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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 22:22:58 UTC

Update Date

2021-09-26 22:53:41 UTC

HMDB ID

HMDB0245296

Secondary Accession Numbers

None

Metabolite Identification

Common Name

2-Phosphonopropionic acid

Description

2-Phosphonopropionic acid belongs to the class of organic compounds known as organic phosphonic acids. These are organic compounds containing phosphonic acid. Based on a literature review a small amount of articles have been published on 2-Phosphonopropionic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). 2-phosphonopropionic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically 2-Phosphonopropionic acid is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
2-Phosphonopropionate	Generator

Chemical Formula

C₃H₇O₅P

Average Molecular Weight

154.058

Monoisotopic Molecular Weight

154.003110323

IUPAC Name

2-phosphonopropanoic acid

Traditional Name

2-phosphonopropanoic acid

CAS Registry Number

Not Available

SMILES

CC(C(O)=O)P(O)(O)=O

InChI Identifier

InChI=1S/C3H7O5P/c1-2(3(4)5)9(6,7)8/h2H,1H3,(H,4,5)(H2,6,7,8)

InChI Key

GUXRZQZCNOHHDO-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as organic phosphonic acids. These are organic compounds containing phosphonic acid.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Organic phosphonic acids and derivatives

Sub Class

Organic phosphonic acids

Direct Parent

Organic phosphonic acids

Alternative Parents

Substituents

Organophosphonic acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organophosphorus compound
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-1.8	ALOGPS
logP	-1.1	ChemAxon
logS	-0.75	ALOGPS
pKa (Strongest Acidic)	1.59	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	28.13 m³·mol⁻¹	ChemAxon
Polarizability	11.66 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	119.426	30932474
DeepCCS	[M-H]-	116.302	30932474
DeepCCS	[M-2H]-	153.174	30932474
DeepCCS	[M+Na]+	127.994	30932474
AllCCS	[M+H]+	135.6	32859911
AllCCS	[M+H-H2O]+	131.6	32859911
AllCCS	[M+NH4]+	139.3	32859911
AllCCS	[M+Na]+	140.3	32859911
AllCCS	[M-H]-	125.9	32859911
AllCCS	[M+Na-2H]-	128.7	32859911
AllCCS	[M+HCOO]-	131.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
2-Phosphonopropionic acid	CC(C(O)=O)P(O)(O)=O	2832.3	Standard polar	33892256
2-Phosphonopropionic acid	CC(C(O)=O)P(O)(O)=O	1215.0	Standard non polar	33892256
2-Phosphonopropionic acid	CC(C(O)=O)P(O)(O)=O	1364.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
2-Phosphonopropionic acid,2TMS,isomer #1	CC(C(=O)O[Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	1439.2	Semi standard non polar	33892256
2-Phosphonopropionic acid,2TMS,isomer #1	CC(C(=O)O[Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	1455.6	Standard non polar	33892256
2-Phosphonopropionic acid,2TMS,isomer #1	CC(C(=O)O[Si](C)(C)C)P(=O)(O)O[Si](C)(C)C	1768.5	Standard polar	33892256
2-Phosphonopropionic acid,2TMS,isomer #2	CC(C(=O)O)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	1503.5	Semi standard non polar	33892256
2-Phosphonopropionic acid,2TMS,isomer #2	CC(C(=O)O)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	1488.7	Standard non polar	33892256
2-Phosphonopropionic acid,2TMS,isomer #2	CC(C(=O)O)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	1712.5	Standard polar	33892256
2-Phosphonopropionic acid,3TMS,isomer #1	CC(C(=O)O[Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	1490.6	Semi standard non polar	33892256
2-Phosphonopropionic acid,3TMS,isomer #1	CC(C(=O)O[Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	1553.7	Standard non polar	33892256
2-Phosphonopropionic acid,3TMS,isomer #1	CC(C(=O)O[Si](C)(C)C)P(=O)(O[Si](C)(C)C)O[Si](C)(C)C	1550.6	Standard polar	33892256
2-Phosphonopropionic acid,2TBDMS,isomer #1	CC(C(=O)O[Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C	1888.2	Semi standard non polar	33892256
2-Phosphonopropionic acid,2TBDMS,isomer #1	CC(C(=O)O[Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C	1911.0	Standard non polar	33892256
2-Phosphonopropionic acid,2TBDMS,isomer #1	CC(C(=O)O[Si](C)(C)C(C)(C)C)P(=O)(O)O[Si](C)(C)C(C)(C)C	2043.6	Standard polar	33892256
2-Phosphonopropionic acid,2TBDMS,isomer #2	CC(C(=O)O)P(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	1930.4	Semi standard non polar	33892256
2-Phosphonopropionic acid,2TBDMS,isomer #2	CC(C(=O)O)P(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	1920.3	Standard non polar	33892256
2-Phosphonopropionic acid,2TBDMS,isomer #2	CC(C(=O)O)P(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2028.6	Standard polar	33892256
2-Phosphonopropionic acid,3TBDMS,isomer #1	CC(C(=O)O[Si](C)(C)C(C)(C)C)P(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2111.1	Semi standard non polar	33892256
2-Phosphonopropionic acid,3TBDMS,isomer #1	CC(C(=O)O[Si](C)(C)C(C)(C)C)P(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2173.4	Standard non polar	33892256
2-Phosphonopropionic acid,3TBDMS,isomer #1	CC(C(=O)O[Si](C)(C)C(C)(C)C)P(=O)(O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	1937.8	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Phosphonopropionic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-001i-9400000000-5937b28b132da836456f	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Phosphonopropionic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Phosphonopropionic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Phosphonopropionic acid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Phosphonopropionic acid GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 2-Phosphonopropionic acid GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-03	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Phosphonopropionic acid 10V, Positive-QTOF	splash10-0a4r-1900000000-13931e74f6f1099da7fc	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Phosphonopropionic acid 20V, Positive-QTOF	splash10-001i-9000000000-78b7020fd5de19fcc3e0	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Phosphonopropionic acid 40V, Positive-QTOF	splash10-06si-9000000000-309b25bac571560a8d8e	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Phosphonopropionic acid 10V, Negative-QTOF	splash10-0gz9-5900000000-6e07a08abe49deb6ab65	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Phosphonopropionic acid 20V, Negative-QTOF	splash10-01t9-9000000000-a29ca570089fed2adf53	2021-10-12	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 2-Phosphonopropionic acid 40V, Negative-QTOF	splash10-004i-9000000000-5709d1c4f97833162146	2021-10-12	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-10-12	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

65949

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

73187

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for 2-Phosphonopropionic acid (HMDB0245296)

MOL for HMDB0245296 (2-Phosphonopropionic acid)

3D MOL for HMDB0245296 (2-Phosphonopropionic acid)

3D SDF for HMDB0245296 (2-Phosphonopropionic acid)

3D-SDF for HMDB0245296 (2-Phosphonopropionic acid)

PDB for HMDB0245296 (2-Phosphonopropionic acid)

3D PDB for HMDB0245296 (2-Phosphonopropionic acid)

SMILES for HMDB0245296 (2-Phosphonopropionic acid)

INCHI for HMDB0245296 (2-Phosphonopropionic acid)

Structure for HMDB0245296 (2-Phosphonopropionic acid)

3D Structure for HMDB0245296 (2-Phosphonopropionic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra