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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2012-09-06 21:03:44 UTC

Update Date

2021-09-14 15:46:12 UTC

HMDB ID

HMDB0029109

Secondary Accession Numbers

HMDB29109

Metabolite Identification

Common Name

Tyrosyl-Leucine

Description

Tyrosyl-Leucine is a dipeptide composed of tyrosine and leucine. 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

HMDB0029109
     RDKit          3D
Tyrosyl-Leucine
 43 43  0  0  0  0  0  0  0  0999 V2000
   -4.0772    2.0826   -1.0795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1493    1.7624    0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1049    1.1388    1.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0876    0.8549   -0.3739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0156    0.4179    0.5669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1137   -0.4425   -0.1196 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0229   -0.8621   -1.2721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8459   -0.4962   -2.2884 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1094   -1.7782   -1.6596 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4776   -3.0099   -2.1211 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1228   -2.1164   -0.6403 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9041   -1.0091   -0.0787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0016   -0.4949   -0.7374 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7751    0.5237   -0.2237 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4451    1.0584    1.0014 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2114    2.0846    1.5348 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3576    0.5561    1.6658 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5932   -0.4641    1.1390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4725   -0.3192    1.7669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3855   -1.5967    1.7732 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9900    0.2316    2.9119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6657    1.1640   -1.2810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7855    2.8757   -0.8126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4611    2.2830   -1.9635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7385    2.7169    0.4475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0967    1.6350    2.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9879    0.0492    1.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1912    1.2783    0.8033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5458    1.3836   -1.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5685   -0.0303   -0.8676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4988    1.3516    0.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3993   -1.2565   -2.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6522   -1.3637   -2.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1782   -3.6801   -2.4989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1058   -3.4290   -1.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6395   -2.7323    0.1554 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8369   -2.8510   -1.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2558   -0.9213   -1.7028 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6336    0.9327   -0.7291 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9872    2.4870    2.4254 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1106    0.9849    2.6255 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7681   -0.7910    1.7660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7960   -0.2084    3.3358 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
  6  7  2  3
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
  5 19  1  0
 19 20  2  0
 19 21  1  0
 18 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  8 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 13 38  1  0
 14 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
 21 43  1  0
M  END

  Mrv1652304032018482D          

 21 21  0  0  0  0            999 V2000
   -2.8579    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    9.4875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    8.2500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    7.0125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    7.4250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    5.7750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   10.7250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  3  1  0  0  0  0
  6  4  2  0  0  0  0
  9  1  1  0  0  0  0
  9  2  1  0  0  0  0
  9  7  1  0  0  0  0
 10  3  2  0  0  0  0
 10  4  1  0  0  0  0
 10  8  1  0  0  0  0
 11  5  2  0  0  0  0
 11  6  1  0  0  0  0
 12  8  1  0  0  0  0
 13  7  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 12  1  0  0  0  0
 17 13  1  4  0  0  0
 17 14  2  0  0  0  0
 18 11  1  0  0  0  0
 19 14  1  0  0  0  0
 20 15  2  0  0  0  0
 21 15  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0029109

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)CC(N=C(O)C(N)CC1=CC=C(O)C=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C15H22N2O4/c1-9(2)7-13(15(20)21)17-14(19)12(16)8-10-3-5-11(18)6-4-10/h3-6,9,12-13,18H,7-8,16H2,1-2H3,(H,17,19)(H,20,21)

> <INCHI_KEY>
AUEJLPRZGVVDNU-UHFFFAOYSA-N

> <FORMULA>
C15H22N2O4

> <MOLECULAR_WEIGHT>
294.3462

> <EXACT_MASS>
294.157957202

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
31.715971085995864

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{[2-amino-1-hydroxy-3-(4-hydroxyphenyl)propylidene]amino}-4-methylpentanoic acid

> <ALOGPS_LOGP>
-1.04

> <JCHEM_LOGP>
-0.17180656580690026

> <ALOGPS_LOGS>
-2.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
4.3030567171404375

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.349452333493798

> <JCHEM_PKA_STRONGEST_BASIC>
9.837215704908331

> <JCHEM_POLAR_SURFACE_AREA>
116.14

> <JCHEM_REFRACTIVITY>
78.58990000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.10e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{[2-amino-1-hydroxy-3-(4-hydroxyphenyl)propylidene]amino}-4-methylpentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029109
     RDKit          3D
Tyrosyl-Leucine
 43 43  0  0  0  0  0  0  0  0999 V2000
   -4.0772    2.0826   -1.0795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1493    1.7624    0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1049    1.1388    1.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0876    0.8549   -0.3739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0156    0.4179    0.5669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1137   -0.4425   -0.1196 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0229   -0.8621   -1.2721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8459   -0.4962   -2.2884 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1094   -1.7782   -1.6596 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4776   -3.0099   -2.1211 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1228   -2.1164   -0.6403 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9041   -1.0091   -0.0787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0016   -0.4949   -0.7374 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7751    0.5237   -0.2237 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4451    1.0584    1.0014 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2114    2.0846    1.5348 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3576    0.5561    1.6658 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5932   -0.4641    1.1390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4725   -0.3192    1.7669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3855   -1.5967    1.7732 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9900    0.2316    2.9119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6657    1.1640   -1.2810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7855    2.8757   -0.8126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4611    2.2830   -1.9635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7385    2.7169    0.4475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0967    1.6350    2.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9879    0.0492    1.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1912    1.2783    0.8033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5458    1.3836   -1.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5685   -0.0303   -0.8676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4988    1.3516    0.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3993   -1.2565   -2.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6522   -1.3637   -2.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1782   -3.6801   -2.4989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1058   -3.4290   -1.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6395   -2.7323    0.1554 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8369   -2.8510   -1.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2558   -0.9213   -1.7028 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6336    0.9327   -0.7291 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9872    2.4870    2.4254 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1106    0.9849    2.6255 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7681   -0.7910    1.7660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7960   -0.2084    3.3358 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
  6  7  2  3
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
  5 19  1  0
 19 20  2  0
 19 21  1  0
 18 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  8 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 13 38  1  0
 14 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
 21 43  1  0
M  END

HEADER    PROTEIN                                 03-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-APR-20         0                                  
HETATM    1  C   UNK     0      -5.335   6.160   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  16.170   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  16.170   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  17.710   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  17.710   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -4.001   8.470   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  13.860   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  15.400   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000  18.480   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -1.334  13.090   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667   9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  11.550   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334   8.470   0.000  0.00  0.00           C+0
HETATM   16  N   UNK     0      -2.667  13.860   0.000  0.00  0.00           N+0
HETATM   17  N   UNK     0      -2.667  10.780   0.000  0.00  0.00           N+0
HETATM   18  O   UNK     0       0.000  20.020   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       0.000  10.780   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       0.000   9.240   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
CONECT    1    9                                                            
CONECT    2    9                                                            
CONECT    3    5   10                                                       
CONECT    4    6   10                                                       
CONECT    5    3   11                                                       
CONECT    6    4   11                                                       
CONECT    7    9   13                                                       
CONECT    8   10   12                                                       
CONECT    9    1    2    7                                                  
CONECT   10    3    4    8                                                  
CONECT   11    5    6   18                                                  
CONECT   12    8   14   16                                                  
CONECT   13    7   15   17                                                  
CONECT   14   12   17   19                                                  
CONECT   15   13   20   21                                                  
CONECT   16   12                                                            
CONECT   17   13   14                                                       
CONECT   18   11                                                            
CONECT   19   14                                                            
CONECT   20   15                                                            
CONECT   21   15                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

COMPND    HMDB0029109
HETATM    1  C1  UNL     1      -4.077   2.083  -1.079  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.149   1.762   0.134  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.105   1.139   1.131  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.088   0.855  -0.374  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.016   0.418   0.567  1.00  0.00           C  
HETATM    6  N1  UNL     1      -0.114  -0.442  -0.120  1.00  0.00           N  
HETATM    7  C6  UNL     1       0.023  -0.862  -1.272  1.00  0.00           C  
HETATM    8  O1  UNL     1      -0.846  -0.496  -2.288  1.00  0.00           O  
HETATM    9  C7  UNL     1       1.109  -1.778  -1.660  1.00  0.00           C  
HETATM   10  N2  UNL     1       0.478  -3.010  -2.121  1.00  0.00           N  
HETATM   11  C8  UNL     1       2.123  -2.116  -0.640  1.00  0.00           C  
HETATM   12  C9  UNL     1       2.904  -1.009  -0.079  1.00  0.00           C  
HETATM   13  C10 UNL     1       4.002  -0.495  -0.737  1.00  0.00           C  
HETATM   14  C11 UNL     1       4.775   0.524  -0.224  1.00  0.00           C  
HETATM   15  C12 UNL     1       4.445   1.058   1.001  1.00  0.00           C  
HETATM   16  O2  UNL     1       5.211   2.085   1.535  1.00  0.00           O  
HETATM   17  C13 UNL     1       3.358   0.556   1.666  1.00  0.00           C  
HETATM   18  C14 UNL     1       2.593  -0.464   1.139  1.00  0.00           C  
HETATM   19  C15 UNL     1      -1.472  -0.319   1.767  1.00  0.00           C  
HETATM   20  O3  UNL     1      -1.385  -1.597   1.773  1.00  0.00           O  
HETATM   21  O4  UNL     1      -1.990   0.232   2.912  1.00  0.00           O  
HETATM   22  H1  UNL     1      -4.666   1.164  -1.281  1.00  0.00           H  
HETATM   23  H2  UNL     1      -4.786   2.876  -0.813  1.00  0.00           H  
HETATM   24  H3  UNL     1      -3.461   2.283  -1.963  1.00  0.00           H  
HETATM   25  H4  UNL     1      -2.738   2.717   0.447  1.00  0.00           H  
HETATM   26  H5  UNL     1      -4.097   1.635   2.122  1.00  0.00           H  
HETATM   27  H6  UNL     1      -3.988   0.049   1.158  1.00  0.00           H  
HETATM   28  H7  UNL     1      -5.191   1.278   0.803  1.00  0.00           H  
HETATM   29  H8  UNL     1      -1.546   1.384  -1.218  1.00  0.00           H  
HETATM   30  H9  UNL     1      -2.569  -0.030  -0.868  1.00  0.00           H  
HETATM   31  H10 UNL     1      -0.499   1.352   0.946  1.00  0.00           H  
HETATM   32  H11 UNL     1      -1.399  -1.257  -2.697  1.00  0.00           H  
HETATM   33  H12 UNL     1       1.652  -1.364  -2.553  1.00  0.00           H  
HETATM   34  H13 UNL     1       1.178  -3.680  -2.499  1.00  0.00           H  
HETATM   35  H14 UNL     1      -0.106  -3.429  -1.363  1.00  0.00           H  
HETATM   36  H15 UNL     1       1.640  -2.732   0.155  1.00  0.00           H  
HETATM   37  H16 UNL     1       2.837  -2.851  -1.130  1.00  0.00           H  
HETATM   38  H17 UNL     1       4.256  -0.921  -1.703  1.00  0.00           H  
HETATM   39  H18 UNL     1       5.634   0.933  -0.729  1.00  0.00           H  
HETATM   40  H19 UNL     1       4.987   2.487   2.425  1.00  0.00           H  
HETATM   41  H20 UNL     1       3.111   0.985   2.626  1.00  0.00           H  
HETATM   42  H21 UNL     1       1.768  -0.791   1.766  1.00  0.00           H  
HETATM   43  H22 UNL     1      -2.796  -0.208   3.336  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3    4   25
CONECT    3   26   27   28
CONECT    4    5   29   30
CONECT    5    6   19   31
CONECT    6    7    7
CONECT    7    8    9
CONECT    8   32
CONECT    9   10   11   33
CONECT   10   34   35
CONECT   11   12   36   37
CONECT   12   13   13   18
CONECT   13   14   38
CONECT   14   15   15   39
CONECT   15   16   17
CONECT   16   40
CONECT   17   18   18   41
CONECT   18   42
CONECT   19   20   20   21
CONECT   21   43
END

HMDB0029109
     RDKit          3D
Tyrosyl-Leucine
 43 43  0  0  0  0  0  0  0  0999 V2000
   -4.0772    2.0826   -1.0795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1493    1.7624    0.1342 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1049    1.1388    1.1308 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0876    0.8549   -0.3739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0156    0.4179    0.5669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1137   -0.4425   -0.1196 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0229   -0.8621   -1.2721 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8459   -0.4962   -2.2884 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1094   -1.7782   -1.6596 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4776   -3.0099   -2.1211 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1228   -2.1164   -0.6403 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9041   -1.0091   -0.0787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0016   -0.4949   -0.7374 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7751    0.5237   -0.2237 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4451    1.0584    1.0014 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2114    2.0846    1.5348 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3576    0.5561    1.6658 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5932   -0.4641    1.1390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4725   -0.3192    1.7669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3855   -1.5967    1.7732 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9900    0.2316    2.9119 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6657    1.1640   -1.2810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7855    2.8757   -0.8126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4611    2.2830   -1.9635 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7385    2.7169    0.4475 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0967    1.6350    2.1217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9879    0.0492    1.1583 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1912    1.2783    0.8033 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5458    1.3836   -1.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5685   -0.0303   -0.8676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4988    1.3516    0.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3993   -1.2565   -2.6967 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6522   -1.3637   -2.5528 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1782   -3.6801   -2.4989 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1058   -3.4290   -1.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6395   -2.7323    0.1554 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8369   -2.8510   -1.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2558   -0.9213   -1.7028 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6336    0.9327   -0.7291 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9872    2.4870    2.4254 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1106    0.9849    2.6255 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7681   -0.7910    1.7660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7960   -0.2084    3.3358 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
  6  7  2  3
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 15 17  1  0
 17 18  2  0
  5 19  1  0
 19 20  2  0
 19 21  1  0
 18 12  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  3 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  8 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 11 36  1  0
 11 37  1  0
 13 38  1  0
 14 39  1  0
 16 40  1  0
 17 41  1  0
 18 42  1  0
 21 43  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
L-Tyrosyl-L-leucine	HMDB
Tyr-leu	HMDB
Tyrosine leucine dipeptide	HMDB
Tyrosine-leucine dipeptide	HMDB
Tyrosylleucine	HMDB
Y-L dipeptide	HMDB
yl Dipeptide	HMDB
2-{[2-amino-1-hydroxy-3-(4-hydroxyphenyl)propylidene]amino}-4-methylpentanoate	HMDB

Chemical Formula

C₁₅H₂₂N₂O₄

Average Molecular Weight

294.3462

Monoisotopic Molecular Weight

294.157957202

IUPAC Name

2-{[2-amino-1-hydroxy-3-(4-hydroxyphenyl)propylidene]amino}-4-methylpentanoic acid

Traditional Name

2-{[2-amino-1-hydroxy-3-(4-hydroxyphenyl)propylidene]amino}-4-methylpentanoic acid

CAS Registry Number

Not Available

SMILES

CC(C)CC(N=C(O)C(N)CC1=CC=C(O)C=C1)C(O)=O

InChI Identifier

InChI=1S/C15H22N2O4/c1-9(2)7-13(15(20)21)17-14(19)12(16)8-10-3-5-11(18)6-4-10/h3-6,9,12-13,18H,7-8,16H2,1-2H3,(H,17,19)(H,20,21)

InChI Key

AUEJLPRZGVVDNU-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
Tyrosine or derivatives
Phenylalanine or derivatives
Leucine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Alpha-amino acid or derivatives
Amphetamine or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Aralkylamine
Benzenoid
Fatty acyl
Monocyclic benzene moiety
Fatty amide
Amino acid
Secondary carboxylic acid amide
Amino acid or derivatives
Carboxamide group
Carboxylic acid
Monocarboxylic acid or derivatives
Amine
Primary aliphatic amine
Organopnictogen compound
Organic oxide
Organonitrogen compound
Carbonyl group
Organooxygen compound
Organic oxygen compound
Organic nitrogen compound
Primary amine
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Feces (PMID: 27275383)

Source

Endogenous

Endogenous (HMDB: HMDB0029109)

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)

Milk and milk product

Unfermented milk

Milk (Cow) (FooDB: FOOD00618)

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	-0.77	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	1.05 g/L	ALOGPS
logP	-1	ALOGPS
logP	-0.17	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	3.35	ChemAxon
pKa (Strongest Basic)	9.84	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.14 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	78.59 m³·mol⁻¹	ChemAxon
Polarizability	31.72 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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]+	170.797	31661259
DarkChem	[M-H]-	166.938	31661259
DeepCCS	[M+H]+	176.912	30932474
DeepCCS	[M-H]-	174.554	30932474
DeepCCS	[M-2H]-	207.44	30932474
DeepCCS	[M+Na]+	183.006	30932474
AllCCS	[M+H]+	170.2	32859911
AllCCS	[M+H-H2O]+	167.2	32859911
AllCCS	[M+NH4]+	173.1	32859911
AllCCS	[M+Na]+	173.9	32859911
AllCCS	[M-H]-	170.8	32859911
AllCCS	[M+Na-2H]-	171.3	32859911
AllCCS	[M+HCOO]-	172.0	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Tyrosyl-Leucine	CC(C)CC(N=C(O)C(N)CC1=CC=C(O)C=C1)C(O)=O	3780.4	Standard polar	33892256
Tyrosyl-Leucine	CC(C)CC(N=C(O)C(N)CC1=CC=C(O)C=C1)C(O)=O	2330.6	Standard non polar	33892256
Tyrosyl-Leucine	CC(C)CC(N=C(O)C(N)CC1=CC=C(O)C=C1)C(O)=O	2632.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Tyrosyl-Leucine,1TMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C)C(N)CC1=CC=C(O)C=C1)C(=O)O	2551.9	Semi standard non polar	33892256
Tyrosyl-Leucine,1TMS,isomer #2	CC(C)CC(N=C(O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O	2622.9	Semi standard non polar	33892256
Tyrosyl-Leucine,1TMS,isomer #3	CC(C)CC(N=C(O)C(N)CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C	2572.6	Semi standard non polar	33892256
Tyrosyl-Leucine,1TMS,isomer #4	CC(C)CC(N=C(O)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C)C(=O)O	2663.4	Semi standard non polar	33892256
Tyrosyl-Leucine,2TMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O	2550.4	Semi standard non polar	33892256
Tyrosyl-Leucine,2TMS,isomer #2	CC(C)CC(N=C(O[Si](C)(C)C)C(N)CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C	2432.3	Semi standard non polar	33892256
Tyrosyl-Leucine,2TMS,isomer #3	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C)C(=O)O	2496.0	Semi standard non polar	33892256
Tyrosyl-Leucine,2TMS,isomer #4	CC(C)CC(N=C(O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	2557.7	Semi standard non polar	33892256
Tyrosyl-Leucine,2TMS,isomer #5	CC(C)CC(N=C(O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O	2625.5	Semi standard non polar	33892256
Tyrosyl-Leucine,2TMS,isomer #6	CC(C)CC(N=C(O)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2567.9	Semi standard non polar	33892256
Tyrosyl-Leucine,2TMS,isomer #7	CC(C)CC(N=C(O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2765.5	Semi standard non polar	33892256
Tyrosyl-Leucine,3TMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	2484.2	Semi standard non polar	33892256
Tyrosyl-Leucine,3TMS,isomer #2	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O	2519.9	Semi standard non polar	33892256
Tyrosyl-Leucine,3TMS,isomer #3	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2424.3	Semi standard non polar	33892256
Tyrosyl-Leucine,3TMS,isomer #4	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2660.5	Semi standard non polar	33892256
Tyrosyl-Leucine,3TMS,isomer #5	CC(C)CC(N=C(O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2566.0	Semi standard non polar	33892256
Tyrosyl-Leucine,3TMS,isomer #6	CC(C)CC(N=C(O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2779.4	Semi standard non polar	33892256
Tyrosyl-Leucine,3TMS,isomer #7	CC(C)CC(N=C(O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2681.5	Semi standard non polar	33892256
Tyrosyl-Leucine,4TMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2505.0	Semi standard non polar	33892256
Tyrosyl-Leucine,4TMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2458.6	Standard non polar	33892256
Tyrosyl-Leucine,4TMS,isomer #2	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2703.5	Semi standard non polar	33892256
Tyrosyl-Leucine,4TMS,isomer #2	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2548.0	Standard non polar	33892256
Tyrosyl-Leucine,4TMS,isomer #3	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2615.4	Semi standard non polar	33892256
Tyrosyl-Leucine,4TMS,isomer #3	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2587.2	Standard non polar	33892256
Tyrosyl-Leucine,4TMS,isomer #4	CC(C)CC(N=C(O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2716.1	Semi standard non polar	33892256
Tyrosyl-Leucine,4TMS,isomer #4	CC(C)CC(N=C(O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2590.7	Standard non polar	33892256
Tyrosyl-Leucine,5TMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2675.1	Semi standard non polar	33892256
Tyrosyl-Leucine,5TMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2592.2	Standard non polar	33892256
Tyrosyl-Leucine,1TBDMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(N)CC1=CC=C(O)C=C1)C(=O)O	2814.5	Semi standard non polar	33892256
Tyrosyl-Leucine,1TBDMS,isomer #2	CC(C)CC(N=C(O)C(N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	2860.2	Semi standard non polar	33892256
Tyrosyl-Leucine,1TBDMS,isomer #3	CC(C)CC(N=C(O)C(N)CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	2815.0	Semi standard non polar	33892256
Tyrosyl-Leucine,1TBDMS,isomer #4	CC(C)CC(N=C(O)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O	2869.0	Semi standard non polar	33892256
Tyrosyl-Leucine,2TBDMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	3066.3	Semi standard non polar	33892256
Tyrosyl-Leucine,2TBDMS,isomer #2	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(N)CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	2923.5	Semi standard non polar	33892256
Tyrosyl-Leucine,2TBDMS,isomer #3	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O	2972.0	Semi standard non polar	33892256
Tyrosyl-Leucine,2TBDMS,isomer #4	CC(C)CC(N=C(O)C(N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	3049.0	Semi standard non polar	33892256
Tyrosyl-Leucine,2TBDMS,isomer #5	CC(C)CC(N=C(O)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O	3099.8	Semi standard non polar	33892256
Tyrosyl-Leucine,2TBDMS,isomer #6	CC(C)CC(N=C(O)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3005.4	Semi standard non polar	33892256
Tyrosyl-Leucine,2TBDMS,isomer #7	CC(C)CC(N=C(O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3150.9	Semi standard non polar	33892256
Tyrosyl-Leucine,3TBDMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	3209.0	Semi standard non polar	33892256
Tyrosyl-Leucine,3TBDMS,isomer #2	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O	3233.0	Semi standard non polar	33892256
Tyrosyl-Leucine,3TBDMS,isomer #3	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3071.1	Semi standard non polar	33892256
Tyrosyl-Leucine,3TBDMS,isomer #4	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3356.9	Semi standard non polar	33892256
Tyrosyl-Leucine,3TBDMS,isomer #5	CC(C)CC(N=C(O)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3251.2	Semi standard non polar	33892256
Tyrosyl-Leucine,3TBDMS,isomer #6	CC(C)CC(N=C(O)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3425.5	Semi standard non polar	33892256
Tyrosyl-Leucine,3TBDMS,isomer #7	CC(C)CC(N=C(O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3333.3	Semi standard non polar	33892256
Tyrosyl-Leucine,4TBDMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3361.4	Semi standard non polar	33892256
Tyrosyl-Leucine,4TBDMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3107.4	Standard non polar	33892256
Tyrosyl-Leucine,4TBDMS,isomer #2	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3651.6	Semi standard non polar	33892256
Tyrosyl-Leucine,4TBDMS,isomer #2	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3177.9	Standard non polar	33892256
Tyrosyl-Leucine,4TBDMS,isomer #3	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3493.1	Semi standard non polar	33892256
Tyrosyl-Leucine,4TBDMS,isomer #3	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3225.3	Standard non polar	33892256
Tyrosyl-Leucine,4TBDMS,isomer #4	CC(C)CC(N=C(O)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3608.0	Semi standard non polar	33892256
Tyrosyl-Leucine,4TBDMS,isomer #4	CC(C)CC(N=C(O)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3284.0	Standard non polar	33892256
Tyrosyl-Leucine,5TBDMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3848.6	Semi standard non polar	33892256
Tyrosyl-Leucine,5TBDMS,isomer #1	CC(C)CC(N=C(O[Si](C)(C)C(C)(C)C)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3377.2	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Tyrosyl-Leucine GC-MS (Non-derivatized) - 70eV, Positive	splash10-000l-4910000000-711a5382e400d3b41cf8	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tyrosyl-Leucine GC-MS (2 TMS) - 70eV, Positive	splash10-0a4i-4191000000-7afee3fd243ab6e3a997	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tyrosyl-Leucine 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 - Tyrosyl-Leucine 10V, Positive-QTOF	splash10-002k-0590000000-c8221005bf43c2415430	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 20V, Positive-QTOF	splash10-00kr-3920000000-e518ddadf89a8ded4dc7	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 40V, Positive-QTOF	splash10-0a4i-4900000000-4fad3ce6a27e0b81e0e8	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 10V, Negative-QTOF	splash10-0006-0190000000-f026d1fddf348ce13ed0	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 20V, Negative-QTOF	splash10-01u4-3980000000-d837848997dc913a9c78	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 40V, Negative-QTOF	splash10-03l0-7900000000-c2bed71df9e81e4b9dda	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 10V, Positive-QTOF	splash10-000b-0890000000-f0d64a37f5588ed3f8d4	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 20V, Positive-QTOF	splash10-0080-2910000000-843e17bab6e7d0ba889c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 40V, Positive-QTOF	splash10-0aba-4900000000-65f15fba6370202f2b6e	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 10V, Negative-QTOF	splash10-001i-0940000000-8d0d3fa06d0e197f3a0a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 20V, Negative-QTOF	splash10-01u0-1900000000-fd1d42b59fc990922cea	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Leucine 40V, Negative-QTOF	splash10-0006-9800000000-abcb371dde8ab0749077	2021-09-22	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

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

Abnormal Concentrations

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

Associated Disorders and Diseases

Disease References

Colorectal cancer

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

FDB098231

KNApSAcK ID

Not Available

Chemspider ID

3664634

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

4466134

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 Tyrosyl-Leucine (HMDB0029109)

MOL for HMDB0029109 (Tyrosyl-Leucine)

3D MOL for HMDB0029109 (Tyrosyl-Leucine)

3D SDF for HMDB0029109 (Tyrosyl-Leucine)

3D-SDF for HMDB0029109 (Tyrosyl-Leucine)

PDB for HMDB0029109 (Tyrosyl-Leucine)

3D PDB for HMDB0029109 (Tyrosyl-Leucine)

SMILES for HMDB0029109 (Tyrosyl-Leucine)

INCHI for HMDB0029109 (Tyrosyl-Leucine)

Structure for HMDB0029109 (Tyrosyl-Leucine)

3D Structure for HMDB0029109 (Tyrosyl-Leucine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra