Showing metabocard for PC(P-18:1(11Z)/18:1(11Z)) (BMDB0011275)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2016-10-03 18:15:40 UTC
Update Date2020-06-04 19:58:03 UTC
BMDB IDBMDB0011275
Secondary Accession Numbers
  • BMDB11275
Metabolite Identification
Common NamePC(P-18:1(11Z)/18:1(11Z))
DescriptionPC(P-18:1(11Z)/18:1(11Z)) is a phosphatidylchloline (PC). It is a glycerophospholipid in which a phosphorylcholine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, phosphatidylcholines can have many different combinations of fatty acids of varying lengths and saturation attached to the C-1 and C-2 positions. PC(P-18:1(11Z)/18:1(11Z)), in particular, consists of one 1Z,11Z-octadecadienyl chain to the C-1 atom, and one 11Z-octadecenoyl to the C-2 atom. In E. coli, PCs can be found in the integral component of the cell outer membrane. They are hydrolyzed by Phospholipases to a 2-acylglycerophosphocholine and a carboxylate.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-(1-Enyl-vaccenoyl)-2-vaccenoyl-sn-glycero-3-phosphocholineHMDB
Gpcho(18:1/18:1)HMDB
Gpcho(18:1n7/18:1n7)HMDB
Gpcho(18:1W7/18:1W7)HMDB
Gpcho(36:2)HMDB
1-(1Z,11Z-Octadecadienyl)-2-cis-vaccenoyl-GPCHMDB
1-(1Z,11Z-Octadecadienyl)-2-cis-vaccenoyl-sn-glycero-3-phosphocholineHMDB
1-(1Z,11Z-Octadecadienyl)-2-cis-vaccenoyl-sn-glycero-phosphatidylcholineHMDB
GPC(18:2/18:1)HMDB
GPC(36:3)HMDB
GPC(O-18:2(1Z,11Z)/18:1(11Z))HMDB
GPC(O-18:2(1Z,11Z)/18:1n7)HMDB
GPC(O-18:2(1Z,11Z)/18:1W7)HMDB
GPC(p-18:1(11Z)/18:1(11Z))HMDB
GPC(p-18:1(11Z)/18:1n7)HMDB
GPC(p-18:1(11Z)/18:1W7)HMDB
GPCho(18:2/18:1)HMDB
GPCho(36:3)HMDB
GPCho(O-18:2(1Z,11Z)/18:1(11Z))HMDB
GPCho(O-18:2(1Z,11Z)/18:1n7)HMDB
GPCho(O-18:2(1Z,11Z)/18:1W7)HMDB
GPCho(p-18:1(11Z)/18:1(11Z))HMDB
GPCho(p-18:1(11Z)/18:1n7)HMDB
GPCho(p-18:1(11Z)/18:1W7)HMDB
PC(18:2/18:1)HMDB
PC(36:3)HMDB
PC(O-18:2(1Z,11Z)/18:1(11Z))HMDB
PC(O-18:2(1Z,11Z)/18:1n7)HMDB
PC(O-18:2(1Z,11Z)/18:1W7)HMDB
PC(p-18:1(11Z)/18:1n7)HMDB
PC(p-18:1(11Z)/18:1W7)HMDB
Phosphatidylcholine(18:2/18:1)HMDB
Phosphatidylcholine(36:3)HMDB
Phosphatidylcholine(O-18:2(1Z,11Z)/18:1(11Z))HMDB
Phosphatidylcholine(O-18:2(1Z,11Z)/18:1n7)HMDB
Phosphatidylcholine(O-18:2(1Z,11Z)/18:1W7)HMDB
Phosphatidylcholine(p-18:1(11Z)/18:1(11Z))HMDB
Phosphatidylcholine(p-18:1(11Z)/18:1n7)HMDB
Phosphatidylcholine(p-18:1(11Z)/18:1W7)HMDB
Chemical FormulaC44H84NO7P
Average Molecular Weight770.114
Monoisotopic Molecular Weight769.598540559
IUPAC Nametrimethyl(2-{[(2R)-2-[(11Z)-octadec-11-enoyloxy]-3-[(1Z,11Z)-octadeca-1,11-dien-1-yloxy]propyl phosphonato]oxy}ethyl)azanium
Traditional Nametrimethyl(2-{[(2R)-2-[(11Z)-octadec-11-enoyloxy]-3-[(1Z,11Z)-octadeca-1,11-dien-1-yloxy]propyl phosphonato]oxy}ethyl)azanium
CAS Registry NumberNot Available
SMILES
CCCCCC\C=C/CCCCCCCCCC(=O)O[C@]([H])(CO\C=C/CCCCCCCC\C=C/CCCCCC)COP([O-])(=O)OCC[N+](C)(C)C
InChI Identifier
InChI=1S/C44H84NO7P/c1-6-8-10-12-14-16-18-20-22-24-26-28-30-32-34-36-39-49-41-43(42-51-53(47,48)50-40-38-45(3,4)5)52-44(46)37-35-33-31-29-27-25-23-21-19-17-15-13-11-9-7-2/h16-19,36,39,43H,6-15,20-35,37-38,40-42H2,1-5H3/b18-16-,19-17-,39-36-/t43-/m1/s1
InChI KeySOSODLPIZNSISY-WDMTWABASA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as 1-(1z-alkenyl),2-acyl-glycerophosphocholines. These are glycerophosphocholines that carry exactly one acyl chain attached to the glycerol moiety through an ester linkage at the O2-position, and one 1Z-alkenyl chain attached through an ether linkage at the O1-position.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerophospholipids
Sub ClassGlycerophosphocholines
Direct Parent1-(1Z-alkenyl),2-acyl-glycerophosphocholines
Alternative Parents
Substituents
  • 1-(1z-alkenyl),2-acyl-glycerophosphocholine
  • Phosphocholine
  • Glycerol vinyl ether
  • Fatty acid ester
  • Dialkyl phosphate
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Alkyl phosphate
  • Fatty acyl
  • Quaternary ammonium salt
  • Tetraalkylammonium salt
  • Carboxylic acid ester
  • Monocarboxylic acid or derivatives
  • Carboxylic acid derivative
  • Amine
  • Organic oxide
  • Organopnictogen compound
  • Organooxygen compound
  • Organonitrogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Carbonyl group
  • Hydrocarbon derivative
  • Organic salt
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cell membrane
  • Intracellular membrane
  • Membrane
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP6.15ALOGPS
logP9.56ChemAxon
logS-7.6ALOGPS
pKa (Strongest Acidic)1.86ChemAxon
pKa (Strongest Basic)-4.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area94.12 ŲChemAxon
Rotatable Bond Count41ChemAxon
Refractivity236.84 m³·mol⁻¹ChemAxon
Polarizability95.12 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash Key
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-9161231300-9d93f924af93de598fafView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-00ks-4292021000-0a28f1faf6e78defbf16View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0079-9085033100-a730b21ab52299c938c1View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0159-0080002900-4c61188879baf621cf99View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0159-1090205300-bc1dd692bb9c11e98f24View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-02cr-4090100000-35051db372b808beb464View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-014i-0000000900-a77b4361de0929ecf0e7View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-014i-0040010900-d77b209932f761a48fcaView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00o0-5182900000-beed5f310ab63867ca7cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00di-0000000900-f8446695140eef013859View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0089-0900000500-cd8c0d0cdfcf2e96697cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0240-0500120900-bb08571f4d1734ff6207View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0udi-0000000090-3d6811548a7d3de72b59View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0udi-0000000090-3d6811548a7d3de72b59View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0ul3-0030911510-f3acb3bfc2ecda08bb52View in MoNA
Biological Properties
Cellular Locations
  • Cell membrane
  • Intracellular membrane
  • Membrane
Biospecimen Locations
  • All Tissues
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
All TissuesExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
 details
Abnormal Concentrations
Not Available
HMDB IDHMDB0011275
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB028022
KNApSAcK IDNot Available
Chemspider ID24767550
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound53480741
PDB IDNot Available
ChEBI ID89939
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available