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About This Item
Empirical Formula (Hill Notation):
C8H20NO6P
Molecular Weight:
257.22
NACRES:
NA.83
PubChem Substance ID:
UNSPSC Code:
12352204
EC Number:
248-962-2
MDL number:
Product Name
L-α-Glycerophosphorylcholine, from soybean, ≥98%, powder
InChI
1S/C8H21NO6P/c1-9(2,3)4-5-14-16(12,13)15-7-8(11)6-10/h8,10-11H,4-7H2,1-3H3,(H,12,13)
InChI key
XGPKIOAEPQZUED-UHFFFAOYSA-N
SMILES string
C[N](C)(C)CCOP(O)(=O)OC[C@@H](O)CO
biological source
soybean
assay
≥98%
form
powder
solubility
water: 50 mg/mL, clear, colorless to very faintly yellow
storage temp.
−20°C
Application
L-α-Glycerophosphorylcholine has been used to rescue choline auxotrophy. It has also been used for the synthesis of glycerophospholipids.
Biochem/physiol Actions
Increases inositol phosphate formation.
General description
L-α-Glycerophosphorylcholine is a phospholipid, which is a derivative of phosphatidylcholine.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Cognitive improvement in mild to moderate Alzheimer's dementia after treatment with the acetylcholine precursor choline alfoscerate: a multicenter, double-blind, randomized, placebo-controlled trial
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Alzheimer's Disease: Current Research In Early Diagnosis (1990)
Cholinergic precursors in the treatment of cognitive impairment of vascular origin: ineffective approaches or need for re-evaluation?
Parnetti L, et al.
Journal of the Neurological Sciences, 257(1-2), 264-269 (2007)
Overproduction of Phospholipids by the Kennedy Pathway Leads to Hypervirulence in Candida albicans
Tams RN, et al.
Frontiers in Microbiology, 10 (2019)
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Huynh K, et al.
Cell Chemical Biology, 26(1), 71-84 (2019)
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