Jump To Section:

Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References XML

Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 19:04:07 UTC

Update Date

2021-09-26 23:14:33 UTC

HMDB ID

HMDB0257920

Secondary Accession Numbers

None

Metabolite Identification

Common Name

(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid

Description

(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Based on a literature review very few articles have been published on (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid. This compound has been identified in human blood as reported by (PMID: 31557052 ). (2s)-2-[(2-carboxy-2-oxoethyl)amino]pentanedioic acid is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic 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


  Mrv1652309112121042D          

 16 15  0  0  0  0            999 V2000
    4.4270    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9980    3.3809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1414    1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559    0.9059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    0.9059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559    2.5559    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.5704    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2849    3.3809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7138    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9993    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0257920

> <DATABASE_NAME>
hmdb

> <SMILES>
OC(=O)CCC(NCC(=O)C(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C8H11NO7/c10-5(8(15)16)3-9-4(7(13)14)1-2-6(11)12/h4,9H,1-3H2,(H,11,12)(H,13,14)(H,15,16)

> <INCHI_KEY>
XREHQPOYORRYEU-UHFFFAOYSA-N

> <FORMULA>
C8H11NO7

> <MOLECULAR_WEIGHT>
233.176

> <EXACT_MASS>
233.053551698

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
27

> <JCHEM_AVERAGE_POLARIZABILITY>
20.359337518201244

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(2-carboxy-2-oxoethyl)amino]pentanedioic acid

> <ALOGPS_LOGP>
-1.37

> <JCHEM_LOGP>
-3.4121780623397133

> <ALOGPS_LOGS>
-1.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
2.2739363231315197

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.0865853824534026

> <JCHEM_PKA_STRONGEST_BASIC>
8.7678201677181

> <JCHEM_POLAR_SURFACE_AREA>
140.99999999999997

> <JCHEM_REFRACTIVITY>
47.492900000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.80e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(2-carboxy-2-oxoethyl)amino]pentanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0       8.264   4.771   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.596   4.771   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.263   4.001   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       5.596   6.311   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       9.597   4.001   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.597   2.461   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.931   1.691   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0       8.264   1.691   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0      10.931   4.771   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      12.265   4.001   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.598   4.771   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      13.598   6.311   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      14.932   4.001   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      16.266   4.771   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      14.932   2.461   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3                                                            
CONECT    6    1    7   10                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    6   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   30    0
END

COMPND    HMDB0257920
HETATM    1  O1  UNL     1       4.112  -0.512  -0.105  1.00  0.00           O  
HETATM    2  C1  UNL     1       3.401   0.371  -0.702  1.00  0.00           C  
HETATM    3  O2  UNL     1       3.534   0.362  -2.095  1.00  0.00           O  
HETATM    4  C2  UNL     1       2.532   1.311  -0.041  1.00  0.00           C  
HETATM    5  C3  UNL     1       1.085   1.111   0.152  1.00  0.00           C  
HETATM    6  C4  UNL     1       0.671  -0.041   0.925  1.00  0.00           C  
HETATM    7  N1  UNL     1      -0.765  -0.100   1.215  1.00  0.00           N  
HETATM    8  C5  UNL     1      -1.618  -0.210   0.089  1.00  0.00           C  
HETATM    9  C6  UNL     1      -3.028  -0.212   0.556  1.00  0.00           C  
HETATM   10  O3  UNL     1      -3.269  -0.102   1.807  1.00  0.00           O  
HETATM   11  C7  UNL     1      -4.162  -0.334  -0.325  1.00  0.00           C  
HETATM   12  O4  UNL     1      -4.018  -0.462  -1.586  1.00  0.00           O  
HETATM   13  O5  UNL     1      -5.453  -0.317   0.142  1.00  0.00           O  
HETATM   14  C8  UNL     1       0.861  -1.329   0.175  1.00  0.00           C  
HETATM   15  O6  UNL     1       0.264  -2.387   0.663  1.00  0.00           O  
HETATM   16  O7  UNL     1       1.557  -1.571  -0.947  1.00  0.00           O  
HETATM   17  H1  UNL     1       4.317   0.756  -2.565  1.00  0.00           H  
HETATM   18  H2  UNL     1       2.718   2.384  -0.476  1.00  0.00           H  
HETATM   19  H3  UNL     1       3.042   1.500   0.993  1.00  0.00           H  
HETATM   20  H4  UNL     1       0.696   2.099   0.556  1.00  0.00           H  
HETATM   21  H5  UNL     1       0.641   1.033  -0.897  1.00  0.00           H  
HETATM   22  H6  UNL     1       1.192  -0.114   1.880  1.00  0.00           H  
HETATM   23  H7  UNL     1      -0.932  -0.789   1.952  1.00  0.00           H  
HETATM   24  H8  UNL     1      -1.482   0.519  -0.698  1.00  0.00           H  
HETATM   25  H9  UNL     1      -1.459  -1.221  -0.376  1.00  0.00           H  
HETATM   26  H10 UNL     1      -5.882   0.548   0.505  1.00  0.00           H  
HETATM   27  H11 UNL     1       1.445  -2.293  -1.615  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   17
CONECT    4    5   18   19
CONECT    5    6   20   21
CONECT    6    7   14   22
CONECT    7    8   23
CONECT    8    9   24   25
CONECT    9   10   10   11
CONECT   11   12   12   13
CONECT   13   26
CONECT   14   15   15   16
CONECT   16   27
END

View in JSmol View Stereo Labels

Synonyms

Value	Source
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioate	Generator
2-[(2-Carboxy-2-oxoethyl)amino]pentanedioate	HMDB

Chemical Formula

C₈H₁₁NO₇

Average Molecular Weight

233.176

Monoisotopic Molecular Weight

233.053551698

IUPAC Name

2-[(2-carboxy-2-oxoethyl)amino]pentanedioic acid

Traditional Name

2-[(2-carboxy-2-oxoethyl)amino]pentanedioic acid

CAS Registry Number

Not Available

SMILES

OC(=O)CCC(NCC(=O)C(O)=O)C(O)=O

InChI Identifier

InChI=1S/C8H11NO7/c10-5(8(15)16)3-9-4(7(13)14)1-2-6(11)12/h4,9H,1-3H2,(H,11,12)(H,13,14)(H,15,16)

InChI Key

XREHQPOYORRYEU-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Glutamic acid and derivatives

Alternative Parents

Substituents

Glutamic acid or derivatives
Alpha-amino acid
Tricarboxylic acid or derivatives
Amino fatty acid
Alpha-keto acid
Fatty acyl
Keto acid
Alpha-aminoketone
Alpha-hydroxy ketone
Amino acid
Ketone
Secondary amine
Secondary aliphatic amine
Carboxylic acid
Organic nitrogen compound
Carbonyl group
Hydrocarbon derivative
Amine
Organic oxide
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
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	-1.4	ALOGPS
logP	-3.4	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	1.09	ChemAxon
pKa (Strongest Basic)	8.77	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	141 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	47.49 m³·mol⁻¹	ChemAxon
Polarizability	20.36 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]+	143.074	30932474
DeepCCS	[M-H]-	140.716	30932474
DeepCCS	[M-2H]-	176.197	30932474
DeepCCS	[M+Na]+	151.736	30932474

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	1.81 minutes	32390414
Predicted by Siyang on May 30, 2022	10.1037 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	8.82 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	513.9 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	291.5 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	41.5 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	170.5 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	63.0 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	278.4 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	234.0 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	842.3 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	596.9 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	44.5 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	812.5 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	187.3 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	245.4 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	693.0 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	405.1 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	485.7 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid	OC(=O)CCC(NCC(=O)C(O)=O)C(O)=O	3155.7	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid	OC(=O)CCC(NCC(=O)C(O)=O)C(O)=O	1494.0	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid	OC(=O)CCC(NCC(=O)C(O)=O)C(O)=O	2076.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(NC=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2192.7	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(NC=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2159.7	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(NC=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2416.7	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(CC(=O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2197.3	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(CC(=O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2155.8	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #2	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(CC(=O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2337.2	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #3	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2306.1	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #3	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2173.4	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #3	C[Si](C)(C)OC(=O)CCC(C(=O)O)N(C=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2635.5	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C=C(O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2364.8	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C=C(O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2214.2	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #4	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C=C(O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2605.9	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #5	C[Si](C)(C)OC(=O)C(=CN(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	2302.0	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #5	C[Si](C)(C)OC(=O)C(=CN(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	2153.2	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TMS,isomer #5	C[Si](C)(C)OC(=O)C(=CN(C(CCC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)O[Si](C)(C)C	2586.1	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2276.8	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2176.0	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C)N(C=C(O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2382.0	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3053.9	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2814.1	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)CCC(NC=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2828.9	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(CC(=O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3032.0	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(CC(=O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2921.0	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(CC(=O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2820.3	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3140.4	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2786.7	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O)N(C=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2949.2	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C=C(O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3185.8	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C=C(O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2856.8	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C=C(O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2937.6	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=CN(C(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3124.9	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=CN(C(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2767.4	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(=CN(C(CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2922.0	Standard polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3286.0	Semi standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2946.6	Standard non polar	33892256
(2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)CCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C=C(O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2875.5	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (Non-derivatized) - 70eV, Positive	splash10-0006-4900000000-24596543d962eab3b57d	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_3_1) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_3_2) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_3_3) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_3_4) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_3_5) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_3_6) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_3_7) - 70eV, Positive	Not Available	2021-11-05	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid GC-MS (TMS_3_8) - 70eV, Positive	Not Available	2021-11-05	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

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21226067

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 (2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid (HMDB0257920)

MOL for HMDB0257920 ((2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid)

3D MOL for HMDB0257920 ((2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid)

3D SDF for HMDB0257920 ((2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid)

3D-SDF for HMDB0257920 ((2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid)

PDB for HMDB0257920 ((2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid)

3D PDB for HMDB0257920 ((2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid)

SMILES for HMDB0257920 ((2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid)

INCHI for HMDB0257920 ((2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid)

Structure for HMDB0257920 ((2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid)

3D Structure for HMDB0257920 ((2S)-2-[(2-Carboxy-2-oxoethyl)amino]pentanedioic acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra