CHEBI:16870 - choline alfoscerate

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ChEBI Name choline alfoscerate
ChEBI ID CHEBI:16870
Definition A member of the class of phosphocholines that is the choline ester of sn-glycero-3-phosphate. It is one of the major osmolyte in the renal medullary cells.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Birgit
Secondary ChEBI IDs CHEBI:76433, CHEBI:41458, CHEBI:10646, CHEBI:12847, CHEBI:12841, CHEBI:26697, CHEBI:55397, CHEBI:14343
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Formula C8H20NO6P
Net Charge 0
Average Mass 257.22130
InChI InChI=1S/C8H20NO6P/c1-9(2,3)4-5-14-16(12,13)15-7-8(11)6-10/h8,10-11H,4-7H2,1-3H3/t8-/m1/s1
InChIKey SUHOQUVVVLNYQR-MRVPVSSYSA-N
SMILES C[N+](C)(C)CCOP([O-])(=O)OC[C@H](O)CO
Metabolite of Species Details
Homo sapiens (NCBI:9606) See: DOI
Roles Classification
Biological Role(s): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
parasympatholytic
Any cholinergic antagonist that inhibits the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the muscarinic antagonists.
Application(s): parasympatholytic
Any cholinergic antagonist that inhibits the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the muscarinic antagonists.
neuroprotective agent
Any compound that can be used for the treatment of neurodegenerative disorders.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing choline alfoscerate (CHEBI:16870) has role human metabolite (CHEBI:77746)
choline alfoscerate (CHEBI:16870) has role neuroprotective agent (CHEBI:63726)
choline alfoscerate (CHEBI:16870) has role parasympatholytic (CHEBI:50370)
choline alfoscerate (CHEBI:16870) is a sn-glycerol 3-phosphates (CHEBI:26706)
choline alfoscerate (CHEBI:16870) is a phosphocholines (CHEBI:36700)
IUPAC Names
(2R)-2,3-dihydroxypropyl 2-(trimethylazaniumyl)ethyl phosphate
2-{[(2R)-2,3-dihydroxypropoxy](hydroxy)phosphoryloxy}-N,N,N-trimethylethanaminium
INNs Sources
alfoscerate de choline ChemIDplus
alfoscerato de colina ChemIDplus
choline alfoscerate ChemIDplus
choline alfoscerate KEGG DRUG
cholini alfosceras ChemIDplus
Synonyms Sources
(2R)-2,3-dihydroxypropyl 2-(trimethylammonio)ethyl phosphate IUPAC
alpha-Glycerophosphorylcholine HMDB
Choline alphoscerate ChemIDplus
Choline glycerophosphate ChemIDplus
Cholini glycerophosphas ChemIDplus
Glicerofosfato de colina ChemIDplus
Glycerol phosphorylcholine HMDB
Glycerol-3-phosphatidylcholine HMDB
glycerol-3-phosphocholine ChEBI
Glycerophosphate de choline ChemIDplus
Glycerophosphocholine ChemIDplus
Glycerophosphocholine KEGG COMPOUND
Glycerophosphocholine KEGG COMPOUND
Glycerophosphorylcholine ChemIDplus
GPCho HMDB
L-alpha-Glycerophosphocholine ChemIDplus
L-alpha-Glycerophosphorylcholine ChemIDplus
L-alpha-Glycerophosphorylcholine HMDB
L-Choline hydroxide 2,3-dihydroxypropyl hydrogen phosphate inner salt HMDB
sn-3-GPC MetaCyc
sn-Glycero-3-phosphocholine ChemIDplus
sn-glycero-3-phosphocholine ChEBI
sn-glycero-3-phosphocholine ChEBI
sn-glycerol 3-phosphocholine UniProt
Database Links Databases
Alpha-GPC Wikipedia
C00670 KEGG COMPOUND
CH5 PDBeChem
D07349 KEGG DRUG
DB04660 DrugBank
HMDB00086 HMDB
L-1-GLYCERO-PHOSPHORYLCHOLINE MetaCyc
View more database links
Registry Numbers Types Sources
28319-77-9 CAS Registry Number ChemIDplus
28319-77-9 CAS Registry Number KEGG DRUG
3908444 Reaxys Registry Number Reaxys
6062450 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
21165396 PubMed citation CiteXplore
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22191561 PubMed citation CiteXplore
22677751 PubMed citation CiteXplore
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Last Modified
24 November 2014