red, blue, and orange for the gas, benzene and water phases respectively. The data in the form of underline and bold represent the lowest value in the same phase. For example, in the gas phase, the 4 OH BDE of ellagic acid is lower than the BDE of the other groups, ETE and all of the PA. Thus, it is in the form of underline and bold. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 2 in Free radical scavenging potency of ellagic acid and its derivatives in multiple H /e processes
Fig. 2. The mechanisms proposed for the radical scavenge reaction of compound 1 in different phases. The values for BDE, PA and ETE are in kcal/mol and in the color of red, blue, and orange for the gas, benzene and water phases respectively. The data in the form of underline and bold represent the lowest value in the same phase. For example, in the gas phase, the 3 OH BDE of ellagic acid is lower than the BDE of the other groups, ETE and all of the PA. Thus, it is in the form of underline and bold. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in Free radical scavenging potency of ellagic acid and its derivatives in multiple H /e processes
Fig. 4. The mechanisms proposed for the radical scavenge reaction of compound 3 in different phases. The values for BDE, PA and ETE are in red, blue, and orange for the gas, benzene and water phases respectively. The data in the form of underline and bold represent the lowest value in the same phase. For example, in the gas phase, the 4 OH BDE of ellagic acid is lower than the BDE of the other groups, ETE and all of the PA. Thus, it is in the form of underline and bold. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 3 in Free radical scavenging potency of ellagic acid and its derivatives in multiple H /e processes
Fig. 3. The mechanisms proposed for the radical scavenge reaction of compound 2 in different phases. The values for BDE, PA and ETE are in red, blue, and orange for the gas, benzene and water phases respectively. The data in the form of underline and bold represent the lowest value in the same phase. For example, in the gas phase, the 3 OH BDE of ellagic acid is lower than the BDE of the other groups, ETE and all of the PA. Thus, it is in the form of underline and bold. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Fig. 1 in Free radical scavenging potency of ellagic acid and its derivatives in multiple H /e processes
Fig. 1. The most stable optimized geometries of the ellagic acid (1) and its derivatives. The derivatives include 3-O-methylellagic acid (2), 3,3′-di-O-methylellagic acid (3), 3,3′,4′-tri-O-methylellagic acid (4) and 2,3,7-trihydroxychromeno [5,4,3-cde]chromene-5,10-dione (5). Intramolecular hydrogen-bonds are identified by the dash lines and the corresponding bond lengths are labeled beside the hydrogen-bond.
Fig. 5 in Are thymol, rosefuran, terpinolene and umbelliferone good scavengers of peroxyl radicals?
Fig. 5. PH effect on the SPLET mechanism rate coefficients of the reaction of Umb and Thy with HOO• in water.
Fig. 4 in Are thymol, rosefuran, terpinolene and umbelliferone good scavengers of peroxyl radicals?
Fig. 4. The acid dissociation equilibrium of the phenolic compounds Thy and Umb in aqueous solution (pH = 7.4).
Fig. 3 in Are thymol, rosefuran, terpinolene and umbelliferone good scavengers of peroxyl radicals?
Fig. 3. Optimized transition states and imaginary frequency (IF) of the reactions of the studied compounds with HOO• in the gas phase. Distances are in Aand angels in ◦.
Fig. 6 in Theoretical study on the free radical scavenging potency and mechanism of natural coumestans: Roles of substituent, noncovalent interaction and solvent
Fig. 6. The optimized structures, imaginary frequencies (Þ) and the main parameters of TS for WEL with HOO• radical in water phase (distances and angles are given in angstroms and degree). COU–H → COU + H+ (3.1) • Data availability COU → COU + e (3.2)
Fig. 3 in Theoretical study on the free radical scavenging potency and mechanism of natural coumestans: Roles of substituent, noncovalent interaction and solvent
Fig. 3. NCI plots of 5-O• radical for DMW (left), AUR (center) and FLC (right). Blue regions refer to strong attractive interactions, green regions refer to weak dispersion-based interactions, and red regions refer to repulsive interactions (isovalue = 0.7). (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Study of the Effect of Oral Zinc Supplementation on Superoxide Radical Scavengers
ClinicalTrials.gov study NCT02217189. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Too much is bad: increasing numbers of livestock and conspecifics reduce body mass in an avian scavenger
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Data from: Climatic factors shape plastic trade-offs in the polyphenic black scavenger fly Sepsis thoracica (Diptera: Sepsidae)
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Data from: Megafires attract avian scavenging but carcasses still persist
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Data from: Dietary changes in predators and scavengers in a nocturnally illuminated riparian ecosystem
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Data from: Do scavengers prevent or promote disease transmission? The effect of invertebrate scavenging on Ranavirus transmission
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Data from: Top carnivore decline has cascading effects on scavengers and carrion persistence
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Data from: Condition dependence and the maintenance of genetic variance in a sexually dimorphic black scavenger fly
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Data from: Effects of vulture exclusion on carrion consumption by facultative scavengers
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ScienceDex guides
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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.