Compound
1-eicosanoyl-2-hexadecanoyl-sn-glycero-3-phosphocholine
A phosphatidylcholine 36:0 where the acyl substituents at positions 1 and 2 are icosanoyl and palmitoyl respectively.
Definition from ChEBI (CHEBI:75294), read 2026-09-23. CC BY 4.0.
Structure
No three-dimensional record for this entry.
- Class
- Organic compound
- Formula
- C44H88NO8P
- Mass
- 790.161 g/mol
- Charge
- 0
- InChIKey
- JJSZXCSTFDBBBZ-HUESYALOSA-N
- SMILES
- CCCCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCC
- Look it up
- ChEBIBy InChIKey
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-eicosanoyl-2-hexadecanoyl-sn-glycero-3-phosphocholine has the functional parent 1-eicosanoyl-sn-glycero-3-phosphocholineCompoundChEBI CHEBI:75294Inferred only
Statements
1 statement
1 statement · 1 reference database · Subject: 1-eicosanoyl-2-hexadecanoyl-sn-glycero-3-phosphocholine · Sources: Rhea
- 1-eicosanoyl-2-hexadecanoyl-sn-glycero-3-phosphocholine is a substrate of LPCAT1ProteinRhea RHEA:37843Inferred only
Reactions
1 reaction
1-eicosanoyl-sn-glycero-3-phosphocholine+hexadecanoyl-CoA1-eicosanoyl-2-hexadecanoyl-sn-glycero-3-phosphocholine+coenzyme A(4-)
Catalysed by LPCAT1
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:37843CC BY 4.0Reference data
Other names
11 names
Resolves to: 1-eicosanoyl-2-hexadecanoyl-sn-glycero-3-phosphocholine
- Also called
- 1-icosanoyl-2-hexadecanoyl-sn-glycero-3-phosphocholine1-icosanoyl-2-palmitoyl-sn-phosphatidylcholineGPCho(20:0/16:0)PC 20:0/16:0PC 36:0PC(16:0_20:0)PC(20:0/16:0)PC(36:0)Phosphatidylcholine(20:0/16:0)
- Systematic name
- (2R)-2-(hexadecanoyloxy)-3-(icosanoyloxy)propyl 2-(trimethylammonio)ethyl phosphate(2R)-2-(hexadecanoyloxy)-3-(icosanoyloxy)propyl 2-(trimethylazaniumyl)ethyl phosphate