MiMeDB: Showing metabocard for 2-hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate (MMDBc0055239)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2022-06-17 19:47:03 UTC

Update Date

2025-10-07 16:09:02 UTC

Metabolite ID

MMDBc0055239

Metabolite Identification

Common Name

2-hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate

Description

2-hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate is a phosphate-containing metabolite. There is limited literature available on this compound, indicating that it has not been extensively studied in the context of metabolic pathways or biological functions.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306172221472D          

 14 13  0  0  0  0            999 V2000
   -0.6039    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6829   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    1.2375    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    4.3974    2.0625    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    5.2224    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3974    1.2375    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    0.4125    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  1  0  0  0  0
  5  2  1  0  0  0  0
  6  4  2  0  0  0  0
  6  5  1  0  0  0  0
  7  5  2  0  0  0  0
  8  6  1  0  0  0  0
  4 12  1  4  0  0  0
 13  9  1  0  0  0  0
 13 10  1  0  0  0  0
 13 11  2  0  0  0  0
 13 12  1  0  0  0  0
 14  1  1  0  0  0  0
 14  3  1  0  0  0  0
M  CHG  2   8  -1   9  -1
M  END
> <DATABASE_ID>
MMDBc0055239

> <DATABASE_NAME>
MIME

> <SMILES>
CSCCC(=O)C([O-])=COP(O)([O-])=O

> <INCHI_IDENTIFIER>
InChI=1S/C6H11O6PS/c1-14-3-2-5(7)6(8)4-12-13(9,10)11/h4,8H,2-3H2,1H3,(H2,9,10,11)/p-2

> <INCHI_KEY>
YIEMFVNCENFBSD-UHFFFAOYSA-L

> <FORMULA>
C6H9O6PS

> <MOLECULAR_WEIGHT>
240.17

> <EXACT_MASS>
239.986843342

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
23

> <JCHEM_AVERAGE_POLARIZABILITY>
19.98912345290521

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
-2

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(hydrogen phosphonooxy)-5-(methylsulfanyl)-3-oxopent-1-en-2-olate

> <JCHEM_LOGP>
0.15778081366666724

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.40082136178022

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.3641115734153981

> <JCHEM_PKA_STRONGEST_BASIC>
-4.556270321103455

> <JCHEM_POLAR_SURFACE_AREA>
109.72000000000001

> <JCHEM_REFRACTIVITY>
62.170300000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
1-(hydrogen phosphonooxy)-5-(methylsulfanyl)-3-oxopent-1-en-2-olate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-JUN-22         0                                  
HETATM    1  C   UNK     0      -1.127   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.874   0.770   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.540   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.875  -0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.207  -0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.541   0.770   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.207  -1.540   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       5.541   2.310   0.000  0.00  0.00           O-1
HETATM    9  O   UNK     0       8.208   3.850   0.000  0.00  0.00           O-1
HETATM   10  O   UNK     0       9.748   2.310   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       8.208   0.770   0.000  0.00  0.00           O+0
HETATM   13  P   UNK     0       8.208   2.310   0.000  0.00  0.00           P+0
HETATM   14  S   UNK     0       0.206   0.770   0.000  0.00  0.00           S+0
CONECT    1   14                                                            
CONECT    2    3    5                                                       
CONECT    3    2   14                                                       
CONECT    4    6   12                                                       
CONECT    5    2    6    7                                                  
CONECT    6    4    5    8                                                  
CONECT    7    5                                                            
CONECT    8    6                                                            
CONECT    9   13                                                            
CONECT   10   13                                                            
CONECT   11   13                                                            
CONECT   12    4   13                                                       
CONECT   13    9   10   11   12                                             
CONECT   14    1    3                                                       
MASTER        0    0    0    0    0    0    0    0   14    0   26    0
END

Synonyms

Value	Source
2-Hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate	ChEBI
2-Hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphoric acid	Generator
2-Hydroxy-5-methylsulphanyl-3-oxopent-1-enyl phosphate	Generator
2-Hydroxy-5-methylsulphanyl-3-oxopent-1-enyl phosphoric acid	Generator
2-Hydroxy-5-(methylsulfanyl)-3-oxopent-1-enyl phosphoric acid(2-)	Generator
2-Hydroxy-5-(methylsulphanyl)-3-oxopent-1-enyl phosphate(2-)	Generator
2-Hydroxy-5-(methylsulphanyl)-3-oxopent-1-enyl phosphoric acid(2-)	Generator

Molecular Formula

C₆H₉O₆PS

Average Mass

240.17

Monoisotopic Mass

239.986843342

IUPAC Name

1-(hydrogen phosphonooxy)-5-(methylsulfanyl)-3-oxopent-1-en-2-olate

Traditional Name

1-(hydrogen phosphonooxy)-5-(methylsulfanyl)-3-oxopent-1-en-2-olate

CAS Registry Number

Not Available

SMILES

CSCCC(=O)C([O-])=COP(O)([O-])=O

InChI Identifier

InChI=1S/C6H11O6PS/c1-14-3-2-5(7)6(8)4-12-13(9,10)11/h4,8H,2-3H2,1H3,(H2,9,10,11)/p-2

InChI Key

YIEMFVNCENFBSD-UHFFFAOYSA-L

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phosphate esters. These are organic compounds containing phosphoric acid ester functional group, with the general structure R1P(=O)(R2)OR3. R1,R2 = O,N, or halogen atom; R3 = organyl group.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Organic phosphoric acids and derivatives

Sub Class

Phosphate esters

Direct Parent

Phosphate esters

Alternative Parents

Substituents

Phosphoric acid ester
Alpha-branched alpha,beta-unsaturated-ketone
Acryloyl-group
Enone
Alpha,beta-unsaturated ketone
Ketone
Sulfenyl compound
Thioether
Dialkylthioether
Hydrocarbon derivative
Organosulfur compound
Organooxygen compound
Organic oxygen compound
Organic oxide
Carbonyl group
Organic anion
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

organophosphate oxoanion (CHEBI:59505 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
logP	0.16	ChemAxon
pKa (Strongest Acidic)	1.36	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	109.72 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	62.17 m³·mol⁻¹	ChemAxon
Polarizability	19.99 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	2022-08-20	View Spectrum

Chromatographic Retention Times and Retention Indices

Retention Times

Chromatography Type	Technique	Column	Deposition Date	Retention Time (s)
Liquid Chromatography	HILIC	Waters Acquity UPLC-BEH Amide column (eluted)	2025-10-24	118.6
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (eluted)	2025-10-24	45.1
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (eluted)	2025-10-24	343.2
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-24	605.6
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-24	355.0
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (void)	2025-10-24	327.4
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	1519.1
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-24	102.0
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-24	671.1
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	275.9
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-24	257.2
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	209.0
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	103.7
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-24	178.9
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-24	434.8
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	104.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (void)	2025-10-24	326.3
Liquid Chromatography	Reversed-phase	Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex (eluted)	2025-10-24	959.9
Liquid Chromatography	Reversed-phase	Waters Atlantis T3 (2.1 x 150 mm, 5 um) (eluted)	2025-10-24	843.5

Retention Indices

Chromatography Type	Peak Label	SMILES	Stationary Phase	Deposition Date	Retention Index
Gas Chromatography	2-hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate_TMS_1	CSCCC(=O)C([O-])=COP(=O)([O-])O[Si](C)(C)C	standard non polar	2025-10-24	1541.16
Gas Chromatography	2-hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate_TMS_2	CSCC=C(O[Si](C)(C)C)C([O-])=COP(=O)([O-])O	standard non polar	2025-10-24	2605.03
Gas Chromatography	2-hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate_TMS_3	CSCC=C(O[Si](C)(C)C)C([O-])=COP(=O)([O-])O[Si](C)(C)C	standard non polar	2025-10-24	1653.6
Gas Chromatography	2-hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate_TMS_1	CSCCC(=O)C([O-])=COP(=O)([O-])O[Si](C)(C)C	standard polar	2025-10-24	2001.74
Gas Chromatography	2-hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate_TMS_2	CSCC=C(O[Si](C)(C)C)C([O-])=COP(=O)([O-])O	standard polar	2025-10-24	1995.59
Gas Chromatography	2-hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate_TMS_3	CSCC=C(O[Si](C)(C)C)C([O-])=COP(=O)([O-])O[Si](C)(C)C	standard polar	2025-10-24	2409.27

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria/Eubacteria	Firmicutes	28	Human ; Human feces
Bacteria/Eubacteria	Cyanobacteria	2	Human

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

26333198

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

75154468

PDB ID

Not Available

ChEBI ID

59505

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for 2-hydroxy-5-methylsulfanyl-3-oxopent-1-enyl phosphate (MMDBc0055239)

MOL for #<Metabolite:0x00007f2de539b470>

3D MOL for #<Metabolite:0x00007f2de539b470>

3D SDF for #<Metabolite:0x00007f2de539b470>

3D-SDF for #<Metabolite:0x00007f2de539b470>

PDB for #<Metabolite:0x00007f2de539b470>

3D PDB for #<Metabolite:0x00007f2de539b470>

SMILES for #<Metabolite:0x00007f2de539b470>

INCHI for #<Metabolite:0x00007f2de539b470>

Structure for #<Metabolite:0x00007f2de539b470>

3D Structure for #<Metabolite:0x00007f2de539b470>