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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 21:03:31 UTC

Update Date

2021-09-14 15:19:02 UTC

HMDB ID

HMDB0029057

Secondary Accession Numbers

HMDB29057

Metabolite Identification

Common Name

Threonylaspartic acid

Description

Threonylaspartic acid is a dipeptide composed of threonine 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

HMDB0029057
     RDKit          3D
Threonylaspartic acid
 30 29  0  0  0  0  0  0  0  0999 V2000
   -3.5487    1.3449    0.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3302    0.5275   -0.1542 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6016   -0.2424   -1.2889 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1615    1.4467   -0.4768 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4812    2.3203   -1.5882 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0079    0.5911   -0.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5267    0.6986   -1.9734 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961   -0.3577    0.0906 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6295   -1.2122   -0.2421 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6976   -1.0439    0.8148 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1745    0.3430    0.9067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7036    1.2307    0.1620 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1524    0.6925    1.8178 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1865   -2.6395   -0.1968 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0103   -2.9724    0.0899 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1000   -3.6430   -0.4801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1888    2.1892    0.8742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2093    0.7257    0.8682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0438    1.7686   -0.6477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0589   -0.0954    0.7062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1074   -1.0397   -0.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9143    2.0528    0.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7654    3.2408   -1.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3147    1.9327   -2.1153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0511   -0.4467    1.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0099   -0.9971   -1.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5518   -1.7304    0.6323 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2382   -1.3049    1.8048 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8757    0.9975    2.7471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3297   -4.3772    0.1668 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  1
  3 21  1  0
  4 22  1  1
  5 23  1  0
  5 24  1  0
  8 25  1  0
  9 26  1  6
 10 27  1  0
 10 28  1  0
 13 29  1  0
 16 30  1  0
M  END


  Mrv1652304062014142D          

 16 15  0  0  0  0            999 V2000
10047.066710047.2380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10047.783810047.6498    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10048.498110047.2380    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10049.212410047.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.926910047.2380    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10049.212410048.4745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10046.353410047.6498    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10045.638010047.2380    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10044.924610047.6498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10045.638010046.4130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10046.353410048.4745    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10047.066710046.4130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10048.498110046.4130    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.214110045.9995    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.930310046.4130    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10049.214110045.1726    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  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
  3 13  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0029057

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C8H14N2O6/c1-3(11)6(9)7(14)10-4(8(15)16)2-5(12)13/h3-4,6,11H,2,9H2,1H3,(H,10,14)(H,12,13)(H,15,16)/t3-,4+,6+/m1/s1

> <INCHI_KEY>
IOWJRKAVLALBQB-IWGUZYHVSA-N

> <FORMULA>
C8H14N2O6

> <MOLECULAR_WEIGHT>
234.208

> <EXACT_MASS>
234.085186179

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
21.059268574003887

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-[(2S,3R)-2-amino-3-hydroxybutanamido]butanedioic acid

> <ALOGPS_LOGP>
-3.42

> <JCHEM_LOGP>
-4.732920778864015

> <ALOGPS_LOGS>
-0.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
5.138292173015183

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.253675803787258

> <JCHEM_PKA_STRONGEST_BASIC>
7.9228550636492265

> <JCHEM_POLAR_SURFACE_AREA>
149.95

> <JCHEM_REFRACTIVITY>
49.79260000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.63e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S,3R)-2-amino-3-hydroxybutanamido]butanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029057
     RDKit          3D
Threonylaspartic acid
 30 29  0  0  0  0  0  0  0  0999 V2000
   -3.5487    1.3449    0.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3302    0.5275   -0.1542 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6016   -0.2424   -1.2889 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1615    1.4467   -0.4768 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4812    2.3203   -1.5882 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0079    0.5911   -0.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5267    0.6986   -1.9734 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961   -0.3577    0.0906 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6295   -1.2122   -0.2421 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6976   -1.0439    0.8148 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1745    0.3430    0.9067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7036    1.2307    0.1620 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1524    0.6925    1.8178 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1865   -2.6395   -0.1968 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0103   -2.9724    0.0899 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1000   -3.6430   -0.4801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1888    2.1892    0.8742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2093    0.7257    0.8682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0438    1.7686   -0.6477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0589   -0.0954    0.7062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1074   -1.0397   -0.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9143    2.0528    0.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7654    3.2408   -1.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3147    1.9327   -2.1153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0511   -0.4467    1.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0099   -0.9971   -1.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5518   -1.7304    0.6323 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2382   -1.3049    1.8048 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8757    0.9975    2.7471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3297   -4.3772    0.1668 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  1
  3 21  1  0
  4 22  1  1
  5 23  1  0
  5 24  1  0
  8 25  1  0
  9 26  1  6
 10 27  1  0
 10 28  1  0
 13 29  1  0
 16 30  1  0
M  END

HEADER    PROTEIN                                 06-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-APR-20         0                                  
HETATM    1  C   UNK     0    8754.5258754.844   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0    8755.8638755.613   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0    8757.1968754.844   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8758.5308755.613   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0    8759.8648754.844   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0    8758.5308757.152   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0    8753.1938755.613   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8751.8588754.844   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8750.5268755.613   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0    8751.8588753.304   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0    8753.1938757.152   0.000  0.00  0.00           N+0
HETATM   12  O   UNK     0    8754.5258753.304   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0    8757.1968753.304   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8758.5338752.532   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0    8759.8708753.304   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0    8758.5338750.989   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   14    3                                                       
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    HMDB0029057
HETATM    1  C1  UNL     1      -3.549   1.345   0.251  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.330   0.527  -0.154  1.00  0.00           C  
HETATM    3  O1  UNL     1      -2.602  -0.242  -1.289  1.00  0.00           O  
HETATM    4  C3  UNL     1      -1.161   1.447  -0.477  1.00  0.00           C  
HETATM    5  N1  UNL     1      -1.481   2.320  -1.588  1.00  0.00           N  
HETATM    6  C4  UNL     1      -0.008   0.591  -0.844  1.00  0.00           C  
HETATM    7  O2  UNL     1       0.527   0.699  -1.973  1.00  0.00           O  
HETATM    8  N2  UNL     1       0.496  -0.358   0.091  1.00  0.00           N  
HETATM    9  C5  UNL     1       1.629  -1.212  -0.242  1.00  0.00           C  
HETATM   10  C6  UNL     1       2.698  -1.044   0.815  1.00  0.00           C  
HETATM   11  C7  UNL     1       3.175   0.343   0.907  1.00  0.00           C  
HETATM   12  O3  UNL     1       2.704   1.231   0.162  1.00  0.00           O  
HETATM   13  O4  UNL     1       4.152   0.692   1.818  1.00  0.00           O  
HETATM   14  C8  UNL     1       1.187  -2.639  -0.197  1.00  0.00           C  
HETATM   15  O5  UNL     1       0.010  -2.972   0.090  1.00  0.00           O  
HETATM   16  O6  UNL     1       2.100  -3.643  -0.480  1.00  0.00           O  
HETATM   17  H1  UNL     1      -3.189   2.189   0.874  1.00  0.00           H  
HETATM   18  H2  UNL     1      -4.209   0.726   0.868  1.00  0.00           H  
HETATM   19  H3  UNL     1      -4.044   1.769  -0.648  1.00  0.00           H  
HETATM   20  H4  UNL     1      -2.059  -0.095   0.706  1.00  0.00           H  
HETATM   21  H5  UNL     1      -3.107  -1.040  -0.956  1.00  0.00           H  
HETATM   22  H6  UNL     1      -0.914   2.053   0.435  1.00  0.00           H  
HETATM   23  H7  UNL     1      -1.765   3.241  -1.173  1.00  0.00           H  
HETATM   24  H8  UNL     1      -2.315   1.933  -2.115  1.00  0.00           H  
HETATM   25  H9  UNL     1       0.051  -0.447   1.029  1.00  0.00           H  
HETATM   26  H10 UNL     1       2.010  -0.997  -1.260  1.00  0.00           H  
HETATM   27  H11 UNL     1       3.552  -1.730   0.632  1.00  0.00           H  
HETATM   28  H12 UNL     1       2.238  -1.305   1.805  1.00  0.00           H  
HETATM   29  H13 UNL     1       3.876   0.998   2.747  1.00  0.00           H  
HETATM   30  H14 UNL     1       2.330  -4.377   0.167  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    4   20
CONECT    3   21
CONECT    4    5    6   22
CONECT    5   23   24
CONECT    6    7    7    8
CONECT    8    9   25
CONECT    9   10   14   26
CONECT   10   11   27   28
CONECT   11   12   12   13
CONECT   13   29
CONECT   14   15   15   16
CONECT   16   30
END

HMDB0029057
     RDKit          3D
Threonylaspartic acid
 30 29  0  0  0  0  0  0  0  0999 V2000
   -3.5487    1.3449    0.2507 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3302    0.5275   -0.1542 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.6016   -0.2424   -1.2889 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1615    1.4467   -0.4768 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4812    2.3203   -1.5882 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0079    0.5911   -0.8437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5267    0.6986   -1.9734 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4961   -0.3577    0.0906 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6295   -1.2122   -0.2421 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6976   -1.0439    0.8148 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1745    0.3430    0.9067 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7036    1.2307    0.1620 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1524    0.6925    1.8178 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1865   -2.6395   -0.1968 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0103   -2.9724    0.0899 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1000   -3.6430   -0.4801 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1888    2.1892    0.8742 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2093    0.7257    0.8682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0438    1.7686   -0.6477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0589   -0.0954    0.7062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1074   -1.0397   -0.9565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9143    2.0528    0.4351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7654    3.2408   -1.1730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3147    1.9327   -2.1153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0511   -0.4467    1.0291 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0099   -0.9971   -1.2595 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5518   -1.7304    0.6323 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2382   -1.3049    1.8048 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8757    0.9975    2.7471 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3297   -4.3772    0.1668 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  1
  3 21  1  0
  4 22  1  1
  5 23  1  0
  5 24  1  0
  8 25  1  0
  9 26  1  6
 10 27  1  0
 10 28  1  0
 13 29  1  0
 16 30  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
L-THR-L-Asp	ChEBI
TD	ChEBI
Threoninyl-aspartate	ChEBI
Threoninyl-aspartic acid	Generator
Threonylaspartate	Generator
L-Threoninyl-L-aspartate	HMDB
L-Threoninyl-L-aspartic acid	HMDB
L-Threonyl-L-aspartate	HMDB
L-Threonyl-L-aspartic acid	HMDB
N-L-Threoninyl-L-aspartate	HMDB
N-L-Threoninyl-L-aspartic acid	HMDB
N-L-Threonyl-L-aspartate	HMDB
N-L-Threonyl-L-aspartic acid	HMDB
N-Threoninylaspartate	HMDB
N-Threoninylaspartic acid	HMDB
N-Threonylaspartate	HMDB
N-Threonylaspartic acid	HMDB
T-D Dipeptide	HMDB
TD Dipeptide	HMDB
THR-Asp	HMDB
Threonine aspartate dipeptide	HMDB
Threonine aspartic acid dipeptide	HMDB
Threonine-aspartate dipeptide	HMDB
Threonine-aspartic acid dipeptide	HMDB
Threoninylaspartate	HMDB
Threoninylaspartic acid	HMDB
Threonyl-aspartate	HMDB
Threonyl-aspartic acid	HMDB
Threonylaspartic acid	ChEBI

Chemical Formula

C₈H₁₄N₂O₆

Average Molecular Weight

234.208

Monoisotopic Molecular Weight

234.085186179

IUPAC Name

(2S)-2-[(2S,3R)-2-amino-3-hydroxybutanamido]butanedioic acid

Traditional Name

(2S)-2-[(2S,3R)-2-amino-3-hydroxybutanamido]butanedioic acid

CAS Registry Number

108320-97-4

SMILES

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

InChI Identifier

InChI=1S/C8H14N2O6/c1-3(11)6(9)7(14)10-4(8(15)16)2-5(12)13/h3-4,6,11H,2,9H2,1H3,(H,10,14)(H,12,13)(H,15,16)/t3-,4+,6+/m1/s1

InChI Key

IOWJRKAVLALBQB-IWGUZYHVSA-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 or derivatives
N-acyl-alpha-amino acid
Acyl-homoserine
Acyl-l-homoserine
N-acyl-l-alpha-amino acid
Alpha-amino acid amide
Alpha-amino acid or derivatives
N-acyl-amine
Fatty amide
Dicarboxylic acid or derivatives
Fatty acid
Fatty acyl
Secondary carboxylic acid amide
Amino acid
Amino acid or derivatives
Carboxamide group
Secondary alcohol
Carboxylic acid
Organooxygen compound
Primary aliphatic amine
Primary amine
Hydrocarbon derivative
Alcohol
Organic oxide
Carbonyl group
Organopnictogen compound
Amine
Organic oxygen compound
Organic nitrogen compound
Organonitrogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

dipeptide (CHEBI:74854 )

Ontology

Not Available

Endogenous (HMDB: HMDB0029057)

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	-4.92	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	26.3 g/L	ALOGPS
logP	-3.4	ALOGPS
logP	-4.7	ChemAxon
logS	-0.95	ALOGPS
pKa (Strongest Acidic)	3.25	ChemAxon
pKa (Strongest Basic)	7.92	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	149.95 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	49.79 m³·mol⁻¹	ChemAxon
Polarizability	21.06 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]+	155.79	30932474
DeepCCS	[M-H]-	153.395	30932474
DeepCCS	[M-2H]-	186.321	30932474
DeepCCS	[M+Na]+	161.756	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.	1.3 minutes	32390414
Predicted by Siyang on May 30, 2022	10.3946 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	9.29 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	431.8 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	486.5 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	287.7 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	31.8 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	167.1 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	65.8 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	311.8 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	231.8 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	863.0 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	596.6 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	44.4 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	751.9 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	187.5 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	277.7 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	643.6 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	535.9 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	476.1 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Threonylaspartic acid	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(O)=O)C(O)=O	3361.9	Standard polar	33892256
Threonylaspartic acid	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(O)=O)C(O)=O	1887.7	Standard non polar	33892256
Threonylaspartic acid	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(O)=O)C(O)=O	2259.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Threonylaspartic acid,1TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CC(=O)O)C(=O)O	2020.7	Semi standard non polar	33892256
Threonylaspartic acid,1TMS,isomer #2	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O	2054.3	Semi standard non polar	33892256
Threonylaspartic acid,1TMS,isomer #3	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C	2017.2	Semi standard non polar	33892256
Threonylaspartic acid,1TMS,isomer #4	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)O	2035.4	Semi standard non polar	33892256
Threonylaspartic acid,1TMS,isomer #5	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2051.7	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O	2064.6	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #10	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2194.9	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #11	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2096.1	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C	2035.6	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)O	2091.4	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2095.2	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #5	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2055.6	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #6	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O	2087.5	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #7	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2048.4	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #8	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C	2079.5	Semi standard non polar	33892256
Threonylaspartic acid,2TMS,isomer #9	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2045.2	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2105.1	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #10	C[C@@H](O)[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	2223.3	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #11	C[C@@H](O)[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	2098.5	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #12	C[C@@H](O)[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	2227.8	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #13	C[C@@H](O)[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	2112.5	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #14	C[C@@H](O)[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	2221.9	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O	2131.9	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2082.8	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C	2128.0	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2089.3	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CC(=O)O)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2253.3	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2117.3	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #8	C[C@@H](O)[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	2125.4	Semi standard non polar	33892256
Threonylaspartic acid,3TMS,isomer #9	C[C@@H](O)[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	2072.7	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #1	C[C@@H](O[Si](C)(C)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	2169.7	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #1	C[C@@H](O[Si](C)(C)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	2169.3	Standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #10	C[C@@H](O)[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	2242.8	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #10	C[C@@H](O)[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	2319.5	Standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #11	C[C@@H](O)[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	2269.1	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #11	C[C@@H](O)[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	2291.2	Standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #2	C[C@@H](O[Si](C)(C)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	2134.5	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #2	C[C@@H](O[Si](C)(C)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	2235.4	Standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #3	C[C@@H](O[Si](C)(C)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	2265.5	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #3	C[C@@H](O[Si](C)(C)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	2261.2	Standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #4	C[C@@H](O[Si](C)(C)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	2138.2	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #4	C[C@@H](O[Si](C)(C)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	2223.2	Standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #5	C[C@@H](O[Si](C)(C)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	2270.1	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #5	C[C@@H](O[Si](C)(C)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	2244.0	Standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #6	C[C@@H](O[Si](C)(C)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	2158.8	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #6	C[C@@H](O[Si](C)(C)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	2195.5	Standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #7	C[C@@H](O[Si](C)(C)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	2296.9	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #7	C[C@@H](O[Si](C)(C)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	2302.6	Standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #8	C[C@@H](O)[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	2247.2	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #8	C[C@@H](O)[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	2252.9	Standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #9	C[C@@H](O)[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	2132.1	Semi standard non polar	33892256
Threonylaspartic acid,4TMS,isomer #9	C[C@@H](O)[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	2188.4	Standard non polar	33892256
Threonylaspartic acid,5TMS,isomer #1	C[C@@H](O[Si](C)(C)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	2284.2	Semi standard non polar	33892256
Threonylaspartic acid,5TMS,isomer #1	C[C@@H](O[Si](C)(C)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	2289.6	Standard non polar	33892256
Threonylaspartic acid,5TMS,isomer #2	C[C@@H](O[Si](C)(C)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	2176.1	Semi standard non polar	33892256
Threonylaspartic acid,5TMS,isomer #2	C[C@@H](O[Si](C)(C)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	2246.4	Standard non polar	33892256
Threonylaspartic acid,5TMS,isomer #3	C[C@@H](O[Si](C)(C)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	2304.4	Semi standard non polar	33892256
Threonylaspartic acid,5TMS,isomer #3	C[C@@H](O[Si](C)(C)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	2343.7	Standard non polar	33892256
Threonylaspartic acid,5TMS,isomer #4	C[C@@H](O[Si](C)(C)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	2318.8	Semi standard non polar	33892256
Threonylaspartic acid,5TMS,isomer #4	C[C@@H](O[Si](C)(C)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	2321.6	Standard non polar	33892256
Threonylaspartic acid,5TMS,isomer #5	C[C@@H](O)[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	2303.2	Semi standard non polar	33892256
Threonylaspartic acid,5TMS,isomer #5	C[C@@H](O)[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	2329.4	Standard non polar	33892256
Threonylaspartic acid,6TMS,isomer #1	C[C@@H](O[Si](C)(C)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	2367.2	Semi standard non polar	33892256
Threonylaspartic acid,6TMS,isomer #1	C[C@@H](O[Si](C)(C)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	2374.1	Standard non polar	33892256
Threonylaspartic acid,1TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CC(=O)O)C(=O)O	2255.2	Semi standard non polar	33892256
Threonylaspartic acid,1TBDMS,isomer #2	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	2295.1	Semi standard non polar	33892256
Threonylaspartic acid,1TBDMS,isomer #3	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	2257.7	Semi standard non polar	33892256
Threonylaspartic acid,1TBDMS,isomer #4	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)O	2272.5	Semi standard non polar	33892256
Threonylaspartic acid,1TBDMS,isomer #5	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	2292.7	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	2528.7	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #10	C[C@@H](O)[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	2631.8	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #11	C[C@@H](O)[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	2545.1	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	2491.7	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC(=O)O)C(=O)O	2524.0	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	2536.5	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #5	C[C@@H](O)[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	2510.2	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #6	C[C@@H](O)[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	2530.1	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #7	C[C@@H](O)[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	2525.9	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #8	C[C@@H](O)[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	2512.4	Semi standard non polar	33892256
Threonylaspartic acid,2TBDMS,isomer #9	C[C@@H](O)[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	2512.8	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)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	2767.6	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #10	C[C@@H](O)[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	2912.4	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #11	C[C@@H](O)[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	2789.4	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #12	C[C@@H](O)[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	2892.5	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #13	C[C@@H](O)[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	2787.4	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #14	C[C@@H](O)[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	2887.8	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)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	2783.3	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)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	2776.7	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)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	2765.4	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)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	2769.9	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)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	2901.2	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)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	2798.4	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #8	C[C@@H](O)[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	2769.7	Semi standard non polar	33892256
Threonylaspartic acid,3TBDMS,isomer #9	C[C@@H](O)[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	2745.4	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)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	3001.2	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)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	2866.8	Standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #10	C[C@@H](O)[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	3128.6	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #10	C[C@@H](O)[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	2984.3	Standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #11	C[C@@H](O)[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	3120.1	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #11	C[C@@H](O)[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	2965.5	Standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)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	2989.3	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)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	2946.6	Standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)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	3169.8	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)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	2929.6	Standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)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	3025.1	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)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	2902.5	Standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)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	3152.2	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)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	2915.5	Standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)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	3025.5	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)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	2888.6	Standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)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	3153.4	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)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	2946.3	Standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #8	C[C@@H](O)[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	3147.1	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #8	C[C@@H](O)[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	2944.0	Standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #9	C[C@@H](O)[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	2986.7	Semi standard non polar	33892256
Threonylaspartic acid,4TBDMS,isomer #9	C[C@@H](O)[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	2905.1	Standard non polar	33892256
Threonylaspartic acid,5TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)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	3383.0	Semi standard non polar	33892256
Threonylaspartic acid,5TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)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	3104.4	Standard non polar	33892256
Threonylaspartic acid,5TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)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	3215.6	Semi standard non polar	33892256
Threonylaspartic acid,5TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)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	3082.9	Standard non polar	33892256
Threonylaspartic acid,5TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)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	3375.4	Semi standard non polar	33892256
Threonylaspartic acid,5TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)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	3156.0	Standard non polar	33892256
Threonylaspartic acid,5TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)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	3376.2	Semi standard non polar	33892256
Threonylaspartic acid,5TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)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	3145.1	Standard non polar	33892256
Threonylaspartic acid,5TBDMS,isomer #5	C[C@@H](O)[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	3333.0	Semi standard non polar	33892256
Threonylaspartic acid,5TBDMS,isomer #5	C[C@@H](O)[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	3180.2	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Threonylaspartic 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 - Threonylaspartic acid 10V, Negative-QTOF	splash10-00m0-5930000000-482bf476ac2a202d4711	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonylaspartic acid 20V, Negative-QTOF	splash10-000i-9400000000-27536cececf6956f01f8	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonylaspartic acid 40V, Negative-QTOF	splash10-000l-9100000000-7fa34ee214321ef757b4	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonylaspartic acid 10V, Positive-QTOF	splash10-0079-7590000000-e01a18e15480324ab60c	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonylaspartic acid 20V, Positive-QTOF	splash10-014i-3900000000-46362d4e382b455a835b	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonylaspartic acid 40V, Positive-QTOF	splash10-06ri-9100000000-256311df7ea09e9ddfdc	2021-09-24	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

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB112063

KNApSAcK ID

Not Available

Chemspider ID

5379089

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

7016067

PDB ID

Not Available

ChEBI ID

74854

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

Van de Bittner GC, Bertozzi CR, Chang CJ: Strategy for dual-analyte luciferin imaging: in vivo bioluminescence detection of hydrogen peroxide and caspase activity in a murine model of acute inflammation. J Am Chem Soc. 2013 Feb 6;135(5):1783-95. doi: 10.1021/ja309078t. Epub 2013 Jan 25. [PubMed:23347279 ]

Showing metabocard for Threonylaspartic acid (HMDB0029057)

MOL for HMDB0029057 (Threonylaspartic acid)

3D MOL for HMDB0029057 (Threonylaspartic acid)

3D SDF for HMDB0029057 (Threonylaspartic acid)

3D-SDF for HMDB0029057 (Threonylaspartic acid)

PDB for HMDB0029057 (Threonylaspartic acid)

3D PDB for HMDB0029057 (Threonylaspartic acid)

SMILES for HMDB0029057 (Threonylaspartic acid)

INCHI for HMDB0029057 (Threonylaspartic acid)

Structure for HMDB0029057 (Threonylaspartic acid)

3D Structure for HMDB0029057 (Threonylaspartic acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra