In brief, LDE was prepared from a lipid mixture composed of 40 mg cholesteryl oleate, 20 mg egg phosphatidylcholine, 1 mg triolein, and 0.5 mg cholesterol [ 808,816 ].) These authors have demonstrated in various studies that their (cremophor-free) nanoemulsion, LDE, is taken up by the low-density lipoprotein, or LDL, receptors [ 808,813–816 ].
Cholesteryl Oleate [Cholesteryl-1,2 -3H(N)]- (30-60 Ci/mmol), 250 µCi quantities of [Cholesteryl-1,2 - 3 H(N)]- Cholesteryl Oleate are available for your research. . Application of [3 H] Cholesteryl Oleate can be found in: metabolism comparisons of labeled lipoproteins in rat in atherosclerosis, labeling and transfer among human/nonhuman primate plasma lipoproteins in analytical biochemistry
Empirical Formula (Hill Notation) C 45 H 78 O 2. Molecular Weight 651.10 . Beilstein/REAXYS Number 2343071 . EC Number 206-142-1. Cholesteryl Oleate [Cholesteryl-1,2 - 3 H (N)]- 250µCi (9.25MBq) Cholesteryl oleate, labeled with tritium. 3 H-cholesteryl oleate is commonly used in lipid transport studies.
81. 2. fatty acid ester of cholesterol - stearate, oleate, or entropy of transition in the order linoleate > oleate > stearate. Dec 9, 2014 Enrichment of LDL with cholesteryl oleate was not associated with increased LDL -biglycan binding. •. Both the high oleic acid canola oil and the Cholesteryl oleate.
Cholesteryl Personeriadistritaldesantamarta.
A comparison between lipase-catalyzed esterification of oleic acid with glycerol in of the precipitation of cholesteryl acetate1992Ingår i: International Journal of
Surface X-ray scattering investigation of cholesteryl oleate, an important cholesterol ester in modelling the tear film lipid layer.” Mahshid abstract = "Preincubation of a triolein/phospholipid/cholesteryl oleate-emulsion in vitro with either pancreatic phospholipase A2 (PLA2) or gastric lipase (GL) Preincubation of a triolein/phospholipid/cholesteryl oleate-emulsion in vitro with either pancreatic phospholipase A2 (PLA2) or gastric lipase (GL) resulted in EC 3.1.1.13. Engelsk definition.
Cholesteryl Oleate labeled with 14C. 50 µCi quantities of [Oleate-1-14 C]-Cholesteryl Oleate are available for your research.Application of [14 C]Cholesteryl Oleate can be found in: uptake of the nanoemulsion by endothelial cells in the presence of HDL and LDL in atherosclerosis, plasma kinetics and uptake by the tumor of a cholesterol-rich microemulsion (LDE) associated to etoposide oleate
The liver is a primary source of cholesteryl oleate that enriches the LDL particles when released into plasma. The secretion of lipoproteins enriched with cholesteryl oleate has close correlation with the pathogenesis of coronary artery atherosclerosis. cholesteryl oleate: ChEBI ID CHEBI:46898: Definition The (Z)-stereoisomer of cholesteryl octadec-9-enoate. Stars This entity has been manually annotated by the ChEBI Team. Secondary ChEBI IDs CHEBI:34634, CHEBI:39859 LEAPChem, a specialized fine chemicals supplier for research, development and production. We are supplier of 2H-Naphth[2,3-d]imidazole-2-thione,1,3-dihydro-.LEAPChem provides nearly 50,000 rare and innovative chemical products to support the evolving needs of our customers in research & bulk manufacturing activities.
3 H-cholesteryl oleate is commonly used in lipid transport studies. Cholesteryl oleate-13 C 18 99 atom % 13 C, 95% (CP) Empirical Formula (Hill Notation) 13 C 18 C 27 H 78 O 2. Molecular Weight 668.97 . MDL number MFCD00003645. PubChem Substance ID 329764486
Cholesteryl oleate is an ester of cholesterol.
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PEG-4 oleate, PEG-100 stearate, dimethicone, carnauba wax, mango seed butter, polyacrylate-13, cetearyl glucoside, sodium polyacrylic Late, cholesteryl Ethylhexyl Salicylate, Glyceryl Citrate/Lactate/Linoleate/Oleate, Glycerin, Phenoxyethanol, Caprylic/Capric Triglyceride, Cholesteryl Hydroxystearate, Extract (10000ppm), Cholesteryl/ Behenyl/ Octyldodecyl Lauroyl Glutamate, Hydrogenated Lecithin, Oligopeptide-68, Sodium Oleate, Ascorbyl Palmitate, GLYCERYL CITRATE/LACTATE/LINOLEATE/OLEATE, GLYCERIN, CHOLESTERYL HYDROXYSTEARATE, SORBITOL, AROMA (FRAGRANCE), GLYCERYL CITRATE/LACTATE/LINOLEATE/OLEATE, GLYCERIN, CHOLESTERYL HYDROXYSTEARATE, SORBITOL, AROMA (FRAGRANCE), aug - Utforska Ebba Sakkos anslagstavla "Saker till skäggagam" cholesteryl oleate structure Pinterest.
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However, cholesteryl oleate (177) proved to be the mounting sex pheromone of the hard tick, Dermacentor variabilis. 483 This compound is secreted by sexually mature females during feeding and accumulates on the surface of the body cuticle, indicating successful parasitism.
Laser diffraction and laser Doppler microelectrophoresis were used to evaluate particle size and zeta potential, respectively. Nanoparticle morphology was analyzed using electron microscopy.
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cholesteryl behenate | cholesteryl behenic acid | 5-cholesten-3β-ol 3-docosanoate | 5-cholesten-3beta-ol 3-docosanoate | cholesteryl docosanoate
662-798-7061. Ethal Sailingcharleston Prior exercise increases dietary oleate, but not palmitate oxidation.
Dihydrocholesteryl oleate | C45H80O2 | CID 69166846 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological
Surface X-ray scattering investigation of cholesteryl oleate, an important cholesterol ester in modelling the tear film lipid layer.” Mahshid abstract = "Preincubation of a triolein/phospholipid/cholesteryl oleate-emulsion in vitro with either pancreatic phospholipase A2 (PLA2) or gastric lipase (GL) Preincubation of a triolein/phospholipid/cholesteryl oleate-emulsion in vitro with either pancreatic phospholipase A2 (PLA2) or gastric lipase (GL) resulted in EC 3.1.1.13. Engelsk definition. An enzyme that catalyzes the hydrolysis of CHOLESTEROL ESTERS and some other sterol esters, to liberate cholesterol plus a Acylhydrolase, Sterol Ester. Cholesterol Ester Hydrolase. Cholesterol Esterase. Cholesteryl Oleate Hydrolase. Cholesterylester Hydrolase.
CHEMBL153910. We have previously reported the use of cholesteryl oleate as a novel excipient for solid lipid nanoparticles (SLNs) for the development of highly efficient and nontoxic nucleic acid delivery carriers. Here, we performed an extensive characterization of this novel formulation to make the scale up under Good Manufacturing Practice (GMP) possible. 1986-01-28 · The model particles were formed by cosonication of cholesteryl oleate and dimyristoylphosphatidylcholine in a 4:1 molar ratio for 45 min at 55-60 degrees C (above both lipid phase transition temperatures). The crude microemulsion was fractionated by low-speed centrifugation and Sepharose CL-2B chromatography. 1982-07-10 · Solubilization and localization of cholesteryl oleate in egg phosphatidylcholine vesicles. A carbon 13 NMR study.