Compound
1-hexadecanoyl-2-dodecanoyl-sn-glycero-3-phospho-(1D-myo-inositol)
A phosphatidylinositol 28:0 in which the phosphatidyl acyl groups at positions 1 and 2 are specified as palmitoyl (hexadecanoyl) and lauroyl (dodecanoyl) respectively.
Definition from ChEBI (CHEBI:75160), read 2026-09-23. CC BY 4.0.
Structure
No three-dimensional record for this entry.
- Class
- Organic compound, anion
- Formula
- C37H70O13P
- Mass
- 753.928 g/mol
- Charge
- -1
- InChIKey
- OOIYGIBLKJXABS-AVVBPMCPSA-M
- SMILES
- CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])O[C@@H]1[C@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H]1O)OC(=O)CCCCCCCCCCC
- 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
Statements
1 statement
1 statement · 1 reference database · Subject: 1-hexadecanoyl-2-dodecanoyl-sn-glycero-3-phospho-(1D-myo-inositol) · Sources: Rhea
- 1-hexadecanoyl-2-dodecanoyl-sn-glycero-3-phospho-(1D-myo-inositol) is a substrate of LCLAT1ProteinRhea RHEA:37639Inferred only
Reactions
1 reaction
1-hexadecanoyl-sn-glycero-3-phospho-(1D-myo-inositol)+dodecanoyl-CoA1-hexadecanoyl-2-dodecanoyl-sn-glycero-3-phospho-(1D-myo-inositol)+coenzyme A(4-)
Catalysed by LCLAT1
Reaction pageLeft to rightBalance undeterminable
Rhea RHEA:37639CC BY 4.0Reference data
Other names
9 names
Resolves to: 1-hexadecanoyl-2-dodecanoyl-sn-glycero-3-phospho-(1D-myo-inositol)
- Also called
- 1-hexadecanoyl-2-dodecanoyl-sn-3-phosphatidylinositol(1-)1-hexadecanoyl-2-dodecanoyl-sn-3-phosphatidylinositol(1−)1-hexadecanoyl-2-dodecanoyl-sn-glycero-3-phospho-1D-myo-inositol1-hexadecanoyl-2-dodecanoyl-sn-glycero-3-phospho-1D-myo-inositol(1-)1-hexadecanoyl-2-dodecanoyl-sn-glycero-3-phospho-1D-myo-inositol(1−)PI(16:0/12:0)PI(16:0/12:0)(1-)PI(16:0/12:0)(1−)
- Systematic name
- (2R)-2-(dodecanoyloxy)-3-(hexadecanoyloxy)propyl (1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl phosphate