| 
	Record Information | 
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| Version | 
		1.0 | 
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| Update Date | 
		1/22/2018 11:54:54 AM | 
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| 
		Metabolite ID | PAMDB004113 | 
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| 
		Identification | 
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| Name: | 
		PG(19:iso/17:0cycw7c) | 
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| Description: | PG(19:iso/17:0cycw7c) 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(19:iso/17:0cycw7c), in particular, consists of one 17-methylocatdecanoyl chain  to the C-1 atom, and one heptadec-9-10-cyclo-anoyl  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: | - 1-17-methylocatdecanoyl-2-heptadec-9-10-cyclo-anoyl-sn-glycero-3-phospho-(1'-glycerol)
 - 1-17-methylocatdecanoyl-2-heptadec-9-10-cyclo-anoyl-sn-glycero-3-phosphoglycerol
 - GPG(19:0/17:0)
 - GPG(36:0)
 - PG(19:0/17:0)
 - PG(36:0)
 - Phosphatidylglycerol(19:0/17:0)
 - Phosphatidylglycerol(36:0)
 
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| 
	Chemical Formula: | 
	C42H81O10P | 
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| Average Molecular Weight: | 
		777.0603 | 
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| Monoisotopic Molecular 
		Weight: | 
		776.556735324 | 
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| InChI Key: | 
		PLDSGIMTTTZWJZ-UHFFFAOYSA-N | 
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| InChI: | InChI=1S/C42H81O10P/c1-4-5-6-22-27-37-31-38(37)28-23-18-16-20-25-30-42(46)52-40(35-51-53(47,48)50-33-39(44)32-43)34-49-41(45)29-24-19-15-13-11-9-7-8-10-12-14-17-21-26-36(2)3/h36-40,43-44H,4-35H2,1-3H3,(H,47,48) | 
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| CAS 
	number: | 
	Not Available | 
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| IUPAC Name: | (2,3-dihydroxypropoxy)(2-{[8-(2-hexylcyclopropyl)octanoyl]oxy}-3-[(17-methyloctadecanoyl)oxy]propoxy)phosphinic acid | 
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| 
	Traditional IUPAC Name: | 
	2,3-dihydroxypropoxy(2-{[8-(2-hexylcyclopropyl)octanoyl]oxy}-3-[(17-methyloctadecanoyl)oxy]propoxy)phosphinic acid | 
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| SMILES: | CCCCCCC1CC1CCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCCCCCC(C)C)COP(O)(=O)OCC(O)CO | 
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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-diacylglycerophosphoglycerol
 - Fatty acid ester
 - Dialkyl phosphate
 - Dicarboxylic acid or derivatives
 - Fatty acyl
 - Alkyl phosphate
 - Organic phosphate
 - Organic phosphoric acid derivative
 - Phosphoric acid ester
 - 1,2-diol
 - Carboxylic acid ester
 - Secondary alcohol
 - Carboxylic acid derivative
 - Hydrocarbon derivative
 - Organic oxide
 - Alcohol
 - Carbonyl group
 - Primary alcohol
 - Organooxygen compound
 - 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: | 
		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: | 
		- Casadei MA, Ma?as P, Niven G, Needs E, Mackey BM. (2002) "Role of membrane fluidity in pressure resistance of Escherichia coli NCTC 8164."  Appl Environ Microbiol. 68(12):5965-72. Pubmed: 12450817 
 - 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 
 - 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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