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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2021-09-10 23:40:41 UTC

Update Date

2021-09-26 22:55:52 UTC

HMDB ID

HMDB0246659

Secondary Accession Numbers

None

Metabolite Identification

Common Name

L-Leucine-p-nitroanilide

Description

L-Leucine-p-nitroanilide belongs to the class of organic compounds known as leucine and derivatives. Leucine and derivatives are compounds containing leucine or a derivative thereof resulting from reaction of leucine 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 L-Leucine-p-nitroanilide. This compound has been identified in human blood as reported by (PMID: 31557052 ). L-leucine-p-nitroanilide is not a naturally occurring metabolite and is only found in those individuals exposed to this compound or its derivatives. Technically L-Leucine-p-nitroanilide 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

HMDB0246659
     RDKit          3D
L-Leucine-p-nitroanilide
 35 35  0  0  0  0  0  0  0  0999 V2000
   -4.0180    1.5119   -0.1630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8019    0.2755   -0.9943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6628   -0.8782   -0.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3671   -0.0802   -1.1490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6293   -0.3607    0.1150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6224    0.7698    1.0174 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2090   -0.6719   -0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0200   -1.6146   -0.9976 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8451    0.0776    0.3336 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2279   -0.0673    0.1377 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7443   -1.0289   -0.6742 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1392   -1.1259   -0.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0202   -0.2878   -0.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4312   -0.4015   -0.3718 N   0  0  0  0  0  4  0  0  0  0  0  0
    7.1643    0.4126    0.2496 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9886   -1.3598   -1.1834 O   0  0  0  0  0  1  0  0  0  0  0  0
    4.4677    0.6740    0.6146 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1079    0.7893    0.7852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9376    1.2829    0.9031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0247    1.9299   -0.3710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2934    2.2768   -0.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1768    0.5368   -2.0285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1242   -1.5659    0.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0146   -1.4876   -1.3979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5590   -0.5289   -0.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3047   -0.9698   -1.8217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8681    0.7519   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0283   -1.2371    0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2663    1.6396    0.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3198    0.5383    1.9663 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5804    0.8878    1.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1304   -1.7312   -1.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5118   -1.8964   -1.4802 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1493    1.3549    1.1303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7397    1.5839    1.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  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  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 13 17  1  0
 17 18  2  0
 18 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  6 29  1  0
  6 30  1  0
  9 31  1  0
 11 32  1  0
 12 33  1  0
 17 34  1  0
 18 35  1  0
M  CHG  2  14   1  16  -1
M  END

  Mrv1652309112101402D          

 18 18  0  0  0  0            999 V2000
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   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
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
    8.5737   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -6.1875    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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
  9 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
  5 18  1  0  0  0  0
M  CHG  2  15   1  17  -1
M  END
> <DATABASE_ID>
HMDB0246659

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)CC(N)C(=O)NC1=CC=C(C=C1)[N+]([O-])=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H17N3O3/c1-8(2)7-11(13)12(16)14-9-3-5-10(6-4-9)15(17)18/h3-6,8,11H,7,13H2,1-2H3,(H,14,16)

> <INCHI_KEY>
AXZJHDNQDSVIDR-UHFFFAOYSA-N

> <FORMULA>
C12H17N3O3

> <MOLECULAR_WEIGHT>
251.286

> <EXACT_MASS>
251.126991419

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
26.418460141564232

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-amino-4-methyl-N-(4-nitrophenyl)pentanamide

> <ALOGPS_LOGP>
1.45

> <JCHEM_LOGP>
2.0496849286666663

> <ALOGPS_LOGS>
-3.45

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.397488883016031

> <JCHEM_PKA_STRONGEST_BASIC>
8.270848709006458

> <JCHEM_POLAR_SURFACE_AREA>
98.25999999999999

> <JCHEM_REFRACTIVITY>
68.76870000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.00e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-amino-4-methyl-N-(4-nitrophenyl)pentanamide

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0246659
     RDKit          3D
L-Leucine-p-nitroanilide
 35 35  0  0  0  0  0  0  0  0999 V2000
   -4.0180    1.5119   -0.1630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8019    0.2755   -0.9943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6628   -0.8782   -0.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3671   -0.0802   -1.1490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6293   -0.3607    0.1150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6224    0.7698    1.0174 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2090   -0.6719   -0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0200   -1.6146   -0.9976 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8451    0.0776    0.3336 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2279   -0.0673    0.1377 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7443   -1.0289   -0.6742 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1392   -1.1259   -0.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0202   -0.2878   -0.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4312   -0.4015   -0.3718 N   0  0  0  0  0  4  0  0  0  0  0  0
    7.1643    0.4126    0.2496 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9886   -1.3598   -1.1834 O   0  0  0  0  0  1  0  0  0  0  0  0
    4.4677    0.6740    0.6146 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1079    0.7893    0.7852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9376    1.2829    0.9031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0247    1.9299   -0.3710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2934    2.2768   -0.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1768    0.5368   -2.0285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1242   -1.5659    0.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0146   -1.4876   -1.3979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5590   -0.5289   -0.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3047   -0.9698   -1.8217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8681    0.7519   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0283   -1.2371    0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2663    1.6396    0.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3198    0.5383    1.9663 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5804    0.8878    1.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1304   -1.7312   -1.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5118   -1.8964   -1.4802 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1493    1.3549    1.1303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7397    1.5839    1.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  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  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 13 17  1  0
 17 18  2  0
 18 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  6 29  1  0
  6 30  1  0
  9 31  1  0
 11 32  1  0
 12 33  1  0
 17 34  1  0
 18 35  1  0
M  CHG  2  14   1  16  -1
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       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0       9.336  -6.930   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      14.670 -10.010   0.000  0.00  0.00           N+1
HETATM   16  O   UNK     0      16.004  -9.240   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      14.670 -11.550   0.000  0.00  0.00           O-1
HETATM   18  N   UNK     0       6.668  -5.390   0.000  0.00  0.00           N+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   18                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18    5                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

COMPND    HMDB0246659
HETATM    1  C1  UNL     1      -4.018   1.512  -0.163  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.802   0.276  -0.994  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.663  -0.878  -0.539  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.367  -0.080  -1.149  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.629  -0.361   0.115  1.00  0.00           C  
HETATM    6  N1  UNL     1      -1.622   0.770   1.017  1.00  0.00           N  
HETATM    7  C6  UNL     1      -0.209  -0.672  -0.218  1.00  0.00           C  
HETATM    8  O1  UNL     1      -0.020  -1.615  -0.998  1.00  0.00           O  
HETATM    9  N2  UNL     1       0.845   0.078   0.334  1.00  0.00           N  
HETATM   10  C7  UNL     1       2.228  -0.067   0.138  1.00  0.00           C  
HETATM   11  C8  UNL     1       2.744  -1.029  -0.674  1.00  0.00           C  
HETATM   12  C9  UNL     1       4.139  -1.126  -0.832  1.00  0.00           C  
HETATM   13  C10 UNL     1       5.020  -0.288  -0.200  1.00  0.00           C  
HETATM   14  N3  UNL     1       6.431  -0.402  -0.372  1.00  0.00           N1+
HETATM   15  O2  UNL     1       7.164   0.413   0.250  1.00  0.00           O  
HETATM   16  O3  UNL     1       6.989  -1.360  -1.183  1.00  0.00           O1-
HETATM   17  C11 UNL     1       4.468   0.674   0.615  1.00  0.00           C  
HETATM   18  C12 UNL     1       3.108   0.789   0.785  1.00  0.00           C  
HETATM   19  H1  UNL     1      -3.938   1.283   0.903  1.00  0.00           H  
HETATM   20  H2  UNL     1      -5.025   1.930  -0.371  1.00  0.00           H  
HETATM   21  H3  UNL     1      -3.293   2.277  -0.494  1.00  0.00           H  
HETATM   22  H4  UNL     1      -4.177   0.537  -2.029  1.00  0.00           H  
HETATM   23  H5  UNL     1      -4.124  -1.566   0.140  1.00  0.00           H  
HETATM   24  H6  UNL     1      -5.015  -1.488  -1.398  1.00  0.00           H  
HETATM   25  H7  UNL     1      -5.559  -0.529  -0.009  1.00  0.00           H  
HETATM   26  H8  UNL     1      -2.305  -0.970  -1.822  1.00  0.00           H  
HETATM   27  H9  UNL     1      -1.868   0.752  -1.698  1.00  0.00           H  
HETATM   28  H10 UNL     1      -2.028  -1.237   0.671  1.00  0.00           H  
HETATM   29  H11 UNL     1      -1.266   1.640   0.610  1.00  0.00           H  
HETATM   30  H12 UNL     1      -1.320   0.538   1.966  1.00  0.00           H  
HETATM   31  H13 UNL     1       0.580   0.888   1.010  1.00  0.00           H  
HETATM   32  H14 UNL     1       2.130  -1.731  -1.211  1.00  0.00           H  
HETATM   33  H15 UNL     1       4.512  -1.896  -1.480  1.00  0.00           H  
HETATM   34  H16 UNL     1       5.149   1.355   1.130  1.00  0.00           H  
HETATM   35  H17 UNL     1       2.740   1.584   1.453  1.00  0.00           H  
CONECT    1    2   19   20   21
CONECT    2    3    4   22
CONECT    3   23   24   25
CONECT    4    5   26   27
CONECT    5    6    7   28
CONECT    6   29   30
CONECT    7    8    8    9
CONECT    9   10   31
CONECT   10   11   11   18
CONECT   11   12   32
CONECT   12   13   13   33
CONECT   13   14   17
CONECT   14   15   15   16
CONECT   17   18   18   34
CONECT   18   35
END

HMDB0246659
     RDKit          3D
L-Leucine-p-nitroanilide
 35 35  0  0  0  0  0  0  0  0999 V2000
   -4.0180    1.5119   -0.1630 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8019    0.2755   -0.9943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6628   -0.8782   -0.5385 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3671   -0.0802   -1.1490 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6293   -0.3607    0.1150 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6224    0.7698    1.0174 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2090   -0.6719   -0.2184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0200   -1.6146   -0.9976 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8451    0.0776    0.3336 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2279   -0.0673    0.1377 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7443   -1.0289   -0.6742 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1392   -1.1259   -0.8320 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0202   -0.2878   -0.1995 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4312   -0.4015   -0.3718 N   0  0  0  0  0  4  0  0  0  0  0  0
    7.1643    0.4126    0.2496 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9886   -1.3598   -1.1834 O   0  0  0  0  0  1  0  0  0  0  0  0
    4.4677    0.6740    0.6146 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1079    0.7893    0.7852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9376    1.2829    0.9031 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0247    1.9299   -0.3710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2934    2.2768   -0.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1768    0.5368   -2.0285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1242   -1.5659    0.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0146   -1.4876   -1.3979 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5590   -0.5289   -0.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3047   -0.9698   -1.8217 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8681    0.7519   -1.6983 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0283   -1.2371    0.6710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2663    1.6396    0.6099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3198    0.5383    1.9663 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5804    0.8878    1.0102 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1304   -1.7312   -1.2112 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5118   -1.8964   -1.4802 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1493    1.3549    1.1303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7397    1.5839    1.4528 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  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  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 13 17  1  0
 17 18  2  0
 18 10  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  6 29  1  0
  6 30  1  0
  9 31  1  0
 11 32  1  0
 12 33  1  0
 17 34  1  0
 18 35  1  0
M  CHG  2  14   1  16  -1
M  END

View in JSmol View Stereo Labels

Synonyms

Value	Source
1-Leucine-4-nitroanilide	HMDB
1-Leucine-4-nitroanilide, (S)-isomer	HMDB
1-Leucyl-4-nitroanilide	HMDB
1-Leucyl-p-nitroanilide	HMDB
L-Leucine-4-nitroanilide	HMDB

Chemical Formula

C₁₂H₁₇N₃O₃

Average Molecular Weight

251.286

Monoisotopic Molecular Weight

251.126991419

IUPAC Name

2-amino-4-methyl-N-(4-nitrophenyl)pentanamide

Traditional Name

2-amino-4-methyl-N-(4-nitrophenyl)pentanamide

CAS Registry Number

Not Available

SMILES

CC(C)CC(N)C(=O)NC1=CC=C(C=C1)[N+]([O-])=O

InChI Identifier

InChI=1S/C12H17N3O3/c1-8(2)7-11(13)12(16)14-9-3-5-10(6-4-9)15(17)18/h3-6,8,11H,7,13H2,1-2H3,(H,14,16)

InChI Key

AXZJHDNQDSVIDR-UHFFFAOYSA-N

Chemical Taxonomy

Description

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

Leucine and derivatives

Alternative Parents

Substituents

Leucine or derivatives
Alpha-amino acid amide
Nitrobenzene
Anilide
Nitroaromatic compound
N-arylamide
Monocyclic benzene moiety
Fatty acyl
Fatty amide
Benzenoid
Organic nitro compound
Carboxamide group
C-nitro compound
Secondary carboxylic acid amide
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic oxoazanium
Allyl-type 1,3-dipolar organic compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Organopnictogen compound
Primary aliphatic amine
Organic oxide
Organic oxygen compound
Carbonyl group
Primary amine
Hydrocarbon derivative
Amine
Organic zwitterion
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	1.45	ALOGPS
logP	2.05	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	12.4	ChemAxon
pKa (Strongest Basic)	8.27	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	98.26 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	68.77 m³·mol⁻¹	ChemAxon
Polarizability	26.42 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

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	165.433	30932474
DeepCCS	[M-H]-	162.023	30932474
DeepCCS	[M-2H]-	196.912	30932474
DeepCCS	[M+Na]+	173.203	30932474
AllCCS	[M+H]+	157.8	32859911
AllCCS	[M+H-H2O]+	154.4	32859911
AllCCS	[M+NH4]+	161.0	32859911
AllCCS	[M+Na]+	161.9	32859911
AllCCS	[M-H]-	159.6	32859911
AllCCS	[M+Na-2H]-	160.0	32859911
AllCCS	[M+HCOO]-	160.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
L-Leucine-p-nitroanilide	CC(C)CC(N)C(=O)NC1=CC=C(C=C1)[N+]([O-])=O	3112.5	Standard polar	33892256
L-Leucine-p-nitroanilide	CC(C)CC(N)C(=O)NC1=CC=C(C=C1)[N+]([O-])=O	2376.1	Standard non polar	33892256
L-Leucine-p-nitroanilide	CC(C)CC(N)C(=O)NC1=CC=C(C=C1)[N+]([O-])=O	2336.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
L-Leucine-p-nitroanilide,1TMS,isomer #1	CC(C)CC(N[Si](C)(C)C)C(=O)NC1=CC=C([N+](=O)[O-])C=C1	2403.9	Semi standard non polar	33892256
L-Leucine-p-nitroanilide,1TMS,isomer #1	CC(C)CC(N[Si](C)(C)C)C(=O)NC1=CC=C([N+](=O)[O-])C=C1	2245.8	Standard non polar	33892256
L-Leucine-p-nitroanilide,1TMS,isomer #1	CC(C)CC(N[Si](C)(C)C)C(=O)NC1=CC=C([N+](=O)[O-])C=C1	3019.6	Standard polar	33892256
L-Leucine-p-nitroanilide,1TMS,isomer #2	CC(C)CC(N)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C	2209.3	Semi standard non polar	33892256
L-Leucine-p-nitroanilide,1TMS,isomer #2	CC(C)CC(N)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C	2187.2	Standard non polar	33892256
L-Leucine-p-nitroanilide,1TMS,isomer #2	CC(C)CC(N)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C	3062.4	Standard polar	33892256
L-Leucine-p-nitroanilide,2TMS,isomer #1	CC(C)CC(C(=O)NC1=CC=C([N+](=O)[O-])C=C1)N([Si](C)(C)C)[Si](C)(C)C	2497.8	Semi standard non polar	33892256
L-Leucine-p-nitroanilide,2TMS,isomer #1	CC(C)CC(C(=O)NC1=CC=C([N+](=O)[O-])C=C1)N([Si](C)(C)C)[Si](C)(C)C	2383.9	Standard non polar	33892256
L-Leucine-p-nitroanilide,2TMS,isomer #1	CC(C)CC(C(=O)NC1=CC=C([N+](=O)[O-])C=C1)N([Si](C)(C)C)[Si](C)(C)C	2846.4	Standard polar	33892256
L-Leucine-p-nitroanilide,2TMS,isomer #2	CC(C)CC(N[Si](C)(C)C)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C	2202.2	Semi standard non polar	33892256
L-Leucine-p-nitroanilide,2TMS,isomer #2	CC(C)CC(N[Si](C)(C)C)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C	2258.3	Standard non polar	33892256
L-Leucine-p-nitroanilide,2TMS,isomer #2	CC(C)CC(N[Si](C)(C)C)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C	2643.2	Standard polar	33892256
L-Leucine-p-nitroanilide,3TMS,isomer #1	CC(C)CC(C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2386.6	Semi standard non polar	33892256
L-Leucine-p-nitroanilide,3TMS,isomer #1	CC(C)CC(C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2397.9	Standard non polar	33892256
L-Leucine-p-nitroanilide,3TMS,isomer #1	CC(C)CC(C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2532.7	Standard polar	33892256
L-Leucine-p-nitroanilide,1TBDMS,isomer #1	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)NC1=CC=C([N+](=O)[O-])C=C1	2645.4	Semi standard non polar	33892256
L-Leucine-p-nitroanilide,1TBDMS,isomer #1	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)NC1=CC=C([N+](=O)[O-])C=C1	2464.2	Standard non polar	33892256
L-Leucine-p-nitroanilide,1TBDMS,isomer #1	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)NC1=CC=C([N+](=O)[O-])C=C1	3040.8	Standard polar	33892256
L-Leucine-p-nitroanilide,1TBDMS,isomer #2	CC(C)CC(N)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C(C)(C)C	2513.1	Semi standard non polar	33892256
L-Leucine-p-nitroanilide,1TBDMS,isomer #2	CC(C)CC(N)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C(C)(C)C	2392.8	Standard non polar	33892256
L-Leucine-p-nitroanilide,1TBDMS,isomer #2	CC(C)CC(N)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C(C)(C)C	3095.8	Standard polar	33892256
L-Leucine-p-nitroanilide,2TBDMS,isomer #1	CC(C)CC(C(=O)NC1=CC=C([N+](=O)[O-])C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2975.4	Semi standard non polar	33892256
L-Leucine-p-nitroanilide,2TBDMS,isomer #1	CC(C)CC(C(=O)NC1=CC=C([N+](=O)[O-])C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2778.6	Standard non polar	33892256
L-Leucine-p-nitroanilide,2TBDMS,isomer #1	CC(C)CC(C(=O)NC1=CC=C([N+](=O)[O-])C=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2922.2	Standard polar	33892256
L-Leucine-p-nitroanilide,2TBDMS,isomer #2	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C(C)(C)C	2730.9	Semi standard non polar	33892256
L-Leucine-p-nitroanilide,2TBDMS,isomer #2	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C(C)(C)C	2683.1	Standard non polar	33892256
L-Leucine-p-nitroanilide,2TBDMS,isomer #2	CC(C)CC(N[Si](C)(C)C(C)(C)C)C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C(C)(C)C	2806.6	Standard polar	33892256
L-Leucine-p-nitroanilide,3TBDMS,isomer #1	CC(C)CC(C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3140.3	Semi standard non polar	33892256
L-Leucine-p-nitroanilide,3TBDMS,isomer #1	CC(C)CC(C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2973.9	Standard non polar	33892256
L-Leucine-p-nitroanilide,3TBDMS,isomer #1	CC(C)CC(C(=O)N(C1=CC=C([N+](=O)[O-])C=C1)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2760.3	Standard polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - L-Leucine-p-nitroanilide GC-MS (Non-derivatized) - 70eV, Positive	splash10-000l-9410000000-397fdc4deb0bbe3080b1	2021-09-24	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - L-Leucine-p-nitroanilide GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	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

108743

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

121895

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 L-Leucine-p-nitroanilide (HMDB0246659)

MOL for HMDB0246659 (L-Leucine-p-nitroanilide)

3D MOL for HMDB0246659 (L-Leucine-p-nitroanilide)

3D SDF for HMDB0246659 (L-Leucine-p-nitroanilide)

3D-SDF for HMDB0246659 (L-Leucine-p-nitroanilide)

PDB for HMDB0246659 (L-Leucine-p-nitroanilide)

3D PDB for HMDB0246659 (L-Leucine-p-nitroanilide)

SMILES for HMDB0246659 (L-Leucine-p-nitroanilide)

INCHI for HMDB0246659 (L-Leucine-p-nitroanilide)

Structure for HMDB0246659 (L-Leucine-p-nitroanilide)

3D Structure for HMDB0246659 (L-Leucine-p-nitroanilide)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra