| Record Information | 
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| Version | 1.0 | 
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| Update Date | 1/22/2018 12:54:54 PM | 
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| Metabolite ID | PAMDB004092 | 
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| Identification | 
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| Name: | PG(17:0cycw7c/12:0(3-OH)) | 
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| Description: | PG(17:0cycw7c/12:0(3-OH)) is a phosphatidylglycerol. Phosphatidylglycerols consist of a glycerol 3-phosphate backbone esterified to either saturated or unsaturated fatty acids on carbons 1 and 2. As is the case with diacylglycerols, phosphatidylglycerols can have many different combinations of fatty acids of varying lengths and saturation attached to the C-1 and C-2 positions. PG(17:0cycw7c/12:0(3-OH)), in particular, consists of one heptadec-9-10-cyclo-anoyl chain  to the C-1 atom, and one 3-hydroxydodecanoyl  to the C-2 atom. In Pseudomonas aeruginosa glycerophospholipid metabolism, phosphatidylglycerol is formed from phosphatidic acid (1,2-diacyl-sn-glycerol 3-phosphate) by a sequence of enzymatic reactions that proceeds via two intermediates, cytidine diphosphate diacylglycerol (CDP-diacylglycerol) and phosphatidylglycerophosphate (PGP, a phosphorylated phosphatidylglycerol). Phosphatidylglycerols, along with CDP-diacylglycerol, also serve as precursor molecules for the synthesis of cardiolipin, a phospholipid found in membranes. | 
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| Structure |  | 
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| Synonyms: | 1-heptadec-9-10-cyclo-anoyl-2-3-hydroxydodecanoyl-sn-glycero-3-phospho-(1'-glycerol)1-heptadec-9-10-cyclo-anoyl-2-3-hydroxydodecanoyl-sn-glycero-3-phosphoglycerol1-heptadec-9-10-cyclo-anoyl-2-3-hydroxydodecanoyl-sn-glycero-3-phosphoglycerolGPG(17:0/12:0)GPG(29:0)PG(17:0/12:0)PG(29:0)Phosphatidylglycerol(17:0/12:0)Phosphatidylglycerol(29:0)
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| Chemical Formula: | C35H67O11P | 
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| Average Molecular Weight: | 694.884 | 
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| Monoisotopic Molecular 
		Weight: | 694.442099975 | 
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| InChI Key: | PBRPHFMBSOADCF-QOGUGHGESA-N | 
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| InChI: | InChI=1S/C35H67O11P/c1-3-5-7-9-10-13-17-21-31(37)24-35(40)43-27-33(28-45-47(41,42)44-26-32(38)25-36)46-34(39)22-18-14-11-12-16-20-30-23-29(30)19-15-8-6-4-2/h29-33,36-38H,3-28H2,1-2H3,(H,41,42)/t29?,30?,31?,32-,33+/m0/s1 | 
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| CAS 
	number: | Not Available | 
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| IUPAC Name: | [(2S)-2,3-dihydroxypropoxy][(2R)-2-{[8-(2-hexylcyclopropyl)octanoyl]oxy}-3-[(3-hydroxydodecanoyl)oxy]propoxy]phosphinic acid | 
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| Traditional IUPAC Name: | (2S)-2,3-dihydroxypropoxy((2R)-2-{[8-(2-hexylcyclopropyl)octanoyl]oxy}-3-[(3-hydroxydodecanoyl)oxy]propoxy)phosphinic acid | 
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| SMILES: | [H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CC(O)CCCCCCCCC)OC(=O)CCCCCCCC1CC1CCCCCC | 
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| Chemical Taxonomy | 
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| Taxonomy Description | This compound belongs to the class of organic compounds known as phosphatidylglycerols. These are glycerophosphoglycerols 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 | Glycerophosphoglycerols | 
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| Direct Parent | Phosphatidylglycerols | 
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| Alternative Parents |  | 
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| Substituents | 1,2-diacylglycerophosphoglycerolBeta-hydroxy acidDialkyl phosphateFatty acid esterFatty acylAlkyl phosphateDicarboxylic acid or derivativesPhosphoric acid esterOrganic phosphoric acid derivativeHydroxy acid1,2-diolCarboxylic acid esterSecondary alcoholCarboxylic acid derivativePrimary alcoholHydrocarbon derivativeOrganic oxygen compoundCarbonyl groupOrganic oxideAlcoholOrganooxygen compoundAliphatic 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: | Solid | 
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| Charge: | -1 | 
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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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| Pathways: |  | 
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| Spectra | 
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| Spectra: |  | 
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| References | 
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| References: | Kanehisa, M., Goto, S., Sato, Y., Furumichi, M., Tanabe, M. (2012). "KEGG for integration and interpretation of large-scale molecular data sets." Nucleic Acids Res 40:D109-D114. Pubmed: 22080510 Taylor SS, Heath EC. (1969) "The incorporation of beta-hydroxy fatty acids into a phospholipid of Escherichia coli B."  J Biol Chem. 244(24):6605-16. Pubmed: 4902888 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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