Record Information |
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Version | 5.0 |
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Status | Expected but not Quantified |
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Creation Date | 2017-09-09 02:42:06 UTC |
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Update Date | 2022-11-30 19:25:54 UTC |
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HMDB ID | HMDB0114785 |
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Secondary Accession Numbers | None |
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Metabolite Identification |
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Common Name | PA(14:0/20:4(5Z,8Z,11Z,14Z)) |
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Description | PA(14:0/20:4(5Z,8Z,11Z,14Z)) is a phosphatidic acid. It is a glycerophospholipid in which a phosphate moiety occupies a glycerol substitution site. As is the case with diacylglycerols, phosphatidic acids 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. PA(14:0/20:4(5Z,8Z,11Z,14Z)), in particular, consists of one chain of myristic acid at the C-1 position and one chain of arachidonic acid at the C-2 position. Phosphatidic acids are quite rare but are extremely important as intermediates in the biosynthesis of triacylglycerols and phospholipids. |
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Structure | [H][C@@](COC(=O)CCCCCCCCCCCCC)(COP(O)(O)=O)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC InChI=1S/C37H65O8P/c1-3-5-7-9-11-13-15-16-17-18-19-20-22-24-26-28-30-32-37(39)45-35(34-44-46(40,41)42)33-43-36(38)31-29-27-25-23-21-14-12-10-8-6-4-2/h11,13,16-17,19-20,24,26,35H,3-10,12,14-15,18,21-23,25,27-34H2,1-2H3,(H2,40,41,42)/b13-11-,17-16-,20-19-,26-24-/t35-/m1/s1 |
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Synonyms | Value | Source |
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1-Myristoyl-2-arachidonoyl-sn-glycero-3-phosphate | HMDB | 1-Myristoyl-2-arachidonoyl-sn-phosphatidic acid | HMDB | PA(14:0/20:4) | HMDB | PA(14:0/20:4N6) | HMDB | PA(14:0/20:4W6) | HMDB | PA(34:4) | HMDB | Phosphatidic acid(14:0/20:4(5Z,8Z,11Z,14Z)) | HMDB | Phosphatidic acid(14:0/20:4) | HMDB | Phosphatidic acid(14:0/20:4n6) | HMDB | Phosphatidic acid(14:0/20:4W6) | HMDB | Phosphatidic acid(34:4) | HMDB | Phosphatidate(14:0/20:4(5Z,8Z,11Z,14Z)) | HMDB | Phosphatidate(14:0/20:4) | HMDB | Phosphatidate(14:0/20:4N6) | HMDB | Phosphatidate(14:0/20:4W6) | HMDB | Phosphatidate(34:4) | HMDB | 1-myristoyl-2-arachidonoyl-sn-glycero-3-phosphate | SMPDB, HMDB | 1-myristoyl-2-arachidonoyl-sn-phosphatidic acid | SMPDB, HMDB | PA(14:0/20:4) | SMPDB, HMDB | PA(14:0/20:4n6) | SMPDB, HMDB | PA(14:0/20:4w6) | SMPDB, HMDB | PA(34:4) | SMPDB, HMDB | Phosphatidic acid(14:0/20:4(5Z,8Z,11Z,14Z)) | SMPDB, HMDB | Phosphatidic acid(14:0/20:4) | SMPDB, HMDB | Phosphatidic acid(14:0/20:4n6) | SMPDB, HMDB | Phosphatidic acid(14:0/20:4w6) | SMPDB, HMDB | Phosphatidic acid(34:4) | SMPDB, HMDB | Phosphatidate(14:0/20:4(5Z,8Z,11Z,14Z)) | SMPDB, HMDB | Phosphatidate(14:0/20:4) | SMPDB, HMDB | Phosphatidate(14:0/20:4n6) | SMPDB, HMDB | Phosphatidate(14:0/20:4w6) | SMPDB, HMDB | PA(14:0/20:4(5Z,8Z,11Z,14Z)) | SMPDB |
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Chemical Formula | C37H65O8P |
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Average Molecular Weight | 668.893 |
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Monoisotopic Molecular Weight | 668.441706051 |
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IUPAC Name | [(2R)-2-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyloxy]-3-(tetradecanoyloxy)propoxy]phosphonic acid |
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Traditional Name | (2R)-2-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoyloxy]-3-(tetradecanoyloxy)propoxyphosphonic acid |
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CAS Registry Number | Not Available |
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SMILES | [H][C@@](COC(=O)CCCCCCCCCCCCC)(COP(O)(O)=O)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC |
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InChI Identifier | InChI=1S/C37H65O8P/c1-3-5-7-9-11-13-15-16-17-18-19-20-22-24-26-28-30-32-37(39)45-35(34-44-46(40,41)42)33-43-36(38)31-29-27-25-23-21-14-12-10-8-6-4-2/h11,13,16-17,19-20,24,26,35H,3-10,12,14-15,18,21-23,25,27-34H2,1-2H3,(H2,40,41,42)/b13-11-,17-16-,20-19-,26-24-/t35-/m1/s1 |
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InChI Key | FXDNJLAQUIAATP-MTRMCENXSA-N |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as 1,2-diacylglycerol-3-phosphates. These are glycerol-3-phosphates in which the glycerol moiety is bonded to two aliphatic chains through ester linkages. |
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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 | Glycerophosphates |
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Direct Parent | 1,2-diacylglycerol-3-phosphates |
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Alternative Parents | |
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Substituents | - 1,2-diacylglycerol-3-phosphate
- Fatty acid ester
- Monoalkyl phosphate
- Dicarboxylic acid or derivatives
- Fatty acyl
- Alkyl phosphate
- Phosphoric acid ester
- Organic phosphoric acid derivative
- Carboxylic acid ester
- Carboxylic acid derivative
- Hydrocarbon derivative
- Organic oxide
- Organic oxygen compound
- Carbonyl group
- Organooxygen compound
- 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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Physiological effect | Not Available |
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Disposition | |
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Process | Naturally occurring processBiological processBiochemical pathwayMetabolic pathway- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z)) (PathBank: SMP0064259)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/22:4(7Z,10Z,13Z,16Z)) (PathBank: SMP0064265)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/24:0) (PathBank: SMP0064269)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/22:0) (PathBank: SMP0088275)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/22:5(4Z,7Z,10Z,13Z,16Z)) (PathBank: SMP0088279)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) (PathBank: SMP0088281)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(8Z,11Z,14Z,17Z)) (PathBank: SMP0064260)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/22:5(7Z,10Z,13Z,16Z,19Z)) (PathBank: SMP0064267)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/22:2(13Z,16Z)) (PathBank: SMP0073014)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/20:5(5Z,8Z,11Z,14Z,17Z)) (PathBank: SMP0085584)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z)/20:4(8Z,11Z,14Z,17Z)) (PathBank: SMP0096959)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/24:1(15Z)) (PathBank: SMP0064270)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z)) (PathBank: SMP0096958)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(8Z,11Z,14Z,17Z)/20:4(8Z,11Z,14Z,17Z)) (PathBank: SMP0096962)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/22:1(13Z)) (PathBank: SMP0064263)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/14:0) (PathBank: SMP0016653)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/15:0) (PathBank: SMP0016654)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/16:0) (PathBank: SMP0016655)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/18:0) (PathBank: SMP0016656)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/20:0) (PathBank: SMP0016657)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/14:1(9Z)) (PathBank: SMP0016660)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/16:1(9Z)) (PathBank: SMP0016661)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/18:1(11Z)) (PathBank: SMP0016662)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/18:1(9Z)) (PathBank: SMP0016663)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/20:1(11Z)) (PathBank: SMP0016664)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/20:3(5Z,8Z,11Z)) (PathBank: SMP0016665)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/18:2(9Z,12Z)) (PathBank: SMP0016668)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/18:3(6Z,9Z,12Z)) (PathBank: SMP0016669)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/18:3(9Z,12Z,15Z)) (PathBank: SMP0016674)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/18:4(6Z,9Z,12Z,15Z)) (PathBank: SMP0016675)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/20:2(11Z,14Z)) (PathBank: SMP0032499)
- De Novo Triacylglycerol Biosynthesis TG(14:0/20:4(5Z,8Z,11Z,14Z)/20:3(8Z,11Z,14Z)) (PathBank: SMP0032500)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z)/20:5(5Z,8Z,11Z,14Z,17Z)) (PathBank: SMP0083349)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(8Z,11Z,14Z,17Z)/20:5(5Z,8Z,11Z,14Z,17Z)) (PathBank: SMP0083351)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/20:5(5Z,8Z,11Z,14Z,17Z)/20:5(5Z,8Z,11Z,14Z,17Z)) (PathBank: SMP0083352)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z)/22:0) (PathBank: SMP0096960)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(5Z,8Z,11Z,14Z)/22:1(13Z)) (PathBank: SMP0096961)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(8Z,11Z,14Z,17Z)/22:0) (PathBank: SMP0096963)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/20:4(8Z,11Z,14Z,17Z)/22:1(13Z)) (PathBank: SMP0096964)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/22:0/22:0) (PathBank: SMP0096965)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/22:0/22:1(13Z)) (PathBank: SMP0096966)
- Cardiolipin Biosynthesis CL(14:0/20:4(5Z,8Z,11Z,14Z)/22:1(13Z)/22:1(13Z)) (PathBank: SMP0096967)
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Role | Not Available |
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Physical Properties |
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State | Solid |
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Experimental Molecular 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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Experimental Chromatographic Properties | Not Available |
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Predicted Molecular Properties | | Show more...
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Predicted Chromatographic Properties | Predicted Collision Cross SectionsPredicted Kovats Retention IndicesUnderivatizedDerivatizedDerivative Name / Structure | SMILES | Kovats RI Value | Column Type | Reference |
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PA(14:0/20:4(5Z,8Z,11Z,14Z)),1TMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O)O[Si](C)(C)C | 4735.1 | Semi standard non polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),1TMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O)O[Si](C)(C)C | 4220.3 | Standard non polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),1TMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O)O[Si](C)(C)C | 5439.3 | Standard polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),2TMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C | 4703.4 | Semi standard non polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),2TMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C | 4200.1 | Standard non polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),2TMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C | 4711.7 | Standard polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),1TBDMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O)O[Si](C)(C)C(C)(C)C | 4952.5 | Semi standard non polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),1TBDMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O)O[Si](C)(C)C(C)(C)C | 4333.4 | Standard non polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),1TBDMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O)O[Si](C)(C)C(C)(C)C | 5423.3 | Standard polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),2TBDMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C | 5148.8 | Semi standard non polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),2TBDMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C | 4381.1 | Standard non polar | 33892256 | PA(14:0/20:4(5Z,8Z,11Z,14Z)),2TBDMS,isomer #1 | CCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)O[C@H](COC(=O)CCCCCCCCCCCCC)COP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C | 4774.3 | Standard polar | 33892256 |
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Spectra |
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| MS/MS SpectraSpectrum Type | Description | Splash Key | Deposition Date | Source | View |
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Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 10V, Positive-QTOF | splash10-014r-1295224000-81eb7b4c20402bae00a9 | 2019-02-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 20V, Positive-QTOF | splash10-014s-2392121000-61931a4f198a27daefde | 2019-02-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 40V, Positive-QTOF | splash10-00ks-1390020000-a30f669209b3db8909c1 | 2019-02-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 10V, Negative-QTOF | splash10-056r-4095002000-01d4d004721d067a2b2e | 2019-02-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 20V, Negative-QTOF | splash10-004i-9050000000-eb651bb66ae57f1b6bab | 2019-02-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 40V, Negative-QTOF | splash10-004i-9000000000-0da5f56fd93ed2ac7e1b | 2019-02-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 10V, Negative-QTOF | splash10-014i-0000009000-97bc48d486ef223a1313 | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 20V, Negative-QTOF | splash10-0jr9-0039404000-19813786175eee3bba8a | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 40V, Negative-QTOF | splash10-0fb9-1189301000-97a3f763d86c4c503d0e | 2021-09-22 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 10V, Positive-QTOF | splash10-0006-0000009000-6c13c0d0af92448808fc | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 20V, Positive-QTOF | splash10-0006-0000099000-e1245ac0e399fb7fc244 | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 40V, Positive-QTOF | splash10-01p6-0003934000-7d48bf473106bfec424e | 2021-09-23 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 10V, Positive-QTOF | splash10-0uxr-0000009000-bc4118d373f2ace63551 | 2021-09-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 20V, Positive-QTOF | splash10-01b9-0000059000-4bcb690eb848e4967651 | 2021-09-25 | Wishart Lab | View Spectrum | Predicted LC-MS/MS | Predicted LC-MS/MS Spectrum - PA(14:0/20:4(5Z,8Z,11Z,14Z)) 40V, Positive-QTOF | splash10-00xu-0006693000-19567edd5e7ceac95d69 | 2021-09-25 | Wishart Lab | View Spectrum |
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Biological Properties |
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Cellular Locations | Not Available |
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Biospecimen Locations | Not Available |
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Tissue Locations | Not Available |
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Pathways | |
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Normal Concentrations |
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Abnormal Concentrations |
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Associated Disorders and Diseases |
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Disease References | None |
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Associated OMIM IDs | None |
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External Links |
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DrugBank ID | Not Available |
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Phenol Explorer Compound ID | Not Available |
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FooDB ID | Not Available |
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KNApSAcK ID | Not Available |
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Chemspider ID | 74876552 |
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KEGG Compound ID | Not Available |
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BioCyc ID | Not Available |
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BiGG ID | Not Available |
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Wikipedia Link | Not Available |
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METLIN ID | Not Available |
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PubChem Compound | 52929514 |
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PDB ID | Not Available |
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ChEBI ID | Not Available |
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Food Biomarker Ontology | Not Available |
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VMH ID | Not Available |
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MarkerDB ID | Not Available |
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Good Scents ID | Not Available |
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References |
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Synthesis Reference | Not Available |
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Material Safety Data Sheet (MSDS) | Not Available |
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General References | - Moritz A, De Graan PN, Gispen WH, Wirtz KW: Phosphatidic acid is a specific activator of phosphatidylinositol-4-phosphate kinase. J Biol Chem. 1992 Apr 15;267(11):7207-10. [PubMed:1313792 ]
- Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
- Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
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