| 
	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 | PAMDB004068 | 
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| 
		Identification | 
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| Name: | 
		PG(14:0(3-OH)/18:1(9Z)) | 
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| Description: | PG(14:0(3-OH)/18:1(9Z)) 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(14:0(3-OH)/18:1(9Z)), in particular, consists of one 3-hydroxytetradecanoyl chain  to the C-1 atom, and one 9Z-octadecenoyl  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: | - 1-3-hydroxytetradecanoyl-2-(9Z-octadecenoyl)-sn-glycero-3-phospho-(1'-glycerol)
 - 1-3-hydroxytetradecanoyl-2-(9Z-octadecenoyl)-sn-glycero-3-phosphoglycerol
 - 1-3-hydroxytetradecanoyl-2-oleoyl-sn-glycero-3-phosphoglycerol
 - GPG(14:0/18:1)
 - GPG(32:1)
 - PG(14:0/18:1)
 - PG(32:1)
 - Phosphatidylglycerol(14:0/18:1)
 - Phosphatidylglycerol(32:1)
 
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| 
	Chemical Formula: | 
	C38H73O11P | 
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| Average Molecular Weight: | 
		736.965 | 
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| Monoisotopic Molecular 
		Weight: | 
		736.489050169 | 
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| InChI Key: | 
		YZWXTZVNFIEAJY-TXMSSCOLSA-N | 
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| InChI: | InChI=1S/C38H73O11P/c1-3-5-7-9-11-13-14-15-16-17-18-20-22-24-26-28-37(42)46-32-36(33-48-50(44,45)47-31-35(41)30-39)49-38(43)29-34(40)27-25-23-21-19-12-10-8-6-4-2/h15-16,34-36,39-41H,3-14,17-33H2,1-2H3,(H,44,45)/b16-15-/t34?,35-,36+/m0/s1 | 
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| CAS 
	number: | 
	Not Available | 
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| IUPAC Name: | [(2S)-2,3-dihydroxypropoxy][(2R)-2-[(3-hydroxytetradecanoyl)oxy]-3-[(9Z)-octadec-9-enoyloxy]propoxy]phosphinic acid | 
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| 
	Traditional IUPAC Name: | 
	(2S)-2,3-dihydroxypropoxy((2R)-2-[(3-hydroxytetradecanoyl)oxy]-3-[(9Z)-octadec-9-enoyloxy]propoxy)phosphinic acid | 
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| SMILES: | [H][C@](O)(CO)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCC\C=C/CCCCCCCC)OC(=O)CC(O)CCCCCCCCCCC | 
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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
 - Beta-hydroxy acid
 - Dialkyl phosphate
 - Fatty acid ester
 - Fatty acyl
 - Alkyl phosphate
 - Dicarboxylic acid or derivatives
 - Phosphoric acid ester
 - Organic phosphoric acid derivative
 - Hydroxy acid
 - 1,2-diol
 - Carboxylic acid ester
 - Secondary alcohol
 - Carboxylic acid derivative
 - Primary alcohol
 - Hydrocarbon derivative
 - Organic oxygen compound
 - Carbonyl group
 - Organic oxide
 - Alcohol
 - Organooxygen compound
 - 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: | 
		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 
 - Yuan Y, Leeds JA, Meredith TC (2012). "Pseudomonas aeruginosa Directly Shunts β-Oxidation Degradation Intermediates into De Novo Fatty Acid Biosynthesis." J Bacteriol. 194(19):5185-96 Pubmed: 22753057 
 - 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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