| 
	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 | PAMDB001675 | 
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| 
		Identification | 
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| Name: | 
		PGP(12:0/12:0) | 
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| Description: | PGP(12:0/12:0) 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(12:0/12:0), in particular, consists of two dodecanoyl chains at positions C-1 and C-2. In Pseudomonas aeruginosa, 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: | - 1,2-didodecanoyl-rac-glycero-3-phospho-(1'-sn-glycerol-3'-phosphate)
 - 1,2-didodecanoyl-rac-glycero-3-phospho-(1'-sn-glycerol-3'-phosphate)
 - 1,2-Didodecanoyl-rac-glycero-3-phospho-(1'-sn-glycerol-3'-phosphoric acid)
 - 3-sn-Phosphatidyl-1'-sn-glycerol 3'-phosphate
 - 3-sn-phosphatidyl-1'-sn-glycerol 3'-phosphoric acid
 - PGP(24:0)
 
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| 
	Chemical Formula: | 
	C30H60O13P2 | 
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| Average Molecular Weight: | 
		690.745 | 
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| Monoisotopic Molecular 
		Weight: | 
		690.350915988 | 
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| InChI Key: | 
		LNEADDPQSRWQGI-VSGBNLITSA-N | 
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| InChI: | InChI=1S/C30H60O13P2/c1-3-5-7-9-11-13-15-17-19-21-29(32)39-25-28(43-30(33)22-20-18-16-14-12-10-8-6-4-2)26-42-45(37,38)41-24-27(31)23-40-44(34,35)36/h27-28,31H,3-26H2,1-2H3,(H,37,38)(H2,34,35,36)/t27-,28-/m1/s1 | 
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| CAS 
	number: | 
	Not Available | 
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| IUPAC Name: | [(2R)-3-({[(2R)-2,3-bis(dodecanoyloxy)propoxy](hydroxy)phosphoryl}oxy)-2-hydroxypropoxy]phosphonic acid | 
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| 
	Traditional IUPAC Name: | 
	(2R)-3-{[(2R)-2,3-bis(dodecanoyloxy)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)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC | 
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| 
	Chemical Taxonomy | 
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		Taxonomy Description | Not Available | 
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		Kingdom | 
		Not Available | 
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| Super Class | Not Available | 
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	Class | 
	Not Available | 
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| Sub Class | Not Available | 
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	Direct Parent | 
	Not Available | 
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| Alternative Parents | 
	Not Available | 
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| Substituents | 
		Not Available | 
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| Molecular Framework | 
		Not Available | 
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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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	Pathways: | 
	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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