| Record Information |
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| Version | 1.0 |
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| Creation Date | 2016-07-13 19:52:15 UTC |
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| Update Date | 2016-07-20 20:44:58 UTC |
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| Lmdb | LMDB00546 |
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| Secondary Accession Numbers | None |
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| Metabolite Identification |
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| Common Name | PC(P-16:0/20:1(11Z)) |
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| Description | PC(P-16:0/20:1(11Z)) is a phosphatidylcholine (PC or GPCho). It is a glycerophospholipid in which a phosphorylcholine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphocholines can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 16, 18 and 20 carbons are the most common. PC(P-16:0/20:1(11Z)), in particular, consists of one chain of plasmalogen 16:0 at the C-1 position and one chain of eicosenoic acid at the C-2 position. The plasmalogen 16:0 moiety is derived from animal fats, liver and kidney, while the eicosenoic acid moiety is derived from vegetable oils and cod oils. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling. While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodeling that occurs while these molecules are in membranes. PCs can be synthesized via three different routes. In one route, choline is activated first by phosphorylation and then by coupling to CDP prior to attachment to phosphatidic acid. PCs can also synthesized by the addition of choline to CDP-activated 1,2-diacylglycerol. A third route to PC synthesis involves the conversion of either PS or PE to PC. Plasmalogens are glycerol ether phospholipids. They are of two types, alkyl ether (-O-CH2-) and alkenyl ether (-O-CH=CH-). Dihydroxyacetone phosphate (DHAP) serves as the glycerol precursor for the synthesis of plasmalogens. Three major classes of plasmalogens have been identified: choline, ethanolamine and serine derivatives. Ethanolamine plasmalogen is prevalent in myelin. Choline plasmalogen is abundant in cardiac tissue. Usually, the highest proportion of the plasmalogen form is in the ethanolamine class with rather less in choline, and commonly little or none in other phospholipids such as phosphatidylinositol. In choline plasmalogens of most tissues, a higher proportion is often of the O-alkyl rather than the O-alkenyl form, but the reverse tends to be true in heart lipids. In animal tissues, the alkyl and alkenyl moieties in both non-polar and phospholipids tend to be rather simple in composition with 16:0, 18:0 and 18:1 (double bond in position 9) predominating. Ether analogues of triacylglycerols, i.e. 1-alkyldiacyl-sn-glycerols, are present at trace levels only if at all in most animal tissues, but they can be major components of some marine lipids. |
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| Structure | |
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| Synonyms | | Value | Source |
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| 1-(1-Enyl-palmitoyl)-2-eicosenoyl-sn-glycero-3-phosphocholine | HMDB | | Gpcho(16:0/20:1) | HMDB | | Gpcho(16:0/20:1n9) | HMDB | | Gpcho(16:0/20:1W9) | HMDB | | Gpcho(36:1) | HMDB | | 1-(1Z-Hexadecenyl)-2-eicosenoyl-GPC | HMDB | | 1-(1Z-Hexadecenyl)-2-eicosenoyl-sn-glycero-3-phosphocholine | HMDB | | 1-(1Z-Hexadecenyl)-2-eicosenoyl-sn-glycero-phosphatidylcholine | HMDB | | GPC(16:1/20:1) | HMDB | | GPC(36:2) | HMDB | | GPC(O-16:1(1Z)/20:1(11Z)) | HMDB | | GPC(O-16:1(1Z)/20:1n9) | HMDB | | GPC(O-16:1(1Z)/20:1W9) | HMDB | | GPC(p-16:0/20:1(11Z)) | HMDB | | GPC(p-16:0/20:1n9) | HMDB | | GPC(p-16:0/20:1W9) | HMDB | | GPCho(16:1/20:1) | HMDB | | GPCho(36:2) | HMDB | | GPCho(O-16:1(1Z)/20:1(11Z)) | HMDB | | GPCho(O-16:1(1Z)/20:1n9) | HMDB | | GPCho(O-16:1(1Z)/20:1W9) | HMDB | | GPCho(p-16:0/20:1(11Z)) | HMDB | | GPCho(p-16:0/20:1n9) | HMDB | | GPCho(p-16:0/20:1W9) | HMDB | | PC(16:1/20:1) | HMDB | | PC(36:2) | HMDB | | PC(O-16:1(1Z)/20:1(11Z)) | HMDB | | PC(O-16:1(1Z)/20:1n9) | HMDB | | PC(O-16:1(1Z)/20:1W9) | HMDB | | PC(p-16:0/20:1n9) | HMDB | | PC(p-16:0/20:1W9) | HMDB | | Phosphatidylcholine(16:1/20:1) | HMDB | | Phosphatidylcholine(36:2) | HMDB | | Phosphatidylcholine(O-16:1(1Z)/20:1(11Z)) | HMDB | | Phosphatidylcholine(O-16:1(1Z)/20:1n9) | HMDB | | Phosphatidylcholine(O-16:1(1Z)/20:1W9) | HMDB | | Phosphatidylcholine(p-16:0/20:1(11Z)) | HMDB | | Phosphatidylcholine(p-16:0/20:1n9) | HMDB | | Phosphatidylcholine(p-16:0/20:1W9) | HMDB |
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| Chemical Formula | C44H86NO7P |
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| Average Molecular Weight | 772.1299 |
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| Monoisotopic Molecular Weight | 771.614190623 |
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| IUPAC Name | (2-{[(2R)-3-[(1Z)-hexadec-1-en-1-yloxy]-2-[(11Z)-icos-11-enoyloxy]propyl phosphonato]oxy}ethyl)trimethylazanium |
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| Traditional Name | (2-{[(2R)-3-[(1Z)-hexadec-1-en-1-yloxy]-2-[(11Z)-icos-11-enoyloxy]propyl phosphonato]oxy}ethyl)trimethylazanium |
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| CAS Registry Number | Not Available |
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| SMILES | CCCCCCCCCCCCCC\C=C/OC[C@]([H])(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCC\C=C/CCCCCCCC |
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| InChI Identifier | InChI=1S/C44H86NO7P/c1-6-8-10-12-14-16-18-20-22-23-24-25-27-29-31-33-35-37-44(46)52-43(42-51-53(47,48)50-40-38-45(3,4)5)41-49-39-36-34-32-30-28-26-21-19-17-15-13-11-9-7-2/h20,22,36,39,43H,6-19,21,23-35,37-38,40-42H2,1-5H3/b22-20-,39-36-/t43-/m1/s1 |
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| InChI Key | WXILBCFZIXHZIG-KOUVQCMKSA-N |
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| Chemical Taxonomy |
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| Description | belongs to the class of organic compounds known as 1-(1z-alkenyl),2-acyl-glycerophosphocholines. These are glycerophosphocholines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position. |
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| Kingdom | Organic compounds |
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| Super Class | Lipids and lipid-like molecules |
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| Class | Glycerophospholipids |
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| Sub Class | Glycerophosphocholines |
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| Direct Parent | 1-(1Z-alkenyl),2-acyl-glycerophosphocholines |
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| Alternative Parents | |
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| Substituents | - 1-(1z-alkenyl),2-acyl-glycerophosphocholine
- Phosphocholine
- Glycerol vinyl ether
- Fatty acid ester
- Dialkyl phosphate
- Organic phosphoric acid derivative
- Phosphoric acid ester
- Alkyl phosphate
- Fatty acyl
- Quaternary ammonium salt
- Tetraalkylammonium salt
- Carboxylic acid ester
- Monocarboxylic acid or derivatives
- Carboxylic acid derivative
- Amine
- Organic oxide
- Organopnictogen compound
- Organooxygen compound
- Organonitrogen compound
- Organic oxygen compound
- Organic nitrogen compound
- Carbonyl group
- Hydrocarbon derivative
- Organic salt
- Aliphatic acyclic compound
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| Molecular Framework | Aliphatic acyclic compounds |
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| External Descriptors | |
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| Ontology |
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| Status | Detected and Quantified |
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| Origin | Not Available |
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| Biofunction | Not Available |
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| Application | Not Available |
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| Cellular locations | Not Available |
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| Physical Properties |
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| State | Not Available |
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| Experimental Properties | | Property | Value | Reference |
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| Melting Point | Not Available | Not Available | | Boiling Point | Not Available | Not Available | | Water Solubility | Not Available | Not Available | | LogP | Not Available | Not Available |
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| Predicted Properties | |
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| Spectra |
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| Spectra | | Spectrum Type | Description | Splash Key | View |
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| Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Positive | splash10-0080-9171321300-232e8b8f43a9d59d286a | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Positive | splash10-0083-3190010000-08d45c5d3a9482dd460e | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Positive | splash10-0080-5090011000-666273d15e4b3a2ac3a0 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Negative | splash10-05fr-0096002800-21aca773e511dacead4f | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Negative | splash10-05tr-1092003200-c347622d212b05e91ada | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Negative | splash10-054o-5095000000-836bc7c3ffd50517f449 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Negative | splash10-00di-0000000900-afeccba552b4299f629b | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Negative | splash10-00dl-0041010900-5139e25ac49189787e31 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Negative | splash10-0a6r-4029301000-9390d72092a9447b1939 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Negative | splash10-0a4i-0000000090-4bddad7d3cb753a851a7 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Negative | splash10-0a4i-0000000090-4bddad7d3cb753a851a7 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Negative | splash10-0a4i-0004921610-681c8b13ded467996f33 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 10V, Positive | splash10-00di-0000000900-c9ee98592191a777e9e5 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 20V, Positive | splash10-0089-0900000500-53bbedc27651cf399473 | Spectrum | | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - 40V, Positive | splash10-01x0-0500210900-83174c8af05511b86972 | Spectrum |
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