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

Functional Ontology

Physical Properties

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-00kf-9630000000-5e0b521e8a713bf14d55	2017-09-20	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (2 TMS) - 70eV, Positive	splash10-0006-9232000000-4f91eb7371a9d5a29dbe	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00l2-0290000000-f9fcb6aff67eadfed17b	2017-10-06	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0ukc-3940000000-7715ceedac8896df0578	2017-10-06	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0006-9400000000-8e62f51deaf8b833dd98	2017-10-06	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-03dj-0090000000-72b66ee6f355894e494d	2017-10-06	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-0fdk-1790000000-20dfc405e198de6edc03	2017-10-06	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0f96-7900000000-442d0c720d4960fc6824	2017-10-06	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00ls-1920000000-807efd3a431bc1593d12	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0fr6-5900000000-5f6fef9619344f55f6fd	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0006-9200000000-077ffea0bedc4fae2d88	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-004i-0900000000-86a874c66903f262ba1c	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-0ufr-0900000000-8323aceb3320d31b04ca	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0f6x-9600000000-fcaab1eab6b2655ad112	2021-09-22	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-18	View Spectrum

Biological Properties

Human Proteins and Enzymes

Human Pathways

Metabolic Reactions

Health Effects and Bioactivity

Microbial Sources

Exposure Sources

Host Biospecimen and Location

External Links

References

Showing metabocard for N-Phenylacetylglutamic acid (MMDBc0000485)

MOL for #<Metabolite:0x00007fb809bffef0>

3D MOL for #<Metabolite:0x00007fb809bffef0>

3D SDF for #<Metabolite:0x00007fb809bffef0>

3D-SDF for #<Metabolite:0x00007fb809bffef0>

PDB for #<Metabolite:0x00007fb809bffef0>

3D PDB for #<Metabolite:0x00007fb809bffef0>

SMILES for #<Metabolite:0x00007fb809bffef0>

INCHI for #<Metabolite:0x00007fb809bffef0>

Structure for #<Metabolite:0x00007fb809bffef0>

3D Structure for #<Metabolite:0x00007fb809bffef0>