90756
CDP-ethanolamine sodium salt hydrate
≥93.0% (HPLC)
Synonym(s):
Cytidine 5′-diphosphate ethanolamine sodium salt hydrate, Cytidine 5′-diphosphoethanolamine sodium salt hydrate, Cytidine diphosphate ethanolamine sodium salt hydrate
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About This Item
Empirical Formula (Hill Notation):
C11H20N4O11P2 · xNa+ · yH2O
Molecular Weight:
446.24 (anhydrous free acid basis)
UNSPSC Code:
12352201
NACRES:
NA.25
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Related Categories
Biochem/physiol Actions
Metabolite of glycerophospholipid metabolism and phosphatidylethanolamine (PE) biosynthesis.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Giuliano Sciara et al.
Nature communications, 5, 4068-4068 (2014-06-14)
The CDP-alcohol phosphotransferase (CDP-AP) family of integral membrane enzymes catalyses the transfer of a substituted phosphate group from a CDP-linked donor to an alcohol acceptor. This is an essential reaction for phospholipid biosynthesis across all kingdoms of life, and it
METABOLISM AND FUNCTION OF BACTERIAL LIPIDS. II. BIOSYNTHESIS OF PHOSPHOLIPIDS IN ESCHERICHIA COLI.
J KANFER et al.
The Journal of biological chemistry, 239, 1720-1726 (1964-06-01)
L B Tijburg et al.
Biochemical and biophysical research communications, 160(3), 1275-1280 (1989-05-15)
In the present study pulse-label and pulse-chase experiments with isolated rat hepatocytes in suspension were designed to investigate the effects of the presence of either serine or ethanolamine in the medium on the rate of phosphatidylethanolamine synthesis via the CDPethanolamine
Martina Gsell et al.
Methods in molecular biology (Clifton, N.J.), 1033, 29-44 (2013-09-03)
The yeast Saccharomyces cerevisiae has become a valuable eukaryotic model organism to study biochemical and cellular processes at a molecular basis. A common strategy for such studies is the use of single and multiple mutants constructed by genetic manipulation which
Kristine Glunde et al.
Nature reviews. Cancer, 11(12), 835-848 (2011-11-18)
Abnormal choline metabolism is emerging as a metabolic hallmark that is associated with oncogenesis and tumour progression. Following transformation, the modulation of enzymes that control anabolic and catabolic pathways causes increased levels of choline-containing precursors and breakdown products of membrane
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