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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-11 14:38:37 UTC

Update Date

2021-09-26 23:09:37 UTC

HMDB ID

HMDB0255088

Secondary Accession Numbers

None

Metabolite Identification

Common Name

N-Benzoyl-L-tyrosine

Description

N-Benzoyl-L-tyrosine belongs to the class of organic compounds known as tyrosine and derivatives. Tyrosine and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. Based on a literature review a significant number of articles have been published on N-Benzoyl-L-tyrosine. This compound has been identified in human blood as reported by (PMID: 31557052 ). N-benzoyl-l-tyrosine is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically N-Benzoyl-L-tyrosine is part of the human exposome. The exposome can be defined as the collection of all the exposures of an individual in a lifetime and how those exposures relate to health. An individual's exposure begins before birth and includes insults from environmental and occupational sources.

Structure

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

HMDB0255088
     RDKit          3D
N-Benzoyl-L-tyrosine
 36 37  0  0  0  0  0  0  0  0999 V2000
   -0.3489    0.3730    2.0861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0173    0.0195    1.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5834   -1.1592    0.4047 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5500   -1.9331    0.8332 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5743   -2.0834   -0.2694 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1002   -0.7955   -0.7366 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4559   -0.1586   -1.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8962    1.0512   -2.2582 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0167    1.6862   -1.7232 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4036    2.8885   -2.2518 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6539    1.0375   -0.6859 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2190   -0.1866   -0.1842 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0895   -3.2950    1.1926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1354   -3.5592    1.0797 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9763   -4.2733    1.6464 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1567    0.8061    0.6486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9001    0.4452   -0.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9991    1.1937   -0.8668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3242    2.3316   -0.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6039    2.7135    0.9666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5174    1.9317    1.3399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0907   -1.5213   -0.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9995   -1.4543    1.7425 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1144   -2.6950   -1.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4314   -2.6517    0.1680 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5880   -0.6203   -2.2079 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672    1.5127   -3.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1738    3.4428   -1.9695 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5293    1.5349   -0.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255   -0.6793    0.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0828   -5.1361    1.1060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6881   -0.4236   -1.0507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5873    0.9170   -1.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1844    2.8940   -0.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8477    3.5868    1.5397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9626    2.2595    2.2144 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
  4 13  1  0
 13 14  2  0
 13 15  1  0
  2 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 12  6  1  0
 21 16  1  0
  3 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  7 26  1  0
  8 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 15 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
 21 36  1  0
M  END


  Mrv1652309112116392D          

 21 22  0  0  0  0            999 V2000
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  1  6  1  0  0  0  0
  4  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
 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
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 15 18  1  0  0  0  0
 10 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0255088

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C16H15NO4/c18-13-8-6-11(7-9-13)10-14(16(20)21)17-15(19)12-4-2-1-3-5-12/h1-9,14,18H,10H2,(H,17,19)(H,20,21)

> <INCHI_KEY>
KUUUDPTUEOKITK-UHFFFAOYSA-N

> <FORMULA>
C16H15NO4

> <MOLECULAR_WEIGHT>
285.299

> <EXACT_MASS>
285.100107967

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
28.979618152530172

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(4-hydroxyphenyl)-2-(phenylformamido)propanoic acid

> <ALOGPS_LOGP>
2.37

> <JCHEM_LOGP>
2.447070772666666

> <ALOGPS_LOGS>
-3.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.504657364725249

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.5737495266550248

> <JCHEM_PKA_STRONGEST_BASIC>
-1.343493949815279

> <JCHEM_POLAR_SURFACE_AREA>
86.63000000000001

> <JCHEM_REFRACTIVITY>
77.2115

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.22e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(4-hydroxyphenyl)-2-(phenylformamido)propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0255088
     RDKit          3D
N-Benzoyl-L-tyrosine
 36 37  0  0  0  0  0  0  0  0999 V2000
   -0.3489    0.3730    2.0861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0173    0.0195    1.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5834   -1.1592    0.4047 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5500   -1.9331    0.8332 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5743   -2.0834   -0.2694 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1002   -0.7955   -0.7366 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4559   -0.1586   -1.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8962    1.0512   -2.2582 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0167    1.6862   -1.7232 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4036    2.8885   -2.2518 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6539    1.0375   -0.6859 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2190   -0.1866   -0.1842 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0895   -3.2950    1.1926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1354   -3.5592    1.0797 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9763   -4.2733    1.6464 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1567    0.8061    0.6486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9001    0.4452   -0.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9991    1.1937   -0.8668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3242    2.3316   -0.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6039    2.7135    0.9666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5174    1.9317    1.3399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0907   -1.5213   -0.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9995   -1.4543    1.7425 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1144   -2.6950   -1.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4314   -2.6517    0.1680 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5880   -0.6203   -2.2079 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672    1.5127   -3.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1738    3.4428   -1.9695 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5293    1.5349   -0.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255   -0.6793    0.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0828   -5.1361    1.1060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6881   -0.4236   -1.0507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5873    0.9170   -1.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1844    2.8940   -0.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8477    3.5868    1.5397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9626    2.2595    2.2144 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
  4 13  1  0
 13 14  2  0
 13 15  1  0
  2 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 12  6  1  0
 21 16  1  0
  3 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  7 26  1  0
  8 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 15 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
 21 36  1  0
M  END

HEADER    PROTEIN                                 11-SEP-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-21         0                                  
HETATM    1  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.000  -6.160   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -8.470   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -6.160   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM    9  N   UNK     0       2.667  -4.620   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       4.001  -3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.335  -1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       9.336   0.770   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.668  -3.850   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       5.335  -6.160   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6                                                       
CONECT    6    5    1                                                       
CONECT    7    4    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   19                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   15                                                            
CONECT   19   10   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   44    0
END

COMPND    HMDB0255088
HETATM    1  O1  UNL     1      -0.349   0.373   2.086  1.00  0.00           O  
HETATM    2  C1  UNL     1      -1.017   0.019   1.071  1.00  0.00           C  
HETATM    3  N1  UNL     1      -0.583  -1.159   0.405  1.00  0.00           N  
HETATM    4  C2  UNL     1       0.550  -1.933   0.833  1.00  0.00           C  
HETATM    5  C3  UNL     1       1.574  -2.083  -0.269  1.00  0.00           C  
HETATM    6  C4  UNL     1       2.100  -0.796  -0.737  1.00  0.00           C  
HETATM    7  C5  UNL     1       1.456  -0.159  -1.772  1.00  0.00           C  
HETATM    8  C6  UNL     1       1.896   1.051  -2.258  1.00  0.00           C  
HETATM    9  C7  UNL     1       3.017   1.686  -1.723  1.00  0.00           C  
HETATM   10  O2  UNL     1       3.404   2.888  -2.252  1.00  0.00           O  
HETATM   11  C8  UNL     1       3.654   1.037  -0.686  1.00  0.00           C  
HETATM   12  C9  UNL     1       3.219  -0.187  -0.184  1.00  0.00           C  
HETATM   13  C10 UNL     1       0.089  -3.295   1.193  1.00  0.00           C  
HETATM   14  O3  UNL     1      -1.135  -3.559   1.080  1.00  0.00           O  
HETATM   15  O4  UNL     1       0.976  -4.273   1.646  1.00  0.00           O  
HETATM   16  C11 UNL     1      -2.157   0.806   0.649  1.00  0.00           C  
HETATM   17  C12 UNL     1      -2.900   0.445  -0.450  1.00  0.00           C  
HETATM   18  C13 UNL     1      -3.999   1.194  -0.867  1.00  0.00           C  
HETATM   19  C14 UNL     1      -4.324   2.332  -0.128  1.00  0.00           C  
HETATM   20  C15 UNL     1      -3.604   2.713   0.967  1.00  0.00           C  
HETATM   21  C16 UNL     1      -2.517   1.932   1.340  1.00  0.00           C  
HETATM   22  H1  UNL     1      -1.091  -1.521  -0.454  1.00  0.00           H  
HETATM   23  H2  UNL     1       1.000  -1.454   1.743  1.00  0.00           H  
HETATM   24  H3  UNL     1       1.114  -2.695  -1.063  1.00  0.00           H  
HETATM   25  H4  UNL     1       2.431  -2.652   0.168  1.00  0.00           H  
HETATM   26  H5  UNL     1       0.588  -0.620  -2.208  1.00  0.00           H  
HETATM   27  H6  UNL     1       1.367   1.513  -3.063  1.00  0.00           H  
HETATM   28  H7  UNL     1       4.174   3.443  -1.970  1.00  0.00           H  
HETATM   29  H8  UNL     1       4.529   1.535  -0.269  1.00  0.00           H  
HETATM   30  H9  UNL     1       3.725  -0.679   0.624  1.00  0.00           H  
HETATM   31  H10 UNL     1       1.083  -5.136   1.106  1.00  0.00           H  
HETATM   32  H11 UNL     1      -2.688  -0.424  -1.051  1.00  0.00           H  
HETATM   33  H12 UNL     1      -4.587   0.917  -1.727  1.00  0.00           H  
HETATM   34  H13 UNL     1      -5.184   2.894  -0.476  1.00  0.00           H  
HETATM   35  H14 UNL     1      -3.848   3.587   1.540  1.00  0.00           H  
HETATM   36  H15 UNL     1      -1.963   2.260   2.214  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3   16
CONECT    3    4   22
CONECT    4    5   13   23
CONECT    5    6   24   25
CONECT    6    7    7   12
CONECT    7    8   26
CONECT    8    9    9   27
CONECT    9   10   11
CONECT   10   28
CONECT   11   12   12   29
CONECT   12   30
CONECT   13   14   14   15
CONECT   15   31
CONECT   16   17   17   21
CONECT   17   18   32
CONECT   18   19   19   33
CONECT   19   20   34
CONECT   20   21   21   35
CONECT   21   36
END

HMDB0255088
     RDKit          3D
N-Benzoyl-L-tyrosine
 36 37  0  0  0  0  0  0  0  0999 V2000
   -0.3489    0.3730    2.0861 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0173    0.0195    1.0713 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5834   -1.1592    0.4047 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5500   -1.9331    0.8332 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5743   -2.0834   -0.2694 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1002   -0.7955   -0.7366 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4559   -0.1586   -1.7716 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8962    1.0512   -2.2582 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0167    1.6862   -1.7232 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4036    2.8885   -2.2518 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6539    1.0375   -0.6859 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2190   -0.1866   -0.1842 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0895   -3.2950    1.1926 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1354   -3.5592    1.0797 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9763   -4.2733    1.6464 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1567    0.8061    0.6486 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9001    0.4452   -0.4496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9991    1.1937   -0.8668 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3242    2.3316   -0.1277 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6039    2.7135    0.9666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5174    1.9317    1.3399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0907   -1.5213   -0.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9995   -1.4543    1.7425 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1144   -2.6950   -1.0631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4314   -2.6517    0.1680 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5880   -0.6203   -2.2079 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3672    1.5127   -3.0634 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1738    3.4428   -1.9695 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5293    1.5349   -0.2688 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7255   -0.6793    0.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0828   -5.1361    1.1060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6881   -0.4236   -1.0507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5873    0.9170   -1.7273 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1844    2.8940   -0.4764 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8477    3.5868    1.5397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9626    2.2595    2.2144 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
  9 11  1  0
 11 12  2  0
  4 13  1  0
 13 14  2  0
 13 15  1  0
  2 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 12  6  1  0
 21 16  1  0
  3 22  1  0
  4 23  1  0
  5 24  1  0
  5 25  1  0
  7 26  1  0
  8 27  1  0
 10 28  1  0
 11 29  1  0
 12 30  1  0
 15 31  1  0
 17 32  1  0
 18 33  1  0
 19 34  1  0
 20 35  1  0
 21 36  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
2-{[hydroxy(phenyl)methylidene]amino}-3-(4-hydroxyphenyl)propanoate	HMDB

Chemical Formula

C₁₆H₁₅NO₄

Average Molecular Weight

285.299

Monoisotopic Molecular Weight

285.100107967

IUPAC Name

3-(4-hydroxyphenyl)-2-(phenylformamido)propanoic acid

Traditional Name

3-(4-hydroxyphenyl)-2-(phenylformamido)propanoic acid

CAS Registry Number

Not Available

SMILES

OC(=O)C(CC1=CC=C(O)C=C1)NC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C16H15NO4/c18-13-8-6-11(7-9-13)10-14(16(20)21)17-15(19)12-4-2-1-3-5-12/h1-9,14,18H,10H2,(H,17,19)(H,20,21)

InChI Key

KUUUDPTUEOKITK-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tyrosine and derivatives. Tyrosine and derivatives are compounds containing tyrosine or a derivative thereof resulting from reaction of tyrosine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Tyrosine and derivatives

Alternative Parents

Substituents

Tyrosine or derivatives
Phenylalanine or derivatives
Hippuric acid or derivatives
Hippuric acid
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
3-phenylpropanoic-acid
Amphetamine or derivatives
Benzamide
Benzoic acid or derivatives
Benzoyl
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Secondary carboxylic acid amide
Carboxamide group
Monocarboxylic acid or derivatives
Carboxylic acid
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Non-excretory biofluid

Biofluid or Excreta

Blood (PMID: 31557052)

Source

Exogenous

Exogenous (PMID: 31557052)

Process

Not Available

Role

Not Available

Physical Properties

State

Not Available

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	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	2.37	ALOGPS
logP	2.45	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	3.57	ChemAxon
pKa (Strongest Basic)	-1.3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	86.63 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	77.21 m³·mol⁻¹	ChemAxon
Polarizability	28.98 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	167.504	30932474
DeepCCS	[M-H]-	165.146	30932474
DeepCCS	[M-2H]-	198.101	30932474
DeepCCS	[M+Na]+	173.597	30932474
AllCCS	[M+H]+	167.0	32859911
AllCCS	[M+H-H2O]+	163.7	32859911
AllCCS	[M+NH4]+	170.1	32859911
AllCCS	[M+Na]+	171.0	32859911
AllCCS	[M-H]-	166.9	32859911
AllCCS	[M+Na-2H]-	166.6	32859911
AllCCS	[M+HCOO]-	166.3	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Predicted by Siyang on May 30, 2022	11.2113 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	2.14 minutes	32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1705.8 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	254.7 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	142.2 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	165.5 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	119.0 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	410.8 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	419.6 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	123.8 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	895.4 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	448.9 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	1230.5 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	263.0 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	319.2 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	311.9 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	144.2 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	115.3 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
N-Benzoyl-L-tyrosine	OC(=O)C(CC1=CC=C(O)C=C1)NC(=O)C1=CC=CC=C1	3715.3	Standard polar	33892256
N-Benzoyl-L-tyrosine	OC(=O)C(CC1=CC=C(O)C=C1)NC(=O)C1=CC=CC=C1	2338.9	Standard non polar	33892256
N-Benzoyl-L-tyrosine	OC(=O)C(CC1=CC=C(O)C=C1)NC(=O)C1=CC=CC=C1	2803.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
N-Benzoyl-L-tyrosine,3TMS,isomer #1	C[Si](C)(C)OC(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C	2626.6	Semi standard non polar	33892256
N-Benzoyl-L-tyrosine,3TMS,isomer #1	C[Si](C)(C)OC(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C	2510.0	Standard non polar	33892256
N-Benzoyl-L-tyrosine,3TMS,isomer #1	C[Si](C)(C)OC(=O)C(CC1=CC=C(O[Si](C)(C)C)C=C1)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C	2938.9	Standard polar	33892256
N-Benzoyl-L-tyrosine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C(C)(C)C	3349.8	Semi standard non polar	33892256
N-Benzoyl-L-tyrosine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C(C)(C)C	3125.5	Standard non polar	33892256
N-Benzoyl-L-tyrosine,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(CC1=CC=C(O[Si](C)(C)C(C)(C)C)C=C1)N(C(=O)C1=CC=CC=C1)[Si](C)(C)C(C)(C)C	3215.1	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-0910000000-a6ce8a5d7a1640fafb06	2021-09-23	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TBDMS_2_1) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TBDMS_2_2) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - N-Benzoyl-L-tyrosine GC-MS (TBDMS_2_3) - 70eV, Positive	Not Available	2021-11-04	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	31557052	details

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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

295436

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

333413

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

Barupal DK, Fiehn O: Generating the Blood Exposome Database Using a Comprehensive Text Mining and Database Fusion Approach. Environ Health Perspect. 2019 Sep;127(9):97008. doi: 10.1289/EHP4713. Epub 2019 Sep 26. [PubMed:31557052 ]

Showing metabocard for N-Benzoyl-L-tyrosine (HMDB0255088)

MOL for HMDB0255088 (N-Benzoyl-L-tyrosine)

3D MOL for HMDB0255088 (N-Benzoyl-L-tyrosine)

3D SDF for HMDB0255088 (N-Benzoyl-L-tyrosine)

3D-SDF for HMDB0255088 (N-Benzoyl-L-tyrosine)

PDB for HMDB0255088 (N-Benzoyl-L-tyrosine)

3D PDB for HMDB0255088 (N-Benzoyl-L-tyrosine)

SMILES for HMDB0255088 (N-Benzoyl-L-tyrosine)

INCHI for HMDB0255088 (N-Benzoyl-L-tyrosine)

Structure for HMDB0255088 (N-Benzoyl-L-tyrosine)

3D Structure for HMDB0255088 (N-Benzoyl-L-tyrosine)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra