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Record Information
Version5.0
StatusDetected and Quantified
Creation Date2006-08-14 00:26:01 UTC
Update Date2022-03-07 02:49:21 UTC
HMDB IDHMDB0004685
Secondary Accession Numbers
  • HMDB04685
Metabolite Identification
Common Name13,14-Dihydro-15-keto PGF2a
Description13,14-dihydro-15-keto PGF2a E1 is an isoprostane. The isoprostanes embody a vast family of novel prostaglandin-like lipids that are produced by nonenzymatic peroxidation of arachidonic acid (AA) in response to free radicals and reactive oxygen species. Although free AA is required for the formation of prostaglandins by cyclooxygenases, the isoprostanes can be generated nonenzymatically from esterified AA in membrane phospholipids before being released by a phospholipase(s). Another dissimilarity is that isoprostanes feature side chains that are almost exclusively orientated cis relative to the cyclopentane ring and are therefore distinct from the prostaglandins, which always have side chains in the trans configuration. Nevertheless, isoprostanes are isomeric with prostaglandins and have been given the prefix D-, E-, and F{alpha}- to denote the prostane ring shared with PGD2, PGE2, and PGF2{alpha} respectively. An additional level of complexity is that peroxidation of AA can occur at one of any of four carbon atoms producing regioisomers, the so-called 5-, 12-, 8-, and 15-series isoprostanes, each consisting of eight racemic diastereomers. Thus, a total of 64 isomers can be generated for each of the D-, E-, and F{alpha}-ring isoprostanes. (PMID: 15528403 ). Prostaglandins are eicosanoids. The eicosanoids consist of the prostaglandins (PGs), thromboxanes (TXs), leukotrienes (LTs), and lipoxins (LXs). The PGs and TXs are collectively identified as prostanoids. Prostaglandins were originally shown to be synthesized in the prostate gland, thromboxanes from platelets (thrombocytes), and leukotrienes from leukocytes, hence the derivation of their names. All mammalian cells except erythrocytes synthesize eicosanoids. These molecules are extremely potent, able to cause profound physiological effects at very dilute concentrations. All eicosanoids function locally at the site of synthesis, through receptor-mediated G-protein linked signalling pathways.
Structure
Data?1582752312
Synonyms
ValueSource
13,14-Dihydro-15-keto-prostaglandin F2aChEBI
13,14-Dihydro-15-ketoprostaglandin F2alphaChEBI
15-Keto-13,14-dihydro-PGF2alphaChEBI
15-Keto-13,14-dihydroprostaglandin F2-alphaChEBI
15-Keto-13,14-dihydroprostaglandin F2alphaChEBI
9S,11S-Dihydroxy-15-oxo-5Z-prostenoic acidChEBI
DHK-PGF2alphaChEBI
PGFMChEBI
13,14-Dihydro-15-ketoprostaglandin F2aGenerator
13,14-Dihydro-15-ketoprostaglandin F2αGenerator
15-Keto-13,14-dihydro-PGF2aGenerator
15-Keto-13,14-dihydro-PGF2αGenerator
15-Keto-13,14-dihydroprostaglandin F2-aGenerator
15-Keto-13,14-dihydroprostaglandin F2-αGenerator
15-Keto-13,14-dihydroprostaglandin F2aGenerator
15-Keto-13,14-dihydroprostaglandin F2αGenerator
9S,11S-Dihydroxy-15-oxo-5Z-prostenoateGenerator
DHK-PGF2aGenerator
DHK-PGF2ΑGenerator
13,14-Dihydro-15-keto-PGF2aGenerator
13,14-Dihydro-15-keto-PGF2αGenerator
13,14-dihydro-15-keto PGF2alphaHMDB
13,14-dihydro-15-keto-PGF2alphaHMDB
13,14-dihydro-15-Ketoprostaglandin FHMDB, MeSH
13,14-dihydro-15-Oxoprostaglandin FHMDB, MeSH
15-keto-dihydro-PGF2alphaMeSH, HMDB
Pulmonary metabolite-PGF2alphaMeSH, HMDB
15-K-DH-PGF(2alpha)MeSH, HMDB
15-keto-13,14-dihydro-Prostaglandin F2alphaMeSH, HMDB
Chemical FormulaC20H34O5
Average Molecular Weight354.481
Monoisotopic Molecular Weight354.240624198
IUPAC Name(5Z)-7-[(1R,2R,3R,5S)-3,5-dihydroxy-2-(3-oxooctyl)cyclopentyl]hept-5-enoic acid
Traditional Name13,14-dihydro-15-keto-PGF2α
CAS Registry Number27376-76-7
SMILES
CCCCCC(=O)CC[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/h4,7,16-19,22-23H,2-3,5-6,8-14H2,1H3,(H,24,25)/b7-4-/t16-,17-,18+,19-/m1/s1
InChI KeyVKTIONYPMSCHQI-XAGFEHLVSA-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
  • Ketone
  • Secondary alcohol
  • Carboxylic acid
  • Carboxylic acid derivative
  • Monocarboxylic acid or derivatives
  • Alcohol
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Carbonyl group
  • Organooxygen compound
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External Descriptors
Ontology
Not AvailableNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.11 g/LALOGPS
logP3.12ALOGPS
logP3.02ChemAxon
logS-3.5ALOGPS
pKa (Strongest Acidic)4.31ChemAxon
pKa (Strongest Basic)-2.9ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area94.83 ŲChemAxon
Rotatable Bond Count13ChemAxon
Refractivity98.48 m³·mol⁻¹ChemAxon
Polarizability41 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+189.61231661259
DarkChem[M-H]-187.34331661259
DeepCCS[M+H]+201.23830932474
DeepCCS[M-H]-198.8830932474
DeepCCS[M-2H]-232.84630932474
DeepCCS[M+Na]+208.07630932474
AllCCS[M+H]+193.932859911
AllCCS[M+H-H2O]+191.332859911
AllCCS[M+NH4]+196.332859911
AllCCS[M+Na]+197.032859911
AllCCS[M-H]-192.432859911
AllCCS[M+Na-2H]-193.832859911
AllCCS[M+HCOO]-195.532859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
13,14-Dihydro-15-keto PGF2aCCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O4430.1Standard polar33892256
13,14-Dihydro-15-keto PGF2aCCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O2662.6Standard non polar33892256
13,14-Dihydro-15-keto PGF2aCCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C\C=C/CCCC(O)=O2849.2Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
13,14-Dihydro-15-keto PGF2a,1TMS,isomer #1CCCCCC(=O)CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O2801.6Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,1TMS,isomer #2CCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O2787.4Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,1TMS,isomer #3CCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C2863.0Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,1TMS,isomer #4CCCCCC(=CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C2956.4Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,1TMS,isomer #5CCCCC=C(CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C2960.6Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TMS,isomer #1CCCCCC(=O)CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O2738.2Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TMS,isomer #2CCCCCC(=O)CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C2765.2Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TMS,isomer #3CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C2820.0Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TMS,isomer #4CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C2834.7Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TMS,isomer #5CCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C2750.4Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TMS,isomer #6CCCCCC(=CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C2799.1Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TMS,isomer #7CCCCC=C(CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C2823.5Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TMS,isomer #8CCCCCC(=CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2884.0Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TMS,isomer #9CCCCC=C(CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2896.3Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TMS,isomer #1CCCCCC(=O)CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C2733.3Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TMS,isomer #2CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C2779.4Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TMS,isomer #3CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C2799.2Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TMS,isomer #4CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2796.4Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TMS,isomer #5CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2812.7Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TMS,isomer #6CCCCCC(=CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2777.8Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TMS,isomer #7CCCCC=C(CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2803.7Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,4TMS,isomer #1CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2793.1Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,4TMS,isomer #1CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2792.1Standard non polar33892256
13,14-Dihydro-15-keto PGF2a,4TMS,isomer #1CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2855.3Standard polar33892256
13,14-Dihydro-15-keto PGF2a,4TMS,isomer #2CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2813.5Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,4TMS,isomer #2CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2815.0Standard non polar33892256
13,14-Dihydro-15-keto PGF2a,4TMS,isomer #2CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C)C[C@H](O[Si](C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C2859.4Standard polar33892256
13,14-Dihydro-15-keto PGF2a,1TBDMS,isomer #1CCCCCC(=O)CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O3018.5Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,1TBDMS,isomer #2CCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O3001.1Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,1TBDMS,isomer #3CCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C3119.9Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,1TBDMS,isomer #4CCCCCC(=CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C3202.5Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,1TBDMS,isomer #5CCCCC=C(CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C3197.0Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TBDMS,isomer #1CCCCCC(=O)CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O3208.8Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TBDMS,isomer #2CCCCCC(=O)CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C3265.8Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TBDMS,isomer #3CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C3274.9Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TBDMS,isomer #4CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C3282.9Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TBDMS,isomer #5CCCCCC(=O)CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C3238.2Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TBDMS,isomer #6CCCCCC(=CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C3267.7Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TBDMS,isomer #7CCCCC=C(CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C3272.7Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TBDMS,isomer #8CCCCCC(=CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3401.1Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,2TBDMS,isomer #9CCCCC=C(CC[C@H]1[C@H](O)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3397.7Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TBDMS,isomer #1CCCCCC(=O)CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C3438.5Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TBDMS,isomer #2CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C3463.1Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TBDMS,isomer #3CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C3473.3Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TBDMS,isomer #4CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3518.2Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TBDMS,isomer #5CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3509.4Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TBDMS,isomer #6CCCCCC(=CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3505.8Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,3TBDMS,isomer #7CCCCC=C(CC[C@H]1[C@H](O)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3499.5Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,4TBDMS,isomer #1CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3670.7Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,4TBDMS,isomer #1CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3446.3Standard non polar33892256
13,14-Dihydro-15-keto PGF2a,4TBDMS,isomer #1CCCCCC(=CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3179.8Standard polar33892256
13,14-Dihydro-15-keto PGF2a,4TBDMS,isomer #2CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3676.7Semi standard non polar33892256
13,14-Dihydro-15-keto PGF2a,4TBDMS,isomer #2CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3463.0Standard non polar33892256
13,14-Dihydro-15-keto PGF2a,4TBDMS,isomer #2CCCCC=C(CC[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C3184.1Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 13,14-Dihydro-15-keto PGF2a GC-MS (Non-derivatized) - 70eV, Positivesplash10-052r-5295000000-d95e54c01cb3298d616e2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 13,14-Dihydro-15-keto PGF2a GC-MS (3 TMS) - 70eV, Positivesplash10-0a4i-4602590000-b6fb23141546245935632017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 13,14-Dihydro-15-keto PGF2a GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 10V, Positive-QTOFsplash10-00kr-0019000000-0052c5e0e660b3771d672017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 20V, Positive-QTOFsplash10-05w3-4296000000-cc7ee649acc113c51a642017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 40V, Positive-QTOFsplash10-010d-8190000000-0206683394d5b384af272017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 10V, Negative-QTOFsplash10-0udr-0009000000-93b074f982565ef968fd2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 20V, Negative-QTOFsplash10-0f79-1249000000-05e9f45f6836457a16c92017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 40V, Negative-QTOFsplash10-0a4i-9332000000-b09a8b002500e86325342017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 10V, Positive-QTOFsplash10-014i-0019000000-3a95b34ff22dc22feebf2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 20V, Positive-QTOFsplash10-014j-9345000000-1d8222def709ccd2049a2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 40V, Positive-QTOFsplash10-0006-9100000000-987d738c18f3047f38b92021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 10V, Negative-QTOFsplash10-0udi-0009000000-31341887ac640cdeb33d2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 20V, Negative-QTOFsplash10-0fki-1196000000-90351d169a5f152c18a12021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 13,14-Dihydro-15-keto PGF2a 40V, Negative-QTOFsplash10-0a6r-9140000000-d704a714c796c185009f2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen Locations
  • Blood
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.000235 +/- 0.000028 uMAdult (>18 years old)BothNormal details
BloodDetected and Quantified0.00016 (0.00018-0.0003) uMAdult (>18 years old)FemaleNormal details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified0.0026 +/- 0.001 uMAdult (>18 years old)Female
Pregnancy with RU486 administration
details
Associated Disorders and Diseases
Disease References
Pregnancy
  1. Yang XL, Wu XR: The dynamic changes of several reproductive hormones during termination of early pregnancy by RU486 in combination with PG-05 in Chinese women. Adv Contracept. 1988 Dec;4(4):319-26. [PubMed:3252730 ]
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound5283039
PDB IDNot Available
ChEBI ID63976
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDMDB00013452
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Download (PDF)
General References
  1. Clarke DL, Belvisi MG, Hardaker E, Newton R, Giembycz MA: E-ring 8-isoprostanes are agonists at EP2- and EP4-prostanoid receptors on human airway smooth muscle cells and regulate the release of colony-stimulating factors by activating cAMP-dependent protein kinase. Mol Pharmacol. 2005 Feb;67(2):383-93. Epub 2004 Nov 4. [PubMed:15528403 ]