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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2012-09-06 21:03:03 UTC

Update Date

2021-09-14 15:45:52 UTC

HMDB ID

HMDB0028939

Secondary Accession Numbers

HMDB28939

Metabolite Identification

Common Name

Leucyl-Threonine

Description

Leucyl-Threonine is a dipeptide composed of leucine and threonine. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an 'Expected' metabolite.

Structure

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

HMDB0028939
     RDKit          3D
Leucyl-Threonine
 36 35  0  0  0  0  0  0  0  0999 V2000
   -3.3742    0.7433    1.4984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3324    0.0391    0.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1352    0.7894   -0.8818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8895   -0.1414   -0.2970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1976   -0.9727    0.7541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9041   -2.2418    0.8264 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2384   -1.1833    0.4415 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6510   -2.3543    0.2856 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0833   -0.0718    0.3312 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5153   -0.1811    0.0255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3165    0.3321    1.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7812    0.7882    2.1595 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6947    0.3316    1.0631 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7165    0.5479   -1.2803 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0734    0.4108   -1.8560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3428    1.8871   -1.1757 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3998    1.1909    1.5792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5935    1.5311    1.5714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2499   -0.0381    2.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8308   -0.9421    0.2951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1365    0.9831   -0.4315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6778    1.7175   -1.2121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3154    0.1088   -1.7360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4154    0.8352   -0.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9208   -0.6754   -1.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3296   -0.4722    1.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8279   -2.6938   -0.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5489   -2.8545    1.5749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7383    0.8999    0.4612 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7185   -1.2638   -0.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2615   -0.5078    1.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9799    0.0902   -2.0023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4774    1.4235   -2.1346 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8224   -0.0695   -1.2365 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0614   -0.1503   -2.8345 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6066    2.1642   -0.2475 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
  5  6  1  0
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 10 14  1  0
 14 15  1  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  9 29  1  0
 10 30  1  0
 13 31  1  0
 14 32  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
M  END


  Mrv1652304062013562D          

 16 15  0  0  0  0            999 V2000
    6.0983    4.8196    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2882    4.9755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0181    5.7551    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7481    4.3519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9379    4.5078    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.3979    3.8842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6679    3.1046    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5877    4.0401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3177    4.8196    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0476    3.4164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6974    2.9487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9675    4.3519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0181    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8283    3.4164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4780    2.9487    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  4 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0028939

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)CC(N)C(=O)NC(C(C)O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C10H20N2O4/c1-5(2)4-7(11)9(14)12-8(6(3)13)10(15)16/h5-8,13H,4,11H2,1-3H3,(H,12,14)(H,15,16)

> <INCHI_KEY>
LRKCBIUDWAXNEG-UHFFFAOYSA-N

> <FORMULA>
C10H20N2O4

> <MOLECULAR_WEIGHT>
232.2768

> <EXACT_MASS>
232.142307138

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
24.25767197380555

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(2-amino-4-methylpentanamido)-3-hydroxybutanoic acid

> <ALOGPS_LOGP>
-1.69

> <JCHEM_LOGP>
-2.7559705475418688

> <ALOGPS_LOGS>
-0.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.97674088588695

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.7992348119622803

> <JCHEM_PKA_STRONGEST_BASIC>
8.432481478007258

> <JCHEM_POLAR_SURFACE_AREA>
112.65

> <JCHEM_REFRACTIVITY>
57.430800000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.95e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(2-amino-4-methylpentanamido)-3-hydroxybutanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0028939
     RDKit          3D
Leucyl-Threonine
 36 35  0  0  0  0  0  0  0  0999 V2000
   -3.3742    0.7433    1.4984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3324    0.0391    0.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1352    0.7894   -0.8818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8895   -0.1414   -0.2970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1976   -0.9727    0.7541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9041   -2.2418    0.8264 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2384   -1.1833    0.4415 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6510   -2.3543    0.2856 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0833   -0.0718    0.3312 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5153   -0.1811    0.0255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3165    0.3321    1.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7812    0.7882    2.1595 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6947    0.3316    1.0631 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7165    0.5479   -1.2803 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0734    0.4108   -1.8560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3428    1.8871   -1.1757 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3998    1.1909    1.5792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5935    1.5311    1.5714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2499   -0.0381    2.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8308   -0.9421    0.2951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1365    0.9831   -0.4315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6778    1.7175   -1.2121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3154    0.1088   -1.7360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4154    0.8352   -0.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9208   -0.6754   -1.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3296   -0.4722    1.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8279   -2.6938   -0.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5489   -2.8545    1.5749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7383    0.8999    0.4612 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7185   -1.2638   -0.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2615   -0.5078    1.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9799    0.0902   -2.0023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4774    1.4235   -2.1346 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8224   -0.0695   -1.2365 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0614   -0.1503   -2.8345 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6066    2.1642   -0.2475 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
  5  6  1  0
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 10 14  1  0
 14 15  1  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  9 29  1  0
 10 30  1  0
 13 31  1  0
 14 32  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
M  END

HEADER    PROTEIN                                 06-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-APR-20         0                                  
HETATM    1  C   UNK     0      11.383   8.997   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.871   9.288   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.367  10.743   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       8.863   8.124   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       7.351   8.415   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       6.343   7.251   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.847   5.795   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.830   7.542   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       4.326   8.997   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       3.822   6.377   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.310   6.668   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.302   5.504   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.806   8.124   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.367   6.668   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.879   6.377   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       8.359   5.504   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   14                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    4   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
MASTER        0    0    0    0    0    0    0    0   16    0   30    0
END

COMPND    HMDB0028939
HETATM    1  C1  UNL     1      -3.374   0.743   1.498  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.332   0.039   0.157  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.135   0.789  -0.882  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.890  -0.141  -0.297  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.198  -0.973   0.754  1.00  0.00           C  
HETATM    6  N1  UNL     1      -1.904  -2.242   0.826  1.00  0.00           N  
HETATM    7  C6  UNL     1       0.238  -1.183   0.442  1.00  0.00           C  
HETATM    8  O1  UNL     1       0.651  -2.354   0.286  1.00  0.00           O  
HETATM    9  N2  UNL     1       1.083  -0.072   0.331  1.00  0.00           N  
HETATM   10  C7  UNL     1       2.515  -0.181   0.025  1.00  0.00           C  
HETATM   11  C8  UNL     1       3.317   0.332   1.126  1.00  0.00           C  
HETATM   12  O2  UNL     1       2.781   0.788   2.159  1.00  0.00           O  
HETATM   13  O3  UNL     1       4.695   0.332   1.063  1.00  0.00           O  
HETATM   14  C9  UNL     1       2.717   0.548  -1.280  1.00  0.00           C  
HETATM   15  C10 UNL     1       4.073   0.411  -1.856  1.00  0.00           C  
HETATM   16  O4  UNL     1       2.343   1.887  -1.176  1.00  0.00           O  
HETATM   17  H1  UNL     1      -4.400   1.191   1.579  1.00  0.00           H  
HETATM   18  H2  UNL     1      -2.593   1.531   1.571  1.00  0.00           H  
HETATM   19  H3  UNL     1      -3.250  -0.038   2.276  1.00  0.00           H  
HETATM   20  H4  UNL     1      -3.831  -0.942   0.295  1.00  0.00           H  
HETATM   21  H5  UNL     1      -5.136   0.983  -0.431  1.00  0.00           H  
HETATM   22  H6  UNL     1      -3.678   1.717  -1.212  1.00  0.00           H  
HETATM   23  H7  UNL     1      -4.315   0.109  -1.736  1.00  0.00           H  
HETATM   24  H8  UNL     1      -1.415   0.835  -0.465  1.00  0.00           H  
HETATM   25  H9  UNL     1      -1.921  -0.675  -1.269  1.00  0.00           H  
HETATM   26  H10 UNL     1      -1.330  -0.472   1.742  1.00  0.00           H  
HETATM   27  H11 UNL     1      -1.828  -2.694  -0.127  1.00  0.00           H  
HETATM   28  H12 UNL     1      -1.549  -2.855   1.575  1.00  0.00           H  
HETATM   29  H13 UNL     1       0.738   0.900   0.461  1.00  0.00           H  
HETATM   30  H14 UNL     1       2.719  -1.264  -0.082  1.00  0.00           H  
HETATM   31  H15 UNL     1       5.261  -0.508   1.101  1.00  0.00           H  
HETATM   32  H16 UNL     1       1.980   0.090  -2.002  1.00  0.00           H  
HETATM   33  H17 UNL     1       4.477   1.423  -2.135  1.00  0.00           H  
HETATM   34  H18 UNL     1       4.822  -0.069  -1.237  1.00  0.00           H  
HETATM   35  H19 UNL     1       4.061  -0.150  -2.835  1.00  0.00           H  
HETATM   36  H20 UNL     1       2.607   2.164  -0.247  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3    4   20
CONECT    3   21   22   23
CONECT    4    5   24   25
CONECT    5    6    7   26
CONECT    6   27   28
CONECT    7    8    8    9
CONECT    9   10   29
CONECT   10   11   14   30
CONECT   11   12   12   13
CONECT   13   31
CONECT   14   15   16   32
CONECT   15   33   34   35
CONECT   16   36
END

HMDB0028939
     RDKit          3D
Leucyl-Threonine
 36 35  0  0  0  0  0  0  0  0999 V2000
   -3.3742    0.7433    1.4984 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3324    0.0391    0.1567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1352    0.7894   -0.8818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8895   -0.1414   -0.2970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1976   -0.9727    0.7541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9041   -2.2418    0.8264 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2384   -1.1833    0.4415 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6510   -2.3543    0.2856 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0833   -0.0718    0.3312 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.5153   -0.1811    0.0255 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3165    0.3321    1.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7812    0.7882    2.1595 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6947    0.3316    1.0631 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7165    0.5479   -1.2803 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0734    0.4108   -1.8560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3428    1.8871   -1.1757 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3998    1.1909    1.5792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5935    1.5311    1.5714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2499   -0.0381    2.2758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8308   -0.9421    0.2951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1365    0.9831   -0.4315 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6778    1.7175   -1.2121 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3154    0.1088   -1.7360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4154    0.8352   -0.4653 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9208   -0.6754   -1.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3296   -0.4722    1.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8279   -2.6938   -0.1269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5489   -2.8545    1.5749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7383    0.8999    0.4612 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7185   -1.2638   -0.0815 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2615   -0.5078    1.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9799    0.0902   -2.0023 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4774    1.4235   -2.1346 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8224   -0.0695   -1.2365 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0614   -0.1503   -2.8345 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6066    2.1642   -0.2475 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
  5  6  1  0
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 10 14  1  0
 14 15  1  0
 14 16  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  3 23  1  0
  4 24  1  0
  4 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  9 29  1  0
 10 30  1  0
 13 31  1  0
 14 32  1  0
 15 33  1  0
 15 34  1  0
 15 35  1  0
 16 36  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
L-Leucyl-L-threonine	HMDB
L-T Dipeptide	HMDB
Leu-THR	HMDB
Leucine threonine dipeptide	HMDB
Leucine-threonine dipeptide	HMDB
Leucylthreonine	HMDB
LT Dipeptide	HMDB
2-[(2-Amino-1-hydroxy-4-methylpentylidene)amino]-3-hydroxybutanoate	HMDB

Chemical Formula

C₁₀H₂₀N₂O₄

Average Molecular Weight

232.2768

Monoisotopic Molecular Weight

232.142307138

IUPAC Name

2-(2-amino-4-methylpentanamido)-3-hydroxybutanoic acid

Traditional Name

2-(2-amino-4-methylpentanamido)-3-hydroxybutanoic acid

CAS Registry Number

Not Available

SMILES

CC(C)CC(N)C(=O)NC(C(C)O)C(O)=O

InChI Identifier

InChI=1S/C10H20N2O4/c1-5(2)4-7(11)9(14)12-8(6(3)13)10(15)16/h5-8,13H,4,11H2,1-3H3,(H,12,14)(H,15,16)

InChI Key

LRKCBIUDWAXNEG-UHFFFAOYSA-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
Leucine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Alpha-amino acid or derivatives
Beta-hydroxy acid
Branched fatty acid
Hydroxy fatty acid
Short-chain hydroxy acid
Fatty amide
Hydroxy acid
N-acyl-amine
Fatty acyl
Fatty acid
Secondary carboxylic acid amide
Secondary alcohol
Amino acid or derivatives
Carboxamide group
Amino acid
Carboxylic acid
Monocarboxylic acid or derivatives
Alcohol
Amine
Organic nitrogen compound
Carbonyl group
Organic oxide
Organopnictogen compound
Hydrocarbon derivative
Organooxygen compound
Primary amine
Organic oxygen compound
Organonitrogen compound
Primary aliphatic amine
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Feces (PMID: 27275383)

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
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)

Equine

Horse (FooDB: FOOD00378)

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)

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	-2.75	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	49.5 g/L	ALOGPS
logP	-1.7	ALOGPS
logP	-2.8	ChemAxon
logS	-0.67	ALOGPS
pKa (Strongest Acidic)	3.8	ChemAxon
pKa (Strongest Basic)	8.43	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	112.65 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	57.43 m³·mol⁻¹	ChemAxon
Polarizability	24.26 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
DarkChem	[M+H]+	154.722	31661259
DarkChem	[M-H]-	151.284	31661259
DeepCCS	[M+H]+	157.276	30932474
DeepCCS	[M-H]-	154.242	30932474
DeepCCS	[M-2H]-	190.167	30932474
DeepCCS	[M+Na]+	165.917	30932474
AllCCS	[M+H]+	154.8	32859911
AllCCS	[M+H-H2O]+	151.5	32859911
AllCCS	[M+NH4]+	157.8	32859911
AllCCS	[M+Na]+	158.6	32859911
AllCCS	[M-H]-	153.4	32859911
AllCCS	[M+Na-2H]-	154.5	32859911
AllCCS	[M+HCOO]-	155.7	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Leucyl-Threonine	CC(C)CC(N)C(=O)NC(C(C)O)C(O)=O	3013.9	Standard polar	33892256
Leucyl-Threonine	CC(C)CC(N)C(=O)NC(C(C)O)C(O)=O	1733.9	Standard non polar	33892256
Leucyl-Threonine	CC(C)CC(N)C(=O)NC(C(C)O)C(O)=O	1889.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Leucyl-Threonine,1TMS,isomer #1	CC(C)CC(N)C(=O)NC(C(=O)O)C(C)O[Si](C)(C)C	1880.2	Semi standard non polar	33892256
Leucyl-Threonine,1TMS,isomer #2	CC(C)CC(N)C(=O)NC(C(=O)O[Si](C)(C)C)C(C)O	1874.3	Semi standard non polar	33892256
Leucyl-Threonine,1TMS,isomer #3	CC(C)CC(N[Si](C)(C)C)C(=O)NC(C(=O)O)C(C)O	1914.0	Semi standard non polar	33892256
Leucyl-Threonine,1TMS,isomer #4	CC(C)CC(N)C(=O)N(C(C(=O)O)C(C)O)[Si](C)(C)C	1879.3	Semi standard non polar	33892256
Leucyl-Threonine,2TMS,isomer #1	CC(C)CC(N)C(=O)NC(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C	1896.7	Semi standard non polar	33892256
Leucyl-Threonine,2TMS,isomer #2	CC(C)CC(N[Si](C)(C)C)C(=O)NC(C(=O)O)C(C)O[Si](C)(C)C	1951.2	Semi standard non polar	33892256
Leucyl-Threonine,2TMS,isomer #3	CC(C)CC(N)C(=O)N(C(C(=O)O)C(C)O[Si](C)(C)C)[Si](C)(C)C	1931.5	Semi standard non polar	33892256
Leucyl-Threonine,2TMS,isomer #4	CC(C)CC(N[Si](C)(C)C)C(=O)NC(C(=O)O[Si](C)(C)C)C(C)O	1940.3	Semi standard non polar	33892256
Leucyl-Threonine,2TMS,isomer #5	CC(C)CC(N)C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O)[Si](C)(C)C	1885.5	Semi standard non polar	33892256
Leucyl-Threonine,2TMS,isomer #6	CC(C)CC(C(=O)NC(C(=O)O)C(C)O)N([Si](C)(C)C)[Si](C)(C)C	2098.5	Semi standard non polar	33892256
Leucyl-Threonine,2TMS,isomer #7	CC(C)CC(N[Si](C)(C)C)C(=O)N(C(C(=O)O)C(C)O)[Si](C)(C)C	1968.7	Semi standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #1	CC(C)CC(N[Si](C)(C)C)C(=O)NC(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C	1953.7	Semi standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #1	CC(C)CC(N[Si](C)(C)C)C(=O)NC(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C	1989.7	Standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #2	CC(C)CC(N)C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C)[Si](C)(C)C	1935.2	Semi standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #2	CC(C)CC(N)C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C)[Si](C)(C)C	2015.6	Standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #3	CC(C)CC(C(=O)NC(C(=O)O)C(C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2117.9	Semi standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #3	CC(C)CC(C(=O)NC(C(=O)O)C(C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2044.7	Standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #4	CC(C)CC(N[Si](C)(C)C)C(=O)N(C(C(=O)O)C(C)O[Si](C)(C)C)[Si](C)(C)C	2008.4	Semi standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #4	CC(C)CC(N[Si](C)(C)C)C(=O)N(C(C(=O)O)C(C)O[Si](C)(C)C)[Si](C)(C)C	2016.2	Standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #5	CC(C)CC(C(=O)NC(C(=O)O[Si](C)(C)C)C(C)O)N([Si](C)(C)C)[Si](C)(C)C	2094.5	Semi standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #5	CC(C)CC(C(=O)NC(C(=O)O[Si](C)(C)C)C(C)O)N([Si](C)(C)C)[Si](C)(C)C	2030.6	Standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #6	CC(C)CC(N[Si](C)(C)C)C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O)[Si](C)(C)C	1952.0	Semi standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #6	CC(C)CC(N[Si](C)(C)C)C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O)[Si](C)(C)C	2008.5	Standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #7	CC(C)CC(C(=O)N(C(C(=O)O)C(C)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2107.8	Semi standard non polar	33892256
Leucyl-Threonine,3TMS,isomer #7	CC(C)CC(C(=O)N(C(C(=O)O)C(C)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2066.5	Standard non polar	33892256
Leucyl-Threonine,4TMS,isomer #1	CC(C)CC(C(=O)NC(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2100.1	Semi standard non polar	33892256
Leucyl-Threonine,4TMS,isomer #1	CC(C)CC(C(=O)NC(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2136.8	Standard non polar	33892256
Leucyl-Threonine,4TMS,isomer #2	CC(C)CC(N[Si](C)(C)C)C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C)[Si](C)(C)C	1997.3	Semi standard non polar	33892256
Leucyl-Threonine,4TMS,isomer #2	CC(C)CC(N[Si](C)(C)C)C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C)[Si](C)(C)C	2096.8	Standard non polar	33892256
Leucyl-Threonine,4TMS,isomer #3	CC(C)CC(C(=O)N(C(C(=O)O)C(C)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2158.5	Semi standard non polar	33892256
Leucyl-Threonine,4TMS,isomer #3	CC(C)CC(C(=O)N(C(C(=O)O)C(C)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2148.5	Standard non polar	33892256
Leucyl-Threonine,4TMS,isomer #4	CC(C)CC(C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2116.9	Semi standard non polar	33892256
Leucyl-Threonine,4TMS,isomer #4	CC(C)CC(C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2148.8	Standard non polar	33892256
Leucyl-Threonine,5TMS,isomer #1	CC(C)CC(C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2184.5	Semi standard non polar	33892256
Leucyl-Threonine,5TMS,isomer #1	CC(C)CC(C(=O)N(C(C(=O)O[Si](C)(C)C)C(C)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2243.5	Standard non polar	33892256
Leucyl-Threonine,1TBDMS,isomer #1	CC(C)CC(N)C(=O)NC(C(=O)O)C(C)O[Si](C)(C)C(C)(C)C	2112.9	Semi standard non polar	33892256
Leucyl-Threonine,1TBDMS,isomer #2	CC(C)CC(N)C(=O)NC(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O	2116.5	Semi standard non polar	33892256
Leucyl-Threonine,1TBDMS,isomer #3	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)NC(C(=O)O)C(C)O	2154.1	Semi standard non polar	33892256
Leucyl-Threonine,1TBDMS,isomer #4	CC(C)CC(N)C(=O)N(C(C(=O)O)C(C)O)[Si](C)(C)C(C)(C)C	2099.6	Semi standard non polar	33892256
Leucyl-Threonine,2TBDMS,isomer #1	CC(C)CC(N)C(=O)NC(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O[Si](C)(C)C(C)(C)C	2344.0	Semi standard non polar	33892256
Leucyl-Threonine,2TBDMS,isomer #2	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)NC(C(=O)O)C(C)O[Si](C)(C)C(C)(C)C	2393.7	Semi standard non polar	33892256
Leucyl-Threonine,2TBDMS,isomer #3	CC(C)CC(N)C(=O)N(C(C(=O)O)C(C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2375.9	Semi standard non polar	33892256
Leucyl-Threonine,2TBDMS,isomer #4	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)NC(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O	2393.2	Semi standard non polar	33892256
Leucyl-Threonine,2TBDMS,isomer #5	CC(C)CC(N)C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O)[Si](C)(C)C(C)(C)C	2336.7	Semi standard non polar	33892256
Leucyl-Threonine,2TBDMS,isomer #6	CC(C)CC(C(=O)NC(C(=O)O)C(C)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2518.8	Semi standard non polar	33892256
Leucyl-Threonine,2TBDMS,isomer #7	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(C(=O)O)C(C)O)[Si](C)(C)C(C)(C)C	2409.0	Semi standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #1	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)NC(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O[Si](C)(C)C(C)(C)C	2598.0	Semi standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #1	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)NC(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O[Si](C)(C)C(C)(C)C	2542.6	Standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #2	CC(C)CC(N)C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2580.5	Semi standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #2	CC(C)CC(N)C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2555.4	Standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #3	CC(C)CC(C(=O)NC(C(=O)O)C(C)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2786.2	Semi standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #3	CC(C)CC(C(=O)NC(C(=O)O)C(C)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2587.1	Standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #4	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(C(=O)O)C(C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2649.4	Semi standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #4	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(C(=O)O)C(C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2551.7	Standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #5	CC(C)CC(C(=O)NC(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2749.3	Semi standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #5	CC(C)CC(C(=O)NC(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2578.9	Standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #6	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O)[Si](C)(C)C(C)(C)C	2606.9	Semi standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #6	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O)[Si](C)(C)C(C)(C)C	2558.7	Standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #7	CC(C)CC(C(=O)N(C(C(=O)O)C(C)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2756.1	Semi standard non polar	33892256
Leucyl-Threonine,3TBDMS,isomer #7	CC(C)CC(C(=O)N(C(C(=O)O)C(C)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2595.0	Standard non polar	33892256
Leucyl-Threonine,4TBDMS,isomer #1	CC(C)CC(C(=O)NC(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2983.6	Semi standard non polar	33892256
Leucyl-Threonine,4TBDMS,isomer #1	CC(C)CC(C(=O)NC(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2827.6	Standard non polar	33892256
Leucyl-Threonine,4TBDMS,isomer #2	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2832.9	Semi standard non polar	33892256
Leucyl-Threonine,4TBDMS,isomer #2	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2804.4	Standard non polar	33892256
Leucyl-Threonine,4TBDMS,isomer #3	CC(C)CC(C(=O)N(C(C(=O)O)C(C)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	3028.8	Semi standard non polar	33892256
Leucyl-Threonine,4TBDMS,isomer #3	CC(C)CC(C(=O)N(C(C(=O)O)C(C)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	2834.0	Standard non polar	33892256
Leucyl-Threonine,4TBDMS,isomer #4	CC(C)CC(C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2977.0	Semi standard non polar	33892256
Leucyl-Threonine,4TBDMS,isomer #4	CC(C)CC(C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2848.1	Standard non polar	33892256
Leucyl-Threonine,5TBDMS,isomer #1	CC(C)CC(C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)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	3256.5	Semi standard non polar	33892256
Leucyl-Threonine,5TBDMS,isomer #1	CC(C)CC(C(=O)N(C(C(=O)O[Si](C)(C)C(C)(C)C)C(C)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	3092.9	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Leucyl-Threonine GC-MS (Non-derivatized) - 70eV, Positive	splash10-000f-9300000000-9277d4fd236762d69123	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucyl-Threonine GC-MS (2 TMS) - 70eV, Positive	splash10-02g9-9521000000-752bb4c83d7e92a2448f	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Leucyl-Threonine 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 - Leucyl-Threonine 10V, Positive-QTOF	splash10-014i-2590000000-9f925dac0f2a83225b51	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 20V, Positive-QTOF	splash10-014r-9610000000-9e83b255aa4e88822968	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 40V, Positive-QTOF	splash10-0ap0-9100000000-b2acbe02f26f5d86a8a3	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 10V, Negative-QTOF	splash10-0019-0980000000-c35f4d7a040269f56c3a	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 20V, Negative-QTOF	splash10-029i-1910000000-483d340388a36e998443	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 40V, Negative-QTOF	splash10-00di-9800000000-4ec0c77ac167f2fc9053	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 10V, Positive-QTOF	splash10-001i-2290000000-f80252f919083d47ce28	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 20V, Positive-QTOF	splash10-000i-9200000000-bde5d0d62f5455b58e8f	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 40V, Positive-QTOF	splash10-00ko-9000000000-cf30dac7d9303f43107d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 10V, Negative-QTOF	splash10-001i-0090000000-4a55876d5da898ee2be8	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 20V, Negative-QTOF	splash10-0fbc-4900000000-410ca6abd7b93891d1e0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Leucyl-Threonine 40V, Negative-QTOF	splash10-0006-9100000000-449213439067387771ee	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-16	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

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

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal Cancer	27275383	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal cancer	27015276	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal cancer	25037050	details

Associated Disorders and Diseases

Disease References

Colorectal cancer

Brown DG, Rao S, Weir TL, O'Malia J, Bazan M, Brown RJ, Ryan EP: Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool. Cancer Metab. 2016 Jun 6;4:11. doi: 10.1186/s40170-016-0151-y. eCollection 2016. [PubMed:27275383 ]
Sinha R, Ahn J, Sampson JN, Shi J, Yu G, Xiong X, Hayes RB, Goedert JJ: Fecal Microbiota, Fecal Metabolome, and Colorectal Cancer Interrelations. PLoS One. 2016 Mar 25;11(3):e0152126. doi: 10.1371/journal.pone.0152126. eCollection 2016. [PubMed:27015276 ]
Goedert JJ, Sampson JN, Moore SC, Xiao Q, Xiong X, Hayes RB, Ahn J, Shi J, Sinha R: Fecal metabolomics: assay performance and association with colorectal cancer. Carcinogenesis. 2014 Sep;35(9):2089-96. doi: 10.1093/carcin/bgu131. Epub 2014 Jul 18. [PubMed:25037050 ]

Associated OMIM IDs

114500 (Colorectal cancer)

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB111963

KNApSAcK ID

Not Available

Chemspider ID

16568334

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

18218222

PDB ID

Not Available

ChEBI ID

Not Available

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 Leucyl-Threonine (HMDB0028939)

MOL for HMDB0028939 (Leucyl-Threonine)

3D MOL for HMDB0028939 (Leucyl-Threonine)

3D SDF for HMDB0028939 (Leucyl-Threonine)

3D-SDF for HMDB0028939 (Leucyl-Threonine)

PDB for HMDB0028939 (Leucyl-Threonine)

3D PDB for HMDB0028939 (Leucyl-Threonine)

SMILES for HMDB0028939 (Leucyl-Threonine)

INCHI for HMDB0028939 (Leucyl-Threonine)

Structure for HMDB0028939 (Leucyl-Threonine)

3D Structure for HMDB0028939 (Leucyl-Threonine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra