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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 21:03:15 UTC

Update Date

2021-09-14 15:45:52 UTC

HMDB ID

HMDB0028985

Secondary Accession Numbers

HMDB28985

Metabolite Identification

Common Name

Methionyl-Tyrosine

Description

Methionyl-Tyrosine is a dipeptide composed of methionine and tyrosine. 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

HMDB0028985
     RDKit          3D
Methionyl-Tyrosine
 41 41  0  0  0  0  0  0  0  0999 V2000
    6.9999    0.7246    0.0311 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2177    0.6379    0.1574 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.6599    0.1652    1.8141 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1522    0.1021    1.8840 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6540   -0.9321    0.8805 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1003   -0.4869   -0.4283 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1764   -0.9900    0.9314 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5876   -1.3500    1.9803 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3927   -0.6441   -0.1924 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0668   -0.6798   -0.2078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6228    0.6836   -0.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0992    0.7056   -0.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8321    0.8183    0.7087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2019    0.8582    0.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9164    0.7879   -0.4999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2892    0.8332   -0.4621 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1912    0.6736   -1.6698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8199    0.6345   -1.6282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5796   -1.6265   -1.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7571   -2.2614   -1.9425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9016   -1.9033   -1.4019 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2703    0.7349   -1.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4409    1.6214    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4963   -0.1902    0.4456 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1227   -0.7879    2.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0038    0.9562    2.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8376   -0.1728    2.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7534    1.0861    1.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0350   -1.9256    1.1378 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1115   -1.2224   -1.1401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7191    0.4239   -0.6953 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681   -0.3457   -1.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3803   -1.0206    0.8126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2801    1.1613   -1.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3277    1.3558    0.4455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3390    0.8778    1.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7523    0.9490    1.6179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8707    0.7865   -1.2877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7533    0.6173   -2.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2843    0.5483   -2.5546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3339   -2.2039   -2.2503 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
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 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
 10 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
  6 31  1  0
  9 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


  Mrv1652304062014042D          

 21 21  0  0  0  0            999 V2000
    5.5583   -4.0145    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.0182   -4.6382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2883   -5.4177    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2081   -4.4823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9381   -3.7027    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.6680   -5.1059    0.0000 C   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
    2.3178   -5.5736    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.5077   -5.4177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3685   -4.1704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9086   -3.5468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7187   -3.7027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2588   -3.0791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0689   -3.2350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3390   -4.0145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.1491   -4.1704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7989   -4.6382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9887   -4.4823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6385   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4486   -5.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0984   -5.5736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  1 10  1  0  0  0  0
 10 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
 10 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0028985

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C14H20N2O4S/c1-21-7-6-11(15)13(18)16-12(14(19)20)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>
PESQCPHRXOFIPX-UHFFFAOYSA-N

> <FORMULA>
C14H20N2O4S

> <MOLECULAR_WEIGHT>
312.385

> <EXACT_MASS>
312.114377828

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
32.83750548731434

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[2-amino-4-(methylsulfanyl)butanamido]-3-(4-hydroxyphenyl)propanoic acid

> <ALOGPS_LOGP>
-0.56

> <JCHEM_LOGP>
-1.3755254518070028

> <ALOGPS_LOGS>
-3.10

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.538659318821937

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.5644972087366185

> <JCHEM_PKA_STRONGEST_BASIC>
8.381814303415084

> <JCHEM_POLAR_SURFACE_AREA>
112.65

> <JCHEM_REFRACTIVITY>
81.48330000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.46e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
met-tyr

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0028985
     RDKit          3D
Methionyl-Tyrosine
 41 41  0  0  0  0  0  0  0  0999 V2000
    6.9999    0.7246    0.0311 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2177    0.6379    0.1574 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.6599    0.1652    1.8141 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1522    0.1021    1.8840 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6540   -0.9321    0.8805 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1003   -0.4869   -0.4283 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1764   -0.9900    0.9314 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5876   -1.3500    1.9803 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3927   -0.6441   -0.1924 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0668   -0.6798   -0.2078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6228    0.6836   -0.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0992    0.7056   -0.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8321    0.8183    0.7087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2019    0.8582    0.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9164    0.7879   -0.4999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2892    0.8332   -0.4621 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1912    0.6736   -1.6698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8199    0.6345   -1.6282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5796   -1.6265   -1.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7571   -2.2614   -1.9425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9016   -1.9033   -1.4019 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2703    0.7349   -1.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4409    1.6214    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4963   -0.1902    0.4456 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1227   -0.7879    2.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0038    0.9562    2.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8376   -0.1728    2.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7534    1.0861    1.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0350   -1.9256    1.1378 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1115   -1.2224   -1.1401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7191    0.4239   -0.6953 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681   -0.3457   -1.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3803   -1.0206    0.8126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2801    1.1613   -1.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3277    1.3558    0.4455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3390    0.8778    1.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7523    0.9490    1.6179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8707    0.7865   -1.2877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7533    0.6173   -2.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2843    0.5483   -2.5546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3339   -2.2039   -2.2503 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
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 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
 10 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
  6 31  1  0
  9 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  N   UNK     0      10.375  -7.494   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       9.367  -8.658   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       9.871 -10.113   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       7.855  -8.367   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       7.351  -6.912   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       6.847  -9.531   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    8  S   UNK     0       4.327 -10.404   0.000  0.00  0.00           S+0
HETATM    9  C   UNK     0       2.814 -10.113   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.888  -7.785   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.896  -6.621   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.408  -6.912   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.416  -5.748   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.929  -6.039   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      17.433  -7.494   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      18.945  -7.785   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      16.425  -8.658   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.912  -8.367   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      12.392  -9.240   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      13.904  -9.531   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      11.384 -10.404   0.000  0.00  0.00           O+0
CONECT    1    2   10                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8                                                            
CONECT   10    1   11   19                                                  
CONECT   11   10   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   10   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

COMPND    HMDB0028985
HETATM    1  C1  UNL     1       7.000   0.725   0.031  1.00  0.00           C  
HETATM    2  S1  UNL     1       5.218   0.638   0.157  1.00  0.00           S  
HETATM    3  C2  UNL     1       4.660   0.165   1.814  1.00  0.00           C  
HETATM    4  C3  UNL     1       3.152   0.102   1.884  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.654  -0.932   0.881  1.00  0.00           C  
HETATM    6  N1  UNL     1       3.100  -0.487  -0.428  1.00  0.00           N  
HETATM    7  C5  UNL     1       1.176  -0.990   0.931  1.00  0.00           C  
HETATM    8  O1  UNL     1       0.588  -1.350   1.980  1.00  0.00           O  
HETATM    9  N2  UNL     1       0.393  -0.644  -0.192  1.00  0.00           N  
HETATM   10  C6  UNL     1      -1.067  -0.680  -0.208  1.00  0.00           C  
HETATM   11  C7  UNL     1      -1.623   0.684  -0.413  1.00  0.00           C  
HETATM   12  C8  UNL     1      -3.099   0.706  -0.439  1.00  0.00           C  
HETATM   13  C9  UNL     1      -3.832   0.818   0.709  1.00  0.00           C  
HETATM   14  C10 UNL     1      -5.202   0.858   0.677  1.00  0.00           C  
HETATM   15  C11 UNL     1      -5.916   0.788  -0.500  1.00  0.00           C  
HETATM   16  O2  UNL     1      -7.289   0.833  -0.462  1.00  0.00           O  
HETATM   17  C12 UNL     1      -5.191   0.674  -1.670  1.00  0.00           C  
HETATM   18  C13 UNL     1      -3.820   0.635  -1.628  1.00  0.00           C  
HETATM   19  C14 UNL     1      -1.580  -1.626  -1.197  1.00  0.00           C  
HETATM   20  O3  UNL     1      -0.757  -2.261  -1.943  1.00  0.00           O  
HETATM   21  O4  UNL     1      -2.902  -1.903  -1.402  1.00  0.00           O  
HETATM   22  H1  UNL     1       7.270   0.735  -1.051  1.00  0.00           H  
HETATM   23  H2  UNL     1       7.441   1.621   0.489  1.00  0.00           H  
HETATM   24  H3  UNL     1       7.496  -0.190   0.446  1.00  0.00           H  
HETATM   25  H4  UNL     1       5.123  -0.788   2.114  1.00  0.00           H  
HETATM   26  H5  UNL     1       5.004   0.956   2.517  1.00  0.00           H  
HETATM   27  H6  UNL     1       2.838  -0.173   2.891  1.00  0.00           H  
HETATM   28  H7  UNL     1       2.753   1.086   1.535  1.00  0.00           H  
HETATM   29  H8  UNL     1       3.035  -1.926   1.138  1.00  0.00           H  
HETATM   30  H9  UNL     1       3.111  -1.222  -1.140  1.00  0.00           H  
HETATM   31  H10 UNL     1       2.719   0.424  -0.695  1.00  0.00           H  
HETATM   32  H11 UNL     1       0.868  -0.346  -1.064  1.00  0.00           H  
HETATM   33  H12 UNL     1      -1.380  -1.021   0.813  1.00  0.00           H  
HETATM   34  H13 UNL     1      -1.280   1.161  -1.356  1.00  0.00           H  
HETATM   35  H14 UNL     1      -1.328   1.356   0.446  1.00  0.00           H  
HETATM   36  H15 UNL     1      -3.339   0.878   1.659  1.00  0.00           H  
HETATM   37  H16 UNL     1      -5.752   0.949   1.618  1.00  0.00           H  
HETATM   38  H17 UNL     1      -7.871   0.786  -1.288  1.00  0.00           H  
HETATM   39  H18 UNL     1      -5.753   0.617  -2.608  1.00  0.00           H  
HETATM   40  H19 UNL     1      -3.284   0.548  -2.555  1.00  0.00           H  
HETATM   41  H20 UNL     1      -3.334  -2.204  -2.250  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    7   29
CONECT    6   30   31
CONECT    7    8    8    9
CONECT    9   10   32
CONECT   10   11   19   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

HMDB0028985
     RDKit          3D
Methionyl-Tyrosine
 41 41  0  0  0  0  0  0  0  0999 V2000
    6.9999    0.7246    0.0311 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2177    0.6379    0.1574 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.6599    0.1652    1.8141 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1522    0.1021    1.8840 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6540   -0.9321    0.8805 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1003   -0.4869   -0.4283 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1764   -0.9900    0.9314 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5876   -1.3500    1.9803 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3927   -0.6441   -0.1924 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0668   -0.6798   -0.2078 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6228    0.6836   -0.4130 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0992    0.7056   -0.4386 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8321    0.8183    0.7087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2019    0.8582    0.6774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9164    0.7879   -0.4999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2892    0.8332   -0.4621 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1912    0.6736   -1.6698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8199    0.6345   -1.6282 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5796   -1.6265   -1.1974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7571   -2.2614   -1.9425 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9016   -1.9033   -1.4019 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2703    0.7349   -1.0506 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4409    1.6214    0.4886 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4963   -0.1902    0.4456 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1227   -0.7879    2.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0038    0.9562    2.5172 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8376   -0.1728    2.8909 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7534    1.0861    1.5349 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0350   -1.9256    1.1378 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1115   -1.2224   -1.1401 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7191    0.4239   -0.6953 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8681   -0.3457   -1.0638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3803   -1.0206    0.8126 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2801    1.1613   -1.3557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3277    1.3558    0.4455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3390    0.8778    1.6589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7523    0.9490    1.6179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8707    0.7865   -1.2877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7533    0.6173   -2.6085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2843    0.5483   -2.5546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3339   -2.2039   -2.2503 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
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 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
 10 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
  6 31  1  0
  9 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-Methionyl-L-tyrosine	HMDB
m-Y dipeptide	HMDB
Met-tyr	HMDB
Methionine tyrosine dipeptide	HMDB
Methionine-tyrosine dipeptide	HMDB
Methionyltyrosine	HMDB
MY dipeptide	HMDB
2-{[2-amino-1-hydroxy-4-(methylsulfanyl)butylidene]amino}-3-(4-hydroxyphenyl)propanoate	HMDB
2-{[2-amino-1-hydroxy-4-(methylsulphanyl)butylidene]amino}-3-(4-hydroxyphenyl)propanoate	HMDB
2-{[2-amino-1-hydroxy-4-(methylsulphanyl)butylidene]amino}-3-(4-hydroxyphenyl)propanoic acid	HMDB

Chemical Formula

C₁₄H₂₀N₂O₄S

Average Molecular Weight

312.385

Monoisotopic Molecular Weight

312.114377828

IUPAC Name

2-[2-amino-4-(methylsulfanyl)butanamido]-3-(4-hydroxyphenyl)propanoic acid

Traditional Name

met-tyr

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C14H20N2O4S/c1-21-7-6-11(15)13(18)16-12(14(19)20)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

PESQCPHRXOFIPX-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
3-phenylpropanoic-acid
Alpha-amino acid or derivatives
Amphetamine or derivatives
1-hydroxy-2-unsubstituted benzenoid
Phenol
Fatty acyl
Monocyclic benzene moiety
Fatty amide
N-acyl-amine
Benzenoid
Amino acid
Secondary carboxylic acid amide
Carboxamide group
Amino acid or derivatives
Dialkylthioether
Sulfenyl compound
Thioether
Carboxylic acid
Monocarboxylic acid or derivatives
Primary amine
Organopnictogen compound
Primary aliphatic amine
Amine
Organic oxide
Organonitrogen compound
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Organosulfur compound
Organic nitrogen compound
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Endogenous (HMDB: HMDB0028985)

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	-1.38	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.25 g/L	ALOGPS
logP	-0.56	ALOGPS
logP	-1.4	ChemAxon
logS	-3.1	ALOGPS
pKa (Strongest Acidic)	3.56	ChemAxon
pKa (Strongest Basic)	8.38	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	32.84 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]+	172.915	31661259
DarkChem	[M-H]-	170.647	31661259
DeepCCS	[M+H]+	173.07	30932474
DeepCCS	[M-H]-	170.712	30932474
DeepCCS	[M-2H]-	203.598	30932474
DeepCCS	[M+Na]+	179.163	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 Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	2.5 minutes	32390414
Predicted by Siyang on May 30, 2022	10.2963 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	7.71 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	179.0 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1126.4 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	204.4 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	108.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	153.5 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	93.8 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	317.1 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	349.6 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	596.7 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	742.5 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	333.0 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	903.2 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	219.6 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	228.3 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	352.2 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	465.4 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	119.4 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Methionyl-Tyrosine	CSCCC(N)C(=O)NC(CC1=CC=C(O)C=C1)C(O)=O	3868.5	Standard polar	33892256
Methionyl-Tyrosine	CSCCC(N)C(=O)NC(CC1=CC=C(O)C=C1)C(O)=O	2650.4	Standard non polar	33892256
Methionyl-Tyrosine	CSCCC(N)C(=O)NC(CC1=CC=C(O)C=C1)C(O)=O	2990.3	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Methionyl-Tyrosine,1TMS,isomer #1	CSCCC(N)C(=O)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O	2813.3	Semi standard non polar	33892256
Methionyl-Tyrosine,1TMS,isomer #2	CSCCC(N)C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C	2741.2	Semi standard non polar	33892256
Methionyl-Tyrosine,1TMS,isomer #3	CSCCC(N[Si](C)(C)C)C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O	2829.8	Semi standard non polar	33892256
Methionyl-Tyrosine,1TMS,isomer #4	CSCCC(N)C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O)[Si](C)(C)C	2763.2	Semi standard non polar	33892256
Methionyl-Tyrosine,2TMS,isomer #1	CSCCC(N)C(=O)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	2789.3	Semi standard non polar	33892256
Methionyl-Tyrosine,2TMS,isomer #2	CSCCC(N[Si](C)(C)C)C(=O)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O	2831.3	Semi standard non polar	33892256
Methionyl-Tyrosine,2TMS,isomer #3	CSCCC(N)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O)[Si](C)(C)C	2767.5	Semi standard non polar	33892256
Methionyl-Tyrosine,2TMS,isomer #4	CSCCC(N[Si](C)(C)C)C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C	2760.0	Semi standard non polar	33892256
Methionyl-Tyrosine,2TMS,isomer #5	CSCCC(N)C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2691.0	Semi standard non polar	33892256
Methionyl-Tyrosine,2TMS,isomer #6	CSCCC(C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2920.4	Semi standard non polar	33892256
Methionyl-Tyrosine,2TMS,isomer #7	CSCCC(N[Si](C)(C)C)C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O)[Si](C)(C)C	2768.9	Semi standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #1	CSCCC(N[Si](C)(C)C)C(=O)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	2798.1	Semi standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #1	CSCCC(N[Si](C)(C)C)C(=O)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C	2682.3	Standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #2	CSCCC(N)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2743.8	Semi standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #2	CSCCC(N)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2694.8	Standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #3	CSCCC(C(=O)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2952.6	Semi standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #3	CSCCC(C(=O)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2785.2	Standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #4	CSCCC(N[Si](C)(C)C)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O)[Si](C)(C)C	2806.8	Semi standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #4	CSCCC(N[Si](C)(C)C)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O)[Si](C)(C)C	2746.8	Standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #5	CSCCC(C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2854.0	Semi standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #5	CSCCC(C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2811.6	Standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #6	CSCCC(N[Si](C)(C)C)C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2712.6	Semi standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #6	CSCCC(N[Si](C)(C)C)C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2756.5	Standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #7	CSCCC(C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2890.9	Semi standard non polar	33892256
Methionyl-Tyrosine,3TMS,isomer #7	CSCCC(C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2872.0	Standard non polar	33892256
Methionyl-Tyrosine,4TMS,isomer #1	CSCCC(C(=O)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2901.7	Semi standard non polar	33892256
Methionyl-Tyrosine,4TMS,isomer #1	CSCCC(C(=O)NC(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2805.0	Standard non polar	33892256
Methionyl-Tyrosine,4TMS,isomer #2	CSCCC(N[Si](C)(C)C)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2779.5	Semi standard non polar	33892256
Methionyl-Tyrosine,4TMS,isomer #2	CSCCC(N[Si](C)(C)C)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2754.4	Standard non polar	33892256
Methionyl-Tyrosine,4TMS,isomer #3	CSCCC(C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2957.0	Semi standard non polar	33892256
Methionyl-Tyrosine,4TMS,isomer #3	CSCCC(C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2863.5	Standard non polar	33892256
Methionyl-Tyrosine,4TMS,isomer #4	CSCCC(C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2885.4	Semi standard non polar	33892256
Methionyl-Tyrosine,4TMS,isomer #4	CSCCC(C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2886.1	Standard non polar	33892256
Methionyl-Tyrosine,5TMS,isomer #1	CSCCC(C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2949.2	Semi standard non polar	33892256
Methionyl-Tyrosine,5TMS,isomer #1	CSCCC(C(=O)N(C(CC1=CC=C(O[Si](C)(C)C)C=C1)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2874.7	Standard non polar	33892256
Methionyl-Tyrosine,1TBDMS,isomer #1	CSCCC(N)C(=O)NC(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	3082.2	Semi standard non polar	33892256
Methionyl-Tyrosine,1TBDMS,isomer #2	CSCCC(N)C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	3031.2	Semi standard non polar	33892256
Methionyl-Tyrosine,1TBDMS,isomer #3	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O	3069.0	Semi standard non polar	33892256
Methionyl-Tyrosine,1TBDMS,isomer #4	CSCCC(N)C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C	3033.9	Semi standard non polar	33892256
Methionyl-Tyrosine,2TBDMS,isomer #1	CSCCC(N)C(=O)NC(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	3337.8	Semi standard non polar	33892256
Methionyl-Tyrosine,2TBDMS,isomer #2	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O	3372.1	Semi standard non polar	33892256
Methionyl-Tyrosine,2TBDMS,isomer #3	CSCCC(N)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C	3321.9	Semi standard non polar	33892256
Methionyl-Tyrosine,2TBDMS,isomer #4	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	3261.5	Semi standard non polar	33892256
Methionyl-Tyrosine,2TBDMS,isomer #5	CSCCC(N)C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3232.4	Semi standard non polar	33892256
Methionyl-Tyrosine,2TBDMS,isomer #6	CSCCC(C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3390.2	Semi standard non polar	33892256
Methionyl-Tyrosine,2TBDMS,isomer #7	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C	3298.9	Semi standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #1	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	3560.0	Semi standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #1	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)NC(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C	3262.9	Standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #2	CSCCC(N)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3533.7	Semi standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #2	CSCCC(N)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3266.9	Standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #3	CSCCC(C(=O)NC(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3707.8	Semi standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #3	CSCCC(C(=O)NC(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3323.6	Standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #4	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C	3594.6	Semi standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #4	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C	3286.0	Standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #5	CSCCC(C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3586.5	Semi standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #5	CSCCC(C(=O)NC(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3357.9	Standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #6	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3464.2	Semi standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #6	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3329.6	Standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #7	CSCCC(C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3621.3	Semi standard non polar	33892256
Methionyl-Tyrosine,3TBDMS,isomer #7	CSCCC(C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3382.3	Standard non polar	33892256
Methionyl-Tyrosine,4TBDMS,isomer #1	CSCCC(C(=O)NC(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3893.0	Semi standard non polar	33892256
Methionyl-Tyrosine,4TBDMS,isomer #1	CSCCC(C(=O)NC(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3482.8	Standard non polar	33892256
Methionyl-Tyrosine,4TBDMS,isomer #2	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3756.2	Semi standard non polar	33892256
Methionyl-Tyrosine,4TBDMS,isomer #2	CSCCC(N[Si](C)(C)C(C)(C)C)C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3451.5	Standard non polar	33892256
Methionyl-Tyrosine,4TBDMS,isomer #3	CSCCC(C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3935.9	Semi standard non polar	33892256
Methionyl-Tyrosine,4TBDMS,isomer #3	CSCCC(C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3514.7	Standard non polar	33892256
Methionyl-Tyrosine,4TBDMS,isomer #4	CSCCC(C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3802.9	Semi standard non polar	33892256
Methionyl-Tyrosine,4TBDMS,isomer #4	CSCCC(C(=O)N(C(CC1=CC=C(O)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3558.3	Standard non polar	33892256
Methionyl-Tyrosine,5TBDMS,isomer #1	CSCCC(C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4102.0	Semi standard non polar	33892256
Methionyl-Tyrosine,5TBDMS,isomer #1	CSCCC(C(=O)N(C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3676.5	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Methionyl-Tyrosine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0pw9-7930000000-be179775439df2f13e95	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Methionyl-Tyrosine GC-MS (2 TMS) - 70eV, Positive	splash10-0pj3-9512200000-f44d269658d585cfaf24	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Methionyl-Tyrosine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Methionyl-Tyrosine 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 - Methionyl-Tyrosine 10V, Positive-QTOF	splash10-0j5a-1974000000-fe0a79980081316a19de	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 20V, Positive-QTOF	splash10-0f79-4920000000-be1102a1bbec00848b6b	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 40V, Positive-QTOF	splash10-0a6r-9300000000-4e5bcc67cbde1b5e1902	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 10V, Negative-QTOF	splash10-03dj-9178000000-b7c159c1a0a11f195ba5	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 20V, Negative-QTOF	splash10-0002-9220000000-b56c83760d54f5d6b658	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 40V, Negative-QTOF	splash10-0002-9300000000-56cf809f41e3c379274c	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 10V, Negative-QTOF	splash10-03di-0009000000-faa9ec499190ebb9d3e1	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 20V, Negative-QTOF	splash10-01x1-5900000000-797a8dd559b140a8ac55	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 40V, Negative-QTOF	splash10-00dj-9400000000-74110cecb6d5f016630a	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 10V, Positive-QTOF	splash10-03di-0319000000-79f53d54a3740f5a0740	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 20V, Positive-QTOF	splash10-03ei-4911000000-2c1e56747fa93b2bb893	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Methionyl-Tyrosine 40V, Positive-QTOF	splash10-0a4r-9400000000-ac8de50ba92b10975999	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

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

FDB112005

KNApSAcK ID

Not Available

Chemspider ID

10441901

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23275780

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 Methionyl-Tyrosine (HMDB0028985)

MOL for HMDB0028985 (Methionyl-Tyrosine)

3D MOL for HMDB0028985 (Methionyl-Tyrosine)

3D SDF for HMDB0028985 (Methionyl-Tyrosine)

3D-SDF for HMDB0028985 (Methionyl-Tyrosine)

PDB for HMDB0028985 (Methionyl-Tyrosine)

3D PDB for HMDB0028985 (Methionyl-Tyrosine)

SMILES for HMDB0028985 (Methionyl-Tyrosine)

INCHI for HMDB0028985 (Methionyl-Tyrosine)

Structure for HMDB0028985 (Methionyl-Tyrosine)

3D Structure for HMDB0028985 (Methionyl-Tyrosine)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra