MiMeDB: Showing metabocard for 4-Fumarylacetoacetic acid (MMDBc0047925)

Plant

Animal

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2021-11-23 23:15:47 UTC

Update Date

2024-04-30 20:32:41 UTC

Metabolite ID

MMDBc0047925

Metabolite Identification

Common Name

4-Fumarylacetoacetic acid

Description

4-Fumarylacetoacetic acid is an intermediate in the metabolism of tyrosine. Fumarylacetoacetate hydrolase (FAH) is an enzyme which catalyzes the hydrolysis of 4-fumarylacetoacetate into fumarate and acetoacetate. FAH is the last enzyme in the tyrosine catabolism pathway. FAH deficiency is associated with Type 1 hereditary tyrosinemia.

Structure

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


  Mrv1652309042000202D          

 14 13  0  0  0  0            999 V2000
10009.830310008.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10009.114810008.9496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10008.400710008.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10007.686010008.9496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10006.970910008.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10006.256210008.9496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10005.541510008.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10006.256210009.7744    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10008.400710007.7121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10010.546010008.9496    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10011.259510008.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10011.975010008.9496    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10011.259510007.7121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10009.830310007.7121    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 10  1  0  0  0  0
  1 14  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  9  2  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0047925

> <DATABASE_NAME>
MIME

> <SMILES>
OC(=O)CC(=O)CC(=O)\C=C\C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C8H8O6/c9-5(1-2-7(11)12)3-6(10)4-8(13)14/h1-2H,3-4H2,(H,11,12)(H,13,14)/b2-1+

> <INCHI_KEY>
GACSIVHAIFQKTC-OWOJBTEDSA-N

> <FORMULA>
C8H8O6

> <MOLECULAR_WEIGHT>
200.1455

> <EXACT_MASS>
200.032087988

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
22

> <JCHEM_AVERAGE_POLARIZABILITY>
17.284079207301815

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2E)-4,6-dioxooct-2-enedioic acid

> <ALOGPS_LOGP>
-0.19

> <JCHEM_LOGP>
0.4027936060000003

> <ALOGPS_LOGS>
-2.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.8947874187334905

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.0462803866743133

> <JCHEM_PKA_STRONGEST_BASIC>
-7.057634181873521

> <JCHEM_POLAR_SURFACE_AREA>
108.74000000000001

> <JCHEM_REFRACTIVITY>
44.3974

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.65e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-fumarylacetoacetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  C   UNK     0    8685.0178682.603   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8683.6818683.373   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8682.3488682.603   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8681.0148683.373   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0    8679.6798682.603   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8678.3458683.373   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0    8677.0118682.603   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0    8678.3458684.912   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0    8682.3488681.063   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0    8686.3538683.373   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8687.6848682.603   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0    8689.0208683.373   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0    8687.6848681.063   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0    8685.0178681.063   0.000  0.00  0.00           O+0
CONECT    1    2   10   14                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    3                                                            
CONECT   10    1   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    1                                                            
MASTER        0    0    0    0    0    0    0    0   14    0   26    0
END

Synonyms

Value	Source
Fumarylacetoacetone	ChEBI
Fumarylacetoacetate	Kegg
Fumarylacetoacetic acid	Generator
4-Fumarylacetoacetate	Generator
4-Fumaryl-acetoacetate	HMDB
(2E)-4,6-Dioxo-2-octenedioic acid	HMDB
4-Fumarylacetoacetic acid	HMDB

Molecular Formula

C₈H₈O₆

Average Mass

200.1455

Monoisotopic Mass

200.032087988

IUPAC Name

(2E)-4,6-dioxooct-2-enedioic acid

Traditional Name

4-fumarylacetoacetic acid

CAS Registry Number

28613-33-4

SMILES

OC(=O)CC(=O)CC(=O)\C=C\C(O)=O

InChI Identifier

InChI=1S/C8H8O6/c9-5(1-2-7(11)12)3-6(10)4-8(13)14/h1-2H,3-4H2,(H,11,12)(H,13,14)/b2-1+

InChI Key

GACSIVHAIFQKTC-OWOJBTEDSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as medium-chain keto acids and derivatives. These are keto acids with a 6 to 12 carbon atoms long side chain.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Keto acids and derivatives

Sub Class

Medium-chain keto acids and derivatives

Direct Parent

Medium-chain keto acids and derivatives

Alternative Parents

Substituents

Medium-chain keto acid
Beta-keto acid
1,3-diketone
Beta-hydroxy ketone
Dicarboxylic acid or derivatives
Unsaturated fatty acid
1,3-dicarbonyl compound
Fatty acyl
Enone
Acryloyl-group
Alpha,beta-unsaturated ketone
Ketone
Carboxylic acid
Carboxylic acid derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

oxo dicarboxylic acid (CHEBI:30907 )
beta-diketone (CHEBI:30907 )
Dicarboxylic acids (LMFA01170066 )

Functional Ontology

Not Available

Physical Properties

State

Solid

Predicted Properties

Property	Value	Source
Water Solubility	1.65 g/L	ALOGPS
logP	-0.19	ALOGPS
logP	0.4	ChemAxon
logS	-2.1	ALOGPS
pKa (Strongest Acidic)	3.05	ChemAxon
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	108.74 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	44.4 m³·mol⁻¹	ChemAxon
Polarizability	17.28 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	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-0007-9300000000-7b2ae90eb353073cb652	2017-09-01	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (2 TMS) - 70eV, Positive	splash10-05bu-7092000000-254fb0c9b4683fd48ef1	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0fsi-1920000000-f36f976fb4a0271e936b	2016-08-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-000i-6900000000-692cbcc9f99aac913e42	2016-08-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-00rj-9200000000-8e21be4180492b988f54	2016-08-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0a4j-1900000000-ea634f49698a94be6311	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-0a4i-5900000000-4d5261faac7c9dc29c36	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0a4i-9500000000-17b0a81ad882f626ac2a	2016-08-03	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0bt9-3900000000-0353447aa417ab1cef29	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-014i-9600000000-fabbd099eded8f7879a9	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-014i-9000000000-e4bd7674e02d56b3573f	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-001r-4900000000-80aa92977bd40f96e740	2021-09-24	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00kb-9100000000-7d688d7f7d7a804690a3	2021-09-24	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0006-9000000000-c0d2eba6487ff950c63d	2021-09-24	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	231.8
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (eluted)	2025-10-24	91.7
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (void)	2025-10-24	145.9
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-24	319.7
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-24	251.3
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (void)	2025-10-24	299.1
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	975.9
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (void)	2025-10-24	215.1
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-24	859.8
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	175.1
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-24	230.6
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	177.3
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	74.8
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-24	287.9
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-24	681.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	56.1
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (void)	2025-10-24	217.5
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	658.4

Retention Indices

Chromatography Type	Peak Label	SMILES	Stationary Phase	Deposition Date	Retention Index
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_1	C[Si](C)(C)OC(=O)CC(=O)CC(=O)/C=C/C(=O)O	standard non polar	2025-10-24	2218.62
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_2	C[Si](C)(C)OC(=O)/C=C/C(=O)CC(=O)CC(=O)O	standard non polar	2025-10-24	1744.71
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_3	C[Si](C)(C)OC(=CC(=O)/C=C/C(=O)O)CC(=O)O	standard non polar	2025-10-24	2167.59
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_4	C[Si](C)(C)OC(=CC(=O)O)CC(=O)/C=C/C(=O)O	standard non polar	2025-10-24	1419.93
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_5	C[Si](C)(C)OC(=CC(=O)CC(=O)O)/C=C/C(=O)O	standard non polar	2025-10-24	1921.57
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_6	C[Si](C)(C)OC(=O)/C=C/C(=O)CC(=O)CC(=O)O[Si](C)(C)C	standard non polar	2025-10-24	1448.86
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_7	C[Si](C)(C)OC(=O)CC(=CC(=O)/C=C/C(=O)O)O[Si](C)(C)C	standard non polar	2025-10-24	2156.89
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_8	C[Si](C)(C)OC(=O)C=C(CC(=O)/C=C/C(=O)O)O[Si](C)(C)C	standard non polar	2025-10-24	2119.91
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_9	C[Si](C)(C)OC(=O)CC(=O)C=C(/C=C/C(=O)O)O[Si](C)(C)C	standard non polar	2025-10-24	1882.26
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_10	C[Si](C)(C)OC(=O)/C=C/C(=CC(=O)CC(=O)O)O[Si](C)(C)C	standard non polar	2025-10-24	2230.63
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_11	C[Si](C)(C)OC(=O)/C=C/C(=O)CC(=CC(=O)O)O[Si](C)(C)C	standard non polar	2025-10-24	2588.49
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_12	C[Si](C)(C)OC(=O)/C=C/C(=O)C=C(CC(=O)O)O[Si](C)(C)C	standard non polar	2025-10-24	1995.4
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_13	C[Si](C)(C)OC(=CC(=O)O)C=C(/C=C/C(=O)O)O[Si](C)(C)C	standard non polar	2025-10-24	2053.13
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_14	C[Si](C)(C)OC(=O)/C=C/C(=CC(=O)CC(=O)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-24	2801.79
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_15	C[Si](C)(C)OC(=O)C=C(CC(=O)/C=C/C(=O)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-24	2043.65
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_16	C[Si](C)(C)OC(=O)/C=C/C(=O)C=C(CC(=O)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-24	1719.08
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_17	C[Si](C)(C)OC(=O)C=C(C=C(/C=C/C(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-24	1964.45
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_18	C[Si](C)(C)OC(=O)/C=C/C(=CC(=CC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-24	2293.12
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_19	C[Si](C)(C)OC(=O)C=C(C=C(/C=C/C(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-24	2916.19
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_1	C[Si](C)(C)OC(=O)CC(=O)CC(=O)/C=C/C(=O)O	standard polar	2025-10-24	2106.63
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_2	C[Si](C)(C)OC(=O)/C=C/C(=O)CC(=O)CC(=O)O	standard polar	2025-10-24	2321.76
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_3	C[Si](C)(C)OC(=CC(=O)/C=C/C(=O)O)CC(=O)O	standard polar	2025-10-24	2584.05
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_4	C[Si](C)(C)OC(=CC(=O)O)CC(=O)/C=C/C(=O)O	standard polar	2025-10-24	2242.0
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_5	C[Si](C)(C)OC(=CC(=O)CC(=O)O)/C=C/C(=O)O	standard polar	2025-10-24	1626.56
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_6	C[Si](C)(C)OC(=O)/C=C/C(=O)CC(=O)CC(=O)O[Si](C)(C)C	standard polar	2025-10-24	2201.21
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_7	C[Si](C)(C)OC(=O)CC(=CC(=O)/C=C/C(=O)O)O[Si](C)(C)C	standard polar	2025-10-24	1725.8
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_8	C[Si](C)(C)OC(=O)C=C(CC(=O)/C=C/C(=O)O)O[Si](C)(C)C	standard polar	2025-10-24	1877.72
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_9	C[Si](C)(C)OC(=O)CC(=O)C=C(/C=C/C(=O)O)O[Si](C)(C)C	standard polar	2025-10-24	2809.11
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_10	C[Si](C)(C)OC(=O)/C=C/C(=CC(=O)CC(=O)O)O[Si](C)(C)C	standard polar	2025-10-24	2154.78
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_11	C[Si](C)(C)OC(=O)/C=C/C(=O)CC(=CC(=O)O)O[Si](C)(C)C	standard polar	2025-10-24	1397.93
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_12	C[Si](C)(C)OC(=O)/C=C/C(=O)C=C(CC(=O)O)O[Si](C)(C)C	standard polar	2025-10-24	1478.16
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_13	C[Si](C)(C)OC(=CC(=O)O)C=C(/C=C/C(=O)O)O[Si](C)(C)C	standard polar	2025-10-24	2431.53
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_14	C[Si](C)(C)OC(=O)/C=C/C(=CC(=O)CC(=O)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-24	2052.68
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_15	C[Si](C)(C)OC(=O)C=C(CC(=O)/C=C/C(=O)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-24	2114.59
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_16	C[Si](C)(C)OC(=O)/C=C/C(=O)C=C(CC(=O)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-24	1277.84
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_17	C[Si](C)(C)OC(=O)C=C(C=C(/C=C/C(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-24	2179.29
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_18	C[Si](C)(C)OC(=O)/C=C/C(=CC(=CC(=O)O)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-24	2472.25
Gas Chromatography	4-Fumarylacetoacetic acid_TMS_19	C[Si](C)(C)OC(=O)C=C(C=C(/C=C/C(=O)O[Si](C)(C)C)O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-24	2207.13

Biological Properties

Cellular Locations

Cytoplasm

Biospecimen Locations

Feces

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
MMDBp0192352	Fumarylacetoacetase	Unknown	P16930	Homo sapiens
MMDBp0192437	Maleylacetoacetate isomerase	Enzyme	O43708	Homo sapiens

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	Proteobacteria	4	Human feces; Human	Metabolic reconstruction
Eukaryota/Fungi	Ascomycota	2

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
Human Feces	Detected but not Quantified									HMDB

External Links

HMDB ID

HMDB0001268

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

4-FUMARYL-ACETOACETATE

BiGG ID

1485275

Wikipedia Link

Fumarylacetoacetic_acid

METLIN ID

6123

PubChem Compound

5280398

PDB ID

Not Available

ChEBI ID

30907

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Noronha A, Modamio J, Jarosz Y, Guerard E, Sompairac N, Preciat G, Danielsdottir AD, Krecke M, Merten D, Haraldsdottir HS, Heinken A, Heirendt L, Magnusdottir S, Ravcheev DA, Sahoo S, Gawron P, Friscioni L, Garcia B, Prendergast M, Puente A, Rodrigues M, Roy A, Rouquaya M, Wiltgen L, Zagare A, John E, Krueger M, Kuperstein I, Zinovyev A, Schneider R, Fleming RMT, Thiele I: The Virtual Metabolic Human database: integrating human and gut microbiome metabolism with nutrition and disease. Nucleic Acids Res. 2019 Jan 8;47(D1):D614-D624. doi: 10.1093/nar/gky992. [PubMed:30371894 ]

Showing metabocard for 4-Fumarylacetoacetic acid (MMDBc0047925)

MOL for #<Metabolite:0x00007f9ab20862c8>

3D MOL for #<Metabolite:0x00007f9ab20862c8>

3D SDF for #<Metabolite:0x00007f9ab20862c8>

3D-SDF for #<Metabolite:0x00007f9ab20862c8>

PDB for #<Metabolite:0x00007f9ab20862c8>

3D PDB for #<Metabolite:0x00007f9ab20862c8>

SMILES for #<Metabolite:0x00007f9ab20862c8>

INCHI for #<Metabolite:0x00007f9ab20862c8>

Structure for #<Metabolite:0x00007f9ab20862c8>

3D Structure for #<Metabolite:0x00007f9ab20862c8>