| Record Information | 
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| Version | 2.0 | 
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| Creation Date | 2015-09-08 19:35:44 -0600 | 
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| Update Date | 2015-12-09 17:20:52 -0700 | 
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| Secondary Accession Numbers |  | 
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| Identification | 
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| Name: | PGP(17:0cycw7c/16:1(9Z)) | 
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| Description | PGP(17:0cycw7c/16:1(9Z)) 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(17:0cycw7c/16:1(9Z)), in particular, consists of one heptadec-9-10-cyclo-anoyl chain  to the C-1 atom, and one 9Z-hexadecenoyl  to the C-2 atom. 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: | C39H74O13P2 | 
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| Weight: | Average: 812.956 Monoisotopic: 812.460466439 | 
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| InChI Key: | CBRAARCYPATVPD-ROKAYYDNSA-N | 
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| InChI: | InChI=1S/C39H74O13P2/c1-3-5-7-9-10-11-12-13-14-15-16-19-24-28-39(42)52-37(33-51-54(46,47)50-31-36(40)30-49-53(43,44)45)32-48-38(41)27-23-20-17-18-22-26-35-29-34(35)25-21-8-6-4-2/h11-12,34-37,40H,3-10,13-33H2,1-2H3,(H,46,47)(H2,43,44,45)/b12-11-/t34?,35?,36-,37-/m1/s1 | 
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| CAS number: | Not Available | 
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| IUPAC Name: | [(2R)-3-({[(2R)-2-[(9Z)-hexadec-9-enoyloxy]-3-{[8-(2-hexylcyclopropyl)octanoyl]oxy}propoxy](hydroxy)phosphoryl}oxy)-2-hydroxypropoxy]phosphonic acid | 
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| Traditional IUPAC Name: | (2R)-3-{[(2R)-2-[(9Z)-hexadec-9-enoyloxy]-3-{[8-(2-hexylcyclopropyl)octanoyl]oxy}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)CCCCCCCC1CC1CCCCCC)OC(=O)CCCCCCC\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 homomonocyclic compound
 
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| Molecular Framework | Aliphatic homomonocyclic 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: |  | 
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| SMPDB Pathways: | | phospholipid biosynthesis CL(16:0/16:0/17:0cycw7c/16:1(9Z)) | PW001273   |     |  
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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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