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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

HMDB0029123

Secondary Accession Numbers

HMDB29123

Metabolite Identification

Common Name

Valylaspartic acid

Description

Valylaspartic acid is a dipeptide composed of valine and aspartic acid. 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

HMDB0029123
     RDKit          3D
Valylaspartic acid
 32 31  0  0  0  0  0  0  0  0999 V2000
   -3.8765    0.8942   -1.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4290    1.1047   -0.7846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3181    1.1852    0.7333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6623   -0.1256   -1.2666 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1869   -1.2676   -0.5887 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2377    0.1183   -1.0157 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3748    1.0893   -1.5589 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4926   -0.7219   -0.1614 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8968   -0.4974    0.0976 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1401   -0.1073    1.5380 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5324    0.1400    1.8858 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3396   -0.7652    2.2103 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0133    1.4423    1.8631 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -1.6737   -0.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0899   -2.6632   -0.8323 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0353   -1.7103   -0.2072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5366    1.3192   -0.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0938   -0.1863   -1.1427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1681    1.3969   -2.0688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9986    2.0130   -1.2230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2624    1.2607    1.0624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8154    0.3505    1.2345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8532    2.1155    1.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8976   -0.1969   -2.3610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2139   -2.1381   -1.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9993   -1.3252    0.4141 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0210   -1.5227    0.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1839    0.4256   -0.4887 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7437   -0.9231    2.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5400    0.8030    1.7599 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8137    1.6194    1.2510 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6658   -1.4534   -0.9764 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  2  0
 11 13  1  0
  9 14  1  0
 14 15  2  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  6
  5 25  1  0
  5 26  1  0
  8 27  1  0
  9 28  1  6
 10 29  1  0
 10 30  1  0
 13 31  1  0
 16 32  1  0
M  END

  Mrv1652304062014242D          

 16 15  0  0  0  0            999 V2000
10047.066710047.2385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10047.783810047.6503    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10048.498110047.2385    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10049.212410047.6503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.926910047.2385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10049.212410048.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10046.353410047.6503    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10045.638010047.2385    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10044.924610047.6503    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10045.638010046.4135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10046.353410048.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10047.066710046.4135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10048.498110046.4135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.214210046.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.930410046.4135    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10049.214210045.1731    0.0000 O   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 16  2  0  0  0  0
 14 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0029123

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C9H16N2O5/c1-4(2)7(10)8(14)11-5(9(15)16)3-6(12)13/h4-5,7H,3,10H2,1-2H3,(H,11,14)(H,12,13)(H,15,16)/t5-,7-/m0/s1

> <INCHI_KEY>
OBTCMSPFOITUIJ-FSPLSTOPSA-N

> <FORMULA>
C9H16N2O5

> <MOLECULAR_WEIGHT>
232.236

> <EXACT_MASS>
232.105921623

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
22.22723264559064

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-3.02

> <JCHEM_LOGP>
-3.237273690588061

> <ALOGPS_LOGS>
-1.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
5.3607668765754575

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.4720943036239142

> <JCHEM_PKA_STRONGEST_BASIC>
8.514729778845123

> <JCHEM_POLAR_SURFACE_AREA>
129.72

> <JCHEM_REFRACTIVITY>
52.825700000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.72e+00 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029123
     RDKit          3D
Valylaspartic acid
 32 31  0  0  0  0  0  0  0  0999 V2000
   -3.8765    0.8942   -1.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4290    1.1047   -0.7846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3181    1.1852    0.7333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6623   -0.1256   -1.2666 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1869   -1.2676   -0.5887 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2377    0.1183   -1.0157 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3748    1.0893   -1.5589 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4926   -0.7219   -0.1614 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8968   -0.4974    0.0976 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1401   -0.1073    1.5380 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5324    0.1400    1.8858 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3396   -0.7652    2.2103 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0133    1.4423    1.8631 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -1.6737   -0.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0899   -2.6632   -0.8323 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0353   -1.7103   -0.2072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5366    1.3192   -0.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0938   -0.1863   -1.1427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1681    1.3969   -2.0688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9986    2.0130   -1.2230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2624    1.2607    1.0624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8154    0.3505    1.2345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8532    2.1155    1.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8976   -0.1969   -2.3610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2139   -2.1381   -1.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9993   -1.3252    0.4141 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0210   -1.5227    0.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1839    0.4256   -0.4887 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7437   -0.9231    2.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5400    0.8030    1.7599 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8137    1.6194    1.2510 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6658   -1.4534   -0.9764 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  2  0
 11 13  1  0
  9 14  1  0
 14 15  2  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  6
  5 25  1  0
  5 26  1  0
  8 27  1  0
  9 28  1  6
 10 29  1  0
 10 30  1  0
 13 31  1  0
 16 32  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    8754.5258754.845   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0    8755.8638755.614   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0    8757.1968754.845   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8758.5308755.614   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0    8759.8648754.845   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0    8758.5308757.153   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0    8753.1938755.614   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8751.8588754.845   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8750.5268755.614   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8751.8588753.305   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0    8753.1938757.153   0.000  0.00  0.00           N+0
HETATM   12  O   UNK     0    8754.5258753.305   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0    8757.1968753.305   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8758.5338752.533   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0    8759.8708753.305   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0    8758.5338750.990   0.000  0.00  0.00           O+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   16   15                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   30    0
END

COMPND    HMDB0029123
HETATM    1  C1  UNL     1      -3.876   0.894  -1.124  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.429   1.105  -0.785  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.318   1.185   0.733  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.662  -0.126  -1.267  1.00  0.00           C  
HETATM    5  N1  UNL     1      -2.187  -1.268  -0.589  1.00  0.00           N  
HETATM    6  C5  UNL     1      -0.238   0.118  -1.016  1.00  0.00           C  
HETATM    7  O1  UNL     1       0.375   1.089  -1.559  1.00  0.00           O  
HETATM    8  N2  UNL     1       0.493  -0.722  -0.161  1.00  0.00           N  
HETATM    9  C6  UNL     1       1.897  -0.497   0.098  1.00  0.00           C  
HETATM   10  C7  UNL     1       2.140  -0.107   1.538  1.00  0.00           C  
HETATM   11  C8  UNL     1       3.532   0.140   1.886  1.00  0.00           C  
HETATM   12  O2  UNL     1       4.340  -0.765   2.210  1.00  0.00           O  
HETATM   13  O3  UNL     1       4.013   1.442   1.863  1.00  0.00           O  
HETATM   14  C9  UNL     1       2.667  -1.674  -0.337  1.00  0.00           C  
HETATM   15  O4  UNL     1       2.090  -2.663  -0.832  1.00  0.00           O  
HETATM   16  O5  UNL     1       4.035  -1.710  -0.207  1.00  0.00           O  
HETATM   17  H1  UNL     1      -4.537   1.319  -0.322  1.00  0.00           H  
HETATM   18  H2  UNL     1      -4.094  -0.186  -1.143  1.00  0.00           H  
HETATM   19  H3  UNL     1      -4.168   1.397  -2.069  1.00  0.00           H  
HETATM   20  H4  UNL     1      -1.999   2.013  -1.223  1.00  0.00           H  
HETATM   21  H5  UNL     1      -1.262   1.261   1.062  1.00  0.00           H  
HETATM   22  H6  UNL     1      -2.815   0.350   1.235  1.00  0.00           H  
HETATM   23  H7  UNL     1      -2.853   2.115   1.049  1.00  0.00           H  
HETATM   24  H8  UNL     1      -1.898  -0.197  -2.361  1.00  0.00           H  
HETATM   25  H9  UNL     1      -2.214  -2.138  -1.125  1.00  0.00           H  
HETATM   26  H10 UNL     1      -1.999  -1.325   0.414  1.00  0.00           H  
HETATM   27  H11 UNL     1       0.021  -1.523   0.297  1.00  0.00           H  
HETATM   28  H12 UNL     1       2.184   0.426  -0.489  1.00  0.00           H  
HETATM   29  H13 UNL     1       1.744  -0.923   2.187  1.00  0.00           H  
HETATM   30  H14 UNL     1       1.540   0.803   1.760  1.00  0.00           H  
HETATM   31  H15 UNL     1       4.814   1.619   1.251  1.00  0.00           H  
HETATM   32  H16 UNL     1       4.666  -1.453  -0.976  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    4   20
CONECT    3   21   22   23
CONECT    4    5    6   24
CONECT    5   25   26
CONECT    6    7    7    8
CONECT    8    9   27
CONECT    9   10   14   28
CONECT   10   11   29   30
CONECT   11   12   12   13
CONECT   13   31
CONECT   14   15   15   16
CONECT   16   32
END

HMDB0029123
     RDKit          3D
Valylaspartic acid
 32 31  0  0  0  0  0  0  0  0999 V2000
   -3.8765    0.8942   -1.1237 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4290    1.1047   -0.7846 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3181    1.1852    0.7333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6623   -0.1256   -1.2666 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1869   -1.2676   -0.5887 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2377    0.1183   -1.0157 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3748    1.0893   -1.5589 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4926   -0.7219   -0.1614 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.8968   -0.4974    0.0976 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1401   -0.1073    1.5380 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5324    0.1400    1.8858 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3396   -0.7652    2.2103 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0133    1.4423    1.8631 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -1.6737   -0.3367 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0899   -2.6632   -0.8323 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0353   -1.7103   -0.2072 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5366    1.3192   -0.3219 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0938   -0.1863   -1.1427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1681    1.3969   -2.0688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9986    2.0130   -1.2230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2624    1.2607    1.0624 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8154    0.3505    1.2345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8532    2.1155    1.0487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8976   -0.1969   -2.3610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2139   -2.1381   -1.1247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9993   -1.3252    0.4141 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0210   -1.5227    0.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1839    0.4256   -0.4887 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7437   -0.9231    2.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5400    0.8030    1.7599 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8137    1.6194    1.2510 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6658   -1.4534   -0.9764 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  2  0
 11 13  1  0
  9 14  1  0
 14 15  2  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  6
  5 25  1  0
  5 26  1  0
  8 27  1  0
  9 28  1  6
 10 29  1  0
 10 30  1  0
 13 31  1  0
 16 32  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
L-Val-L-asp	ChEBI
Valyl-aspartate	ChEBI
VD	ChEBI
Valyl-aspartic acid	Generator
Valylaspartate	Generator
L-Valyl-L-aspartate	HMDB
L-Valyl-L-aspartic acid	HMDB
N-L-Valyl-L-aspartate	HMDB
N-L-Valyl-L-aspartic acid	HMDB
N-Valylaspartate	HMDB
N-Valylaspartic acid	HMDB
V-D Dipeptide	HMDB
VD Dipeptide	HMDB
Val-asp	HMDB
Valine aspartate dipeptide	HMDB
Valine aspartic acid dipeptide	HMDB
Valine-aspartate dipeptide	HMDB
Valine-aspartic acid dipeptide	HMDB
Valylaspartic acid	HMDB

Chemical Formula

C₉H₁₆N₂O₅

Average Molecular Weight

232.236

Monoisotopic Molecular Weight

232.105921623

IUPAC Name

(2S)-2-[(2S)-2-amino-3-methylbutanamido]butanedioic acid

Traditional Name

(2S)-2-[(2S)-2-amino-3-methylbutanamido]butanedioic acid

CAS Registry Number

20556-16-5

SMILES

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

InChI Identifier

InChI=1S/C9H16N2O5/c1-4(2)7(10)8(14)11-5(9(15)16)3-6(12)13/h4-5,7H,3,10H2,1-2H3,(H,11,14)(H,12,13)(H,15,16)/t5-,7-/m0/s1

InChI Key

OBTCMSPFOITUIJ-FSPLSTOPSA-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
Aspartic acid or derivatives
N-acyl-alpha-amino acid
Valine or derivatives
N-acyl-alpha amino acid or derivatives
Acyl-homoserine
N-acyl-l-alpha-amino acid
Acyl-l-homoserine
Alpha-amino acid amide
Alpha-amino acid or derivatives
Branched fatty acid
N-acyl-amine
Fatty amide
Dicarboxylic acid or derivatives
Fatty acyl
Fatty acid
Secondary carboxylic acid amide
Carboxamide group
Amino acid or derivatives
Amino acid
Carboxylic acid
Organic nitrogen compound
Primary aliphatic amine
Organonitrogen compound
Organooxygen compound
Primary amine
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Amine
Organic oxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

dipeptide (CHEBI:75009 )

Ontology

Not Available

Feces (PMID: 25037050)

Source

Endogenous

Endogenous (HMDB: HMDB0029123)

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	-3.47	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	9.72 g/L	ALOGPS
logP	-3	ALOGPS
logP	-3.2	ChemAxon
logS	-1.4	ALOGPS
pKa (Strongest Acidic)	3.47	ChemAxon
pKa (Strongest Basic)	8.51	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	129.72 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	52.83 m³·mol⁻¹	ChemAxon
Polarizability	22.23 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]+	156.521	30932474
DeepCCS	[M-H]-	154.163	30932474
DeepCCS	[M-2H]-	187.087	30932474
DeepCCS	[M+Na]+	162.614	30932474

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Valylaspartic acid	CC(C)[C@H](N)C(=O)N[C@@H](CC(O)=O)C(O)=O	3067.7	Standard polar	33892256
Valylaspartic acid	CC(C)[C@H](N)C(=O)N[C@@H](CC(O)=O)C(O)=O	1867.0	Standard non polar	33892256
Valylaspartic acid	CC(C)[C@H](N)C(=O)N[C@@H](CC(O)=O)C(O)=O	2020.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Valylaspartic acid,1TMS,isomer #1	CC(C)[C@H](N)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O	1989.7	Semi standard non polar	33892256
Valylaspartic acid,1TMS,isomer #2	CC(C)[C@H](N)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C	1950.6	Semi standard non polar	33892256
Valylaspartic acid,1TMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)O	1977.0	Semi standard non polar	33892256
Valylaspartic acid,1TMS,isomer #4	CC(C)[C@H](N)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	1979.6	Semi standard non polar	33892256
Valylaspartic acid,2TMS,isomer #1	CC(C)[C@H](N)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	1987.9	Semi standard non polar	33892256
Valylaspartic acid,2TMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O	2034.5	Semi standard non polar	33892256
Valylaspartic acid,2TMS,isomer #3	CC(C)[C@H](N)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	1977.9	Semi standard non polar	33892256
Valylaspartic acid,2TMS,isomer #4	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C	2019.3	Semi standard non polar	33892256
Valylaspartic acid,2TMS,isomer #5	CC(C)[C@H](N)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	1985.0	Semi standard non polar	33892256
Valylaspartic acid,2TMS,isomer #6	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2137.7	Semi standard non polar	33892256
Valylaspartic acid,2TMS,isomer #7	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2038.9	Semi standard non polar	33892256
Valylaspartic acid,3TMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2060.0	Semi standard non polar	33892256
Valylaspartic acid,3TMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2047.2	Standard non polar	33892256
Valylaspartic acid,3TMS,isomer #2	CC(C)[C@H](N)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2009.2	Semi standard non polar	33892256
Valylaspartic acid,3TMS,isomer #2	CC(C)[C@H](N)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2119.6	Standard non polar	33892256
Valylaspartic acid,3TMS,isomer #3	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2163.9	Semi standard non polar	33892256
Valylaspartic acid,3TMS,isomer #3	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2132.2	Standard non polar	33892256
Valylaspartic acid,3TMS,isomer #4	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2025.1	Semi standard non polar	33892256
Valylaspartic acid,3TMS,isomer #4	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2090.6	Standard non polar	33892256
Valylaspartic acid,3TMS,isomer #5	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2160.7	Semi standard non polar	33892256
Valylaspartic acid,3TMS,isomer #5	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2133.9	Standard non polar	33892256
Valylaspartic acid,3TMS,isomer #6	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2052.9	Semi standard non polar	33892256
Valylaspartic acid,3TMS,isomer #6	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2062.2	Standard non polar	33892256
Valylaspartic acid,3TMS,isomer #7	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2162.2	Semi standard non polar	33892256
Valylaspartic acid,3TMS,isomer #7	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2166.3	Standard non polar	33892256
Valylaspartic acid,4TMS,isomer #1	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2173.5	Semi standard non polar	33892256
Valylaspartic acid,4TMS,isomer #1	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2178.8	Standard non polar	33892256
Valylaspartic acid,4TMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2057.1	Semi standard non polar	33892256
Valylaspartic acid,4TMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2113.9	Standard non polar	33892256
Valylaspartic acid,4TMS,isomer #3	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2182.7	Semi standard non polar	33892256
Valylaspartic acid,4TMS,isomer #3	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2234.4	Standard non polar	33892256
Valylaspartic acid,4TMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2220.1	Semi standard non polar	33892256
Valylaspartic acid,4TMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2210.9	Standard non polar	33892256
Valylaspartic acid,5TMS,isomer #1	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2257.8	Semi standard non polar	33892256
Valylaspartic acid,5TMS,isomer #1	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2262.2	Standard non polar	33892256
Valylaspartic acid,1TBDMS,isomer #1	CC(C)[C@H](N)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	2222.8	Semi standard non polar	33892256
Valylaspartic acid,1TBDMS,isomer #2	CC(C)[C@H](N)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	2182.2	Semi standard non polar	33892256
Valylaspartic acid,1TBDMS,isomer #3	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)O	2203.4	Semi standard non polar	33892256
Valylaspartic acid,1TBDMS,isomer #4	CC(C)[C@H](N)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	2223.0	Semi standard non polar	33892256
Valylaspartic acid,2TBDMS,isomer #1	CC(C)[C@H](N)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2439.9	Semi standard non polar	33892256
Valylaspartic acid,2TBDMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	2475.5	Semi standard non polar	33892256
Valylaspartic acid,2TBDMS,isomer #3	CC(C)[C@H](N)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2453.0	Semi standard non polar	33892256
Valylaspartic acid,2TBDMS,isomer #4	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	2445.4	Semi standard non polar	33892256
Valylaspartic acid,2TBDMS,isomer #5	CC(C)[C@H](N)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2436.0	Semi standard non polar	33892256
Valylaspartic acid,2TBDMS,isomer #6	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2582.5	Semi standard non polar	33892256
Valylaspartic acid,2TBDMS,isomer #7	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	2474.1	Semi standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2691.2	Semi standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #1	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2595.9	Standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #2	CC(C)[C@H](N)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2656.3	Semi standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #2	CC(C)[C@H](N)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2685.7	Standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #3	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O[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	2859.3	Semi standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #3	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O[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	2651.2	Standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #4	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2713.8	Semi standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #4	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2604.6	Standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #5	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)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	2835.4	Semi standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #5	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)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	2628.8	Standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #6	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2706.7	Semi standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #6	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2585.1	Standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #7	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)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	2831.7	Semi standard non polar	33892256
Valylaspartic acid,3TBDMS,isomer #7	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)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	2652.6	Standard non polar	33892256
Valylaspartic acid,4TBDMS,isomer #1	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O[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	3072.3	Semi standard non polar	33892256
Valylaspartic acid,4TBDMS,isomer #1	CC(C)[C@@H](C(=O)N[C@@H](CC(=O)O[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	2850.8	Standard non polar	33892256
Valylaspartic acid,4TBDMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2899.6	Semi standard non polar	33892256
Valylaspartic acid,4TBDMS,isomer #2	CC(C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2813.3	Standard non polar	33892256
Valylaspartic acid,4TBDMS,isomer #3	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O[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	3067.9	Semi standard non polar	33892256
Valylaspartic acid,4TBDMS,isomer #3	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O[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	2891.3	Standard non polar	33892256
Valylaspartic acid,4TBDMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)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	3058.1	Semi standard non polar	33892256
Valylaspartic acid,4TBDMS,isomer #4	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)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	2872.7	Standard non polar	33892256
Valylaspartic acid,5TBDMS,isomer #1	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3302.5	Semi standard non polar	33892256
Valylaspartic acid,5TBDMS,isomer #1	CC(C)[C@@H](C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3103.6	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Valylaspartic acid GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Valylaspartic acid 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 - Valylaspartic acid 10V, Negative-QTOF	splash10-01q9-4980000000-5c705dc66a76bcea9f7d	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Valylaspartic acid 20V, Negative-QTOF	splash10-000i-9500000000-9ee65587f16d24e95224	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Valylaspartic acid 40V, Negative-QTOF	splash10-000f-9200000000-07f773f77ffd7d72c122	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Valylaspartic acid 10V, Positive-QTOF	splash10-001i-2690000000-33109a79a58dd4ff52b3	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Valylaspartic acid 20V, Positive-QTOF	splash10-01b9-4900000000-5e7666ae99f6c8ef887f	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Valylaspartic acid 40V, Positive-QTOF	splash10-05fu-9000000000-e3f3e0404b57ed936753	2021-09-25	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	25037050	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	27275383	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

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 ]
Brown DG, Rao S, Weir TL, O'Malia J, Bazan M, Brown RJ, Ryan EP: Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool. Cancer Metab. 2016 Jun 6;4:11. doi: 10.1186/s40170-016-0151-y. eCollection 2016. [PubMed:27275383 ]
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 ]

Associated OMIM IDs

114500 (Colorectal cancer)

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB112125

KNApSAcK ID

Not Available

Chemspider ID

5373188

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

7009608

PDB ID

Not Available

ChEBI ID

75009

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 Valylaspartic acid (HMDB0029123)

MOL for HMDB0029123 (Valylaspartic acid)

3D MOL for HMDB0029123 (Valylaspartic acid)

3D SDF for HMDB0029123 (Valylaspartic acid)

3D-SDF for HMDB0029123 (Valylaspartic acid)

PDB for HMDB0029123 (Valylaspartic acid)

3D PDB for HMDB0029123 (Valylaspartic acid)

SMILES for HMDB0029123 (Valylaspartic acid)

INCHI for HMDB0029123 (Valylaspartic acid)

Structure for HMDB0029123 (Valylaspartic acid)

3D Structure for HMDB0029123 (Valylaspartic acid)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra