Compound
a 1-O-alkyl-sn-glycero-3-phosphoethanolamine
A glycerophosphoethanolamine zwitterion obtained by transfer of a proton from the phosphate to the amino group of any 1-alkyl-sn-glycero-3-phosphoethanolamine.
Definition from ChEBI (CHEBI:76168), read 2026-09-23. CC BY 4.0.
Structure
- Class
- Organic compound
- Formula
- C5H13NO6PR
- Mass
- 214.134 g/mol
- Charge
- 0
- SMILES
- *OC[C@@]([H])(O)COP(=O)([O-])OCC[NH3+]
- Look it up
- ChEBI
Identity from ChEBI. Not evidence.
What it touches on the way
Mechanistic reach
1 entity
1 entities reached.
0 reported hops1 assembled from the scaffold
What the reference databases state
Statements
1 statement
1 statement · 1 reference database · Subject: a 1-O-alkyl-sn-glycero-3-phosphoethanolamine · Sources: Rhea
- a 1-O-alkyl-sn-glycero-3-phosphoethanolamine is a substrate of ENPP2ProteinRhea RHEA:15965Inferred only
Reactions
3 reactions
CHEBI:28894+a 1-O-alkyl-sn-glycero-3-phosphoethanolamineCHEBI:76251+a 1-O-alkyl-sn-glycero-3-phosphocholine
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:15409CC BY 4.0Reference data
a 1-O-alkyl-sn-glycero-3-phosphoethanolamine+watera 1-O-alkyl-sn-glycero-3-phosphate+ethanolamine+hydron
Catalysed by ENPP2
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:15965CC BY 4.0Reference data
a 1-O-alkyl-sn-glycero-3-phosphoethanolamine+a 1-O-alkyl-2-acyl-sn-glycero-3-phosphocholinea 1-O-alkyl-2-acyl-sn-glycero-3-phosphoethanolamine+a 1-O-alkyl-sn-glycero-3-phosphocholine
Reaction pageDirection not assertedBalance undeterminable
Rhea RHEA:20972CC BY 4.0Reference data
Other names
5 names
Resolves to: a 1-O-alkyl-sn-glycero-3-phosphoethanolamine
- Also called
- 1-O-alkyl-2-hydroxy-sn-glycero-3-phosphoethanolamine zwitterion1-O-alkyl-sn-glycero-3-phosphoethanolamine1-O-alkyl-sn-glycero-3-phosphoethanolamine zwitterion1-O-alkyllysophosphatidylethanolamine zwitterionLPE(O-)