MiMeDB: Showing metabocard for Histidylalanine (MMDBc0000662)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-12-10 18:52:11 UTC

Update Date

2024-04-30 19:33:26 UTC

Metabolite ID

MMDBc0000662

Metabolite Identification

Common Name

Histidylalanine

Description

Histidylalanine is a dipeptide composed of histidine and alanine. It is an incomplete breakdown product of protein digestion or protein catabolism. Dipeptides are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond. Some dipeptides are known to have physiological or cell-signalling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis.

Structure

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

HMDB0028878
     RDKit          3D
Histidylalanine
 30 30  0  0  0  0  0  0  0  0999 V2000
    3.6565   -0.1355    0.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3102    0.5667    0.2900 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2358   -0.3795    0.0624 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2189   -0.6183    1.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2674    0.0198    2.0903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8595   -1.5869    0.7564 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8551   -1.5900    1.8140 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5634   -1.4223   -0.5442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2437   -0.1589   -0.7712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9279    0.2015   -1.9406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4187    1.4264   -1.7580 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0957    1.8770   -0.5499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3806    0.8941    0.0319 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2695    1.5996   -0.7548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4047    1.6038   -1.6807 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1996    2.6247   -0.7572 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8816   -0.5457   -0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6402   -1.0216    0.9395 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4440    0.5268    0.6299 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2311    1.0564    1.2707 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2580   -0.8814   -0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3861   -2.6172    0.8101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4884   -1.0874    2.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2571   -2.5087    2.0044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3252   -2.2492   -0.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8150   -1.6668   -1.3519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0228   -0.4200   -2.8123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3378    2.8320   -0.0891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0024    0.9821    0.9909 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9618    2.6783   -0.0996 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  2  0
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
  2 14  1  0
 14 15  2  0
 14 16  1  0
 13  9  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  1
  3 21  1  0
  6 22  1  6
  7 23  1  0
  7 24  1  0
  8 25  1  0
  8 26  1  0
 10 27  1  0
 12 28  1  0
 13 29  1  0
 16 30  1  0
M  END


  Mrv1652304062013472D          

 16 16  0  0  0  0            999 V2000
 9998.856310000.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.5710 9999.7990    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10000.284910000.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.0006 9999.7990    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10001.716310000.2111    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10002.4320 9999.7990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.145710000.2111    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.4320 9998.9737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.716310001.0362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.284910001.0362    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.5710 9998.9737    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9997.470710000.2930    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9996.8033 9999.8080    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.0582 9999.0234    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9997.8832 9999.0234    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.1381 9999.8080    0.0000 C   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 11  1  1  0  0  0
  3  4  1  0  0  0  0
  3 10  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  9  1  1  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
 15 16  2  0  0  0  0
 12 13  1  0  0  0  0
 12 16  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
  1 16  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0000662

> <DATABASE_NAME>
MIME

> <SMILES>
C[C@H](NC(=O)[C@@H](N)CC1=CN=CN1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C9H14N4O3/c1-5(9(15)16)13-8(14)7(10)2-6-3-11-4-12-6/h3-5,7H,2,10H2,1H3,(H,11,12)(H,13,14)(H,15,16)/t5-,7-/m0/s1

> <INCHI_KEY>
FRJIAZKQGSCKPQ-FSPLSTOPSA-N

> <FORMULA>
C9H14N4O3

> <MOLECULAR_WEIGHT>
226.236

> <EXACT_MASS>
226.106590327

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
30

> <JCHEM_AVERAGE_POLARIZABILITY>
22.202296766433424

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-[(2S)-2-amino-3-(1H-imidazol-5-yl)propanamido]propanoic acid

> <ALOGPS_LOGP>
-2.84

> <JCHEM_LOGP>
-3.9182224567181616

> <ALOGPS_LOGS>
-1.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.80936009749242

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3876704112606513

> <JCHEM_PKA_STRONGEST_BASIC>
8.022226429560167

> <JCHEM_POLAR_SURFACE_AREA>
121.10000000000001

> <JCHEM_REFRACTIVITY>
55.356399999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.14e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S)-2-amino-3-(3H-imidazol-4-yl)propanamido]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0028878
     RDKit          3D
Histidylalanine
 30 30  0  0  0  0  0  0  0  0999 V2000
    3.6565   -0.1355    0.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3102    0.5667    0.2900 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2358   -0.3795    0.0624 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2189   -0.6183    1.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2674    0.0198    2.0903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8595   -1.5869    0.7564 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8551   -1.5900    1.8140 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5634   -1.4223   -0.5442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2437   -0.1589   -0.7712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9279    0.2015   -1.9406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4187    1.4264   -1.7580 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0957    1.8770   -0.5499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3806    0.8941    0.0319 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2695    1.5996   -0.7548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4047    1.6038   -1.6807 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1996    2.6247   -0.7572 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8816   -0.5457   -0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6402   -1.0216    0.9395 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4440    0.5268    0.6299 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2311    1.0564    1.2707 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2580   -0.8814   -0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3861   -2.6172    0.8101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4884   -1.0874    2.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2571   -2.5087    2.0044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3252   -2.2492   -0.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8150   -1.6668   -1.3519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0228   -0.4200   -2.8123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3378    2.8320   -0.0891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0024    0.9821    0.9909 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9618    2.6783   -0.0996 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  2  0
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
  2 14  1  0
 14 15  2  0
 14 16  1  0
 13  9  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  1
  3 21  1  0
  6 22  1  6
  7 23  1  0
  7 24  1  0
  8 25  1  0
  8 26  1  0
 10 27  1  0
 12 28  1  0
 13 29  1  0
 16 30  1  0
M  END

HEADER    PROTEIN                                 06-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-APR-20         0                                  
HETATM    1  C   UNK     0    8664.5328667.061   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8665.8668666.291   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8667.1988667.061   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0    8668.5348666.291   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0    8669.8708667.061   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8671.2068666.291   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0    8672.5398667.061   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0    8671.2068664.751   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0    8669.8708668.601   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0    8667.1988668.601   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0    8665.8668664.751   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0    8661.9458667.214   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0    8660.6998666.308   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0    8661.1758664.844   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0    8662.7158664.844   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8663.1918666.308   0.000  0.00  0.00           C+0
CONECT    1    2   16                                                       
CONECT    2    1    3   11                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    9                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    5                                                            
CONECT   10    3                                                            
CONECT   11    2                                                            
CONECT   12   13   16                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   16   14                                                       
CONECT   16   15   12    1                                                  
MASTER        0    0    0    0    0    0    0    0   16    0   32    0
END

COMPND    HMDB0028878
HETATM    1  C1  UNL     1       3.657  -0.136   0.240  1.00  0.00           C  
HETATM    2  C2  UNL     1       2.310   0.567   0.290  1.00  0.00           C  
HETATM    3  N1  UNL     1       1.236  -0.380   0.062  1.00  0.00           N  
HETATM    4  C3  UNL     1       0.219  -0.618   1.018  1.00  0.00           C  
HETATM    5  O1  UNL     1       0.267   0.020   2.090  1.00  0.00           O  
HETATM    6  C4  UNL     1      -0.859  -1.587   0.756  1.00  0.00           C  
HETATM    7  N2  UNL     1      -1.855  -1.590   1.814  1.00  0.00           N  
HETATM    8  C5  UNL     1      -1.563  -1.422  -0.544  1.00  0.00           C  
HETATM    9  C6  UNL     1      -2.244  -0.159  -0.771  1.00  0.00           C  
HETATM   10  C7  UNL     1      -2.928   0.202  -1.941  1.00  0.00           C  
HETATM   11  N3  UNL     1      -3.419   1.426  -1.758  1.00  0.00           N  
HETATM   12  C8  UNL     1      -3.096   1.877  -0.550  1.00  0.00           C  
HETATM   13  N4  UNL     1      -2.381   0.894   0.032  1.00  0.00           N  
HETATM   14  C9  UNL     1       2.269   1.600  -0.755  1.00  0.00           C  
HETATM   15  O2  UNL     1       1.405   1.604  -1.681  1.00  0.00           O  
HETATM   16  O3  UNL     1       3.200   2.625  -0.757  1.00  0.00           O  
HETATM   17  H1  UNL     1       3.882  -0.546  -0.761  1.00  0.00           H  
HETATM   18  H2  UNL     1       3.640  -1.022   0.940  1.00  0.00           H  
HETATM   19  H3  UNL     1       4.444   0.527   0.630  1.00  0.00           H  
HETATM   20  H4  UNL     1       2.231   1.056   1.271  1.00  0.00           H  
HETATM   21  H5  UNL     1       1.258  -0.881  -0.863  1.00  0.00           H  
HETATM   22  H6  UNL     1      -0.386  -2.617   0.810  1.00  0.00           H  
HETATM   23  H7  UNL     1      -1.488  -1.087   2.649  1.00  0.00           H  
HETATM   24  H8  UNL     1      -2.257  -2.509   2.004  1.00  0.00           H  
HETATM   25  H9  UNL     1      -2.325  -2.249  -0.667  1.00  0.00           H  
HETATM   26  H10 UNL     1      -0.815  -1.667  -1.352  1.00  0.00           H  
HETATM   27  H11 UNL     1      -3.023  -0.420  -2.812  1.00  0.00           H  
HETATM   28  H12 UNL     1      -3.338   2.832  -0.089  1.00  0.00           H  
HETATM   29  H13 UNL     1      -2.002   0.982   0.991  1.00  0.00           H  
HETATM   30  H14 UNL     1       3.962   2.678  -0.100  1.00  0.00           H  
CONECT    1    2   17   18   19
CONECT    2    3   14   20
CONECT    3    4   21
CONECT    4    5    5    6
CONECT    6    7    8   22
CONECT    7   23   24
CONECT    8    9   25   26
CONECT    9   10   10   13
CONECT   10   11   27
CONECT   11   12   12
CONECT   12   13   28
CONECT   13   29
CONECT   14   15   15   16
CONECT   16   30
END

HMDB0028878
     RDKit          3D
Histidylalanine
 30 30  0  0  0  0  0  0  0  0999 V2000
    3.6565   -0.1355    0.2400 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3102    0.5667    0.2900 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2358   -0.3795    0.0624 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2189   -0.6183    1.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2674    0.0198    2.0903 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8595   -1.5869    0.7564 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8551   -1.5900    1.8140 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5634   -1.4223   -0.5442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2437   -0.1589   -0.7712 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9279    0.2015   -1.9406 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4187    1.4264   -1.7580 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0957    1.8770   -0.5499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3806    0.8941    0.0319 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2695    1.5996   -0.7548 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4047    1.6038   -1.6807 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1996    2.6247   -0.7572 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8816   -0.5457   -0.7608 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6402   -1.0216    0.9395 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4440    0.5268    0.6299 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2311    1.0564    1.2707 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2580   -0.8814   -0.8625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3861   -2.6172    0.8101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4884   -1.0874    2.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2571   -2.5087    2.0044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3252   -2.2492   -0.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8150   -1.6668   -1.3519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0228   -0.4200   -2.8123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3378    2.8320   -0.0891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0024    0.9821    0.9909 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9618    2.6783   -0.0996 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  2  0
  4  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
  2 14  1  0
 14 15  2  0
 14 16  1  0
 13  9  1  0
  1 17  1  0
  1 18  1  0
  1 19  1  0
  2 20  1  1
  3 21  1  0
  6 22  1  6
  7 23  1  0
  7 24  1  0
  8 25  1  0
  8 26  1  0
 10 27  1  0
 12 28  1  0
 13 29  1  0
 16 30  1  0
M  END

Synonyms

Value	Source
HA	ChEBI
Histidinoalanine	ChEBI
Histidinyl-alanine	ChEBI
L-His-L-ala	ChEBI
N-(2-Amino-2-carboxyethyl)histidine	ChEBI
Histidinylalanine	HMDB
Histidinoalanine, (beta)-isomer	HMDB
H-a Dipeptide	HMDB
HA dipeptide	HMDB
His-ala	HMDB
Histidine alanine dipeptide	HMDB
Histidine-alanine dipeptide	HMDB
Histidyl-alanine	HMDB
L-Histidinyl-L-alanine	HMDB
L-Histidyl-L-alanine	HMDB
N-Histidinylalanine	HMDB
N-Histidylalanine	HMDB
N-L-Histidinyl-L-alanine	HMDB
N-L-Histidyl-L-alanine	HMDB
Histidylalanine	ChEBI

Molecular Formula

C₉H₁₄N₄O₃

Average Mass

226.236

Monoisotopic Mass

226.106590327

IUPAC Name

(2S)-2-[(2S)-2-amino-3-(1H-imidazol-5-yl)propanamido]propanoic acid

Traditional Name

(2S)-2-[(2S)-2-amino-3-(3H-imidazol-4-yl)propanamido]propanoic acid

CAS Registry Number

Not Available

SMILES

C[C@H](NC(=O)[C@@H](N)CC1=CN=CN1)C(O)=O

InChI Identifier

InChI=1S/C9H14N4O3/c1-5(9(15)16)13-8(14)7(10)2-6-3-11-4-12-6/h3-5,7H,2,10H2,1H3,(H,11,12)(H,13,14)(H,15,16)/t5-,7-/m0/s1

InChI Key

FRJIAZKQGSCKPQ-FSPLSTOPSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as peptides. Peptides are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Peptides

Alternative Parents

Substituents

Alpha peptide
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alanine or derivatives
Alpha-amino acid or derivatives
Imidazolyl carboxylic acid derivative
Aralkylamine
Azole
Imidazole
Heteroaromatic compound
Amino acid or derivatives
Amino acid
Carboximidic acid
Carboximidic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Primary aliphatic amine
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organopnictogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Organic nitrogen compound
Primary amine
Amine
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

dipeptide (CHEBI:73924 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	11.4 g/L	ALOGPS
logP	-2.8	ALOGPS
logP	-3.9	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	3.39	ChemAxon
pKa (Strongest Basic)	8.02	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	121.1 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	55.36 m³·mol⁻¹	ChemAxon
Polarizability	22.2 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

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	Bacteroidetes	1	Human feces; Human stool	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 Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	25037050
Human Feces	Detected but not Quantified						Adult (>18 years old)	Both	Normal	HMDB	29808030

External Links

HMDB ID

HMDB0028878

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB111907

KNApSAcK ID

Not Available

Chemspider ID

91418

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101180

PDB ID

Not Available

ChEBI ID

73924

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Nath M, Singh H, Eng G, Song X: New diorganotin(IV) derivatives of dipeptides: synthesis and characteristic spectral studies. Spectrochim Acta A Mol Biomol Spectrosc. 2008 Nov 15;71(2):529-36. doi: 10.1016/j.saa.2008.01.006. Epub 2008 Jan 11. [PubMed:18289925 ]
Gucinski AC, Chamot-Rooke J, Nicol E, Somogyi A, Wysocki VH: Structural influences on preferential oxazolone versus diketopiperazine b(2+) ion formation for histidine analogue-containing peptides. J Phys Chem A. 2012 May 3;116(17):4296-304. doi: 10.1021/jp300262d. Epub 2012 Apr 24. [PubMed:22448972 ]

Showing metabocard for Histidylalanine (MMDBc0000662)

MOL for #<Metabolite:0x00007f920a5f6d58>

3D MOL for #<Metabolite:0x00007f920a5f6d58>

3D SDF for #<Metabolite:0x00007f920a5f6d58>

3D-SDF for #<Metabolite:0x00007f920a5f6d58>

PDB for #<Metabolite:0x00007f920a5f6d58>

3D PDB for #<Metabolite:0x00007f920a5f6d58>

SMILES for #<Metabolite:0x00007f920a5f6d58>

INCHI for #<Metabolite:0x00007f920a5f6d58>

Structure for #<Metabolite:0x00007f920a5f6d58>

3D Structure for #<Metabolite:0x00007f920a5f6d58>