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Phosphorylethanolamine or phosphoethanolamine is an ethanolamine derivative that is used to construct two different categories of phospholipids. One category termed a glycerophospholipid and the other a sphingomyelin , or more specifically within the sphingomyelin class, a sphingophospholipid .
The levels of Amadori-phosphatidylethanolamine products are higher in foods with high lipid and sugar concentrations that have high temperatures in processing. [13] Additional studies have found that Amadori-phosphatidylethanolamine may play a role in vascular disease , [ 15 ] act as the mechanism by which diabetes can increase the incidence of ...
Ethanolamine (2-aminoethanol, monoethanolamine, ETA, or MEA) is a naturally occurring organic chemical compound with the formula HOCH 2 CH 2 NH 2 or C 2 H 7 NO. [8] The molecule is bifunctional, containing both a primary amine and a primary alcohol.
Hypophosphatasia (/ ˌ h aɪ p oʊ ˈ f ɒ s f eɪ t ˌ eɪ ʒ ə /; also called deficiency of alkaline phosphatase, phosphoethanolaminuria, [5] or Rathbun's syndrome; [1] sometimes abbreviated HPP [6]) is a rare, and sometimes fatal, inherited [7] metabolic bone disease. [8]
Other names in common use include O-phosphoethanolamine-phospholyase, amino alcohol O-phosphate phospholyase, O-phosphorylethanol-amine phospho-lyase, and ethanolamine-phosphate phospho-lyase (deaminating).
Hyperuricosuria is a medical term referring to the presence of excessive amounts of uric acid in the urine. For men this is at a rate greater than 800 mg/day, and for women, 750 mg/day. [1] Notable direct causes of hyperuricosuria are dissolution of uric acid crystals in the kidneys or urinary bladder, and hyperuricemia.
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(1) O-phosphoethanolamine + H 2 O ethanolamine + phosphate (2) phosphocholine + H 2 O ⇌ {\displaystyle \rightleftharpoons } choline + phosphate The enzyme is a member of the haloacid dehalogenase superfamily.