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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 21:03:44 UTC

Update Date

2021-09-14 15:46:12 UTC

HMDB ID

HMDB0029111

Secondary Accession Numbers

HMDB29111

Metabolite Identification

Common Name

Tyrosyl-Methionine

Description

Tyrosyl-Methionine is a dipeptide composed of tyrosine and methionine. 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

HMDB0029111
     RDKit          3D
Tyrosyl-Methionine
 41 41  0  0  0  0  0  0  0  0999 V2000
    6.0110   -0.5540   -2.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3047   -0.4358   -2.8287 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.3700    0.4874   -1.5653 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3368   -0.3487   -0.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5954    0.2772    0.8168 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2184    0.5557    0.5280 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2033   -0.0545    1.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5205   -0.8370    2.2255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2060    0.2196    1.0137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4035    1.1298   -0.0807 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8992   -1.0950    0.6871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3127   -0.7943    0.4071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2376   -0.8001    1.4162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5716   -0.5142    1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0056   -0.2194   -0.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3510    0.0678   -0.4166 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0506   -0.2214   -1.1375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7150   -0.5058   -0.8694 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2813    1.5206    1.2744 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6390    2.5871    1.3525 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6348    1.4794    1.6108 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2203    0.2095   -1.4995 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1503   -1.5636   -1.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7474   -0.4152   -3.0770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3598    0.7353   -1.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8988    1.4519   -1.4345 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3965   -0.4799    0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9546   -1.3555   -0.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6590   -0.4320    1.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9146    1.2047   -0.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6409    0.6925    1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1113    0.7772   -0.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9718    2.0632    0.1427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4356   -1.5857   -0.1864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8374   -1.7892    1.5770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9913   -1.0197    2.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3241   -0.5160    1.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9345   -0.7342   -0.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3457    0.0046   -2.1577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0192   -0.4860   -1.7188 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9480    1.8880    2.5031 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  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
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  6 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 13 36  1  0
 14 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 21 41  1  0
M  END


  Mrv1652304062014222D          

 21 21  0  0  0  0            999 V2000
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.2881   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0026   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0029111

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C14H20N2O4S/c1-21-7-6-12(14(19)20)16-13(18)11(15)8-9-2-4-10(17)5-3-9/h2-5,11-12,17H,6-8,15H2,1H3,(H,16,18)(H,19,20)

> <INCHI_KEY>
KYPMKDGKAYQCHO-UHFFFAOYSA-N

> <FORMULA>
C14H20N2O4S

> <MOLECULAR_WEIGHT>
312.385

> <EXACT_MASS>
312.114377828

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
32.69638323572675

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[2-amino-3-(4-hydroxyphenyl)propanamido]-4-(methylsulfanyl)butanoic acid

> <ALOGPS_LOGP>
-0.56

> <JCHEM_LOGP>
-1.3759503623140266

> <ALOGPS_LOGS>
-3.11

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.51860334882835

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.626182376219533

> <JCHEM_PKA_STRONGEST_BASIC>
8.020690924899268

> <JCHEM_POLAR_SURFACE_AREA>
112.65

> <JCHEM_REFRACTIVITY>
81.48330000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.43e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[2-amino-3-(4-hydroxyphenyl)propanamido]-4-(methylsulfanyl)butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029111
     RDKit          3D
Tyrosyl-Methionine
 41 41  0  0  0  0  0  0  0  0999 V2000
    6.0110   -0.5540   -2.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3047   -0.4358   -2.8287 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.3700    0.4874   -1.5653 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3368   -0.3487   -0.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5954    0.2772    0.8168 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2184    0.5557    0.5280 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2033   -0.0545    1.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5205   -0.8370    2.2255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2060    0.2196    1.0137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4035    1.1298   -0.0807 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8992   -1.0950    0.6871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3127   -0.7943    0.4071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2376   -0.8001    1.4162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5716   -0.5142    1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0056   -0.2194   -0.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3510    0.0678   -0.4166 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0506   -0.2214   -1.1375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7150   -0.5058   -0.8694 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2813    1.5206    1.2744 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6390    2.5871    1.3525 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6348    1.4794    1.6108 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2203    0.2095   -1.4995 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1503   -1.5636   -1.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7474   -0.4152   -3.0770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3598    0.7353   -1.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8988    1.4519   -1.4345 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3965   -0.4799    0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9546   -1.3555   -0.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6590   -0.4320    1.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9146    1.2047   -0.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6409    0.6925    1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1113    0.7772   -0.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9718    2.0632    0.1427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4356   -1.5857   -0.1864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8374   -1.7892    1.5770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9913   -1.0197    2.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3241   -0.5160    1.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9345   -0.7342   -0.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3457    0.0046   -2.1577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0192   -0.4860   -1.7188 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9480    1.8880    2.5031 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  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
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  6 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 13 36  1  0
 14 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 21 41  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       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM    2  S   UNK     0       4.001 -10.010   0.000  0.00  0.00           S+0
HETATM    3  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0       9.336 -10.010   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      10.669  -7.700   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   10  N   UNK     0      12.003 -11.550   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.671 -10.010   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.004  -9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.338 -10.010   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      18.672 -12.320   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.671 -11.550   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.336  -6.930   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       6.668  -6.930   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   19                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   12                                                       
CONECT   19    5   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

COMPND    HMDB0029111
HETATM    1  C1  UNL     1       6.011  -0.554  -2.260  1.00  0.00           C  
HETATM    2  S1  UNL     1       4.305  -0.436  -2.829  1.00  0.00           S  
HETATM    3  C2  UNL     1       3.370   0.487  -1.565  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.337  -0.349  -0.332  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.595   0.277   0.817  1.00  0.00           C  
HETATM    6  N1  UNL     1       1.218   0.556   0.528  1.00  0.00           N  
HETATM    7  C5  UNL     1       0.203  -0.055   1.296  1.00  0.00           C  
HETATM    8  O1  UNL     1       0.520  -0.837   2.225  1.00  0.00           O  
HETATM    9  C6  UNL     1      -1.206   0.220   1.014  1.00  0.00           C  
HETATM   10  N2  UNL     1      -1.403   1.130  -0.081  1.00  0.00           N  
HETATM   11  C7  UNL     1      -1.899  -1.095   0.687  1.00  0.00           C  
HETATM   12  C8  UNL     1      -3.313  -0.794   0.407  1.00  0.00           C  
HETATM   13  C9  UNL     1      -4.238  -0.800   1.416  1.00  0.00           C  
HETATM   14  C10 UNL     1      -5.572  -0.514   1.138  1.00  0.00           C  
HETATM   15  C11 UNL     1      -6.006  -0.219  -0.143  1.00  0.00           C  
HETATM   16  O2  UNL     1      -7.351   0.068  -0.417  1.00  0.00           O  
HETATM   17  C12 UNL     1      -5.051  -0.221  -1.137  1.00  0.00           C  
HETATM   18  C13 UNL     1      -3.715  -0.506  -0.869  1.00  0.00           C  
HETATM   19  C14 UNL     1       3.281   1.521   1.274  1.00  0.00           C  
HETATM   20  O3  UNL     1       2.639   2.587   1.352  1.00  0.00           O  
HETATM   21  O4  UNL     1       4.635   1.479   1.611  1.00  0.00           O  
HETATM   22  H1  UNL     1       6.220   0.210  -1.500  1.00  0.00           H  
HETATM   23  H2  UNL     1       6.150  -1.564  -1.825  1.00  0.00           H  
HETATM   24  H3  UNL     1       6.747  -0.415  -3.077  1.00  0.00           H  
HETATM   25  H4  UNL     1       2.360   0.735  -1.957  1.00  0.00           H  
HETATM   26  H5  UNL     1       3.899   1.452  -1.435  1.00  0.00           H  
HETATM   27  H6  UNL     1       4.397  -0.480   0.008  1.00  0.00           H  
HETATM   28  H7  UNL     1       2.955  -1.355  -0.586  1.00  0.00           H  
HETATM   29  H8  UNL     1       2.659  -0.432   1.666  1.00  0.00           H  
HETATM   30  H9  UNL     1       0.915   1.205  -0.242  1.00  0.00           H  
HETATM   31  H10 UNL     1      -1.641   0.693   1.914  1.00  0.00           H  
HETATM   32  H11 UNL     1      -1.111   0.777  -0.998  1.00  0.00           H  
HETATM   33  H12 UNL     1      -0.972   2.063   0.143  1.00  0.00           H  
HETATM   34  H13 UNL     1      -1.436  -1.586  -0.186  1.00  0.00           H  
HETATM   35  H14 UNL     1      -1.837  -1.789   1.577  1.00  0.00           H  
HETATM   36  H15 UNL     1      -3.991  -1.020   2.450  1.00  0.00           H  
HETATM   37  H16 UNL     1      -6.324  -0.516   1.942  1.00  0.00           H  
HETATM   38  H17 UNL     1      -7.935  -0.734  -0.654  1.00  0.00           H  
HETATM   39  H18 UNL     1      -5.346   0.005  -2.158  1.00  0.00           H  
HETATM   40  H19 UNL     1      -3.019  -0.486  -1.719  1.00  0.00           H  
HETATM   41  H20 UNL     1       4.948   1.888   2.503  1.00  0.00           H  
CONECT    1    2   22   23   24
CONECT    2    3
CONECT    3    4   25   26
CONECT    4    5   27   28
CONECT    5    6   19   29
CONECT    6    7   30
CONECT    7    8    8    9
CONECT    9   10   11   31
CONECT   10   32   33
CONECT   11   12   34   35
CONECT   12   13   13   18
CONECT   13   14   36
CONECT   14   15   15   37
CONECT   15   16   17
CONECT   16   38
CONECT   17   18   18   39
CONECT   18   40
CONECT   19   20   20   21
CONECT   21   41
END

HMDB0029111
     RDKit          3D
Tyrosyl-Methionine
 41 41  0  0  0  0  0  0  0  0999 V2000
    6.0110   -0.5540   -2.2595 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3047   -0.4358   -2.8287 S   0  0  0  0  0  0  0  0  0  0  0  0
    3.3700    0.4874   -1.5653 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3368   -0.3487   -0.3319 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5954    0.2772    0.8168 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2184    0.5557    0.5280 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2033   -0.0545    1.2956 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5205   -0.8370    2.2255 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2060    0.2196    1.0137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4035    1.1298   -0.0807 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8992   -1.0950    0.6871 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3127   -0.7943    0.4071 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2376   -0.8001    1.4162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5716   -0.5142    1.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0056   -0.2194   -0.1426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3510    0.0678   -0.4166 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0506   -0.2214   -1.1375 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7150   -0.5058   -0.8694 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2813    1.5206    1.2744 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6390    2.5871    1.3525 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6348    1.4794    1.6108 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2203    0.2095   -1.4995 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1503   -1.5636   -1.8250 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7474   -0.4152   -3.0770 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3598    0.7353   -1.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8988    1.4519   -1.4345 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3965   -0.4799    0.0082 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9546   -1.3555   -0.5859 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6590   -0.4320    1.6664 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9146    1.2047   -0.2424 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6409    0.6925    1.9136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1113    0.7772   -0.9981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9718    2.0632    0.1427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4356   -1.5857   -0.1864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8374   -1.7892    1.5770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9913   -1.0197    2.4498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3241   -0.5160    1.9420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9345   -0.7342   -0.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3457    0.0046   -2.1577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0192   -0.4860   -1.7188 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9480    1.8880    2.5031 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  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
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  6 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 13 36  1  0
 14 37  1  0
 16 38  1  0
 17 39  1  0
 18 40  1  0
 21 41  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
L-Tyrosyl-L-methionine	HMDB
Tyr-met	HMDB
Tyrosine methionine dipeptide	HMDB
Tyrosine-methionine dipeptide	HMDB
Tyrosylmethionine	HMDB
Y-m dipeptide	HMDB
YM dipeptide	HMDB
2-{[2-amino-1-hydroxy-3-(4-hydroxyphenyl)propylidene]amino}-4-(methylsulfanyl)butanoate	HMDB
2-{[2-amino-1-hydroxy-3-(4-hydroxyphenyl)propylidene]amino}-4-(methylsulphanyl)butanoate	HMDB
2-{[2-amino-1-hydroxy-3-(4-hydroxyphenyl)propylidene]amino}-4-(methylsulphanyl)butanoic acid	HMDB

Chemical Formula

C₁₄H₂₀N₂O₄S

Average Molecular Weight

312.385

Monoisotopic Molecular Weight

312.114377828

IUPAC Name

2-[2-amino-3-(4-hydroxyphenyl)propanamido]-4-(methylsulfanyl)butanoic acid

Traditional Name

2-[2-amino-3-(4-hydroxyphenyl)propanamido]-4-(methylsulfanyl)butanoic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C14H20N2O4S/c1-21-7-6-12(14(19)20)16-13(18)11(15)8-9-2-4-10(17)5-3-9/h2-5,11-12,17H,6-8,15H2,1H3,(H,16,18)(H,19,20)

InChI Key

KYPMKDGKAYQCHO-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
Methionine 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
Hydroxy fatty acid
Phenol
Thia fatty acid
Aralkylamine
Benzenoid
Fatty amide
Fatty acyl
Monocyclic benzene moiety
Secondary carboxylic acid amide
Carboxamide group
Amino acid or derivatives
Amino acid
Sulfenyl compound
Thioether
Monocarboxylic acid or derivatives
Carboxylic acid
Dialkylthioether
Organic nitrogen compound
Primary aliphatic amine
Organonitrogen compound
Organooxygen compound
Organosulfur compound
Primary amine
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Amine
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

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	-1.38	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.24 g/L	ALOGPS
logP	-0.56	ALOGPS
logP	-1.4	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	3.63	ChemAxon
pKa (Strongest Basic)	8.02	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	8	ChemAxon
Refractivity	81.48 m³·mol⁻¹	ChemAxon
Polarizability	32.7 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
DarkChem	[M+H]+	170.858	31661259
DarkChem	[M-H]-	171.804	31661259
DeepCCS	[M+H]+	173.664	30932474
DeepCCS	[M-H]-	171.306	30932474
DeepCCS	[M-2H]-	204.192	30932474
DeepCCS	[M+Na]+	179.757	30932474
AllCCS	[M+H]+	171.7	32859911
AllCCS	[M+H-H2O]+	168.8	32859911
AllCCS	[M+NH4]+	174.4	32859911
AllCCS	[M+Na]+	175.1	32859911
AllCCS	[M-H]-	171.8	32859911
AllCCS	[M+Na-2H]-	172.3	32859911
AllCCS	[M+HCOO]-	172.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Tyrosyl-Methionine	CSCCC(NC(=O)C(N)CC1=CC=C(O)C=C1)C(O)=O	3860.2	Standard polar	33892256
Tyrosyl-Methionine	CSCCC(NC(=O)C(N)CC1=CC=C(O)C=C1)C(O)=O	2599.2	Standard non polar	33892256
Tyrosyl-Methionine	CSCCC(NC(=O)C(N)CC1=CC=C(O)C=C1)C(O)=O	2988.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Tyrosyl-Methionine,1TMS,isomer #1	CSCCC(NC(=O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O	2816.6	Semi standard non polar	33892256
Tyrosyl-Methionine,1TMS,isomer #2	CSCCC(NC(=O)C(N)CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C	2742.2	Semi standard non polar	33892256
Tyrosyl-Methionine,1TMS,isomer #3	CSCCC(NC(=O)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C)C(=O)O	2829.2	Semi standard non polar	33892256
Tyrosyl-Methionine,1TMS,isomer #4	CSCCC(C(=O)O)N(C(=O)C(N)CC1=CC=C(O)C=C1)[Si](C)(C)C	2746.6	Semi standard non polar	33892256
Tyrosyl-Methionine,2TMS,isomer #1	CSCCC(NC(=O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	2772.3	Semi standard non polar	33892256
Tyrosyl-Methionine,2TMS,isomer #2	CSCCC(NC(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O	2816.8	Semi standard non polar	33892256
Tyrosyl-Methionine,2TMS,isomer #3	CSCCC(C(=O)O)N(C(=O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C	2758.6	Semi standard non polar	33892256
Tyrosyl-Methionine,2TMS,isomer #4	CSCCC(NC(=O)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2738.6	Semi standard non polar	33892256
Tyrosyl-Methionine,2TMS,isomer #5	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(N)CC1=CC=C(O)C=C1)[Si](C)(C)C	2673.3	Semi standard non polar	33892256
Tyrosyl-Methionine,2TMS,isomer #6	CSCCC(C(=O)O)N(C(=O)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C	2759.7	Semi standard non polar	33892256
Tyrosyl-Methionine,2TMS,isomer #7	CSCCC(NC(=O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2942.1	Semi standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #1	CSCCC(NC(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2776.8	Semi standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #1	CSCCC(NC(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2672.8	Standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #2	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C	2743.7	Semi standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #2	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(N)CC1=CC=C(O[Si](C)(C)C)C=C1)[Si](C)(C)C	2669.4	Standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #3	CSCCC(C(=O)O)N(C(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C	2806.1	Semi standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #3	CSCCC(C(=O)O)N(C(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C	2741.0	Standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #4	CSCCC(NC(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2960.8	Semi standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #4	CSCCC(NC(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2798.4	Standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #5	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C	2706.0	Semi standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #5	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C)[Si](C)(C)C	2743.7	Standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #6	CSCCC(NC(=O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2861.5	Semi standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #6	CSCCC(NC(=O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2814.1	Standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #7	CSCCC(C(=O)O)N(C(=O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2869.4	Semi standard non polar	33892256
Tyrosyl-Methionine,3TMS,isomer #7	CSCCC(C(=O)O)N(C(=O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2869.6	Standard non polar	33892256
Tyrosyl-Methionine,4TMS,isomer #1	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C	2773.8	Semi standard non polar	33892256
Tyrosyl-Methionine,4TMS,isomer #1	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N[Si](C)(C)C)[Si](C)(C)C	2747.0	Standard non polar	33892256
Tyrosyl-Methionine,4TMS,isomer #2	CSCCC(NC(=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	2882.3	Semi standard non polar	33892256
Tyrosyl-Methionine,4TMS,isomer #2	CSCCC(NC(=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	2798.9	Standard non polar	33892256
Tyrosyl-Methionine,4TMS,isomer #3	CSCCC(C(=O)O)N(C(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2944.8	Semi standard non polar	33892256
Tyrosyl-Methionine,4TMS,isomer #3	CSCCC(C(=O)O)N(C(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2864.4	Standard non polar	33892256
Tyrosyl-Methionine,4TMS,isomer #4	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2871.9	Semi standard non polar	33892256
Tyrosyl-Methionine,4TMS,isomer #4	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(CC1=CC=C(O)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2880.8	Standard non polar	33892256
Tyrosyl-Methionine,5TMS,isomer #1	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2935.7	Semi standard non polar	33892256
Tyrosyl-Methionine,5TMS,isomer #1	CSCCC(C(=O)O[Si](C)(C)C)N(C(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2869.9	Standard non polar	33892256
Tyrosyl-Methionine,1TBDMS,isomer #1	CSCCC(NC(=O)C(N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	3083.3	Semi standard non polar	33892256
Tyrosyl-Methionine,1TBDMS,isomer #2	CSCCC(NC(=O)C(N)CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	3029.1	Semi standard non polar	33892256
Tyrosyl-Methionine,1TBDMS,isomer #3	CSCCC(NC(=O)C(CC1=CC=C(O)C=C1)N[Si](C)(C)C(C)(C)C)C(=O)O	3071.9	Semi standard non polar	33892256
Tyrosyl-Methionine,1TBDMS,isomer #4	CSCCC(C(=O)O)N(C(=O)C(N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C	3018.5	Semi standard non polar	33892256
Tyrosyl-Methionine,2TBDMS,isomer #1	CSCCC(NC(=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	3316.3	Semi standard non polar	33892256
Tyrosyl-Methionine,2TBDMS,isomer #2	CSCCC(NC(=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	3364.3	Semi standard non polar	33892256
Tyrosyl-Methionine,2TBDMS,isomer #3	CSCCC(C(=O)O)N(C(=O)C(N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	3299.9	Semi standard non polar	33892256
Tyrosyl-Methionine,2TBDMS,isomer #4	CSCCC(NC(=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	3245.3	Semi standard non polar	33892256
Tyrosyl-Methionine,2TBDMS,isomer #5	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(N)CC1=CC=C(O)C=C1)[Si](C)(C)C(C)(C)C	3211.9	Semi standard non polar	33892256
Tyrosyl-Methionine,2TBDMS,isomer #6	CSCCC(C(=O)O)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	3270.9	Semi standard non polar	33892256
Tyrosyl-Methionine,2TBDMS,isomer #7	CSCCC(NC(=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	3401.1	Semi standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #1	CSCCC(NC(=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	3535.4	Semi standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #1	CSCCC(NC(=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	3254.8	Standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #2	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	3518.5	Semi standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #2	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(N)CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)[Si](C)(C)C(C)(C)C	3235.0	Standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #3	CSCCC(C(=O)O)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	3571.6	Semi standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #3	CSCCC(C(=O)O)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	3286.3	Standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #4	CSCCC(NC(=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	3720.2	Semi standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #4	CSCCC(NC(=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	3339.4	Standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #5	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)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	3439.3	Semi standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #5	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)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	3319.2	Standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #6	CSCCC(NC(=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	3598.3	Semi standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #6	CSCCC(NC(=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	3358.9	Standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #7	CSCCC(C(=O)O)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)[Si](C)(C)C(C)(C)C	3611.6	Semi standard non polar	33892256
Tyrosyl-Methionine,3TBDMS,isomer #7	CSCCC(C(=O)O)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)[Si](C)(C)C(C)(C)C	3379.1	Standard non polar	33892256
Tyrosyl-Methionine,4TBDMS,isomer #1	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)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	3734.0	Semi standard non polar	33892256
Tyrosyl-Methionine,4TBDMS,isomer #1	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)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	3448.8	Standard non polar	33892256
Tyrosyl-Methionine,4TBDMS,isomer #2	CSCCC(NC(=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	3903.0	Semi standard non polar	33892256
Tyrosyl-Methionine,4TBDMS,isomer #2	CSCCC(NC(=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	3475.0	Standard non polar	33892256
Tyrosyl-Methionine,4TBDMS,isomer #3	CSCCC(C(=O)O)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)[Si](C)(C)C(C)(C)C	3930.0	Semi standard non polar	33892256
Tyrosyl-Methionine,4TBDMS,isomer #3	CSCCC(C(=O)O)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)[Si](C)(C)C(C)(C)C	3514.3	Standard non polar	33892256
Tyrosyl-Methionine,4TBDMS,isomer #4	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)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)[Si](C)(C)C(C)(C)C	3802.2	Semi standard non polar	33892256
Tyrosyl-Methionine,4TBDMS,isomer #4	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)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)[Si](C)(C)C(C)(C)C	3552.8	Standard non polar	33892256
Tyrosyl-Methionine,5TBDMS,isomer #1	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)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)[Si](C)(C)C(C)(C)C	4093.4	Semi standard non polar	33892256
Tyrosyl-Methionine,5TBDMS,isomer #1	CSCCC(C(=O)O[Si](C)(C)C(C)(C)C)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)[Si](C)(C)C(C)(C)C	3674.7	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-Methionine GC-MS (Non-derivatized) - 70eV, Positive	splash10-01p9-2910000000-589e301aedb28d41cd3b	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tyrosyl-Methionine GC-MS (2 TMS) - 70eV, Positive	splash10-001i-6592200000-4163aa634d636f10c531	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tyrosyl-Methionine 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-Methionine 10V, Positive-QTOF	splash10-03ds-1975000000-584521eb213f7ea71e24	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 20V, Positive-QTOF	splash10-0gbi-0910000000-346eb1f1053fed219fda	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 40V, Positive-QTOF	splash10-0a4r-2900000000-f7cc617222206e88e298	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 10V, Negative-QTOF	splash10-03dj-9168000000-487b47b44be81f849527	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 20V, Negative-QTOF	splash10-0002-9310000000-c9dee56f66f7a2de31b0	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 40V, Negative-QTOF	splash10-0002-9200000000-4e1f309a7a43f494451f	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 10V, Positive-QTOF	splash10-03di-0977000000-c893708fbd6361eff016	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 20V, Positive-QTOF	splash10-0079-0920000000-f3ad4779c78fb20855ae	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 40V, Positive-QTOF	splash10-0bt9-7900000000-f84fa0bdad8deb102a6d	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 10V, Negative-QTOF	splash10-03di-0049000000-2c6b904b8a13ff8fc39a	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 20V, Negative-QTOF	splash10-0002-9554000000-70d8565b9d97cc132b08	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tyrosyl-Methionine 40V, Negative-QTOF	splash10-0002-9300000000-2383dcd12ec64cda5028	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	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

FDB112114

KNApSAcK ID

Not Available

Chemspider ID

16568404

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

18218252

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

Zhang H, Zielonka J, Sikora A, Joseph J, Xu Y, Kalyanaraman B: The effect of neighboring methionine residue on tyrosine nitration and oxidation in peptides treated with MPO, H2O2, and NO2(-) or peroxynitrite and bicarbonate: role of intramolecular electron transfer mechanism? Arch Biochem Biophys. 2009 Apr 15;484(2):134-45. doi: 10.1016/j.abb.2008.11.018. Epub 2008 Nov 24. [PubMed:19056332 ]

Showing metabocard for Tyrosyl-Methionine (HMDB0029111)

MOL for HMDB0029111 (Tyrosyl-Methionine)

3D MOL for HMDB0029111 (Tyrosyl-Methionine)

3D SDF for HMDB0029111 (Tyrosyl-Methionine)

3D-SDF for HMDB0029111 (Tyrosyl-Methionine)

PDB for HMDB0029111 (Tyrosyl-Methionine)

3D PDB for HMDB0029111 (Tyrosyl-Methionine)

SMILES for HMDB0029111 (Tyrosyl-Methionine)

INCHI for HMDB0029111 (Tyrosyl-Methionine)

Structure for HMDB0029111 (Tyrosyl-Methionine)

3D Structure for HMDB0029111 (Tyrosyl-Methionine)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra