InChI=1S/C44H80NO8P/c1-6-8-10-12-14-16-18-20-21-22-23-25-27-29-31-33-35-37-44(47)53-42(41-52-54(48,49)51-39-38-45(3,4)5)40-50-43(46)36-34-32-30-28-26-24-19-17-15-13-11-9-7-2/h14,16,20-21,23,25,29,31,42H,6-13,15,17-19,22,24,26-28,30,32-41H2,1-5H3/b16-14-,21-20-,25-23-,31-29-/t42-/m1/s1 |
IIZPXYDJLKNOIY-JXPKJXOSSA-N |
C(C[N+](C)(C)C)OP(=O)([O-])OC[C@H](OC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O)COC(=O)CCCCCCCCCCCCCCC |
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mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via phosphatidylcholine 36:4 )
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(2R)-3-(hexadecanoyloxy)-2-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyloxy]propyl 2-(trimethylammonio)ethyl phosphate
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(2R)-3-(hexadecanoyloxy)-2-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyloxy]propyl 2-(trimethylazaniumyl)ethyl phosphate
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1-hexadecanoyl-2-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphocholine
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UniProt
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1-hexadecanoyl-2-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phosphocholine
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ChEBI
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1-hexadecanoyl-2-(5Z,8Z,11Z,14Z-icosatetraenoyl)-sn-glycero-3-phosphocholine
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ChEBI
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1-O-hexadecanoyl-2-O-arachidonoyl-sn-glycero-3-phosphocholine
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ChEBI
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1-palmitoyl-2-arachidonoyl-GPC
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ChEBI
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1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4)
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ChEBI
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1-Palmitoyl-2-arachidonyl-gpc
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ChemIDplus
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1-Palmitoyl-2-arachidonyl-phosphatidylcholine
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ChemIDplus
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GPC(16:0/20:4)
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ChEBI
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GPCho(16:0/20:4)
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HMDB
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GPCho(16:0/20:4ω6)
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HMDB
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GPCho(16:0/5Z,8Z,11Z,14Z-20:4)
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LIPID MAPS
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GPCho(36:4)
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HMDB
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Lecithin
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ChEBI
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PAPC
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ChEBI
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PC(16:0/20:4(5Z,8Z,11Z,14Z))
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LIPID MAPS
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PC(16:0/20:4)
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LIPID MAPS
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PC(16:0/20:4ω6)
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HMDB
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PC(36:4)
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ChEBI
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PC(36:4)
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HMDB
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PC[16:0/20:4(5Z,8Z,11Z,14Z)]
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LIPID MAPS
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Phosphatidylcholine(16:0/20:4)
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HMDB
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Phosphatidylcholine(16:0/20:4ω6)
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HMDB
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Phosphatidylcholine(16:0/20:4w6)
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ChEBI
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Phosphatidylcholine(36:4)
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HMDB
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6931-56-2
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CAS Registry Number
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ChemIDplus
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7738062
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Beilstein Registry Number
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Beilstein
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7738602
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Reaxys Registry Number
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Reaxys
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