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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 21:03:33 UTC

Update Date

2021-09-14 15:19:02 UTC

HMDB ID

HMDB0029063

Secondary Accession Numbers

HMDB29063

Metabolite Identification

Common Name

Threonylhistidine

Description

Threonylhistidine is a dipeptide composed of threonine and histidine. 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

HMDB0029063
     RDKit          3D
Threonylhistidine
 34 34  0  0  0  0  0  0  0  0999 V2000
   -2.9749   -0.1295    1.3569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1263    0.0007   -0.1234 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2401    0.8067   -0.3648 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9413    0.6410   -0.8199 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3329    0.6787   -2.2394 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7388   -0.2131   -0.7291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3843   -0.8004   -1.7839 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0051   -0.3794    0.4904 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1626   -1.1983    0.5935 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4240   -0.4518    0.9390 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7374    0.5816   -0.0999 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5059    0.4001   -1.2322 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5674    1.5382   -1.9236 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8425    2.4306   -1.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3327    1.8631   -0.1216 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0022   -2.3142    1.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0946   -2.4139    2.1507 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9801   -3.2475    1.8325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4051   -0.9965    1.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0173   -0.2495    1.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5810    0.7783    1.8531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2797   -0.9950   -0.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9403    1.7385   -0.4487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7727    1.6743   -0.4723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2185    1.2265   -2.3074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4841   -0.3126   -2.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3501    0.1440    1.3120 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3470   -1.6524   -0.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4143    0.0353    1.9082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2583   -1.1825    0.9275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9616   -0.5612   -1.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7035    3.4547   -1.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7337    2.3198    0.5968 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9039   -3.2141    1.4387 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
 12 13  1  0
 13 14  2  0
 14 15  1  0
  9 16  1  0
 16 17  2  0
 16 18  1  0
 15 11  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  6
  3 23  1  0
  4 24  1  1
  5 25  1  0
  5 26  1  0
  8 27  1  0
  9 28  1  6
 10 29  1  0
 10 30  1  0
 12 31  1  0
 14 32  1  0
 15 33  1  0
 18 34  1  0
M  END


  Mrv1652304062014152D          

 18 18  0  0  0  0            999 V2000
10047.067410047.2383    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10047.784510047.6501    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10048.498810047.2383    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10049.213110047.6501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.927610047.2383    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10049.213110048.4748    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10046.354110047.6501    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10045.638710047.2383    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10044.925310047.6501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10045.638710046.4133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10046.354110048.4748    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10047.067410046.4133    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10048.498810046.4133    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.214910045.9998    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.301410045.1776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10050.110210045.0056    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10050.523810045.7218    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.970510046.3362    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  7  1  0  0  0  0
  1 12  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  7  8  1  0  0  0  0
  7 11  1  6  0  0  0
  8  9  1  0  0  0  0
  3 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 17 18  1  0  0  0  0
 14 18  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
  8 10  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0029063

> <DATABASE_NAME>
hmdb

> <SMILES>
C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C10H16N4O4/c1-5(15)8(11)9(16)14-7(10(17)18)2-6-3-12-4-13-6/h3-5,7-8,15H,2,11H2,1H3,(H,12,13)(H,14,16)(H,17,18)/t5-,7+,8+/m1/s1

> <INCHI_KEY>
WXVIGTAUZBUDPZ-DTLFHODZSA-N

> <FORMULA>
C10H16N4O4

> <MOLECULAR_WEIGHT>
256.262

> <EXACT_MASS>
256.117155011

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
24.24516216896314

> <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]-3-(1H-imidazol-5-yl)propanoic acid

> <ALOGPS_LOGP>
-2.86

> <JCHEM_LOGP>
-4.541520837335837

> <ALOGPS_LOGS>
-1.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
12.672291085892738

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3322130177713767

> <JCHEM_PKA_STRONGEST_BASIC>
7.950446371190433

> <JCHEM_POLAR_SURFACE_AREA>
141.33

> <JCHEM_REFRACTIVITY>
61.3189

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.04e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S,3R)-2-amino-3-hydroxybutanamido]-3-(3H-imidazol-4-yl)propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029063
     RDKit          3D
Threonylhistidine
 34 34  0  0  0  0  0  0  0  0999 V2000
   -2.9749   -0.1295    1.3569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1263    0.0007   -0.1234 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2401    0.8067   -0.3648 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9413    0.6410   -0.8199 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3329    0.6787   -2.2394 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7388   -0.2131   -0.7291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3843   -0.8004   -1.7839 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0051   -0.3794    0.4904 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1626   -1.1983    0.5935 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4240   -0.4518    0.9390 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7374    0.5816   -0.0999 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5059    0.4001   -1.2322 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5674    1.5382   -1.9236 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8425    2.4306   -1.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3327    1.8631   -0.1216 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0022   -2.3142    1.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0946   -2.4139    2.1507 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9801   -3.2475    1.8325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4051   -0.9965    1.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0173   -0.2495    1.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5810    0.7783    1.8531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2797   -0.9950   -0.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9403    1.7385   -0.4487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7727    1.6743   -0.4723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2185    1.2265   -2.3074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4841   -0.3126   -2.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3501    0.1440    1.3120 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3470   -1.6524   -0.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4143    0.0353    1.9082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2583   -1.1825    0.9275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9616   -0.5612   -1.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7035    3.4547   -1.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7337    2.3198    0.5968 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9039   -3.2141    1.4387 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
 12 13  1  0
 13 14  2  0
 14 15  1  0
  9 16  1  0
 16 17  2  0
 16 18  1  0
 15 11  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  6
  3 23  1  0
  4 24  1  1
  5 25  1  0
  5 26  1  0
  8 27  1  0
  9 28  1  6
 10 29  1  0
 10 30  1  0
 12 31  1  0
 14 32  1  0
 15 33  1  0
 18 34  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    8754.5268754.845   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0    8755.8648755.614   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0    8757.1988754.845   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8758.5318755.614   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0    8759.8658754.845   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0    8758.5318757.153   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0    8753.1948755.614   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8751.8598754.845   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8750.5278755.614   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0    8751.8598753.305   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0    8753.1948757.153   0.000  0.00  0.00           N+0
HETATM   12  O   UNK     0    8754.5268753.305   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0    8757.1988753.305   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8758.5348752.533   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8758.6968750.998   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0    8760.2068750.677   0.000  0.00  0.00           N+0
HETATM   17  C   UNK     0    8760.9788752.014   0.000  0.00  0.00           C+0
HETATM   18  N   UNK     0    8759.9458753.161   0.000  0.00  0.00           N+0
CONECT    1    2    7   12                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4                                                            
CONECT    7    1    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7                                                            
CONECT   12    1                                                            
CONECT   13    3   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   18   16                                                       
CONECT   18   17   14                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

COMPND    HMDB0029063
HETATM    1  C1  UNL     1      -2.975  -0.129   1.357  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.126   0.001  -0.123  1.00  0.00           C  
HETATM    3  O1  UNL     1      -4.240   0.807  -0.365  1.00  0.00           O  
HETATM    4  C3  UNL     1      -1.941   0.641  -0.820  1.00  0.00           C  
HETATM    5  N1  UNL     1      -2.333   0.679  -2.239  1.00  0.00           N  
HETATM    6  C4  UNL     1      -0.739  -0.213  -0.729  1.00  0.00           C  
HETATM    7  O2  UNL     1      -0.384  -0.800  -1.784  1.00  0.00           O  
HETATM    8  N2  UNL     1       0.005  -0.379   0.490  1.00  0.00           N  
HETATM    9  C5  UNL     1       1.163  -1.198   0.594  1.00  0.00           C  
HETATM   10  C6  UNL     1       2.424  -0.452   0.939  1.00  0.00           C  
HETATM   11  C7  UNL     1       2.737   0.582  -0.100  1.00  0.00           C  
HETATM   12  C8  UNL     1       3.506   0.400  -1.232  1.00  0.00           C  
HETATM   13  N3  UNL     1       3.567   1.538  -1.924  1.00  0.00           N  
HETATM   14  C9  UNL     1       2.843   2.431  -1.231  1.00  0.00           C  
HETATM   15  N4  UNL     1       2.333   1.863  -0.122  1.00  0.00           N  
HETATM   16  C10 UNL     1       1.002  -2.314   1.554  1.00  0.00           C  
HETATM   17  O3  UNL     1      -0.095  -2.414   2.151  1.00  0.00           O  
HETATM   18  O4  UNL     1       1.980  -3.248   1.832  1.00  0.00           O  
HETATM   19  H1  UNL     1      -2.405  -0.996   1.699  1.00  0.00           H  
HETATM   20  H2  UNL     1      -4.017  -0.250   1.765  1.00  0.00           H  
HETATM   21  H3  UNL     1      -2.581   0.778   1.853  1.00  0.00           H  
HETATM   22  H4  UNL     1      -3.280  -0.995  -0.561  1.00  0.00           H  
HETATM   23  H5  UNL     1      -3.940   1.739  -0.449  1.00  0.00           H  
HETATM   24  H6  UNL     1      -1.773   1.674  -0.472  1.00  0.00           H  
HETATM   25  H7  UNL     1      -3.219   1.226  -2.307  1.00  0.00           H  
HETATM   26  H8  UNL     1      -2.484  -0.313  -2.534  1.00  0.00           H  
HETATM   27  H9  UNL     1      -0.350   0.144   1.312  1.00  0.00           H  
HETATM   28  H10 UNL     1       1.347  -1.652  -0.424  1.00  0.00           H  
HETATM   29  H11 UNL     1       2.414   0.035   1.908  1.00  0.00           H  
HETATM   30  H12 UNL     1       3.258  -1.183   0.927  1.00  0.00           H  
HETATM   31  H13 UNL     1       3.962  -0.561  -1.459  1.00  0.00           H  
HETATM   32  H14 UNL     1       2.704   3.455  -1.543  1.00  0.00           H  
HETATM   33  H15 UNL     1       1.734   2.320   0.597  1.00  0.00           H  
HETATM   34  H16 UNL     1       2.904  -3.214   1.439  1.00  0.00           H  
CONECT    1    2   19   20   21
CONECT    2    3    4   22
CONECT    3   23
CONECT    4    5    6   24
CONECT    5   25   26
CONECT    6    7    7    8
CONECT    8    9   27
CONECT    9   10   16   28
CONECT   10   11   29   30
CONECT   11   12   12   15
CONECT   12   13   31
CONECT   13   14   14
CONECT   14   15   32
CONECT   15   33
CONECT   16   17   17   18
CONECT   18   34
END

HMDB0029063
     RDKit          3D
Threonylhistidine
 34 34  0  0  0  0  0  0  0  0999 V2000
   -2.9749   -0.1295    1.3569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1263    0.0007   -0.1234 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.2401    0.8067   -0.3648 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9413    0.6410   -0.8199 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3329    0.6787   -2.2394 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7388   -0.2131   -0.7291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3843   -0.8004   -1.7839 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0051   -0.3794    0.4904 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1626   -1.1983    0.5935 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4240   -0.4518    0.9390 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7374    0.5816   -0.0999 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5059    0.4001   -1.2322 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5674    1.5382   -1.9236 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8425    2.4306   -1.2314 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3327    1.8631   -0.1216 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0022   -2.3142    1.5540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0946   -2.4139    2.1507 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9801   -3.2475    1.8325 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4051   -0.9965    1.6991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0173   -0.2495    1.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5810    0.7783    1.8531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2797   -0.9950   -0.5605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9403    1.7385   -0.4487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7727    1.6743   -0.4723 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2185    1.2265   -2.3074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4841   -0.3126   -2.5339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3501    0.1440    1.3120 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3470   -1.6524   -0.4236 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4143    0.0353    1.9082 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2583   -1.1825    0.9275 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9616   -0.5612   -1.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7035    3.4547   -1.5432 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7337    2.3198    0.5968 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9039   -3.2141    1.4387 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
 12 13  1  0
 13 14  2  0
 14 15  1  0
  9 16  1  0
 16 17  2  0
 16 18  1  0
 15 11  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  6
  3 23  1  0
  4 24  1  1
  5 25  1  0
  5 26  1  0
  8 27  1  0
  9 28  1  6
 10 29  1  0
 10 30  1  0
 12 31  1  0
 14 32  1  0
 15 33  1  0
 18 34  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
L-THR-L-His	ChEBI
T-H	ChEBI
TH	ChEBI
L-Threoninyl-L-histidine	HMDB
L-Threonyl-L-histidine	HMDB
N-L-Threoninyl-L-histidine	HMDB
N-L-Threonyl-L-histidine	HMDB
N-Threoninylhistidine	HMDB
N-Threonylhistidine	HMDB
T-H Dipeptide	HMDB
TH Dipeptide	HMDB
THR-His	HMDB
Threonine histidine dipeptide	HMDB
Threonine-histidine dipeptide	HMDB
Threoninyl-histidine	HMDB
Threoninylhistidine	HMDB
Threonyl-histidine	HMDB
Threonylhistidine	HMDB

Chemical Formula

C₁₀H₁₆N₄O₄

Average Molecular Weight

256.262

Monoisotopic Molecular Weight

256.117155011

IUPAC Name

(2S)-2-[(2S,3R)-2-amino-3-hydroxybutanamido]-3-(1H-imidazol-5-yl)propanoic acid

Traditional Name

(2S)-2-[(2S,3R)-2-amino-3-hydroxybutanamido]-3-(3H-imidazol-4-yl)propanoic acid

CAS Registry Number

55831-93-1

SMILES

C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1)C(O)=O

InChI Identifier

InChI=1S/C10H16N4O4/c1-5(15)8(11)9(16)14-7(10(17)18)2-6-3-12-4-13-6/h3-5,7-8,15H,2,11H2,1H3,(H,12,13)(H,14,16)(H,17,18)/t5-,7+,8+/m1/s1

InChI Key

WXVIGTAUZBUDPZ-DTLFHODZSA-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
Histidine or derivatives
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
N-acyl-l-alpha-amino acid
Alpha-amino acid amide
Alpha-amino acid or derivatives
Imidazolyl carboxylic acid derivative
N-acyl-amine
Fatty acyl
Fatty amide
Azole
Imidazole
Heteroaromatic compound
Secondary alcohol
Carboxamide group
Secondary carboxylic acid amide
Amino acid or derivatives
Amino acid
Carboxylic acid
Azacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Primary amine
Organic oxygen compound
Organic nitrogen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Primary aliphatic amine
Amine
Organooxygen compound
Organonitrogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

dipeptide (CHEBI:73663 )

Ontology

Not Available

Endogenous (HMDB: HMDB0029063)

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	-4.55	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	20.4 g/L	ALOGPS
logP	-2.9	ALOGPS
logP	-4.5	ChemAxon
logS	-1.1	ALOGPS
pKa (Strongest Acidic)	3.33	ChemAxon
pKa (Strongest Basic)	7.95	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	141.33 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	61.32 m³·mol⁻¹	ChemAxon
Polarizability	24.25 Å³	ChemAxon
Number of Rings	1	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]+	159.933	30932474
DeepCCS	[M-H]-	157.575	30932474
DeepCCS	[M-2H]-	191.231	30932474
DeepCCS	[M+Na]+	166.458	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.	1.66 minutes	32390414
Predicted by Siyang on May 30, 2022	10.0209 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	9.22 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	464.7 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	398.7 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	261.2 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	34.1 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	164.0 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	73.9 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	325.1 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	239.3 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	995.3 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	576.4 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	47.5 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	690.9 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	187.0 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	319.3 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	656.9 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	744.6 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	434.5 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Threonylhistidine	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1)C(O)=O	3522.7	Standard polar	33892256
Threonylhistidine	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1)C(O)=O	2154.0	Standard non polar	33892256
Threonylhistidine	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1)C(O)=O	2719.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Threonylhistidine,1TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O	2456.3	Semi standard non polar	33892256
Threonylhistidine,1TMS,isomer #2	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C	2419.3	Semi standard non polar	33892256
Threonylhistidine,1TMS,isomer #3	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O	2455.2	Semi standard non polar	33892256
Threonylhistidine,1TMS,isomer #4	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C	2376.7	Semi standard non polar	33892256
Threonylhistidine,1TMS,isomer #5	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O	2501.8	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C	2447.8	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O	2546.5	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #11	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2482.5	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O	2477.6	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C	2405.6	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O	2538.1	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #5	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C	2448.0	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #6	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2373.9	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #7	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C	2522.1	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #8	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2525.6	Semi standard non polar	33892256
Threonylhistidine,2TMS,isomer #9	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C	2405.7	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C	2475.3	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C	2399.5	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C	2573.2	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C	2424.2	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #11	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2508.4	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #11	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2495.2	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #12	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2489.4	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #12	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2610.8	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #13	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2662.6	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #13	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2586.3	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #14	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2546.0	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #14	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2523.6	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2411.5	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2422.3	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C	2579.1	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C	2396.4	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2560.8	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2565.5	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C	2427.7	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C	2485.7	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O	2583.5	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O	2480.4	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2538.1	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2522.8	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #8	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2500.8	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #8	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2518.4	Standard non polar	33892256
Threonylhistidine,3TMS,isomer #9	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2393.1	Semi standard non polar	33892256
Threonylhistidine,3TMS,isomer #9	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2438.8	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2559.7	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2519.2	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2547.8	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2520.2	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #11	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2658.0	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #11	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2678.3	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2440.8	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2466.4	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C	2610.6	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C	2470.6	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2551.1	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2541.9	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2559.8	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2600.5	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2719.4	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2610.6	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2580.2	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2560.5	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #8	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2517.6	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #8	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2577.2	Standard non polar	33892256
Threonylhistidine,4TMS,isomer #9	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2665.0	Semi standard non polar	33892256
Threonylhistidine,4TMS,isomer #9	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2584.4	Standard non polar	33892256
Threonylhistidine,5TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2626.4	Semi standard non polar	33892256
Threonylhistidine,5TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2586.0	Standard non polar	33892256
Threonylhistidine,5TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2726.4	Semi standard non polar	33892256
Threonylhistidine,5TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2606.9	Standard non polar	33892256
Threonylhistidine,5TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2600.3	Semi standard non polar	33892256
Threonylhistidine,5TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2561.0	Standard non polar	33892256
Threonylhistidine,5TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2732.1	Semi standard non polar	33892256
Threonylhistidine,5TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2693.9	Standard non polar	33892256
Threonylhistidine,5TMS,isomer #5	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2691.4	Semi standard non polar	33892256
Threonylhistidine,5TMS,isomer #5	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2679.8	Standard non polar	33892256
Threonylhistidine,6TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2786.2	Semi standard non polar	33892256
Threonylhistidine,6TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2695.9	Standard non polar	33892256
Threonylhistidine,1TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O	2690.8	Semi standard non polar	33892256
Threonylhistidine,1TBDMS,isomer #2	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C	2664.0	Semi standard non polar	33892256
Threonylhistidine,1TBDMS,isomer #3	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O	2670.0	Semi standard non polar	33892256
Threonylhistidine,1TBDMS,isomer #4	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C(C)(C)C	2619.6	Semi standard non polar	33892256
Threonylhistidine,1TBDMS,isomer #5	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O	2762.1	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C	2915.0	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O	3001.0	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,isomer #11	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2966.7	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,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](CC1=CN=C[NH]1)C(=O)O	2908.8	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C(C)(C)C	2886.7	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O	3037.2	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,isomer #5	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C	2896.9	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,isomer #6	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2857.3	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,isomer #7	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3005.7	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,isomer #8	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2970.7	Semi standard non polar	33892256
Threonylhistidine,2TBDMS,isomer #9	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C(C)(C)C	2865.9	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,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](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C	3121.9	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,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](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C	2972.3	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3234.9	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3033.4	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #11	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3177.2	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #11	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3093.2	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #12	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)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	3157.9	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #12	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)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	3138.7	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #13	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[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	3358.9	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #13	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[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	3139.0	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #14	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3219.6	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #14	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3100.9	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3103.1	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3000.1	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3280.7	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3000.7	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3233.7	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3095.7	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #5	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](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C(C)(C)C	3104.0	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #5	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](CC1=CN=C[NH]1)C(=O)O)[Si](C)(C)C(C)(C)C	3030.2	Standard non polar	33892256
Threonylhistidine,3TBDMS,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](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O	3245.7	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,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](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O	3072.4	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3225.9	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3096.3	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #8	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)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	3200.3	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #8	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3066.8	Standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #9	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3084.0	Semi standard non polar	33892256
Threonylhistidine,3TBDMS,isomer #9	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3011.5	Standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)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	3454.1	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=C[NH]1)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	3181.8	Standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3404.1	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3264.9	Standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #11	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[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	3528.9	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #11	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[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	3364.7	Standard non polar	33892256
Threonylhistidine,4TBDMS,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](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3292.9	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,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](CC1=CN=C[NH]1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3149.4	Standard non polar	33892256
Threonylhistidine,4TBDMS,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](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3432.7	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,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](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3198.6	Standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3422.2	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3261.8	Standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)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	3415.3	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)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	3259.5	Standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[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	3603.8	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[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	3306.5	Standard non polar	33892256
Threonylhistidine,4TBDMS,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](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3444.9	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,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](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3264.3	Standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #8	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)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	3375.0	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #8	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)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	3271.2	Standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #9	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[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	3553.4	Semi standard non polar	33892256
Threonylhistidine,4TBDMS,isomer #9	C[C@@H](O)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[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	3307.6	Standard non polar	33892256
Threonylhistidine,5TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)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	3648.2	Semi standard non polar	33892256
Threonylhistidine,5TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=C[NH]1)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	3393.9	Standard non polar	33892256
Threonylhistidine,5TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[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	3779.4	Semi standard non polar	33892256
Threonylhistidine,5TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CC1=CN=CN1[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	3438.2	Standard non polar	33892256
Threonylhistidine,5TBDMS,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](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3605.9	Semi standard non polar	33892256
Threonylhistidine,5TBDMS,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](CC1=CN=CN1[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3424.1	Standard non polar	33892256
Threonylhistidine,5TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[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	3767.9	Semi standard non polar	33892256
Threonylhistidine,5TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[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	3518.2	Standard non polar	33892256
Threonylhistidine,5TBDMS,isomer #5	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[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	3712.6	Semi standard non polar	33892256
Threonylhistidine,5TBDMS,isomer #5	C[C@@H](O)[C@@H](C(=O)N([C@@H](CC1=CN=CN1[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	3541.0	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Threonylhistidine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Threonylhistidine 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 - Threonylhistidine 10V, Positive-QTOF	splash10-0a4i-1590000000-a18e8e307338583df9c0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonylhistidine 20V, Positive-QTOF	splash10-08g0-3900000000-28ef6a936f5ac506c1b2	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonylhistidine 40V, Positive-QTOF	splash10-06si-9600000000-fea5361d4bcebbca47e6	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonylhistidine 10V, Negative-QTOF	splash10-0zfr-0930000000-fb2408089cfb5caf7233	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonylhistidine 20V, Negative-QTOF	splash10-0a4i-4900000000-5866aa1aeb00b025f39f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonylhistidine 40V, Negative-QTOF	splash10-066u-9600000000-2875e494d2cafdc6faf7	2021-09-22	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

FDB112069

KNApSAcK ID

Not Available

Chemspider ID

8118661

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

9943049

PDB ID

Not Available

ChEBI ID

73663

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 Threonylhistidine (HMDB0029063)

MOL for HMDB0029063 (Threonylhistidine)

3D MOL for HMDB0029063 (Threonylhistidine)

3D SDF for HMDB0029063 (Threonylhistidine)

3D-SDF for HMDB0029063 (Threonylhistidine)

PDB for HMDB0029063 (Threonylhistidine)

3D PDB for HMDB0029063 (Threonylhistidine)

SMILES for HMDB0029063 (Threonylhistidine)

INCHI for HMDB0029063 (Threonylhistidine)

Structure for HMDB0029063 (Threonylhistidine)

3D Structure for HMDB0029063 (Threonylhistidine)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra