MiMeDB: Showing metabocard for N-Phenylacetylglutamic acid (MMDBc0000485)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-12-10 18:38:50 UTC

Update Date

2022-08-31 06:07:01 UTC

Metabolite ID

MMDBc0000485

Metabolite Identification

Common Name

N-Phenylacetylglutamic acid

Description

N-Phenylacetylglutamic acid belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom. These are compounds containing an alpha amino acid which bears an acyl group at his terminal nitrogen atom. N-Phenylacetylglutamic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

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

HMDB0059772
     RDKit          3D
N-Phenylacetylglutamic acid
 34 34  0  0  0  0  0  0  0  0999 V2000
    5.0410    2.2682   -1.1424 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6387    1.4708   -0.2574 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3755    1.2400    0.9090 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3340    0.7737   -0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0133   -0.1166    0.6829 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7268   -0.8519    0.5468 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6385    0.1214    0.4091 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3442   -0.0204   -0.5969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2650   -1.0074   -1.3697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4201    0.9521   -0.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7882    0.3945   -0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4945    0.3447    0.5818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7638   -0.1945    0.6509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3568   -0.7085   -0.5082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6685   -0.6682   -1.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3996   -0.1183   -1.7103 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4750   -1.5254    1.8732 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5407   -1.2487    2.6283 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4018   -2.5167    2.1985 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8780    1.9991    1.3618 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4431    0.1588   -1.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5658    1.5747   -0.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8294   -0.8768    0.7194 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0790    0.4742    1.6246 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7318   -1.5826   -0.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5753    0.9293    1.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3117    1.7912    0.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3891    1.4822   -1.7296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0175    0.7463    1.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3290   -0.2429    1.5607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3485   -1.1385   -0.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1568   -1.0767   -2.5714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8949   -0.1092   -2.6772 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6604   -2.7180    3.1588 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  6 17  1  0
 17 18  2  0
 17 19  1  0
 16 11  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  6
  7 26  1  0
 10 27  1  0
 10 28  1  0
 12 29  1  0
 13 30  1  0
 14 31  1  0
 15 32  1  0
 16 33  1  0
 19 34  1  0
M  END


  Mrv0541 02261312032D          

 19 19  0  0  1  0            999 V2000
    2.1434   -5.3625    0.0000 O   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
    2.8579   -4.1250    0.0000 O   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 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 N   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 O   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
    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
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    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
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
  6 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0000485

> <DATABASE_NAME>
MIME

> <SMILES>
OC(=O)CC[C@H](NC(=O)CC1=CC=CC=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C13H15NO5/c15-11(8-9-4-2-1-3-5-9)14-10(13(18)19)6-7-12(16)17/h1-5,10H,6-8H2,(H,14,15)(H,16,17)(H,18,19)/t10-/m0/s1

> <INCHI_KEY>
PTSRBZOZSRJCKX-JTQLQIEISA-N

> <FORMULA>
C13H15NO5

> <MOLECULAR_WEIGHT>
265.2619

> <EXACT_MASS>
265.095022595

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
25.764069079087477

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S)-2-(2-phenylacetamido)pentanedioic acid

> <ALOGPS_LOGP>
0.50

> <JCHEM_LOGP>
0.7213244029999999

> <ALOGPS_LOGS>
-2.58

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.327779283360969

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.580818443871302

> <JCHEM_PKA_STRONGEST_BASIC>
-2.2866498593508844

> <JCHEM_POLAR_SURFACE_AREA>
103.70000000000002

> <JCHEM_REFRACTIVITY>
65.45340000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.96e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-(2-phenylacetamido)pentanedioic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0059772
     RDKit          3D
N-Phenylacetylglutamic acid
 34 34  0  0  0  0  0  0  0  0999 V2000
    5.0410    2.2682   -1.1424 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6387    1.4708   -0.2574 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3755    1.2400    0.9090 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3340    0.7737   -0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0133   -0.1166    0.6829 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7268   -0.8519    0.5468 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6385    0.1214    0.4091 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3442   -0.0204   -0.5969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2650   -1.0074   -1.3697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4201    0.9521   -0.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7882    0.3945   -0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4945    0.3447    0.5818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7638   -0.1945    0.6509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3568   -0.7085   -0.5082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6685   -0.6682   -1.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3996   -0.1183   -1.7103 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4750   -1.5254    1.8732 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5407   -1.2487    2.6283 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4018   -2.5167    2.1985 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8780    1.9991    1.3618 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4431    0.1588   -1.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5658    1.5747   -0.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8294   -0.8768    0.7194 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0790    0.4742    1.6246 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7318   -1.5826   -0.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5753    0.9293    1.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3117    1.7912    0.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3891    1.4822   -1.7296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0175    0.7463    1.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3290   -0.2429    1.5607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3485   -1.1385   -0.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1568   -1.0767   -2.5714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8949   -0.1092   -2.6772 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6604   -2.7180    3.1588 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  6 17  1  0
 17 18  2  0
 17 19  1  0
 16 11  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  6
  7 26  1  0
 10 27  1  0
 10 28  1  0
 12 29  1  0
 13 30  1  0
 14 31  1  0
 15 32  1  0
 16 33  1  0
 19 34  1  0
M  END

HEADER    PROTEIN                                 26-FEB-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-FEB-13         0                                  
HETATM    1  O   UNK     0       4.001 -10.010   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O+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  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      10.669  -9.240   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      12.003 -11.550   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.671 -10.010   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      16.004  -9.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      17.338 -10.010   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.338 -11.550   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      16.004 -12.320   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.671 -11.550   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.669 -12.320   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       8.002 -12.320   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17    6   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   38    0
END

COMPND    HMDB0059772
HETATM    1  O1  UNL     1       5.041   2.268  -1.142  1.00  0.00           O  
HETATM    2  C1  UNL     1       4.639   1.471  -0.257  1.00  0.00           C  
HETATM    3  O2  UNL     1       5.375   1.240   0.909  1.00  0.00           O  
HETATM    4  C2  UNL     1       3.334   0.774  -0.500  1.00  0.00           C  
HETATM    5  C3  UNL     1       3.013  -0.117   0.683  1.00  0.00           C  
HETATM    6  C4  UNL     1       1.727  -0.852   0.547  1.00  0.00           C  
HETATM    7  N1  UNL     1       0.639   0.121   0.409  1.00  0.00           N  
HETATM    8  C5  UNL     1      -0.344  -0.020  -0.597  1.00  0.00           C  
HETATM    9  O3  UNL     1      -0.265  -1.007  -1.370  1.00  0.00           O  
HETATM   10  C6  UNL     1      -1.420   0.952  -0.733  1.00  0.00           C  
HETATM   11  C7  UNL     1      -2.788   0.395  -0.594  1.00  0.00           C  
HETATM   12  C8  UNL     1      -3.495   0.345   0.582  1.00  0.00           C  
HETATM   13  C9  UNL     1      -4.764  -0.195   0.651  1.00  0.00           C  
HETATM   14  C10 UNL     1      -5.357  -0.708  -0.508  1.00  0.00           C  
HETATM   15  C11 UNL     1      -4.668  -0.668  -1.691  1.00  0.00           C  
HETATM   16  C12 UNL     1      -3.400  -0.118  -1.710  1.00  0.00           C  
HETATM   17  C13 UNL     1       1.475  -1.525   1.873  1.00  0.00           C  
HETATM   18  O4  UNL     1       0.541  -1.249   2.628  1.00  0.00           O  
HETATM   19  O5  UNL     1       2.402  -2.517   2.199  1.00  0.00           O  
HETATM   20  H1  UNL     1       5.878   1.999   1.362  1.00  0.00           H  
HETATM   21  H2  UNL     1       3.443   0.159  -1.408  1.00  0.00           H  
HETATM   22  H3  UNL     1       2.566   1.575  -0.583  1.00  0.00           H  
HETATM   23  H4  UNL     1       3.829  -0.877   0.719  1.00  0.00           H  
HETATM   24  H5  UNL     1       3.079   0.474   1.625  1.00  0.00           H  
HETATM   25  H6  UNL     1       1.732  -1.583  -0.261  1.00  0.00           H  
HETATM   26  H7  UNL     1       0.575   0.929   1.052  1.00  0.00           H  
HETATM   27  H8  UNL     1      -1.312   1.791   0.007  1.00  0.00           H  
HETATM   28  H9  UNL     1      -1.389   1.482  -1.730  1.00  0.00           H  
HETATM   29  H10 UNL     1      -3.018   0.746   1.461  1.00  0.00           H  
HETATM   30  H11 UNL     1      -5.329  -0.243   1.561  1.00  0.00           H  
HETATM   31  H12 UNL     1      -6.349  -1.138  -0.490  1.00  0.00           H  
HETATM   32  H13 UNL     1      -5.157  -1.077  -2.571  1.00  0.00           H  
HETATM   33  H14 UNL     1      -2.895  -0.109  -2.677  1.00  0.00           H  
HETATM   34  H15 UNL     1       2.660  -2.718   3.159  1.00  0.00           H  
CONECT    1    2    2
CONECT    2    3    4
CONECT    3   20
CONECT    4    5   21   22
CONECT    5    6   23   24
CONECT    6    7   17   25
CONECT    7    8   26
CONECT    8    9    9   10
CONECT   10   11   27   28
CONECT   11   12   12   16
CONECT   12   13   29
CONECT   13   14   14   30
CONECT   14   15   31
CONECT   15   16   16   32
CONECT   16   33
CONECT   17   18   18   19
CONECT   19   34
END

HMDB0059772
     RDKit          3D
N-Phenylacetylglutamic acid
 34 34  0  0  0  0  0  0  0  0999 V2000
    5.0410    2.2682   -1.1424 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6387    1.4708   -0.2574 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3755    1.2400    0.9090 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3340    0.7737   -0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0133   -0.1166    0.6829 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7268   -0.8519    0.5468 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6385    0.1214    0.4091 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3442   -0.0204   -0.5969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2650   -1.0074   -1.3697 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4201    0.9521   -0.7329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7882    0.3945   -0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4945    0.3447    0.5818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7638   -0.1945    0.6509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3568   -0.7085   -0.5082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6685   -0.6682   -1.6906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3996   -0.1183   -1.7103 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4750   -1.5254    1.8732 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5407   -1.2487    2.6283 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4018   -2.5167    2.1985 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8780    1.9991    1.3618 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4431    0.1588   -1.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5658    1.5747   -0.5826 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8294   -0.8768    0.7194 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0790    0.4742    1.6246 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7318   -1.5826   -0.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5753    0.9293    1.0522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3117    1.7912    0.0073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3891    1.4822   -1.7296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0175    0.7463    1.4614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3290   -0.2429    1.5607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3485   -1.1385   -0.4897 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1568   -1.0767   -2.5714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8949   -0.1092   -2.6772 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6604   -2.7180    3.1588 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  6 17  1  0
 17 18  2  0
 17 19  1  0
 16 11  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  5 24  1  0
  6 25  1  6
  7 26  1  0
 10 27  1  0
 10 28  1  0
 12 29  1  0
 13 30  1  0
 14 31  1  0
 15 32  1  0
 16 33  1  0
 19 34  1  0
M  END

Synonyms

Value	Source
N-Phenylacetylglutamate	Generator
(2S)-2-[(1-Hydroxy-2-phenylethylidene)amino]pentanedioate	Generator

Molecular Formula

C₁₃H₁₅NO₅

Average Mass

265.2619

Monoisotopic Mass

265.095022595

IUPAC Name

(2S)-2-(2-phenylacetamido)pentanedioic acid

Traditional Name

(2S)-2-(2-phenylacetamido)pentanedioic acid

CAS Registry Number

Not Available

SMILES

OC(=O)CC[C@H](NC(=O)CC1=CC=CC=C1)C(O)=O

InChI Identifier

InChI=1S/C13H15NO5/c15-11(8-9-4-2-1-3-5-9)14-10(13(18)19)6-7-12(16)17/h1-5,10H,6-8H2,(H,14,15)(H,16,17)(H,18,19)/t10-/m0/s1

InChI Key

PTSRBZOZSRJCKX-JTQLQIEISA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glutamic acid and derivatives. Glutamic acid and derivatives are compounds containing glutamic acid or a derivative thereof resulting from reaction of glutamic acid 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

Glutamic acid and derivatives

Alternative Parents

Substituents

Glutamic acid or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
N-acyl-l-alpha-amino acid
Phenylacetamide
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Benzenoid
Secondary carboxylic acid amide
Carboxamide group
Carboxylic acid
Organopnictogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Organic nitrogen compound
Carbonyl group
Organic oxide
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.7 g/L	ALOGPS
logP	0.5	ALOGPS
logP	0.72	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	3.58	ChemAxon
pKa (Strongest Basic)	-2.3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	103.7 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	65.45 m³·mol⁻¹	ChemAxon
Polarizability	25.76 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces
Urine

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria/Eubacteria	Firmicutes	1	Human stool; Human ; Human feces	Indirect association between microbiota composition and metabolites measured in host biospecimen

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference
Human Urine	Detected but not Quantified						Not Specified	Not Specified	Normal	HMDB	2338430
Human Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	29808030

External Links

HMDB ID

HMDB0059772

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11579826

PDB ID

Not Available

ChEBI ID

89860

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Showing metabocard for N-Phenylacetylglutamic acid (MMDBc0000485)

MOL for #<Metabolite:0x00007f921801e080>

3D MOL for #<Metabolite:0x00007f921801e080>

3D SDF for #<Metabolite:0x00007f921801e080>

3D-SDF for #<Metabolite:0x00007f921801e080>

PDB for #<Metabolite:0x00007f921801e080>

3D PDB for #<Metabolite:0x00007f921801e080>

SMILES for #<Metabolite:0x00007f921801e080>

INCHI for #<Metabolite:0x00007f921801e080>

Structure for #<Metabolite:0x00007f921801e080>

3D Structure for #<Metabolite:0x00007f921801e080>