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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 21:02:39 UTC

Update Date

2021-09-14 15:36:53 UTC

HMDB ID

HMDB0028828

Secondary Accession Numbers

HMDB28828

Metabolite Identification

Common Name

Glutamylserine

Description

Glutamylserine is a dipeptide composed of glutamate and serine, and is a proteolytic breakdown product of larger proteins. It belongs to the family of N-acyl-alpha amino acids and derivatives. These are compounds containing an alpha amino acid which bears an acyl group at its terminal nitrogen atom. Glutamylserine is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis.

Structure

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

HMDB0028828
     RDKit          3D
Glutamylserine
 30 29  0  0  0  0  0  0  0  0999 V2000
    1.0169    0.6561   -2.7913 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6902    0.0686   -1.5443 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7167    0.4291   -0.4906 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0554   -0.0993   -0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1335    0.2078   -0.0106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2935   -0.1796   -0.3053 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8794    0.8986    1.1864 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6827    0.3716   -1.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4129    1.0765   -1.8490 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1859   -0.1267    0.0875 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5285    0.1273    0.5704 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2025   -1.2227    0.7161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4177   -1.9426    1.6482 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4061    0.7153    1.9210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3154    0.9347    2.5003 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5806    1.0502    2.6006 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4686    1.5563   -2.7911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1065    0.0478   -3.5926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7564   -1.0471   -1.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7678    1.5219   -0.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4805   -0.0113    0.4915 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3289    0.4079   -1.9301 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0314   -1.1820   -1.1724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7131    0.3293    2.0254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5847   -0.7261    0.7160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1126    0.7567   -0.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1294   -1.8019   -0.2283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2301   -1.1566    1.0929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9014   -2.7647    1.9230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7484    0.7958    3.5510 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  2  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  2  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  6
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  7 24  1  0
 10 25  1  0
 11 26  1  6
 12 27  1  0
 12 28  1  0
 13 29  1  0
 16 30  1  0
M  END

  Mrv1652304062013402D          

 16 15  0  0  0  0            999 V2000
 2501.7850 2500.0010    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2501.0710 2499.5877    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 2500.3570 2500.0010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2499.6429 2499.5877    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2498.9289 2500.0010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2498.2149 2499.5877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2497.5009 2500.0010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2496.7869 2499.5877    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2497.5009 2500.8255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2499.6429 2498.7633    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 2500.3570 2500.8255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2502.4990 2499.5877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2503.2130 2500.0010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2502.4990 2498.7633    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2501.7850 2500.8255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2502.4990 2501.2366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1 12  1  0  0  0  0
  1 15  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3 11  2  0  0  0  0
  4  5  1  0  0  0  0
  4 10  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  2  0  0  0  0
 15 16  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0028828

> <DATABASE_NAME>
hmdb

> <SMILES>
N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C8H14N2O6/c9-4(1-2-6(12)13)7(14)10-5(3-11)8(15)16/h4-5,11H,1-3,9H2,(H,10,14)(H,12,13)(H,15,16)/t4-,5-/m0/s1

> <INCHI_KEY>
UQHGAYSULGRWRG-WHFBIAKZSA-N

> <FORMULA>
C8H14N2O6

> <MOLECULAR_WEIGHT>
234.208

> <EXACT_MASS>
234.085186179

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
21.684350549630484

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(4S)-4-amino-4-{[(1S)-1-carboxy-2-hydroxyethyl]carbamoyl}butanoic acid

> <ALOGPS_LOGP>
-3.55

> <JCHEM_LOGP>
-5.122600711260628

> <ALOGPS_LOGS>
-1.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
3.945593981999139

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1121955815753095

> <JCHEM_PKA_STRONGEST_BASIC>
8.44954048473961

> <JCHEM_POLAR_SURFACE_AREA>
149.95

> <JCHEM_REFRACTIVITY>
50.128800000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.37e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4S)-4-amino-4-{[(1S)-1-carboxy-2-hydroxyethyl]carbamoyl}butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0028828
     RDKit          3D
Glutamylserine
 30 29  0  0  0  0  0  0  0  0999 V2000
    1.0169    0.6561   -2.7913 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6902    0.0686   -1.5443 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7167    0.4291   -0.4906 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0554   -0.0993   -0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1335    0.2078   -0.0106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2935   -0.1796   -0.3053 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8794    0.8986    1.1864 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6827    0.3716   -1.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4129    1.0765   -1.8490 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1859   -0.1267    0.0875 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5285    0.1273    0.5704 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2025   -1.2227    0.7161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4177   -1.9426    1.6482 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4061    0.7153    1.9210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3154    0.9347    2.5003 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5806    1.0502    2.6006 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4686    1.5563   -2.7911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1065    0.0478   -3.5926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7564   -1.0471   -1.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7678    1.5219   -0.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4805   -0.0113    0.4915 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3289    0.4079   -1.9301 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0314   -1.1820   -1.1724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7131    0.3293    2.0254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5847   -0.7261    0.7160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1126    0.7567   -0.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1294   -1.8019   -0.2283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2301   -1.1566    1.0929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9014   -2.7647    1.9230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7484    0.7958    3.5510 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  2  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  2  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  6
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  7 24  1  0
 10 25  1  0
 11 26  1  6
 12 27  1  0
 12 28  1  0
 13 29  1  0
 16 30  1  0
M  END

HEADER    PROTEIN                                 06-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-APR-20         0                                  
HETATM    1  C   UNK     0    4669.9994666.669   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0    4668.6664665.897   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0    4667.3334666.669   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    4666.0004665.897   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0    4664.6674666.669   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    4663.3344665.897   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    4662.0024666.669   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0    4660.6694665.897   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0    4662.0024668.208   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0    4666.0004664.358   0.000  0.00  0.00           N+0
HETATM   11  O   UNK     0    4667.3334668.208   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0    4671.3314665.897   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0    4672.6644666.669   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0    4671.3314664.358   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0    4669.9994668.208   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0    4671.3314668.975   0.000  0.00  0.00           O+0
CONECT    1    2   12   15                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   11                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    4                                                            
CONECT   11    3                                                            
CONECT   12    1   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    1   16                                                       
CONECT   16   15                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   30    0
END

COMPND    HMDB0028828
HETATM    1  N1  UNL     1       1.017   0.656  -2.791  1.00  0.00           N  
HETATM    2  C1  UNL     1       0.690   0.069  -1.544  1.00  0.00           C  
HETATM    3  C2  UNL     1       1.717   0.429  -0.491  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.055  -0.099  -0.983  1.00  0.00           C  
HETATM    5  C4  UNL     1       4.133   0.208  -0.011  1.00  0.00           C  
HETATM    6  O1  UNL     1       5.293  -0.180  -0.305  1.00  0.00           O  
HETATM    7  O2  UNL     1       3.879   0.899   1.186  1.00  0.00           O  
HETATM    8  C5  UNL     1      -0.683   0.372  -1.126  1.00  0.00           C  
HETATM    9  O3  UNL     1      -1.413   1.077  -1.849  1.00  0.00           O  
HETATM   10  N2  UNL     1      -1.186  -0.127   0.088  1.00  0.00           N  
HETATM   11  C6  UNL     1      -2.528   0.127   0.570  1.00  0.00           C  
HETATM   12  C7  UNL     1      -3.203  -1.223   0.716  1.00  0.00           C  
HETATM   13  O4  UNL     1      -2.418  -1.943   1.648  1.00  0.00           O  
HETATM   14  C8  UNL     1      -2.406   0.715   1.921  1.00  0.00           C  
HETATM   15  O5  UNL     1      -1.315   0.935   2.500  1.00  0.00           O  
HETATM   16  O6  UNL     1      -3.581   1.050   2.601  1.00  0.00           O  
HETATM   17  H1  UNL     1       1.469   1.556  -2.791  1.00  0.00           H  
HETATM   18  H2  UNL     1       1.106   0.048  -3.593  1.00  0.00           H  
HETATM   19  H3  UNL     1       0.756  -1.047  -1.662  1.00  0.00           H  
HETATM   20  H4  UNL     1       1.768   1.522  -0.432  1.00  0.00           H  
HETATM   21  H5  UNL     1       1.481  -0.011   0.492  1.00  0.00           H  
HETATM   22  H6  UNL     1       3.329   0.408  -1.930  1.00  0.00           H  
HETATM   23  H7  UNL     1       3.031  -1.182  -1.172  1.00  0.00           H  
HETATM   24  H8  UNL     1       3.713   0.329   2.025  1.00  0.00           H  
HETATM   25  H9  UNL     1      -0.585  -0.726   0.716  1.00  0.00           H  
HETATM   26  H10 UNL     1      -3.113   0.757  -0.122  1.00  0.00           H  
HETATM   27  H11 UNL     1      -3.129  -1.802  -0.228  1.00  0.00           H  
HETATM   28  H12 UNL     1      -4.230  -1.157   1.093  1.00  0.00           H  
HETATM   29  H13 UNL     1      -2.901  -2.765   1.923  1.00  0.00           H  
HETATM   30  H14 UNL     1      -3.748   0.796   3.551  1.00  0.00           H  
CONECT    1    2   17   18
CONECT    2    3    8   19
CONECT    3    4   20   21
CONECT    4    5   22   23
CONECT    5    6    6    7
CONECT    7   24
CONECT    8    9    9   10
CONECT   10   11   25
CONECT   11   12   14   26
CONECT   12   13   27   28
CONECT   13   29
CONECT   14   15   15   16
CONECT   16   30
END

HMDB0028828
     RDKit          3D
Glutamylserine
 30 29  0  0  0  0  0  0  0  0999 V2000
    1.0169    0.6561   -2.7913 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.6902    0.0686   -1.5443 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7167    0.4291   -0.4906 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0554   -0.0993   -0.9834 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1335    0.2078   -0.0106 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2935   -0.1796   -0.3053 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8794    0.8986    1.1864 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6827    0.3716   -1.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4129    1.0765   -1.8490 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1859   -0.1267    0.0875 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5285    0.1273    0.5704 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.2025   -1.2227    0.7161 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4177   -1.9426    1.6482 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4061    0.7153    1.9210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3154    0.9347    2.5003 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5806    1.0502    2.6006 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4686    1.5563   -2.7911 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1065    0.0478   -3.5926 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7564   -1.0471   -1.6620 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7678    1.5219   -0.4317 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4805   -0.0113    0.4915 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3289    0.4079   -1.9301 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0314   -1.1820   -1.1724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7131    0.3293    2.0254 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5847   -0.7261    0.7160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1126    0.7567   -0.1219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1294   -1.8019   -0.2283 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2301   -1.1566    1.0929 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9014   -2.7647    1.9230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7484    0.7958    3.5510 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  2  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  2  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  6
  3 20  1  0
  3 21  1  0
  4 22  1  0
  4 23  1  0
  7 24  1  0
 10 25  1  0
 11 26  1  6
 12 27  1  0
 12 28  1  0
 13 29  1  0
 16 30  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
alpha-Glu-ser	ChEBI
alpha-Glutamylserine	ChEBI
E-S	ChEBI
ES	ChEBI
L-Glu-L-ser	ChEBI
a-Glu-ser	Generator
Α-glu-ser	Generator
a-Glutamylserine	Generator
Α-glutamylserine	Generator
e-S Dipeptide	HMDB
ES dipeptide	HMDB
Glu-ser	HMDB
Glutamate serine dipeptide	HMDB
Glutamate-serine dipeptide	HMDB
L-Glutamyl-L-serine	HMDB
Α-L-glu-L-ser	HMDB
Α-L-glutamyl-L-serine	HMDB
L-Α-glutamyl-L-serine	HMDB
N-Α-glutamylserine	HMDB
N-Α-L-glutamyl-L-serine	HMDB
N-L-Α-glutamylserine	HMDB
N-L-Α-glutamyl-L-serine	HMDB
alpha-L-Glu-L-ser	HMDB
alpha-L-Glutamyl-L-serine	HMDB
L-alpha-Glutamyl-L-serine	HMDB
N-alpha-Glutamylserine	HMDB
N-alpha-L-Glutamyl-L-serine	HMDB
N-L-alpha-Glutamylserine	HMDB
N-L-alpha-Glutamyl-L-serine	HMDB
N-Glutamylserine	HMDB
N-L-Glutamyl-L-serine	HMDB
Glutamyl-serine	HMDB
Glutamic acid serine dipeptide	HMDB
Glutamic acid-serine dipeptide	HMDB
Glutamylserine	HMDB, ChEBI

Chemical Formula

C₈H₁₄N₂O₆

Average Molecular Weight

234.208

Monoisotopic Molecular Weight

234.085186179

IUPAC Name

(4S)-4-amino-4-{[(1S)-1-carboxy-2-hydroxyethyl]carbamoyl}butanoic acid

Traditional Name

(4S)-4-amino-4-{[(1S)-1-carboxy-2-hydroxyethyl]carbamoyl}butanoic acid

CAS Registry Number

5875-38-7

SMILES

N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(O)=O

InChI Identifier

InChI=1S/C8H14N2O6/c9-4(1-2-6(12)13)7(14)10-5(3-11)8(15)16/h4-5,11H,1-3,9H2,(H,10,14)(H,12,13)(H,15,16)/t4-,5-/m0/s1

InChI Key

UQHGAYSULGRWRG-WHFBIAKZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Dipeptides

Alternative Parents

Substituents

Alpha-dipeptide
Glutamic acid or derivatives
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
N-acyl-l-alpha-amino acid
Alpha-amino acid amide
Serine or derivatives
Alpha-amino acid or derivatives
Amino fatty acid
Beta-hydroxy acid
Hydroxy fatty acid
Fatty acid
Hydroxy acid
Fatty acyl
N-acyl-amine
Fatty amide
Dicarboxylic acid or derivatives
Amino acid or derivatives
Carboxamide group
Amino acid
Secondary carboxylic acid amide
Carboxylic acid
Primary amine
Organic oxygen compound
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Organic oxide
Organopnictogen compound
Alcohol
Amine
Primary aliphatic amine
Primary alcohol
Organooxygen compound
Organonitrogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

dipeptide (CHEBI:73509 )

Ontology

Not Available

Endogenous (HMDB: HMDB0028828)

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

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	-5.11	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	59.6 g/L	ALOGPS
logP	-3.6	ALOGPS
logP	-5.1	ChemAxon
logS	-1	ALOGPS
pKa (Strongest Acidic)	3.11	ChemAxon
pKa (Strongest Basic)	8.45	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	149.95 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	50.13 m³·mol⁻¹	ChemAxon
Polarizability	21.68 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]+	153.767	30932474
DeepCCS	[M-H]-	151.372	30932474
DeepCCS	[M-2H]-	184.436	30932474
DeepCCS	[M+Na]+	159.791	30932474
AllCCS	[M+H]+	150.2	32859911
AllCCS	[M+H-H2O]+	146.8	32859911
AllCCS	[M+NH4]+	153.3	32859911
AllCCS	[M+Na]+	154.2	32859911
AllCCS	[M-H]-	147.7	32859911
AllCCS	[M+Na-2H]-	148.2	32859911
AllCCS	[M+HCOO]-	148.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Glutamylserine	N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(O)=O	3262.1	Standard polar	33892256
Glutamylserine	N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(O)=O	1918.9	Standard non polar	33892256
Glutamylserine	N[C@@H](CCC(O)=O)C(=O)N[C@@H](CO)C(O)=O	2359.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Glutamylserine,1TMS,isomer #1	C[Si](C)(C)OC(=O)CC[C@H](N)C(=O)N[C@@H](CO)C(=O)O	2181.2	Semi standard non polar	33892256
Glutamylserine,1TMS,isomer #2	C[Si](C)(C)OC[C@H](NC(=O)[C@@H](N)CCC(=O)O)C(=O)O	2160.6	Semi standard non polar	33892256
Glutamylserine,1TMS,isomer #3	C[Si](C)(C)OC(=O)[C@H](CO)NC(=O)[C@@H](N)CCC(=O)O	2157.6	Semi standard non polar	33892256
Glutamylserine,1TMS,isomer #4	C[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)O	2206.7	Semi standard non polar	33892256
Glutamylserine,1TMS,isomer #5	C[Si](C)(C)N(C(=O)[C@@H](N)CCC(=O)O)[C@@H](CO)C(=O)O	2150.0	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #1	C[Si](C)(C)OC[C@H](NC(=O)[C@@H](N)CCC(=O)O[Si](C)(C)C)C(=O)O	2165.3	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #10	C[Si](C)(C)N([C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)O)[Si](C)(C)C	2375.4	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #11	C[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N([C@@H](CO)C(=O)O)[Si](C)(C)C	2224.0	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #2	C[Si](C)(C)OC(=O)CC[C@H](N)C(=O)N[C@@H](CO)C(=O)O[Si](C)(C)C	2196.0	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #3	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N[C@@H](CO)C(=O)O	2242.1	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #4	C[Si](C)(C)OC(=O)CC[C@H](N)C(=O)N([C@@H](CO)C(=O)O)[Si](C)(C)C	2140.5	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #5	C[Si](C)(C)OC[C@H](NC(=O)[C@@H](N)CCC(=O)O)C(=O)O[Si](C)(C)C	2142.9	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #6	C[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO[Si](C)(C)C)C(=O)O	2214.5	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #7	C[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@@H](N)CCC(=O)O)[Si](C)(C)C	2175.2	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #8	C[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)O[Si](C)(C)C	2229.8	Semi standard non polar	33892256
Glutamylserine,2TMS,isomer #9	C[Si](C)(C)OC(=O)[C@H](CO)N(C(=O)[C@@H](N)CCC(=O)O)[Si](C)(C)C	2156.0	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #1	C[Si](C)(C)OC[C@H](NC(=O)[C@@H](N)CCC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2178.0	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #10	C[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2335.9	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #11	C[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N([C@@H](CO[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2225.1	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #12	C[Si](C)(C)OC(=O)[C@H](CO)NC(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2364.0	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #13	C[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2215.5	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #14	C[Si](C)(C)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CO)C(=O)O	2340.0	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #2	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N[C@@H](CO[Si](C)(C)C)C(=O)O	2234.3	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #3	C[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@@H](N)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C	2175.1	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #4	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N[C@@H](CO)C(=O)O[Si](C)(C)C	2254.6	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #5	C[Si](C)(C)OC(=O)CC[C@H](N)C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2164.5	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #6	C[Si](C)(C)OC(=O)CC[C@@H](C(=O)N[C@@H](CO)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2372.0	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #7	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N([C@@H](CO)C(=O)O)[Si](C)(C)C	2200.6	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #8	C[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO[Si](C)(C)C)C(=O)O[Si](C)(C)C	2224.1	Semi standard non polar	33892256
Glutamylserine,3TMS,isomer #9	C[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@@H](N)CCC(=O)O)[Si](C)(C)C	2177.4	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #1	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N[C@@H](CO[Si](C)(C)C)C(=O)O[Si](C)(C)C	2233.6	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #1	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N[C@@H](CO[Si](C)(C)C)C(=O)O[Si](C)(C)C	2264.7	Standard non polar	33892256
Glutamylserine,4TMS,isomer #10	C[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2386.0	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #10	C[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2378.4	Standard non polar	33892256
Glutamylserine,4TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H](CO)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2362.6	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H](CO)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2364.6	Standard non polar	33892256
Glutamylserine,4TMS,isomer #2	C[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@@H](N)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C	2192.3	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #2	C[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@@H](N)CCC(=O)O[Si](C)(C)C)[Si](C)(C)C	2221.5	Standard non polar	33892256
Glutamylserine,4TMS,isomer #3	C[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2377.6	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #3	C[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2366.6	Standard non polar	33892256
Glutamylserine,4TMS,isomer #4	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N([C@@H](CO[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2229.5	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #4	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N([C@@H](CO[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2305.1	Standard non polar	33892256
Glutamylserine,4TMS,isomer #5	C[Si](C)(C)OC(=O)CC[C@@H](C(=O)N[C@@H](CO)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2394.8	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #5	C[Si](C)(C)OC(=O)CC[C@@H](C(=O)N[C@@H](CO)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2335.2	Standard non polar	33892256
Glutamylserine,4TMS,isomer #6	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2216.1	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #6	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2283.8	Standard non polar	33892256
Glutamylserine,4TMS,isomer #7	C[Si](C)(C)OC(=O)CC[C@@H](C(=O)N([C@@H](CO)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2348.3	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #7	C[Si](C)(C)OC(=O)CC[C@@H](C(=O)N([C@@H](CO)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2394.3	Standard non polar	33892256
Glutamylserine,4TMS,isomer #8	C[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2365.6	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #8	C[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2337.2	Standard non polar	33892256
Glutamylserine,4TMS,isomer #9	C[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N([C@@H](CO[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2235.7	Semi standard non polar	33892256
Glutamylserine,4TMS,isomer #9	C[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N([C@@H](CO[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2281.7	Standard non polar	33892256
Glutamylserine,5TMS,isomer #1	C[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2340.4	Semi standard non polar	33892256
Glutamylserine,5TMS,isomer #1	C[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2379.7	Standard non polar	33892256
Glutamylserine,5TMS,isomer #2	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N([C@@H](CO[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2220.0	Semi standard non polar	33892256
Glutamylserine,5TMS,isomer #2	C[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C)C(=O)N([C@@H](CO[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2323.9	Standard non polar	33892256
Glutamylserine,5TMS,isomer #3	C[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@H](CCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2400.1	Semi standard non polar	33892256
Glutamylserine,5TMS,isomer #3	C[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@H](CCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2415.9	Standard non polar	33892256
Glutamylserine,5TMS,isomer #4	C[Si](C)(C)OC(=O)CC[C@@H](C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2388.3	Semi standard non polar	33892256
Glutamylserine,5TMS,isomer #4	C[Si](C)(C)OC(=O)CC[C@@H](C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2401.8	Standard non polar	33892256
Glutamylserine,5TMS,isomer #5	C[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2407.8	Semi standard non polar	33892256
Glutamylserine,5TMS,isomer #5	C[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2393.8	Standard non polar	33892256
Glutamylserine,6TMS,isomer #1	C[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2429.2	Semi standard non polar	33892256
Glutamylserine,6TMS,isomer #1	C[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2434.6	Standard non polar	33892256
Glutamylserine,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](N)C(=O)N[C@@H](CO)C(=O)O	2451.9	Semi standard non polar	33892256
Glutamylserine,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@@H](N)CCC(=O)O)C(=O)O	2423.9	Semi standard non polar	33892256
Glutamylserine,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CO)NC(=O)[C@@H](N)CCC(=O)O	2428.9	Semi standard non polar	33892256
Glutamylserine,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)O	2481.5	Semi standard non polar	33892256
Glutamylserine,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N(C(=O)[C@@H](N)CCC(=O)O)[C@@H](CO)C(=O)O	2427.3	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@@H](N)CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	2642.0	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N([C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)O)[Si](C)(C)C(C)(C)C	2819.4	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N([C@@H](CO)C(=O)O)[Si](C)(C)C(C)(C)C	2692.9	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](N)C(=O)N[C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C	2669.3	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CO)C(=O)O	2712.7	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](N)C(=O)N([C@@H](CO)C(=O)O)[Si](C)(C)C(C)(C)C	2650.6	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@@H](N)CCC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	2617.1	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O	2661.1	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@@H](N)CCC(=O)O)[Si](C)(C)C(C)(C)C	2647.3	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C	2688.1	Semi standard non polar	33892256
Glutamylserine,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CO)N(C(=O)[C@@H](N)CCC(=O)O)[Si](C)(C)C(C)(C)C	2641.5	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@@H](N)CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2861.4	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3016.9	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N([C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2909.0	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CO)NC(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3043.5	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2913.0	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](CO)C(=O)O	3024.6	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O	2893.5	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@@H](N)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2868.2	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C	2908.1	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)CC[C@H](N)C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2855.4	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)N[C@@H](CO)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3074.4	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CO)C(=O)O)[Si](C)(C)C(C)(C)C	2925.6	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N[C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2880.9	Semi standard non polar	33892256
Glutamylserine,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@@H](N)CCC(=O)O)[Si](C)(C)C(C)(C)C	2851.0	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3100.5	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2961.6	Standard non polar	33892256
Glutamylserine,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3252.4	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3024.3	Standard non polar	33892256
Glutamylserine,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CO)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3251.2	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CO)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3024.6	Standard non polar	33892256
Glutamylserine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@@H](N)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3060.2	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@@H](N)CCC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2954.8	Standard non polar	33892256
Glutamylserine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3276.0	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3026.7	Standard non polar	33892256
Glutamylserine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3118.0	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2971.4	Standard non polar	33892256
Glutamylserine,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)N[C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3289.9	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)N[C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3016.5	Standard non polar	33892256
Glutamylserine,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3108.5	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2979.8	Standard non polar	33892256
Glutamylserine,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)N([C@@H](CO)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3272.3	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)N([C@@H](CO)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3041.7	Standard non polar	33892256
Glutamylserine,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3256.1	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2999.7	Standard non polar	33892256
Glutamylserine,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N([C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3108.5	Semi standard non polar	33892256
Glutamylserine,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O)C(=O)N([C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2958.1	Standard non polar	33892256
Glutamylserine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3480.0	Semi standard non polar	33892256
Glutamylserine,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC[C@H](NC(=O)[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3178.5	Standard non polar	33892256
Glutamylserine,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3300.8	Semi standard non polar	33892256
Glutamylserine,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N[C@@H](CCC(=O)O[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CO[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3129.3	Standard non polar	33892256
Glutamylserine,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3487.9	Semi standard non polar	33892256
Glutamylserine,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O)N(C(=O)[C@H](CCC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3207.5	Standard non polar	33892256
Glutamylserine,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3463.4	Semi standard non polar	33892256
Glutamylserine,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)CC[C@@H](C(=O)N([C@@H](CO)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3222.5	Standard non polar	33892256
Glutamylserine,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3467.8	Semi standard non polar	33892256
Glutamylserine,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3197.9	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Glutamylserine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Glutamylserine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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 - Glutamylserine 10V, Positive-QTOF	splash10-014i-1690000000-12bdd77ba3ce2078efc0	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 20V, Positive-QTOF	splash10-0f79-8920000000-2a3b52471b6b4d372e2a	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 40V, Positive-QTOF	splash10-0a4i-9100000000-fd2c7a38d03428014c2d	2019-02-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 10V, Negative-QTOF	splash10-00m0-0590000000-7e013ef10f20fd9b53f7	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 20V, Negative-QTOF	splash10-000i-2930000000-933f6a28d2a96b640aa2	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 40V, Negative-QTOF	splash10-0pbi-9600000000-15e2ba3b626d5337c4f7	2019-02-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 10V, Positive-QTOF	splash10-0a4r-3930000000-7c4331efa54cdee65d58	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 20V, Positive-QTOF	splash10-0ka9-9300000000-758e950fd86b25cb9306	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 40V, Positive-QTOF	splash10-0a4i-9000000000-f936d2b14ca4806b0ac4	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 10V, Negative-QTOF	splash10-001i-0490000000-5db40a750aeb02714042	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 20V, Negative-QTOF	splash10-0umi-6910000000-a6d043f352644254210c	2021-10-11	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Glutamylserine 40V, Negative-QTOF	splash10-00di-9100000000-43c899255fb5b075e2e5	2021-10-11	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

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

FDB111870

KNApSAcK ID

Not Available

Chemspider ID

5363587

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6995653

PDB ID

Not Available

ChEBI ID

73509

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

Kanazawa A, Kakimoto Y, Nakajima T, Sano I: Identification of gamma-glutamylserine, gamma-glutamylalanine, gamma-glutamylvaline and S-methylglutathione of bovine brain. Biochim Biophys Acta. 1965 Nov 15;111(1):90-5. [PubMed:5867340 ]

Showing metabocard for Glutamylserine (HMDB0028828)

MOL for HMDB0028828 (Glutamylserine)

3D MOL for HMDB0028828 (Glutamylserine)

3D SDF for HMDB0028828 (Glutamylserine)

3D-SDF for HMDB0028828 (Glutamylserine)

PDB for HMDB0028828 (Glutamylserine)

3D PDB for HMDB0028828 (Glutamylserine)

SMILES for HMDB0028828 (Glutamylserine)

INCHI for HMDB0028828 (Glutamylserine)

Structure for HMDB0028828 (Glutamylserine)

3D Structure for HMDB0028828 (Glutamylserine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra