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Record Information
Version5.0
StatusDetected but not Quantified
Creation Date2006-05-22 14:17:55 UTC
Update Date2023-02-21 17:16:25 UTC
HMDB IDHMDB0002520
Secondary Accession Numbers
  • HMDB02520
Metabolite Identification
Common Namebeta-Glycerophosphoric acid
Descriptionbeta-Glycerophosphoric acid, also known as b-glycerophosphate, belongs to the class of organic compounds known as glycerophosphates. Glycerophosphates are compounds containing a glycerol linked to a phosphate group. Based on a literature review a significant number of articles have been published on beta-Glycerophosphoric acid.
Structure
Data?1676999785
Synonyms
ValueSource
1,2,3-Propanetriol, 2-(dihydrogen phosphate)ChEBI
1,3-Hydroxy-2-propyl dihydrogen phosphateChEBI
2-GlycerophosphateChEBI
2-HYDROXY-1-(hydroxymethyl)ethyl dihydrogen phosphATEChEBI
beta-GlycerophosphateChEBI
1,2,3-Propanetriol, 2-(dihydrogen phosphoric acid)Generator
1,3-Hydroxy-2-propyl dihydrogen phosphoric acidGenerator
2-Glycerophosphoric acidGenerator
2-HYDROXY-1-(hydroxymethyl)ethyl dihydrogen phosphoric acidGenerator
b-GlycerophosphateGenerator
b-Glycerophosphoric acidGenerator
Β-glycerophosphateGenerator
Β-glycerophosphoric acidGenerator
Glycerol 2-phosphateMeSH
beta-Glycerol phosphateMeSH
beta-Glycerophosphoric acid, calcium saltMeSH
beta-Glycerophosphoric acid, calcium salt (1:1)MeSH
beta-Glycerophosphoric acid, disodium saltMeSH
beta-Glycerophosphoric acid, iron saltMeSH
beta-Glycerophosphoric acid, iron(3+) salt(3:2)MeSH
beta-Glycerophosphoric acid, sodium saltMeSH
beta-GlycerophosphorateHMDB
Glycerol-2-phosphateHMDB
beta-Glycerophosphoric acidChEBI
Glycerol 2-phosphoric acidGenerator, HMDB
BGAHMDB
Dihydrogen beta-glycerophosphateHMDB
Dihydrogen β-glycerophosphateHMDB
beta-Glyceryl phosphateHMDB
β-Glyceryl phosphateHMDB
Glycerol-2-phosphoric acidGenerator
Chemical FormulaC3H9O6P
Average Molecular Weight172.0737
Monoisotopic Molecular Weight172.013674532
IUPAC Name[(1,3-dihydroxypropan-2-yl)oxy]phosphonic acid
Traditional Nameβ-glycerophosphorate
CAS Registry Number17181-54-3
SMILES
OCC(CO)OP(O)(O)=O
InChI Identifier
InChI=1S/C3H9O6P/c4-1-3(2-5)9-10(6,7)8/h3-5H,1-2H2,(H2,6,7,8)
InChI KeyDHCLVCXQIBBOPH-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as glycerophosphates. Glycerophosphates are compounds containing a glycerol linked to a phosphate group.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerophospholipids
Sub ClassGlycerophosphates
Direct ParentGlycerophosphates
Alternative Parents
Substituents
  • Sn-glycerol-2-phosphate
  • Monoalkyl phosphate
  • Alkyl phosphate
  • Phosphoric acid ester
  • Organic phosphoric acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Primary alcohol
  • Organooxygen compound
  • Alcohol
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effect
Disposition
Process
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic Properties

Experimental Collision Cross Sections

Adduct TypeData SourceCCS Value (Å2)Reference
[M-H]-Not Available126.5http://allccs.zhulab.cn/database/detail?ID=AllCCS00002142
Predicted Molecular Properties
PropertyValueSource
Water Solubility30.7 g/LALOGPS
logP-1.8ALOGPS
logP-2ChemAxon
logS-0.75ALOGPS
pKa (Strongest Acidic)1.13ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count5ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area107.22 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity31.39 m³·mol⁻¹ChemAxon
Polarizability13.29 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+135.55831661259
DarkChem[M-H]-132.02331661259
DeepCCS[M+H]+131.58230932474
DeepCCS[M-H]-128.830932474
DeepCCS[M-2H]-165.71430932474
DeepCCS[M+Na]+140.3930932474
AllCCS[M+H]+138.932859911
AllCCS[M+H-H2O]+135.032859911
AllCCS[M+NH4]+142.532859911
AllCCS[M+Na]+143.632859911
AllCCS[M-H]-129.032859911
AllCCS[M+Na-2H]-131.332859911
AllCCS[M+HCOO]-133.932859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
beta-Glycerophosphoric acidOCC(CO)OP(O)(O)=O2742.3Standard polar33892256
beta-Glycerophosphoric acidOCC(CO)OP(O)(O)=O1523.8Standard non polar33892256
beta-Glycerophosphoric acidOCC(CO)OP(O)(O)=O1627.7Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
beta-Glycerophosphoric acid,1TMS,isomer #1C[Si](C)(C)OCC(CO)OP(=O)(O)O1683.8Semi standard non polar33892256
beta-Glycerophosphoric acid,1TMS,isomer #2C[Si](C)(C)OP(=O)(O)OC(CO)CO1660.6Semi standard non polar33892256
beta-Glycerophosphoric acid,2TMS,isomer #1C[Si](C)(C)OCC(CO[Si](C)(C)C)OP(=O)(O)O1721.3Semi standard non polar33892256
beta-Glycerophosphoric acid,2TMS,isomer #2C[Si](C)(C)OCC(CO)OP(=O)(O)O[Si](C)(C)C1709.3Semi standard non polar33892256
beta-Glycerophosphoric acid,2TMS,isomer #3C[Si](C)(C)OP(=O)(OC(CO)CO)O[Si](C)(C)C1676.8Semi standard non polar33892256
beta-Glycerophosphoric acid,3TMS,isomer #1C[Si](C)(C)OCC(CO[Si](C)(C)C)OP(=O)(O)O[Si](C)(C)C1727.1Semi standard non polar33892256
beta-Glycerophosphoric acid,3TMS,isomer #1C[Si](C)(C)OCC(CO[Si](C)(C)C)OP(=O)(O)O[Si](C)(C)C1682.4Standard non polar33892256
beta-Glycerophosphoric acid,3TMS,isomer #1C[Si](C)(C)OCC(CO[Si](C)(C)C)OP(=O)(O)O[Si](C)(C)C1983.4Standard polar33892256
beta-Glycerophosphoric acid,3TMS,isomer #2C[Si](C)(C)OCC(CO)OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C1712.3Semi standard non polar33892256
beta-Glycerophosphoric acid,3TMS,isomer #2C[Si](C)(C)OCC(CO)OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C1698.9Standard non polar33892256
beta-Glycerophosphoric acid,3TMS,isomer #2C[Si](C)(C)OCC(CO)OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C1850.1Standard polar33892256
beta-Glycerophosphoric acid,4TMS,isomer #1C[Si](C)(C)OCC(CO[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C1720.8Semi standard non polar33892256
beta-Glycerophosphoric acid,4TMS,isomer #1C[Si](C)(C)OCC(CO[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C1728.4Standard non polar33892256
beta-Glycerophosphoric acid,4TMS,isomer #1C[Si](C)(C)OCC(CO[Si](C)(C)C)OP(=O)(O[Si](C)(C)C)O[Si](C)(C)C1783.8Standard polar33892256
beta-Glycerophosphoric acid,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC(CO)OP(=O)(O)O1935.0Semi standard non polar33892256
beta-Glycerophosphoric acid,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OP(=O)(O)OC(CO)CO1901.9Semi standard non polar33892256
beta-Glycerophosphoric acid,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)OP(=O)(O)O2140.9Semi standard non polar33892256
beta-Glycerophosphoric acid,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC(CO)OP(=O)(O)O[Si](C)(C)C(C)(C)C2127.2Semi standard non polar33892256
beta-Glycerophosphoric acid,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OP(=O)(OC(CO)CO)O[Si](C)(C)C(C)(C)C2112.2Semi standard non polar33892256
beta-Glycerophosphoric acid,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)OP(=O)(O)O[Si](C)(C)C(C)(C)C2360.0Semi standard non polar33892256
beta-Glycerophosphoric acid,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)OP(=O)(O)O[Si](C)(C)C(C)(C)C2298.3Standard non polar33892256
beta-Glycerophosphoric acid,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)OP(=O)(O)O[Si](C)(C)C(C)(C)C2315.2Standard polar33892256
beta-Glycerophosphoric acid,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC(CO)OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2345.4Semi standard non polar33892256
beta-Glycerophosphoric acid,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC(CO)OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2257.3Standard non polar33892256
beta-Glycerophosphoric acid,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC(CO)OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2196.9Standard polar33892256
beta-Glycerophosphoric acid,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2579.7Semi standard non polar33892256
beta-Glycerophosphoric acid,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2438.4Standard non polar33892256
beta-Glycerophosphoric acid,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC(CO[Si](C)(C)C(C)(C)C)OP(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C2232.6Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental GC-MSGC-MS Spectrum - beta-Glycerophosphoric acid GC-MS (4 TMS)splash10-0gvp-1792000000-c48ad0477aac597f9e482014-06-16HMDB team, MONA, MassBankView Spectrum
Experimental GC-MSGC-MS Spectrum - beta-Glycerophosphoric acid GC-EI-TOF (Non-derivatized)splash10-0gwe-0981000000-ffc7c737ad151bab34f42017-09-12HMDB team, MONA, MassBankView Spectrum
Experimental GC-MSGC-MS Spectrum - beta-Glycerophosphoric acid GC-MS (Non-derivatized)splash10-0gvp-1792000000-c48ad0477aac597f9e482017-09-12HMDB team, MONA, MassBankView Spectrum
Experimental GC-MSGC-MS Spectrum - beta-Glycerophosphoric acid GC-EI-TOF (Non-derivatized)splash10-0gvn-0971000000-02ef7a6a93f26d18e2e92017-09-12HMDB team, MONA, MassBankView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - beta-Glycerophosphoric acid GC-MS (Non-derivatized) - 70eV, Positivesplash10-0002-9100000000-f3b980cd6beaf038fb5c2016-09-22Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - beta-Glycerophosphoric acid GC-MS (2 TMS) - 70eV, Positivesplash10-0gi0-5930000000-043db2c19de48a1a22ad2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - beta-Glycerophosphoric acid GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid LC-ESI-QTOF , negative-QTOFsplash10-004i-9200000000-494acb690fc0f406808a2017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 20V, Positive-QTOFsplash10-0002-9000000000-4944c6b0c8f6d1d30e932021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 10V, Positive-QTOFsplash10-0002-9000000000-178dacbbcce6f01b32e42021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 40V, Positive-QTOFsplash10-001i-9000000000-0d15a9e9ccd8f0340deb2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 35V, Positive-QTOFsplash10-0002-9000000000-0ea1a0eba5ca2510e52a2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 20V, Positive-QTOFsplash10-0002-9000000000-9b83578d72246c176ae22021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 35V, Positive-QTOFsplash10-0002-9100000000-44e85363da094bc399582021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 35V, Positive-QTOFsplash10-0002-9000000000-e6b7983e77544a2cf2de2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 35V, Positive-QTOFsplash10-0002-9000000000-5d410b074c244fb15b592021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 10V, Positive-QTOFsplash10-0002-9000000000-814132cc0e794598b88a2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 40V, Positive-QTOFsplash10-001i-9000000000-415393e808bbb4c6847c2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 10V, Negative-QTOFsplash10-004i-9200000000-a6921adb8e95e92d80152021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 40V, Negative-QTOFsplash10-004i-9000000000-1391ae42d78e238c73782021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 35V, Negative-QTOFsplash10-004i-9100000000-b7bb3126c390b73c7eb12021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 35V, Negative-QTOFsplash10-004i-9200000000-a2e1932c879b8360e2a52021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - beta-Glycerophosphoric acid 20V, Negative-QTOFsplash10-004i-9000000000-eaf5bd1508ba8779087f2021-09-20HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - beta-Glycerophosphoric acid 10V, Positive-QTOFsplash10-00ba-9100000000-767830ab29256b7438a72015-09-14Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - beta-Glycerophosphoric acid 20V, Positive-QTOFsplash10-0002-9300000000-ea2a52269bc5d4ed4c522015-09-14Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - beta-Glycerophosphoric acid 40V, Positive-QTOFsplash10-0a4i-9000000000-6692d72b52d1a7b9adee2015-09-14Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - beta-Glycerophosphoric acid 10V, Negative-QTOFsplash10-00di-5900000000-6fc5f19f68de2c6954f82015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - beta-Glycerophosphoric acid 20V, Negative-QTOFsplash10-004i-9300000000-ff45373c539658924e8c2015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - beta-Glycerophosphoric acid 40V, Negative-QTOFsplash10-004i-9000000000-3c7e37432300e646a9002015-09-15Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - beta-Glycerophosphoric acid 10V, Negative-QTOFsplash10-004i-9100000000-e8c9470a4d96519f535a2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - beta-Glycerophosphoric acid 20V, Negative-QTOFsplash10-004i-9000000000-a5e502a2627af2048a1f2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - beta-Glycerophosphoric acid 40V, Negative-QTOFsplash10-004i-9000000000-a5e502a2627af2048a1f2021-09-22Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum

IR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M-H]-)2023-02-03FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+H]+)2023-02-03FELIX labView Spectrum
Predicted IR SpectrumIR Ion Spectrum (Predicted IRIS Spectrum, Adduct: [M+Na]+)2023-02-03FELIX labView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm (predicted from logP)
Biospecimen Locations
  • Feces
Tissue LocationsNot Available
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
FecesDetected but not QuantifiedNot QuantifiedAdult (>18 years old)Both
Normal
details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
FecesDetected but not QuantifiedNot QuantifiedAdult (>18 years old)Both
Colorectal cancer
details
Associated Disorders and Diseases
Disease References
Colorectal cancer
  1. Goedert JJ, Sampson JN, Moore SC, Xiao Q, Xiong X, Hayes RB, Ahn J, Shi J, Sinha R: Fecal metabolomics: assay performance and association with colorectal cancer. Carcinogenesis. 2014 Sep;35(9):2089-96. doi: 10.1093/carcin/bgu131. Epub 2014 Jul 18. [PubMed:25037050 ]
Associated OMIM IDs
DrugBank IDDB01779
Phenol Explorer Compound IDNot Available
FooDB IDFDB023021
KNApSAcK IDC00007407
Chemspider ID2431
KEGG Compound IDC02979
BioCyc IDCPD-536
BiGG IDNot Available
Wikipedia LinkGlycerol_2-phosphate
METLIN ID6708
PubChem Compound2526
PDB IDNot Available
ChEBI ID17270
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Chamberlin BA, Sweeley CC: Metabolic profiles of urinary organic acids recovered from absorbent filter paper. Clin Chem. 1987 Apr;33(4):572-6. [PubMed:3829393 ]