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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2012-09-06 21:03:47 UTC

Update Date

2021-09-14 15:45:33 UTC

HMDB ID

HMDB0029125

Secondary Accession Numbers

HMDB29125

Metabolite Identification

Common Name

Valylglutamine

Description

Valylglutamine is a dipeptide composed of valine and glutamine. It is an incomplete breakdown product of protein digestion or protein catabolism. Dipeptides are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Some dipeptides are known to have physiological or cell-signalling 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

HMDB0029125
     RDKit          3D
Valylglutamine
 36 35  0  0  0  0  0  0  0  0999 V2000
   -3.4083   -0.6496    1.4523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3360   -0.2006    0.0125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9653    1.2357   -0.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4589   -1.1170   -0.8145 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0155   -2.4821   -0.7861 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0798   -1.2100   -0.2949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6740   -2.3318    0.1865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2341   -0.1090   -0.3253 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1762   -0.2645    0.2263 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0298    0.0949   -0.9132 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -0.0514   -0.9160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107    0.5227    0.0992 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1489    1.6762   -0.1535 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3482    0.0252    1.2650 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1758    0.6909    1.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1093    0.6784    2.1136 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    1.5611    1.7549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3656   -0.8985    1.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1040   -1.5030    1.5838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7682    0.1872    2.0928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3802   -0.2858   -0.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8916    1.8408    0.2131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6720    1.6146   -1.0325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2285    1.5477    0.7202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4161   -0.8013   -1.8671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3332   -3.1567   -1.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2578   -2.7519    0.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4665    0.8081   -0.6908 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2471   -1.2811    0.5521 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6095   -0.5154   -1.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7085    1.1495   -1.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8488    0.3962   -1.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894   -1.1533   -1.0626 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6421    2.1633    0.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2610    2.0204   -1.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0501    2.5499    1.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
  9 15  1  0
 15 16  2  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  6
  5 26  1  0
  5 27  1  0
  8 28  1  0
  9 29  1  1
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 17 36  1  0
M  END


  Mrv1652304062014252D          

 17 16  0  0  0  0            999 V2000
10023.927210024.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10024.644310024.5123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10025.358710024.1004    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10026.073110024.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10026.787610024.1004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10026.073110025.3371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10023.213810024.5123    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10022.498410024.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10021.784910024.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10022.498410023.2754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10023.213810025.3371    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10023.927210023.2754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10025.358710023.2754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10026.074910022.8619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10026.074910022.0349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10025.358710021.6214    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10026.791110021.6214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  7  1  0  0  0  0
  1 12  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  7  8  1  0  0  0  0
  7 11  1  6  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  3 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0029125

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C10H19N3O4/c1-5(2)8(12)9(15)13-6(10(16)17)3-4-7(11)14/h5-6,8H,3-4,12H2,1-2H3,(H2,11,14)(H,13,15)(H,16,17)/t6-,8-/m0/s1

> <INCHI_KEY>
XXDVDTMEVBYRPK-XPUUQOCRSA-N

> <FORMULA>
C10H19N3O4

> <MOLECULAR_WEIGHT>
245.279

> <EXACT_MASS>
245.137556104

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
24.84550380558548

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-[(2S)-2-amino-3-methylbutanamido]-4-carbamoylbutanoic acid

> <ALOGPS_LOGP>
-2.94

> <JCHEM_LOGP>
-3.6522753476248138

> <ALOGPS_LOGS>
-1.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.640319980005692

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.7173694336519865

> <JCHEM_PKA_STRONGEST_BASIC>
8.514442273244482

> <JCHEM_POLAR_SURFACE_AREA>
135.51

> <JCHEM_REFRACTIVITY>
59.40290000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.37e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S)-2-amino-3-methylbutanamido]-4-carbamoylbutanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029125
     RDKit          3D
Valylglutamine
 36 35  0  0  0  0  0  0  0  0999 V2000
   -3.4083   -0.6496    1.4523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3360   -0.2006    0.0125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9653    1.2357   -0.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4589   -1.1170   -0.8145 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0155   -2.4821   -0.7861 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0798   -1.2100   -0.2949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6740   -2.3318    0.1865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2341   -0.1090   -0.3253 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1762   -0.2645    0.2263 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0298    0.0949   -0.9132 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -0.0514   -0.9160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107    0.5227    0.0992 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1489    1.6762   -0.1535 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3482    0.0252    1.2650 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1758    0.6909    1.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1093    0.6784    2.1136 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    1.5611    1.7549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3656   -0.8985    1.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1040   -1.5030    1.5838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7682    0.1872    2.0928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3802   -0.2858   -0.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8916    1.8408    0.2131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6720    1.6146   -1.0325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2285    1.5477    0.7202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4161   -0.8013   -1.8671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3332   -3.1567   -1.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2578   -2.7519    0.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4665    0.8081   -0.6908 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2471   -1.2811    0.5521 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6095   -0.5154   -1.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7085    1.1495   -1.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8488    0.3962   -1.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894   -1.1533   -1.0626 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6421    2.1633    0.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2610    2.0204   -1.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0501    2.5499    1.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
  9 15  1  0
 15 16  2  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  6
  5 26  1  0
  5 27  1  0
  8 28  1  0
  9 29  1  1
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 17 36  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    8711.3318711.654   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0    8712.6698712.423   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0    8714.0038711.654   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8715.3368712.423   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0    8716.6708711.654   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0    8715.3368713.963   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0    8709.9998712.423   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8708.6648711.654   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8707.3328712.423   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8708.6648710.114   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0    8709.9998713.963   0.000  0.00  0.00           N+0
HETATM   12  O   UNK     0    8711.3318710.114   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0    8714.0038710.114   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8715.3408709.342   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8715.3408707.798   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0    8714.0038707.027   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0    8716.6778707.027   0.000  0.00  0.00           N+0
CONECT    1    2    7   12                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4                                                            
CONECT    7    1    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7                                                            
CONECT   12    1                                                            
CONECT   13    3   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   32    0
END

COMPND    HMDB0029125
HETATM    1  C1  UNL     1      -3.408  -0.650   1.452  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.336  -0.201   0.012  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.965   1.236  -0.042  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.459  -1.117  -0.814  1.00  0.00           C  
HETATM    5  N1  UNL     1      -3.016  -2.482  -0.786  1.00  0.00           N  
HETATM    6  C5  UNL     1      -1.080  -1.210  -0.295  1.00  0.00           C  
HETATM    7  O1  UNL     1      -0.674  -2.332   0.187  1.00  0.00           O  
HETATM    8  N2  UNL     1      -0.234  -0.109  -0.325  1.00  0.00           N  
HETATM    9  C6  UNL     1       1.176  -0.264   0.226  1.00  0.00           C  
HETATM   10  C7  UNL     1       2.030   0.095  -0.913  1.00  0.00           C  
HETATM   11  C8  UNL     1       3.479  -0.051  -0.916  1.00  0.00           C  
HETATM   12  C9  UNL     1       4.311   0.523   0.099  1.00  0.00           C  
HETATM   13  N3  UNL     1       5.149   1.676  -0.153  1.00  0.00           N  
HETATM   14  O2  UNL     1       4.348   0.025   1.265  1.00  0.00           O  
HETATM   15  C10 UNL     1       1.176   0.691   1.380  1.00  0.00           C  
HETATM   16  O3  UNL     1       0.109   0.678   2.114  1.00  0.00           O  
HETATM   17  O4  UNL     1       2.121   1.561   1.755  1.00  0.00           O  
HETATM   18  H1  UNL     1      -2.366  -0.899   1.776  1.00  0.00           H  
HETATM   19  H2  UNL     1      -4.104  -1.503   1.584  1.00  0.00           H  
HETATM   20  H3  UNL     1      -3.768   0.187   2.093  1.00  0.00           H  
HETATM   21  H4  UNL     1      -4.380  -0.286  -0.377  1.00  0.00           H  
HETATM   22  H5  UNL     1      -3.892   1.841   0.213  1.00  0.00           H  
HETATM   23  H6  UNL     1      -2.672   1.615  -1.033  1.00  0.00           H  
HETATM   24  H7  UNL     1      -2.229   1.548   0.720  1.00  0.00           H  
HETATM   25  H8  UNL     1      -2.416  -0.801  -1.867  1.00  0.00           H  
HETATM   26  H9  UNL     1      -2.333  -3.157  -1.176  1.00  0.00           H  
HETATM   27  H10 UNL     1      -3.258  -2.752   0.198  1.00  0.00           H  
HETATM   28  H11 UNL     1      -0.466   0.808  -0.691  1.00  0.00           H  
HETATM   29  H12 UNL     1       1.247  -1.281   0.552  1.00  0.00           H  
HETATM   30  H13 UNL     1       1.610  -0.515  -1.804  1.00  0.00           H  
HETATM   31  H14 UNL     1       1.709   1.150  -1.218  1.00  0.00           H  
HETATM   32  H15 UNL     1       3.849   0.396  -1.918  1.00  0.00           H  
HETATM   33  H16 UNL     1       3.789  -1.153  -1.063  1.00  0.00           H  
HETATM   34  H17 UNL     1       5.642   2.163   0.632  1.00  0.00           H  
HETATM   35  H18 UNL     1       5.261   2.020  -1.114  1.00  0.00           H  
HETATM   36  H19 UNL     1       2.050   2.550   1.866  1.00  0.00           H  
CONECT    1    2   18   19   20
CONECT    2    3    4   21
CONECT    3   22   23   24
CONECT    4    5    6   25
CONECT    5   26   27
CONECT    6    7    7    8
CONECT    8    9   28
CONECT    9   10   15   29
CONECT   10   11   30   31
CONECT   11   12   32   33
CONECT   12   13   14   14
CONECT   13   34   35
CONECT   15   16   16   17
CONECT   17   36
END

HMDB0029125
     RDKit          3D
Valylglutamine
 36 35  0  0  0  0  0  0  0  0999 V2000
   -3.4083   -0.6496    1.4523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3360   -0.2006    0.0125 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9653    1.2357   -0.0420 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4589   -1.1170   -0.8145 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0155   -2.4821   -0.7861 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0798   -1.2100   -0.2949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6740   -2.3318    0.1865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2341   -0.1090   -0.3253 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1762   -0.2645    0.2263 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0298    0.0949   -0.9132 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4793   -0.0514   -0.9160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3107    0.5227    0.0992 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1489    1.6762   -0.1535 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.3482    0.0252    1.2650 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1758    0.6909    1.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1093    0.6784    2.1136 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1211    1.5611    1.7549 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3656   -0.8985    1.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1040   -1.5030    1.5838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7682    0.1872    2.0928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3802   -0.2858   -0.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8916    1.8408    0.2131 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6720    1.6146   -1.0325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2285    1.5477    0.7202 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4161   -0.8013   -1.8671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3332   -3.1567   -1.1760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2578   -2.7519    0.1985 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4665    0.8081   -0.6908 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2471   -1.2811    0.5521 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6095   -0.5154   -1.8038 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7085    1.1495   -1.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8488    0.3962   -1.9178 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7894   -1.1533   -1.0626 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6421    2.1633    0.6315 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2610    2.0204   -1.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0501    2.5499    1.8661 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
  9 15  1  0
 15 16  2  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  3 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  6
  5 26  1  0
  5 27  1  0
  8 28  1  0
  9 29  1  1
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 17 36  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
L-Val-L-GLN	ChEBI
Valyl-glutamine	ChEBI
VQ	ChEBI
L-Valyl-L-glutamine	HMDB
N2-L-Valyl-L-glutamine	HMDB
N2-Valylglutamine	HMDB
V-Q Dipeptide	HMDB
VQ Dipeptide	HMDB
Val-GLN	HMDB
Valine glutamine dipeptide	HMDB
Valine-glutamine dipeptide	HMDB
Valylglutamine	ChEBI

Chemical Formula

C₁₀H₁₉N₃O₄

Average Molecular Weight

245.279

Monoisotopic Molecular Weight

245.137556104

IUPAC Name

(2S)-2-[(2S)-2-amino-3-methylbutanamido]-4-carbamoylbutanoic acid

Traditional Name

(2S)-2-[(2S)-2-amino-3-methylbutanamido]-4-carbamoylbutanoic acid

CAS Registry Number

42854-54-6

SMILES

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

InChI Identifier

InChI=1S/C10H19N3O4/c1-5(2)8(12)9(15)13-6(10(16)17)3-4-7(11)14/h5-6,8H,3-4,12H2,1-2H3,(H2,11,14)(H,13,15)(H,16,17)/t6-,8-/m0/s1

InChI Key

XXDVDTMEVBYRPK-XPUUQOCRSA-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
Glutamine or derivatives
N-acyl-alpha amino acid or derivatives
Valine or derivatives
N-acyl-alpha-amino acid
N-acyl-l-alpha-amino acid
Alpha-amino acid amide
N-acyl-l-glutamine
Alpha-amino acid or derivatives
Branched fatty acid
N-acyl-amine
Fatty amide
Fatty acid
Fatty acyl
Amino acid
Secondary carboxylic acid amide
Carboxylic acid salt
Amino acid or derivatives
Primary carboxylic acid amide
Carboxamide group
Carboxylic acid
Monocarboxylic acid or derivatives
Primary amine
Organic nitrogen compound
Primary aliphatic amine
Organic zwitterion
Organic salt
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Amine
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

dipeptide (CHEBI:75010 )

Ontology

Not Available

Feces (PMID: 27543620)

Source

Endogenous

Endogenous (HMDB: HMDB0029125)

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	-3.65	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	7.37 g/L	ALOGPS
logP	-2.9	ALOGPS
logP	-3.7	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	3.72	ChemAxon
pKa (Strongest Basic)	8.51	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	135.51 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	59.4 m³·mol⁻¹	ChemAxon
Polarizability	24.85 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]+	162.3	30932474
DeepCCS	[M-H]-	159.942	30932474
DeepCCS	[M-2H]-	192.829	30932474
DeepCCS	[M+Na]+	168.394	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.	1.46 minutes	32390414
Predicted by Siyang on May 30, 2022	9.6246 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	8.96 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	344.4 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	662.1 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	216.8 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	64.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	154.6 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	48.7 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	288.2 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	258.5 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	750.7 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	589.6 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	80.5 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	764.6 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	165.6 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	190.2 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	516.3 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	550.3 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	323.2 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Valylglutamine	CC(C)[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(O)=O	3009.2	Standard polar	33892256
Valylglutamine	CC(C)[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(O)=O	2020.3	Standard non polar	33892256
Valylglutamine	CC(C)[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(O)=O	2284.5	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Valylglutamine,1TMS,isomer #1	CC(C)[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C	2197.1	Semi standard non polar	33892256
Valylglutamine,1TMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)O	2226.8	Semi standard non polar	33892256
Valylglutamine,1TMS,isomer #3	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O	2269.2	Semi standard non polar	33892256
Valylglutamine,1TMS,isomer #4	CC(C)[C@H](N)C(=O)N([C@@H](CCC(N)=O)C(=O)O)[Si](C)(C)C	2191.8	Semi standard non polar	33892256
Valylglutamine,2TMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C	2261.5	Semi standard non polar	33892256
Valylglutamine,2TMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C	2156.0	Standard non polar	33892256
Valylglutamine,2TMS,isomer #2	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2262.8	Semi standard non polar	33892256
Valylglutamine,2TMS,isomer #2	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2217.5	Standard non polar	33892256
Valylglutamine,2TMS,isomer #3	CC(C)[C@H](N)C(=O)N([C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2182.9	Semi standard non polar	33892256
Valylglutamine,2TMS,isomer #3	CC(C)[C@H](N)C(=O)N([C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2171.5	Standard non polar	33892256
Valylglutamine,2TMS,isomer #4	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O	2312.4	Semi standard non polar	33892256
Valylglutamine,2TMS,isomer #4	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O	2266.2	Standard non polar	33892256
Valylglutamine,2TMS,isomer #5	CC(C)[C@@H](C(=O)N[C@@H](CCC(N)=O)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2386.0	Semi standard non polar	33892256
Valylglutamine,2TMS,isomer #5	CC(C)[C@@H](C(=O)N[C@@H](CCC(N)=O)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2234.5	Standard non polar	33892256
Valylglutamine,2TMS,isomer #6	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(N)=O)C(=O)O)[Si](C)(C)C	2245.0	Semi standard non polar	33892256
Valylglutamine,2TMS,isomer #6	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(N)=O)C(=O)O)[Si](C)(C)C	2173.5	Standard non polar	33892256
Valylglutamine,2TMS,isomer #7	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2233.4	Semi standard non polar	33892256
Valylglutamine,2TMS,isomer #7	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2273.1	Standard non polar	33892256
Valylglutamine,2TMS,isomer #8	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2382.5	Semi standard non polar	33892256
Valylglutamine,2TMS,isomer #8	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2257.1	Standard non polar	33892256
Valylglutamine,3TMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2351.2	Semi standard non polar	33892256
Valylglutamine,3TMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2284.5	Standard non polar	33892256
Valylglutamine,3TMS,isomer #10	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2314.9	Semi standard non polar	33892256
Valylglutamine,3TMS,isomer #10	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2382.4	Standard non polar	33892256
Valylglutamine,3TMS,isomer #2	CC(C)[C@@H](C(=O)N[C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2395.9	Semi standard non polar	33892256
Valylglutamine,3TMS,isomer #2	CC(C)[C@@H](C(=O)N[C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2295.1	Standard non polar	33892256
Valylglutamine,3TMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2235.9	Semi standard non polar	33892256
Valylglutamine,3TMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2206.5	Standard non polar	33892256
Valylglutamine,3TMS,isomer #4	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2234.8	Semi standard non polar	33892256
Valylglutamine,3TMS,isomer #4	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2339.2	Standard non polar	33892256
Valylglutamine,3TMS,isomer #5	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2347.4	Semi standard non polar	33892256
Valylglutamine,3TMS,isomer #5	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2314.9	Standard non polar	33892256
Valylglutamine,3TMS,isomer #6	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2418.0	Semi standard non polar	33892256
Valylglutamine,3TMS,isomer #6	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2372.5	Standard non polar	33892256
Valylglutamine,3TMS,isomer #7	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2279.3	Semi standard non polar	33892256
Valylglutamine,3TMS,isomer #7	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2315.6	Standard non polar	33892256
Valylglutamine,3TMS,isomer #8	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2390.6	Semi standard non polar	33892256
Valylglutamine,3TMS,isomer #8	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2328.8	Standard non polar	33892256
Valylglutamine,3TMS,isomer #9	CC(C)[C@@H](C(=O)N([C@@H](CCC(N)=O)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2354.5	Semi standard non polar	33892256
Valylglutamine,3TMS,isomer #9	CC(C)[C@@H](C(=O)N([C@@H](CCC(N)=O)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2328.1	Standard non polar	33892256
Valylglutamine,4TMS,isomer #1	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2406.9	Semi standard non polar	33892256
Valylglutamine,4TMS,isomer #1	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2408.8	Standard non polar	33892256
Valylglutamine,4TMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2272.7	Semi standard non polar	33892256
Valylglutamine,4TMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2334.1	Standard non polar	33892256
Valylglutamine,4TMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2385.2	Semi standard non polar	33892256
Valylglutamine,4TMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2361.8	Standard non polar	33892256
Valylglutamine,4TMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2404.5	Semi standard non polar	33892256
Valylglutamine,4TMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2372.7	Standard non polar	33892256
Valylglutamine,4TMS,isomer #5	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2320.6	Semi standard non polar	33892256
Valylglutamine,4TMS,isomer #5	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2445.5	Standard non polar	33892256
Valylglutamine,4TMS,isomer #6	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2389.1	Semi standard non polar	33892256
Valylglutamine,4TMS,isomer #6	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2457.0	Standard non polar	33892256
Valylglutamine,4TMS,isomer #7	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2525.3	Semi standard non polar	33892256
Valylglutamine,4TMS,isomer #7	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2449.4	Standard non polar	33892256
Valylglutamine,4TMS,isomer #8	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2350.4	Semi standard non polar	33892256
Valylglutamine,4TMS,isomer #8	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2397.8	Standard non polar	33892256
Valylglutamine,5TMS,isomer #1	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2421.0	Semi standard non polar	33892256
Valylglutamine,5TMS,isomer #1	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2476.9	Standard non polar	33892256
Valylglutamine,5TMS,isomer #2	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2530.4	Semi standard non polar	33892256
Valylglutamine,5TMS,isomer #2	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2493.3	Standard non polar	33892256
Valylglutamine,5TMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2362.0	Semi standard non polar	33892256
Valylglutamine,5TMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2425.0	Standard non polar	33892256
Valylglutamine,5TMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2552.1	Semi standard non polar	33892256
Valylglutamine,5TMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2542.2	Standard non polar	33892256
Valylglutamine,6TMS,isomer #1	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2608.2	Semi standard non polar	33892256
Valylglutamine,6TMS,isomer #1	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2576.6	Standard non polar	33892256
Valylglutamine,1TBDMS,isomer #1	CC(C)[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C(C)(C)C	2445.7	Semi standard non polar	33892256
Valylglutamine,1TBDMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)O	2468.3	Semi standard non polar	33892256
Valylglutamine,1TBDMS,isomer #3	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O	2520.5	Semi standard non polar	33892256
Valylglutamine,1TBDMS,isomer #4	CC(C)[C@H](N)C(=O)N([C@@H](CCC(N)=O)C(=O)O)[Si](C)(C)C(C)(C)C	2434.4	Semi standard non polar	33892256
Valylglutamine,2TBDMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C(C)(C)C	2691.6	Semi standard non polar	33892256
Valylglutamine,2TBDMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C(C)(C)C	2552.2	Standard non polar	33892256
Valylglutamine,2TBDMS,isomer #2	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2718.6	Semi standard non polar	33892256
Valylglutamine,2TBDMS,isomer #2	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2590.8	Standard non polar	33892256
Valylglutamine,2TBDMS,isomer #3	CC(C)[C@H](N)C(=O)N([C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2641.8	Semi standard non polar	33892256
Valylglutamine,2TBDMS,isomer #3	CC(C)[C@H](N)C(=O)N([C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2582.2	Standard non polar	33892256
Valylglutamine,2TBDMS,isomer #4	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O	2761.8	Semi standard non polar	33892256
Valylglutamine,2TBDMS,isomer #4	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O	2606.7	Standard non polar	33892256
Valylglutamine,2TBDMS,isomer #5	CC(C)[C@@H](C(=O)N[C@@H](CCC(N)=O)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2823.0	Semi standard non polar	33892256
Valylglutamine,2TBDMS,isomer #5	CC(C)[C@@H](C(=O)N[C@@H](CCC(N)=O)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2589.7	Standard non polar	33892256
Valylglutamine,2TBDMS,isomer #6	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(N)=O)C(=O)O)[Si](C)(C)C(C)(C)C	2699.4	Semi standard non polar	33892256
Valylglutamine,2TBDMS,isomer #6	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(N)=O)C(=O)O)[Si](C)(C)C(C)(C)C	2547.0	Standard non polar	33892256
Valylglutamine,2TBDMS,isomer #7	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2715.8	Semi standard non polar	33892256
Valylglutamine,2TBDMS,isomer #7	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2626.6	Standard non polar	33892256
Valylglutamine,2TBDMS,isomer #8	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2816.5	Semi standard non polar	33892256
Valylglutamine,2TBDMS,isomer #8	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2629.7	Standard non polar	33892256
Valylglutamine,3TBDMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2965.1	Semi standard non polar	33892256
Valylglutamine,3TBDMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2793.4	Standard non polar	33892256
Valylglutamine,3TBDMS,isomer #10	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=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	2985.6	Semi standard non polar	33892256
Valylglutamine,3TBDMS,isomer #10	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=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	2906.9	Standard non polar	33892256
Valylglutamine,3TBDMS,isomer #2	CC(C)[C@@H](C(=O)N[C@@H](CCC(N)=O)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	3050.0	Semi standard non polar	33892256
Valylglutamine,3TBDMS,isomer #2	CC(C)[C@@H](C(=O)N[C@@H](CCC(N)=O)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	2807.0	Standard non polar	33892256
Valylglutamine,3TBDMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2893.6	Semi standard non polar	33892256
Valylglutamine,3TBDMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(N)=O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2758.0	Standard non polar	33892256
Valylglutamine,3TBDMS,isomer #4	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2892.2	Semi standard non polar	33892256
Valylglutamine,3TBDMS,isomer #4	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2869.6	Standard non polar	33892256
Valylglutamine,3TBDMS,isomer #5	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=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	3004.5	Semi standard non polar	33892256
Valylglutamine,3TBDMS,isomer #5	CC(C)[C@H](N)C(=O)N[C@@H](CCC(=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	2866.8	Standard non polar	33892256
Valylglutamine,3TBDMS,isomer #6	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3119.7	Semi standard non polar	33892256
Valylglutamine,3TBDMS,isomer #6	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2844.1	Standard non polar	33892256
Valylglutamine,3TBDMS,isomer #7	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2949.3	Semi standard non polar	33892256
Valylglutamine,3TBDMS,isomer #7	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2787.6	Standard non polar	33892256
Valylglutamine,3TBDMS,isomer #8	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3067.5	Semi standard non polar	33892256
Valylglutamine,3TBDMS,isomer #8	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2848.3	Standard non polar	33892256
Valylglutamine,3TBDMS,isomer #9	CC(C)[C@@H](C(=O)N([C@@H](CCC(N)=O)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	3026.8	Semi standard non polar	33892256
Valylglutamine,3TBDMS,isomer #9	CC(C)[C@@H](C(=O)N([C@@H](CCC(N)=O)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	2827.0	Standard non polar	33892256
Valylglutamine,4TBDMS,isomer #1	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)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	3321.5	Semi standard non polar	33892256
Valylglutamine,4TBDMS,isomer #1	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)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	3039.6	Standard non polar	33892256
Valylglutamine,4TBDMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3121.9	Semi standard non polar	33892256
Valylglutamine,4TBDMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2987.7	Standard non polar	33892256
Valylglutamine,4TBDMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(=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	3249.7	Semi standard non polar	33892256
Valylglutamine,4TBDMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCC(=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	3029.8	Standard non polar	33892256
Valylglutamine,4TBDMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CCC(N)=O)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	3247.6	Semi standard non polar	33892256
Valylglutamine,4TBDMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CCC(N)=O)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	3050.1	Standard non polar	33892256
Valylglutamine,4TBDMS,isomer #5	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=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)[Si](C)(C)C(C)(C)C	3174.9	Semi standard non polar	33892256
Valylglutamine,4TBDMS,isomer #5	CC(C)[C@H](N)C(=O)N([C@@H](CCC(=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)[Si](C)(C)C(C)(C)C	3128.1	Standard non polar	33892256
Valylglutamine,4TBDMS,isomer #6	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)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	3285.7	Semi standard non polar	33892256
Valylglutamine,4TBDMS,isomer #6	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)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	3066.2	Standard non polar	33892256
Valylglutamine,4TBDMS,isomer #7	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3411.4	Semi standard non polar	33892256
Valylglutamine,4TBDMS,isomer #7	CC(C)[C@@H](C(=O)N[C@@H](CCC(=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3091.4	Standard non polar	33892256
Valylglutamine,4TBDMS,isomer #8	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(=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	3240.6	Semi standard non polar	33892256
Valylglutamine,4TBDMS,isomer #8	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(=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	3037.9	Standard non polar	33892256
Valylglutamine,5TBDMS,isomer #1	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)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	3476.1	Semi standard non polar	33892256
Valylglutamine,5TBDMS,isomer #1	CC(C)[C@@H](C(=O)N([C@@H](CCC(=O)N[Si](C)(C)C(C)(C)C)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	3268.9	Standard non polar	33892256
Valylglutamine,5TBDMS,isomer #2	CC(C)[C@@H](C(=O)N[C@@H](CCC(=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)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3609.1	Semi standard non polar	33892256
Valylglutamine,5TBDMS,isomer #2	CC(C)[C@@H](C(=O)N[C@@H](CCC(=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)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3279.8	Standard non polar	33892256
Valylglutamine,5TBDMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(=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)[Si](C)(C)C(C)(C)C	3406.2	Semi standard non polar	33892256
Valylglutamine,5TBDMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCC(=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)[Si](C)(C)C(C)(C)C	3236.1	Standard non polar	33892256
Valylglutamine,5TBDMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CCC(=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)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3578.2	Semi standard non polar	33892256
Valylglutamine,5TBDMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CCC(=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)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3315.2	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Valylglutamine 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 - Valylglutamine 10V, Negative-QTOF	splash10-004j-0920000000-baece3a2ee7786f786b6	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Valylglutamine 20V, Negative-QTOF	splash10-004m-2910000000-5edcb182c526bd0cd683	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Valylglutamine 40V, Negative-QTOF	splash10-0006-9400000000-be93387653c6d42d587e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Valylglutamine 10V, Positive-QTOF	splash10-0002-0390000000-908438ac65e86d819911	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Valylglutamine 20V, Positive-QTOF	splash10-00ea-9820000000-6e14b89c6983caa6007f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Valylglutamine 40V, Positive-QTOF	splash10-0089-9100000000-9fbe1c4c86a1c93975b7	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	27543620	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	25037050	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	29808030	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal cancer	27015276	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal cancer	25037050	details

Associated Disorders and Diseases

Disease References

Colorectal cancer

Sinha R, Ahn J, Sampson JN, Shi J, Yu G, Xiong X, Hayes RB, Goedert JJ: Fecal Microbiota, Fecal Metabolome, and Colorectal Cancer Interrelations. PLoS One. 2016 Mar 25;11(3):e0152126. doi: 10.1371/journal.pone.0152126. eCollection 2016. [PubMed:27015276 ]
Goedert JJ, Sampson JN, Moore SC, Xiao Q, Xiong X, Hayes RB, Ahn J, Shi J, Sinha R: Fecal metabolomics: assay performance and association with colorectal cancer. Carcinogenesis. 2014 Sep;35(9):2089-96. doi: 10.1093/carcin/bgu131. Epub 2014 Jul 18. [PubMed:25037050 ]

Associated OMIM IDs

114500 (Colorectal cancer)

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB112127

KNApSAcK ID

Not Available

Chemspider ID

5379066

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

7016044

PDB ID

Not Available

ChEBI ID

75010

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

Not Available

Showing metabocard for Valylglutamine (HMDB0029125)

MOL for HMDB0029125 (Valylglutamine)

3D MOL for HMDB0029125 (Valylglutamine)

3D SDF for HMDB0029125 (Valylglutamine)

3D-SDF for HMDB0029125 (Valylglutamine)

PDB for HMDB0029125 (Valylglutamine)

3D PDB for HMDB0029125 (Valylglutamine)

SMILES for HMDB0029125 (Valylglutamine)

INCHI for HMDB0029125 (Valylglutamine)

Structure for HMDB0029125 (Valylglutamine)

3D Structure for HMDB0029125 (Valylglutamine)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra