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259 results for “sucrose”
Pilot Study of Sucrose to Reduce Pain in Sick Babies
ClinicalTrials.gov study NCT01438008. IPD Sharing: Not stated. Countries: 1. Publications: 8.
Glucose Variability in Patients With Type 1 Diabetes With a Sucrose-added Diet
ClinicalTrials.gov study NCT02758483. IPD Sharing: UNDECIDED. Countries: 1. Publications: 1.
A Trial Comparing Ferumoxytol With Iron Sucrose for the Treatment of Iron Deficiency Anemia
ClinicalTrials.gov study NCT01114204. IPD Sharing: Not stated. Countries: 14. Publications: 2.
Ferric Carboxymaltose Versus Iron Sucrose for Treating Anemia in Pregnant Women
ClinicalTrials.gov study NCT06911034. IPD Sharing: NO. Countries: 1. Publications: 1.
Iron Isomaltoside/Ferric Derisomaltose vs Iron Sucrose for the Treatment of Iron Deficiency Anemia (IDA)
ClinicalTrials.gov study NCT02940886. IPD Sharing: NO. Countries: 1. Publications: 1.
Sucrose-preferring gut microbes prevent host obesity by producing exopolysaccharides
Open the record for dataset details and reuse information.
Vacuolar sucrose homeostasis is critical for development, seed properties and survival of dark phases of Arabidopsis
Open the record for dataset details and reuse information.
Gliflozins, sucrose and flavonoids are allosteric activators of lecithin-cholesterol acyltransferase
<p>Computational data of publication "Gliflozins, sucrose and flavonoids are allosteric activators of lecithin-cholesterol acyltransferase" by Akseli Niemelä, Laura Giorgi, Sirine Nouri, Betül Yurttaş, Khushbu Rauniyar, Michael Jeltsch and Artturi Koivuniemi.</p>
Fig. 2 in Agrocinopine C, a Ti-plasmid-coded enzyme-product, is a 2-O, 6-O linked phosphodiester of D-Glucose and sucrose
Fig. 2. Diffuse reflectance mid infra-red spectrum of agrocinopine C. (For interpretation of the references to colour in this figure legend, the reader is referred to the Web version of this article.)
Fig. 4 in Agrocinopine C, a Ti-plasmid-coded enzyme-product, is a 2-O, 6-O linked phosphodiester of D-Glucose and sucrose
Fig. 4. Bioassay detection of agrocinopine C. The left plate shows detection of agrocinopine C in the pH 1.7, anionic paper electrophoretogram segment marked C, by its induction of antibiotic activity in the normally insensitive K478 (syn. A281) overlay, from a source of agrocin 84 produced by the chloroformsterilised, colony of R. rhizogenes strain K84 grown at the centre of both plates. The radius of the normal toxic concentration range of agrocin 84 extends approximately to the location of the paper squares. The right plate demonstrates that glucose 2-phosphate (square A) induces no detectable sensitivity to agrocin 84, glucose 6-phosphate (square B) no detectable sensitivity and purified agrocinopine C (C) induces a very strong uptake of the antibiotic. It is noteworthy that unlike agrocinopine A, which extends the inhibition zone perimeter (Ellis and Murphy, 1981; Ryder et al., 1984) beyond the squares, agrocinopine C only induces sensitivity inwards towards the original agrocin 84 producer colony.
Fig. 3 in Agrocinopine C, a Ti-plasmid-coded enzyme-product, is a 2-O, 6-O linked phosphodiester of D-Glucose and sucrose
Fig. 3. Relative electrophoretic mobilities (RmDNBS) of ribose-5-P (triangle; pKa1 =1.32, pKa2 =6.58), agrocinopine C (circle) and agrocinopine D (square) between pH 1.7 and 10.
Fig. 5 in Agrocinopine C, a Ti-plasmid-coded enzyme-product, is a 2-O, 6-O linked phosphodiester of D-Glucose and sucrose
Fig. 5. (a) 31P NMR signals for agrocinopine C, α/β pyranosyl anomers (-2.80 ppm), α/β furanosyl anomers (-3.24 ppm) and the aldehyde anomer and/or its hydrate (-4.03 ppm). No evidence for a detectable amount of the hydrated aldehyde as a separate 6th signal was observed in these 31P NMR observations. Peaks at -3.09 and -3.12 ppm are not correlated to any agrocinopine C protons by 31P gHMBC. (b) Agrocinopine C31P NMR signals collapse to a singlet after borohydride reduction (-1.55 ppm).
Fig. 6. Structural relationships for agrocinopine C in Agrocinopine C, a Ti-plasmid-coded enzyme-product, is a 2-O, 6-O linked phosphodiester of D-Glucose and sucrose
Fig. 6. Structural relationships for agrocinopine C and its various anomeric equilibria. The presence of the aldehyde anomer and/or its hydrate and α/β pyranosyl and α/β furanosyl anomers is consistent with the three signals detected in the 31P NMR and five anomeric proton signals observed in the 1H NMR (Table 2, Table S1). (ChemBioDraw, 2014).
Fig. 2 in Feruloyl sucrose derivatives from the root of Xerophyllum tenax
Fig. 2. Selected HMBC (solid arrows) and NOESY (dashed arrows) correlations for compounds 1, 3 and 5.
Fig. 4 in Feruloyl sucrose derivatives from the root of Xerophyllum tenax
Fig. 4. Proposed fragmentation pathway of compound 1–5. A. The MS2 spectrum of compounds 1 and 5; positive mode. B. The MS2 spectrum of compound 1 and 5; negative mode. C. Proposed fragmentation pathway of compound 1; positive mode. D. Proposed fragmentation pathway of compounds 1 and 5; negative mode.
Fig. 12 in Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds
Fig. 12. NSEs extracted from Prunus padus, Smilax glabra, Bistorta manshuriensis and Aristolochia cretica.
Fig. 3 in Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds
Fig. 3. Examples of SEs synthesis. (A) heterogeneous catalysis approach and (B) total synthesis of phenylpropanoid SEs.
Fig. 8 in Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds
Fig. 8. Structure of NSEs extracted from Bidens parviflora, Phyllanthus cochinchinensis and Oryza sativa.
Fig. 2 in Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds
Fig. 2. Examples of SEs synthesis. (A) protection and unprotection approach and (B) biocatalysis approach.
Fig. 9 in Natural sucrose esters: Perspectives on the chemical and physiological use of an under investigated chemical class of compounds
Fig. 9. NSEs with phenylpropanoid substitutes extracted from Prunus tomentosa, Polygonum lapathifolium and Polygonum perfoliatum.
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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.