| Record Information | 
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| Version | 2.0 | 
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| Creation Date | 2015-09-08 17:49:51 -0600 | 
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| Update Date | 2015-12-09 12:05:40 -0700 | 
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| Secondary Accession Numbers |  | 
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| Identification | 
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| Name: | PGP(18:2(9Z,12Z)/18:2(9Z,12Z)) | 
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| Description | PGP(18:2(9Z,12Z)/18:2(9Z,12Z)) belongs to the class of glycerophosphoglycerophosphates, also called phosphatidylglycerophosphates (PGPs). These lipids contain a common glycerophosphate skeleton linked to at least one fatty acyl chain and a glycero-3-phosphate moiety. As is the case with diacylglycerols, phosphatidylglycerophosphates can have many different combinations of fatty acids of varying lengths and saturation attached to the C-1 and C-2 positions. PGP(18:2(9Z,12Z)/18:2(9Z,12Z)), in particular, consists of two 9Z,12Z-octadecadienoyl chains at positions C-1 and C-2. In E. coli, PGPs can be found in the cytoplasmic membrane. The are synthesized by the addition of glycerol 3-phosphate to a CDP-diacylglycerol. In turn, PGPs are dephosphorylated to Phosphatidylglycerols (PGs) by the enzyme Phosphatidylglycerophosphatase. | 
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| Structure |  | 
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| Synonyms: | Not Available | 
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| Chemical Formula: | C44H80O13P2 | 
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| Weight: | Average: 879.059 Monoisotopic: 878.507416632 | 
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| InChI Key: | LTCGYYIQFPFMIB-NHPPMFAOSA-N | 
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| InChI: | InChI=1S/C44H80O13P2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-43(46)53-39-42(40-56-59(51,52)55-38-41(45)37-54-58(48,49)50)57-44(47)36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h13-16,19-22,41-42,45H,3-12,17-18,23-40H2,1-2H3,(H,51,52)(H2,48,49,50)/b15-13-,16-14-,21-19-,22-20-/t41-,42+/m0/s1 | 
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| CAS number: | Not Available | 
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| IUPAC Name: | [(2S)-3-({[(2R)-2,3-bis[(9Z,12Z)-nonadeca-9,12-dienoyloxy]propoxy](hydroxy)phosphoryl}oxy)-2-hydroxypropoxy]phosphonic acid | 
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| Traditional IUPAC Name: | (2S)-3-{[(2R)-2,3-bis[(9Z,12Z)-nonadeca-9,12-dienoyloxy]propoxy(hydroxy)phosphoryl]oxy}-2-hydroxypropoxyphosphonic acid | 
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| SMILES: | [H][C@](O)(COP(O)(O)=O)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCC\C=C/C\C=C/CCCCCC)OC(=O)CCCCCCC\C=C/C\C=C/CCCCCC | 
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| Chemical Taxonomy | 
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| Description |  belongs to the class of organic compounds known as phosphatidylglycerophosphates. These are glycerophosphoglycerophosphates in which two fatty acids are bonded to the 1-glycerol moiety 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 | Glycerophosphoglycerophosphates   | 
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| Direct Parent | Phosphatidylglycerophosphates   | 
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| Alternative Parents |  | 
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| Substituents | - Diacylglycerophosphoglycerophosphate
 
- Sn-glycerol-3-phosphate
 
- Fatty acid ester
 
- Monoalkyl phosphate
 
- Dialkyl phosphate
 
- Dicarboxylic acid or derivatives
 
- Organic phosphoric acid derivative
 
- Phosphoric acid ester
 
- Alkyl phosphate
 
- Fatty acyl
 
- Secondary alcohol
 
- Carboxylic acid ester
 
- Carboxylic acid derivative
 
- Organooxygen compound
 
- Organic oxide
 
- Organic oxygen compound
 
- Alcohol
 
- Carbonyl group
 
- Hydrocarbon derivative
 
- Aliphatic acyclic compound
 
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| Molecular Framework | Aliphatic acyclic compounds | 
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| External Descriptors | Not Available | 
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| Physical Properties | 
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| State: | Not Available | 
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| Charge: | -3 | 
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| Melting point: | Not Available | 
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| Experimental Properties: |  | 
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| Predicted Properties |  | 
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| Biological Properties | 
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| Cellular Locations: | Membrane | 
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| Reactions: |  CDP-DG(18:1(11Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) + Glycerol 3-phosphate + CDP-DG(18:1(11Z)/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) > PGP(18:2(9Z,12Z)/18:2(9Z,12Z)) + Hydrogen ion + Cytidine monophosphate + Cytidine monophosphatePGP(18:2(9Z,12Z)/18:2(9Z,12Z)) + Water > Phosphate + PG(18:2(9Z,12Z)/18:2(9Z,12Z))  | 
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| SMPDB Pathways: | | phospholipid biosynthesis I (CL(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)) ) | PW001025   |     |  
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| KEGG Pathways: | Not Available | 
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| EcoCyc Pathways: | Not Available | 
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| Concentrations | 
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 | Not Available | 
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| Spectra | 
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| Spectra: |  | 
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| References | 
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| References: | - Yurtsever D. (2007). Fatty acid methyl ester profiling of Enterococcus and Esherichia coli for microbial source tracking. M.sc. Thesis. Villanova University: U.S.A
 
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| Synthesis Reference: | Not Available | 
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| Material Safety Data Sheet (MSDS) | Not Available | 
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| Links | 
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| External Links: | | Resource | Link | 
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 | CHEBI ID | Not Available |  | HMDB ID | Not Available |  | Pubchem Compound ID | Not Available |  | Kegg ID | Not Available |  | ChemSpider ID | Not Available |  | Wikipedia ID | Not Available |  | BioCyc ID | Not Available |  
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