Showing metabocard for 8-Isoprostaglandin F2a (BMDB0005083)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2016-09-30 23:15:17 UTC
Update Date2020-04-22 15:15:19 UTC
BMDB IDBMDB0005083
Secondary Accession Numbers
  • BMDB05083
Metabolite Identification
Common Name8-Isoprostaglandin F2a
Description8-Isoprostaglandin F2a, also known as 8-iso-PGF2a or 8-epi-PGF2alpha, belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid. Thus, 8-isoprostaglandin F2A is considered to be an eicosanoid. Based on a literature review a significant number of articles have been published on 8-Isoprostaglandin F2a.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
8-Epi-PGF2alphaChEBI
8-Epiprostaglandin F2alphaChEBI
8-Iso-PGF2aChEBI
8-Iso-PGF2alphaChEBI
8-Iso-PGF2alpha-IIIChEBI
8-IsoPChEBI
8-Isoprostaglandin F2alphaChEBI
8-IsoprostaneChEBI
9,11,15-Trihydroxy-prosta-5,13-dien-1-Oic acidChEBI
8-Epi-prostaglandin F2alphaKegg
8-Epi-PGF2aGenerator
8-Epi-PGF2αGenerator
8-Epiprostaglandin F2aGenerator
8-Epiprostaglandin F2αGenerator
8-Iso-PGF2αGenerator
8-Iso-PGF2a-IIIGenerator
8-Iso-PGF2α-IIIGenerator
8-Isoprostaglandin F2αGenerator
9,11,15-Trihydroxy-prosta-5,13-dien-1-OateGenerator
8-Epi-prostaglandin F2aGenerator
8-Epi-prostaglandin F2αGenerator
(5Z,13E,15S)-9alpha,11alpha,15-Trihydroxy-8beta-prosta-5,13-dien-1-OateHMDB
(5Z,13E,15S)-9alpha,11alpha,15-Trihydroxy-8beta-prosta-5,13-dien-1-Oic acidHMDB
8-Epi PGF-2alphaHMDB
9,11,15-Trihydroxy prosta-5,13-dien-1-OateHMDB
9,11,15-Trihydroxy prosta-5,13-dien-1-Oic acidHMDB
9S,11R,15S-Trihydroxy-5Z,13E-prostadienoateHMDB
9S,11R,15S-Trihydroxy-5Z,13E-prostadienoic acidHMDB
9S,11R,15S-Trihydroxy-5Z,13E-prostadienoic acid-cyclo[8S,12R]HMDB
15-F(2t)-IsoPHMDB
15-F(2t)-IsoprostaneHMDB
8-F(2t)-IsoprostaneHMDB
8-Epi-PGF2 alphaHMDB
8-Iso-PGF(2alpha)HMDB
Isoprostaglandin F2alpha type-IIIHMDB
15-F2t-IsoPHMDB
15-F2t-IsoprostaneHMDB
8-Isoprostaglandin F2aGenerator
Chemical FormulaC20H34O5
Average Molecular Weight354.481
Monoisotopic Molecular Weight354.240624198
IUPAC Name(5Z)-7-[(1S,2R,3R,5S)-3,5-dihydroxy-2-[(1E,3S)-3-hydroxyoct-1-en-1-yl]cyclopentyl]hept-5-enoic acid
Traditional Name8-isoprostane
CAS Registry Number27415-26-5
SMILES
CCCCC[C@H](O)\C=C\[C@H]1[C@H](O)C[C@H](O)[C@H]1C\C=C/CCCC(O)=O
InChI Identifier
InChI=1S/C20H34O5/c1-2-3-6-9-15(21)12-13-17-16(18(22)14-19(17)23)10-7-4-5-8-11-20(24)25/h4,7,12-13,15-19,21-23H,2-3,5-6,8-11,14H2,1H3,(H,24,25)/b7-4-,13-12+/t15-,16-,17+,18-,19+/m0/s1
InChI KeyPXGPLTODNUVGFL-NAPLMKITSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as prostaglandins and related compounds. These are unsaturated carboxylic acids consisting of a 20 carbon skeleton that also contains a five member ring, and are based upon the fatty acid arachidonic acid.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassEicosanoids
Direct ParentProstaglandins and related compounds
Alternative Parents
Substituents
  • Prostaglandin skeleton
  • Long-chain fatty acid
  • Hydroxy fatty acid
  • Cyclopentanol
  • Fatty acid
  • Unsaturated fatty acid
  • Cyclic alcohol
  • Secondary alcohol
  • Carboxylic acid derivative
  • Carboxylic acid
  • Monocarboxylic acid or derivatives
  • Organic oxide
  • Organic oxygen compound
  • Alcohol
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External Descriptors
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cell membrane
  • Cytoplasm
  • Membrane
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogP2.183Not Available
Predicted Properties
PropertyValueSource
logP3.11ALOGPS
logP2.61ChemAxon
logS-3.5ALOGPS
pKa (Strongest Acidic)4.36ChemAxon
pKa (Strongest Basic)-1.6ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area97.99 ŲChemAxon
Rotatable Bond Count12ChemAxon
Refractivity100.47 m³·mol⁻¹ChemAxon
Polarizability41.71 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash Key
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positivesplash10-0019-6489000000-bf681ff653e664e9cde0View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (4 TMS) - 70eV, Positivesplash10-004i-9100177000-79583ccaf34002541a28View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableView in JSpectraViewer
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableView in JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014r-0019000000-2c9767841fa4893c60b5View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-01bi-2297000000-8aa402b01c233708c42eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0103-9170000000-b6c0e28782ad3916af75View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0udi-0019000000-43645725f77edc02f608View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0f7c-1049000000-d2fc6ca599de8bc5b9a5View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0a4i-9611000000-80d02fb42a0a241d8e2bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014r-0019000000-ece58dc4c35634d7fe3fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-014i-9255000000-c6aef7e365cba872a558View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-05mo-9300000000-552900f74505f7605b0bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0udi-0009000000-4f29fd22c6b0dfe3ac77View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0udr-0098000000-06ede09931efe0fba78eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00el-9182000000-f1a4c9aba7f705d2868dView in MoNA
Biological Properties
Cellular Locations
  • Cell membrane
  • Cytoplasm
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0005083
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB023622
KNApSAcK IDNot Available
Chemspider ID4445435
KEGG Compound IDC13809
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound5282263
PDB IDNot Available
ChEBI ID34505
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available