Compound
1-acyl-2-hexadecanoyl-sn-glycero-3-phosphoethanolamine
1,2-diacyl-sn-glycero-3-phosphoethanolamine zwitterion in which the acyl group at position 1 is unspecified while that at position 2 is specified as palmitoyl.
Definition from ChEBI (CHEBI:75265), read 2026-09-23. CC BY 4.0.
Structure
- Class
- Organic compound
- Formula
- C22H43NO8PR
- Mass
- 480.553 g/mol
- Charge
- 0
- SMILES
- *C(=O)OC[C@@H](COP(=O)([O-])OCC[NH3+])OC(=O)CCCCCCCCCCCCCCC
- 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
Chemical structure
- 1-acyl-2-hexadecanoyl-sn-glycero-3-phosphoethanolamine has the functional parent hexadecanoic acidCompoundChEBI CHEBI:75265Inferred only
Statements
1 statement
1 statement · 1 reference database · Subject: 1-acyl-2-hexadecanoyl-sn-glycero-3-phosphoethanolamine · Sources: Rhea
- 1-acyl-2-hexadecanoyl-sn-glycero-3-phosphoethanolamine is a substrate of LPCAT4ProteinRhea RHEA:37767Inferred only
Reactions
1 reaction
a 1-acyl-sn-glycero-3-phosphoethanolamine+hexadecanoyl-CoA1-acyl-2-hexadecanoyl-sn-glycero-3-phosphoethanolamine+coenzyme A(4-)
Catalysed by LPCAT4
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:37767CC BY 4.0Reference data
Other names
2 names
Resolves to: 1-acyl-2-hexadecanoyl-sn-glycero-3-phosphoethanolamine
- Also called
- 1-acyl-2-hexadecanoyl-sn-glycero-3-phosphoethanolamine zwitterion1-acyl-2-hexadecanoyl-sn-phosphatidylethanolamine zwitterion