MiMeDB: Showing metabocard for N2-Hexanoyl-L-glutamine (MMDBc0057166)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-11-09 19:21:02 UTC

Update Date

2022-11-09 19:21:02 UTC

Metabolite ID

MMDBc0057166

Metabolite Identification

Common Name

N2-Hexanoyl-L-glutamine

Description

Hexanoylglutamine belongs to the class of organic compounds known as glutamine and derivatives. Glutamine and derivatives are compounds containing glutamine or a derivative thereof resulting from reaction of glutamine 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 very few articles have been published on Hexanoylglutamine.

Structure

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

HMDB0242182
     RDKit          3D
Hexanoylglutamine
 37 36  0  0  0  0  0  0  0  0999 V2000
   -4.5494    1.4256    0.0377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1337    0.0232    0.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4152   -0.6682   -0.7328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1588   -0.0371   -1.1883 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0926    0.1110   -0.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6411   -1.1717    0.4329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5881   -1.9375    1.1750 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5358   -1.6474    0.3252 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5769   -0.9759   -0.3943 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3042   -0.0083    0.5086 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3771    0.7008   -0.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0969    1.6898    0.6145 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3567    1.5376    0.7940 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4435    2.7447    1.2188 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5304   -2.0620   -0.8265 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4172   -3.2095   -0.3593 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5301   -1.8166   -1.7349 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0697    2.1848    0.6930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6543    1.5906    0.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3513    1.6422   -1.0474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5845   -0.0314    1.3497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0807   -0.5533    0.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2272   -1.7218   -0.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1593   -0.7516   -1.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4004    0.9855   -1.5686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7192   -0.5738   -2.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4076    0.7424    0.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2129    0.6263   -0.5704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5725   -2.9263    1.0137 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2381   -0.4702   -1.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7678   -0.5717    1.3551 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6141    0.7421    0.9296 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9225    1.2989   -1.0734 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1384    0.0350   -0.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8976    0.7567    0.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9624    3.5810    1.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3089   -1.2839   -2.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  2  3
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  3
 12 14  1  0
  9 15  1  0
 15 16  2  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  0
  4 26  1  0
  5 27  1  0
  5 28  1  0
  7 29  1  0
  9 30  1  6
 10 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 13 35  1  0
 14 36  1  0
 17 37  1  0
M  END


  Mrv1652308282100562D          

 18 17  0  0  1  0            999 V2000
    7.4250    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0125    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    2.8579    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    3.5724    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.1434    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  7  6  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  5  1  0  0  0  0
 11  8  1  0  0  0  0
 12  9  2  0  0  0  0
  8 13  1  1  0  0  0
 13 10  2  0  0  0  0
 14  9  1  0  0  0  0
 10 15  1  4  0  0  0
 16 11  2  0  0  0  0
 17 11  1  0  0  0  0
  8 18  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0057166

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@](CCC(O)=N)(N=C(O)CCCCC)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C11H20N2O4/c1-2-3-4-5-10(15)13-8(11(16)17)6-7-9(12)14/h8H,2-7H2,1H3,(H2,12,14)(H,13,15)(H,16,17)/t8-/m0/s1

> <INCHI_KEY>
NONGMLDQXRDGIT-QMMMGPOBSA-N

> <FORMULA>
C11H20N2O4

> <MOLECULAR_WEIGHT>
244.291

> <EXACT_MASS>
244.142307132

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
26.17228603614376

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-4-(C-hydroxycarbonimidoyl)-2-[(1-hydroxyhexylidene)amino]butanoic acid

> <JCHEM_LOGP>
-0.9438229377120051

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
4.088674326828256

> <JCHEM_PKA_STRONGEST_ACIDIC>
-0.4428799690310603

> <JCHEM_PKA_STRONGEST_BASIC>
12.924574557571821

> <JCHEM_POLAR_SURFACE_AREA>
113.97000000000001

> <JCHEM_REFRACTIVITY>
72.4419

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-4-(C-hydroxycarbonimidoyl)-2-[(1-hydroxyhexylidene)amino]butanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0242182
     RDKit          3D
Hexanoylglutamine
 37 36  0  0  0  0  0  0  0  0999 V2000
   -4.5494    1.4256    0.0377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1337    0.0232    0.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4152   -0.6682   -0.7328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1588   -0.0371   -1.1883 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0926    0.1110   -0.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6411   -1.1717    0.4329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5881   -1.9375    1.1750 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5358   -1.6474    0.3252 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5769   -0.9759   -0.3943 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3042   -0.0083    0.5086 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3771    0.7008   -0.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0969    1.6898    0.6145 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3567    1.5376    0.7940 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4435    2.7447    1.2188 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5304   -2.0620   -0.8265 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4172   -3.2095   -0.3593 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5301   -1.8166   -1.7349 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0697    2.1848    0.6930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6543    1.5906    0.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3513    1.6422   -1.0474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5845   -0.0314    1.3497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0807   -0.5533    0.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2272   -1.7218   -0.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1593   -0.7516   -1.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4004    0.9855   -1.5686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7192   -0.5738   -2.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4076    0.7424    0.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2129    0.6263   -0.5704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5725   -2.9263    1.0137 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2381   -0.4702   -1.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7678   -0.5717    1.3551 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6141    0.7421    0.9296 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9225    1.2989   -1.0734 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1384    0.0350   -0.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8976    0.7567    0.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9624    3.5810    1.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3089   -1.2839   -2.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  2  3
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  3
 12 14  1  0
  9 15  1  0
 15 16  2  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  0
  4 26  1  0
  5 27  1  0
  5 28  1  0
  7 29  1  0
  9 30  1  6
 10 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 13 35  1  0
 14 36  1  0
 17 37  1  0
M  END

HEADER    PROTEIN                                 28-AUG-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-AUG-21         0                                  
HETATM    1  C   UNK     0      13.860  10.669   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.090   9.336   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.550   9.336   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.780   8.002   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.240   8.002   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.620   5.335   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.850   4.001   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.160   5.335   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.310   4.001   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.470   6.668   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       1.540   2.667   0.000  0.00  0.00           N+0
HETATM   13  N   UNK     0       6.930   6.668   0.000  0.00  0.00           N+0
HETATM   14  O   UNK     0       1.540   5.335   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       9.240   5.335   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       8.470   4.001   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       6.160   2.667   0.000  0.00  0.00           O+0
HETATM   18  H   UNK     0       5.390   4.001   0.000  0.00  0.00           H+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4   10                                                       
CONECT    6    7    8                                                       
CONECT    7    6    9                                                       
CONECT    8    6   11   13   18                                             
CONECT    9    7   12   14                                                  
CONECT   10    5   13   15                                                  
CONECT   11    8   16   17                                                  
CONECT   12    9                                                            
CONECT   13    8   10                                                       
CONECT   14    9                                                            
CONECT   15   10                                                            
CONECT   16   11                                                            
CONECT   17   11                                                            
CONECT   18    8                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   34    0
END

COMPND    HMDB0242182
HETATM    1  C1  UNL     1      -4.549   1.426   0.038  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.134   0.023   0.370  1.00  0.00           C  
HETATM    3  C3  UNL     1      -3.415  -0.668  -0.733  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.159  -0.037  -1.188  1.00  0.00           C  
HETATM    5  C5  UNL     1      -1.093   0.111  -0.154  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.641  -1.172   0.433  1.00  0.00           C  
HETATM    7  O1  UNL     1      -1.588  -1.938   1.175  1.00  0.00           O  
HETATM    8  N1  UNL     1       0.536  -1.647   0.325  1.00  0.00           N  
HETATM    9  C7  UNL     1       1.577  -0.976  -0.394  1.00  0.00           C  
HETATM   10  C8  UNL     1       2.304  -0.008   0.509  1.00  0.00           C  
HETATM   11  C9  UNL     1       3.377   0.701  -0.257  1.00  0.00           C  
HETATM   12  C10 UNL     1       4.097   1.690   0.614  1.00  0.00           C  
HETATM   13  N2  UNL     1       5.357   1.538   0.794  1.00  0.00           N  
HETATM   14  O2  UNL     1       3.443   2.745   1.219  1.00  0.00           O  
HETATM   15  C11 UNL     1       2.530  -2.062  -0.826  1.00  0.00           C  
HETATM   16  O3  UNL     1       2.417  -3.209  -0.359  1.00  0.00           O  
HETATM   17  O4  UNL     1       3.530  -1.817  -1.735  1.00  0.00           O  
HETATM   18  H1  UNL     1      -4.070   2.185   0.693  1.00  0.00           H  
HETATM   19  H2  UNL     1      -5.654   1.591   0.153  1.00  0.00           H  
HETATM   20  H3  UNL     1      -4.351   1.642  -1.047  1.00  0.00           H  
HETATM   21  H4  UNL     1      -3.584  -0.031   1.350  1.00  0.00           H  
HETATM   22  H5  UNL     1      -5.081  -0.553   0.559  1.00  0.00           H  
HETATM   23  H6  UNL     1      -3.227  -1.722  -0.447  1.00  0.00           H  
HETATM   24  H7  UNL     1      -4.159  -0.752  -1.580  1.00  0.00           H  
HETATM   25  H8  UNL     1      -2.400   0.986  -1.569  1.00  0.00           H  
HETATM   26  H9  UNL     1      -1.719  -0.574  -2.054  1.00  0.00           H  
HETATM   27  H10 UNL     1      -1.408   0.742   0.708  1.00  0.00           H  
HETATM   28  H11 UNL     1      -0.213   0.626  -0.570  1.00  0.00           H  
HETATM   29  H12 UNL     1      -1.573  -2.926   1.014  1.00  0.00           H  
HETATM   30  H13 UNL     1       1.238  -0.470  -1.303  1.00  0.00           H  
HETATM   31  H14 UNL     1       2.768  -0.572   1.355  1.00  0.00           H  
HETATM   32  H15 UNL     1       1.614   0.742   0.930  1.00  0.00           H  
HETATM   33  H16 UNL     1       2.923   1.299  -1.073  1.00  0.00           H  
HETATM   34  H17 UNL     1       4.138   0.035  -0.665  1.00  0.00           H  
HETATM   35  H18 UNL     1       5.898   0.757   0.360  1.00  0.00           H  
HETATM   36  H19 UNL     1       3.962   3.581   1.458  1.00  0.00           H  
HETATM   37  H20 UNL     1       3.309  -1.284  -2.585  1.00  0.00           H  
CONECT    1    2   18   19   20
CONECT    2    3   21   22
CONECT    3    4   23   24
CONECT    4    5   25   26
CONECT    5    6   27   28
CONECT    6    7    8    8
CONECT    7   29
CONECT    8    9
CONECT    9   10   15   30
CONECT   10   11   31   32
CONECT   11   12   33   34
CONECT   12   13   13   14
CONECT   13   35
CONECT   14   36
CONECT   15   16   16   17
CONECT   17   37
END

HMDB0242182
     RDKit          3D
Hexanoylglutamine
 37 36  0  0  0  0  0  0  0  0999 V2000
   -4.5494    1.4256    0.0377 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1337    0.0232    0.3695 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4152   -0.6682   -0.7328 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1588   -0.0371   -1.1883 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0926    0.1110   -0.1543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6411   -1.1717    0.4329 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5881   -1.9375    1.1750 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5358   -1.6474    0.3252 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.5769   -0.9759   -0.3943 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3042   -0.0083    0.5086 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3771    0.7008   -0.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0969    1.6898    0.6145 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3567    1.5376    0.7940 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4435    2.7447    1.2188 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5304   -2.0620   -0.8265 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4172   -3.2095   -0.3593 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5301   -1.8166   -1.7349 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0697    2.1848    0.6930 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6543    1.5906    0.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3513    1.6422   -1.0474 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5845   -0.0314    1.3497 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0807   -0.5533    0.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2272   -1.7218   -0.4472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1593   -0.7516   -1.5805 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4004    0.9855   -1.5686 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7192   -0.5738   -2.0537 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4076    0.7424    0.7080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2129    0.6263   -0.5704 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5725   -2.9263    1.0137 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2381   -0.4702   -1.3031 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7678   -0.5717    1.3551 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6141    0.7421    0.9296 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9225    1.2989   -1.0734 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1384    0.0350   -0.6649 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8976    0.7567    0.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9624    3.5810    1.4576 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3089   -1.2839   -2.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  2  3
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  3
 12 14  1  0
  9 15  1  0
 15 16  2  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  0
  2 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  0
  4 26  1  0
  5 27  1  0
  5 28  1  0
  7 29  1  0
  9 30  1  6
 10 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 13 35  1  0
 14 36  1  0
 17 37  1  0
M  END

Synonyms

Not Available

Molecular Formula

C₁₁H₂₀N₂O₄

Average Mass

244.291

Monoisotopic Mass

244.142307132

IUPAC Name

(2S)-4-(C-hydroxycarbonimidoyl)-2-[(1-hydroxyhexylidene)amino]butanoic acid

Traditional Name

(2S)-4-(C-hydroxycarbonimidoyl)-2-[(1-hydroxyhexylidene)amino]butanoic acid

CAS Registry Number

Not Available

SMILES

[H][C@@](CCC(O)=N)(N=C(O)CCCCC)C(O)=O

InChI Identifier

InChI=1S/C11H20N2O4/c1-2-3-4-5-10(15)13-8(11(16)17)6-7-9(12)14/h8H,2-7H2,1H3,(H2,12,14)(H,13,15)(H,16,17)/t8-/m0/s1

InChI Key

NONGMLDQXRDGIT-QMMMGPOBSA-N

Chemical Taxonomy

Description

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

Glutamine and derivatives

Alternative Parents

Substituents

Glutamine or derivatives
N-acyl-alpha-amino acid
N-acyl-l-alpha-amino acid
N-acyl-alpha amino acid or derivatives
N-acyl-l-glutamine
Fatty amide
N-acyl-amine
Fatty acyl
Fatty acid
Carboxamide group
Secondary carboxylic acid amide
Primary carboxylic acid amide
Carboxylic acid
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Not Available

Predicted Properties

Property	Value	Source
logP	-0.94	ChemAxon
pKa (Strongest Acidic)	-0.44	ChemAxon
pKa (Strongest Basic)	12.92	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	113.97 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	72.44 m³·mol⁻¹	ChemAxon
Polarizability	26.17 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Chromatographic Retention Times and Retention Indices

Retention Times

Not Available

Retention Indices

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

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

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated 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

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

External Links

HMDB ID

HMDB0242182

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

67156842

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

28880746

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for N2-Hexanoyl-L-glutamine (MMDBc0057166)

MOL for #<Metabolite:0x0000560be1f9bb20>

3D MOL for #<Metabolite:0x0000560be1f9bb20>

3D SDF for #<Metabolite:0x0000560be1f9bb20>

3D-SDF for #<Metabolite:0x0000560be1f9bb20>

PDB for #<Metabolite:0x0000560be1f9bb20>

3D PDB for #<Metabolite:0x0000560be1f9bb20>

SMILES for #<Metabolite:0x0000560be1f9bb20>

INCHI for #<Metabolite:0x0000560be1f9bb20>

Structure for #<Metabolite:0x0000560be1f9bb20>

3D Structure for #<Metabolite:0x0000560be1f9bb20>