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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2012-09-06 21:02:54 UTC

Update Date

2021-09-14 15:45:45 UTC

HMDB ID

HMDB0028898

Secondary Accession Numbers

HMDB28898

Metabolite Identification

Common Name

Histidylvaline

Description

Histidylvaline is a dipeptide composed of histidine and valine. 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

HMDB0028898
     RDKit          3D
Histidylvaline
 36 36  0  0  0  0  0  0  0  0999 V2000
   -4.2297    0.8051    0.8863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8153    0.8895    0.3784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6639    1.8126   -0.7909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3418   -0.5134    0.1016 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9843   -0.4664   -0.3884 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0802   -1.0403    0.3431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1142   -1.6107    1.4431 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4586   -0.9729   -0.1905 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4519   -0.2913   -1.4333 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3115   -0.3148    0.8699 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7209   -0.1746    0.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2773    0.8904   -0.1626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5889    0.6007   -0.3146 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8388   -0.5945    0.2162 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7106   -1.0877    0.7114 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2377   -1.2598   -0.8025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7253   -1.7500   -1.8589 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5707   -1.4678   -0.5993 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2979   -0.0639    1.5829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9784    0.7543    0.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4012    1.7116    1.5220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1910    1.2846    1.2071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8435    1.3519   -1.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6212    2.2428   -0.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3411    2.6864   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3462   -1.0455    1.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8499    0.0169   -1.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8954   -1.9811   -0.3535 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3412   -0.9093   -2.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1203    0.4690   -1.5544 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8563    0.6685    1.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2404   -0.9535    1.7754 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8112    1.8125   -0.5105 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2846    1.2376   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7967   -1.0977    0.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2315   -1.6391   -1.3217 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
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
  4 16  1  0
 16 17  2  0
 16 18  1  0
 15 11  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  1
  5 27  1  0
  8 28  1  6
  9 29  1  0
  9 30  1  0
 10 31  1  0
 10 32  1  0
 12 33  1  0
 13 34  1  0
 14 35  1  0
 18 36  1  0
M  END


  Mrv1652304062013502D          

 18 18  0  0  0  0            999 V2000
 9998.880610000.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.5954 9999.7892    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10000.309310000.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.0248 9999.7892    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10001.742510000.2013    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10002.4560 9999.7892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.171610000.2013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.309310001.0261    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9999.5954 9998.9638    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9997.494910000.2836    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9996.8275 9999.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.0824 9999.0140    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9997.9074 9999.0140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.1623 9999.7986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.743510001.0263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.458510001.4379    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.029610001.4397    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.4555 9998.9642    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  9  1  1  0  0  0
  3  4  1  0  0  0  0
  3  8  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
 13 14  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 10 11  2  0  0  0  0
 10 14  1  0  0  0  0
  1 14  1  0  0  0  0
  5 15  1  6  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
  6  7  1  0  0  0  0
  6 18  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0028898

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)[C@H](NC(=O)[C@@H](N)CC1=CNC=N1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C11H18N4O3/c1-6(2)9(11(17)18)15-10(16)8(12)3-7-4-13-5-14-7/h4-6,8-9H,3,12H2,1-2H3,(H,13,14)(H,15,16)(H,17,18)/t8-,9-/m0/s1

> <INCHI_KEY>
VLDVBZICYBVQHB-IUCAKERBSA-N

> <FORMULA>
C11H18N4O3

> <MOLECULAR_WEIGHT>
254.29

> <EXACT_MASS>
254.137890456

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
26.22660616645966

> <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-4-yl)propanamido]-3-methylbutanoic acid

> <ALOGPS_LOGP>
-2.44

> <JCHEM_LOGP>
-2.865725631498453

> <ALOGPS_LOGS>
-1.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.912569625865302

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.5381421344849358

> <JCHEM_PKA_STRONGEST_BASIC>
7.838527544356267

> <JCHEM_POLAR_SURFACE_AREA>
121.10000000000002

> <JCHEM_REFRACTIVITY>
63.7863

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.55e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S)-2-amino-3-(1H-imidazol-4-yl)propanamido]-3-methylbutanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0028898
     RDKit          3D
Histidylvaline
 36 36  0  0  0  0  0  0  0  0999 V2000
   -4.2297    0.8051    0.8863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8153    0.8895    0.3784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6639    1.8126   -0.7909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3418   -0.5134    0.1016 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9843   -0.4664   -0.3884 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0802   -1.0403    0.3431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1142   -1.6107    1.4431 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4586   -0.9729   -0.1905 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4519   -0.2913   -1.4333 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3115   -0.3148    0.8699 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7209   -0.1746    0.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2773    0.8904   -0.1626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5889    0.6007   -0.3146 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8388   -0.5945    0.2162 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7106   -1.0877    0.7114 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2377   -1.2598   -0.8025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7253   -1.7500   -1.8589 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5707   -1.4678   -0.5993 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2979   -0.0639    1.5829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9784    0.7543    0.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4012    1.7116    1.5220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1910    1.2846    1.2071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8435    1.3519   -1.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6212    2.2428   -0.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3411    2.6864   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3462   -1.0455    1.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8499    0.0169   -1.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8954   -1.9811   -0.3535 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3412   -0.9093   -2.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1203    0.4690   -1.5544 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8563    0.6685    1.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2404   -0.9535    1.7754 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8112    1.8125   -0.5105 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2846    1.2376   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7967   -1.0977    0.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2315   -1.6391   -1.3217 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
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
  4 16  1  0
 16 17  2  0
 16 18  1  0
 15 11  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  1
  5 27  1  0
  8 28  1  6
  9 29  1  0
  9 30  1  0
 10 31  1  0
 10 32  1  0
 12 33  1  0
 13 34  1  0
 14 35  1  0
 18 36  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    8664.5778667.042   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8665.9118666.273   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8667.2448667.042   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0    8668.5808666.273   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0    8669.9198667.042   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8671.2518666.273   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    8672.5878667.042   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0    8667.2448668.582   0.000  0.00  0.00           O+0
HETATM    9  N   UNK     0    8665.9118664.732   0.000  0.00  0.00           N+0
HETATM   10  N   UNK     0    8661.9908667.196   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0    8660.7458666.291   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0    8661.2208664.826   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0    8662.7608664.826   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8663.2368666.291   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8669.9218668.582   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0    8671.2568669.351   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0    8668.5898669.354   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0    8671.2508664.733   0.000  0.00  0.00           C+0
CONECT    1    2   14                                                       
CONECT    2    1    3    9                                                  
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    7   18                                                  
CONECT    7    6                                                            
CONECT    8    3                                                            
CONECT    9    2                                                            
CONECT   10   11   14                                                       
CONECT   11   12   10                                                       
CONECT   12   11   13                                                       
CONECT   13   14   12                                                       
CONECT   14   13   10    1                                                  
CONECT   15    5   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
CONECT   18    6                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   36    0
END

COMPND    HMDB0028898
HETATM    1  C1  UNL     1      -4.230   0.805   0.886  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.815   0.889   0.378  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.664   1.813  -0.791  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.342  -0.513   0.102  1.00  0.00           C  
HETATM    5  N1  UNL     1      -0.984  -0.466  -0.388  1.00  0.00           N  
HETATM    6  C5  UNL     1       0.080  -1.040   0.343  1.00  0.00           C  
HETATM    7  O1  UNL     1      -0.114  -1.611   1.443  1.00  0.00           O  
HETATM    8  C6  UNL     1       1.459  -0.973  -0.190  1.00  0.00           C  
HETATM    9  N2  UNL     1       1.452  -0.291  -1.433  1.00  0.00           N  
HETATM   10  C7  UNL     1       2.312  -0.315   0.870  1.00  0.00           C  
HETATM   11  C8  UNL     1       3.721  -0.175   0.485  1.00  0.00           C  
HETATM   12  C9  UNL     1       4.277   0.890  -0.163  1.00  0.00           C  
HETATM   13  N3  UNL     1       5.589   0.601  -0.315  1.00  0.00           N  
HETATM   14  C10 UNL     1       5.839  -0.595   0.216  1.00  0.00           C  
HETATM   15  N4  UNL     1       4.711  -1.088   0.711  1.00  0.00           N  
HETATM   16  C11 UNL     1      -3.238  -1.260  -0.803  1.00  0.00           C  
HETATM   17  O2  UNL     1      -2.725  -1.750  -1.859  1.00  0.00           O  
HETATM   18  O3  UNL     1      -4.571  -1.468  -0.599  1.00  0.00           O  
HETATM   19  H1  UNL     1      -4.298  -0.064   1.583  1.00  0.00           H  
HETATM   20  H2  UNL     1      -4.978   0.754   0.070  1.00  0.00           H  
HETATM   21  H3  UNL     1      -4.401   1.712   1.522  1.00  0.00           H  
HETATM   22  H4  UNL     1      -2.191   1.285   1.207  1.00  0.00           H  
HETATM   23  H5  UNL     1      -2.844   1.352  -1.761  1.00  0.00           H  
HETATM   24  H6  UNL     1      -1.621   2.243  -0.829  1.00  0.00           H  
HETATM   25  H7  UNL     1      -3.341   2.686  -0.657  1.00  0.00           H  
HETATM   26  H8  UNL     1      -2.346  -1.046   1.076  1.00  0.00           H  
HETATM   27  H9  UNL     1      -0.850   0.017  -1.312  1.00  0.00           H  
HETATM   28  H10 UNL     1       1.895  -1.981  -0.354  1.00  0.00           H  
HETATM   29  H11 UNL     1       1.341  -0.909  -2.267  1.00  0.00           H  
HETATM   30  H12 UNL     1       2.120   0.469  -1.554  1.00  0.00           H  
HETATM   31  H13 UNL     1       1.856   0.668   1.153  1.00  0.00           H  
HETATM   32  H14 UNL     1       2.240  -0.953   1.775  1.00  0.00           H  
HETATM   33  H15 UNL     1       3.811   1.812  -0.511  1.00  0.00           H  
HETATM   34  H16 UNL     1       6.285   1.238  -0.783  1.00  0.00           H  
HETATM   35  H17 UNL     1       6.797  -1.098   0.248  1.00  0.00           H  
HETATM   36  H18 UNL     1      -5.231  -1.639  -1.322  1.00  0.00           H  
CONECT    1    2   19   20   21
CONECT    2    3    4   22
CONECT    3   23   24   25
CONECT    4    5   16   26
CONECT    5    6   27
CONECT    6    7    7    8
CONECT    8    9   10   28
CONECT    9   29   30
CONECT   10   11   31   32
CONECT   11   12   12   15
CONECT   12   13   33
CONECT   13   14   34
CONECT   14   15   15   35
CONECT   16   17   17   18
CONECT   18   36
END

HMDB0028898
     RDKit          3D
Histidylvaline
 36 36  0  0  0  0  0  0  0  0999 V2000
   -4.2297    0.8051    0.8863 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8153    0.8895    0.3784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6639    1.8126   -0.7909 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3418   -0.5134    0.1016 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9843   -0.4664   -0.3884 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0802   -1.0403    0.3431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1142   -1.6107    1.4431 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4586   -0.9729   -0.1905 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4519   -0.2913   -1.4333 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.3115   -0.3148    0.8699 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7209   -0.1746    0.4852 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2773    0.8904   -0.1626 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5889    0.6007   -0.3146 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.8388   -0.5945    0.2162 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7106   -1.0877    0.7114 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2377   -1.2598   -0.8025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7253   -1.7500   -1.8589 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5707   -1.4678   -0.5993 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2979   -0.0639    1.5829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9784    0.7543    0.0703 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4012    1.7116    1.5220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1910    1.2846    1.2071 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8435    1.3519   -1.7611 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6212    2.2428   -0.8286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3411    2.6864   -0.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3462   -1.0455    1.0759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8499    0.0169   -1.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8954   -1.9811   -0.3535 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3412   -0.9093   -2.2672 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1203    0.4690   -1.5544 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8563    0.6685    1.1534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2404   -0.9535    1.7754 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8112    1.8125   -0.5105 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2846    1.2376   -0.7835 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7967   -1.0977    0.2483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2315   -1.6391   -1.3217 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
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
  4 16  1  0
 16 17  2  0
 16 18  1  0
 15 11  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  1
  5 27  1  0
  8 28  1  6
  9 29  1  0
  9 30  1  0
 10 31  1  0
 10 32  1  0
 12 33  1  0
 13 34  1  0
 14 35  1  0
 18 36  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Histidinyl-valine	ChEBI
HV	ChEBI
L-His-L-val	ChEBI
H-V Dipeptide	HMDB
HV Dipeptide	HMDB
His-val	HMDB
Histidine valine dipeptide	HMDB
Histidine-valine dipeptide	HMDB
Histidinylvaline	HMDB
Histidyl-valine	HMDB
L-Histidinyl-L-valine	HMDB
L-Histidyl-L-valine	HMDB
N-Histidinylvaline	HMDB
N-Histidylvaline	HMDB
N-L-Histidinyl-L-valine	HMDB
N-L-Histidyl-L-valine	HMDB
Histidylvaline	ChEBI

Chemical Formula

C₁₁H₁₈N₄O₃

Average Molecular Weight

254.29

Monoisotopic Molecular Weight

254.137890456

IUPAC Name

(2S)-2-[(2S)-2-amino-3-(1H-imidazol-4-yl)propanamido]-3-methylbutanoic acid

Traditional Name

(2S)-2-[(2S)-2-amino-3-(1H-imidazol-4-yl)propanamido]-3-methylbutanoic acid

CAS Registry Number

76019-15-3

SMILES

CC(C)[C@H](NC(=O)[C@@H](N)CC1=CNC=N1)C(O)=O

InChI Identifier

InChI=1S/C11H18N4O3/c1-6(2)9(11(17)18)15-10(16)8(12)3-7-4-13-5-14-7/h4-6,8-9H,3,12H2,1-2H3,(H,13,14)(H,15,16)(H,17,18)/t8-,9-/m0/s1

InChI Key

VLDVBZICYBVQHB-IUCAKERBSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Dipeptides

Alternative Parents

Substituents

Alpha-dipeptide
Histidine or derivatives
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
Valine or derivatives
N-acyl-l-alpha-amino acid
Alpha-amino acid amide
Alpha-amino acid or derivatives
Imidazolyl carboxylic acid derivative
Aralkylamine
Fatty amide
Fatty acyl
Azole
Imidazole
Heteroaromatic compound
Carboxamide group
Amino acid or derivatives
Amino acid
Secondary carboxylic acid amide
Carboxylic acid salt
Azacycle
Carboxylic acid
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Primary aliphatic amine
Organic zwitterion
Organic salt
Amine
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Primary amine
Organooxygen compound
Organonitrogen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

dipeptide (CHEBI:74060 )

Ontology

Not Available

Feces (PMID: 27275383)

Source

Endogenous

Endogenous (HMDB: HMDB0028898)

Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)
Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Equine

Horse (FooDB: FOOD00378)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

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	-3.22	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	6.2 g/L	ALOGPS
logP	-2.4	ALOGPS
logP	-2.9	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	3.54	ChemAxon
pKa (Strongest Basic)	7.84	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	6	ChemAxon
Refractivity	63.79 m³·mol⁻¹	ChemAxon
Polarizability	26.23 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

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	161.956	30932474
DeepCCS	[M-H]-	159.598	30932474
DeepCCS	[M-2H]-	192.485	30932474
DeepCCS	[M+Na]+	168.049	30932474

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	1.82 minutes	32390414
Predicted by Siyang on May 30, 2022	9.9164 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	8.76 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	409.8 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	421.3 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	238.9 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	49.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	157.6 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	44.4 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	317.0 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	249.4 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	865.5 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	581.9 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	42.7 seconds	40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid	664.2 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	163.9 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	250.0 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	517.5 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	668.6 seconds	40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water	364.7 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Histidylvaline	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CNC=N1)C(O)=O	3195.5	Standard polar	33892256
Histidylvaline	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CNC=N1)C(O)=O	2101.2	Standard non polar	33892256
Histidylvaline	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CNC=N1)C(O)=O	2411.0	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Histidylvaline,1TMS,isomer #1	CC(C)[C@H](NC(=O)[C@@H](N)CC1=C[NH]C=N1)C(=O)O[Si](C)(C)C	2341.5	Semi standard non polar	33892256
Histidylvaline,1TMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C)C(=O)O	2400.3	Semi standard non polar	33892256
Histidylvaline,1TMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[Si](C)(C)C	2266.6	Semi standard non polar	33892256
Histidylvaline,1TMS,isomer #4	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)C(=O)O	2445.1	Semi standard non polar	33892256
Histidylvaline,2TMS,isomer #1	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2385.4	Semi standard non polar	33892256
Histidylvaline,2TMS,isomer #1	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2318.5	Standard non polar	33892256
Histidylvaline,2TMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[Si](C)(C)C	2278.0	Semi standard non polar	33892256
Histidylvaline,2TMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[Si](C)(C)C	2254.6	Standard non polar	33892256
Histidylvaline,2TMS,isomer #3	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)C(=O)O[Si](C)(C)C	2457.7	Semi standard non polar	33892256
Histidylvaline,2TMS,isomer #3	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)C(=O)O[Si](C)(C)C	2238.7	Standard non polar	33892256
Histidylvaline,2TMS,isomer #4	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C)[Si](C)(C)C	2311.5	Semi standard non polar	33892256
Histidylvaline,2TMS,isomer #4	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C)[Si](C)(C)C	2352.0	Standard non polar	33892256
Histidylvaline,2TMS,isomer #5	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N[Si](C)(C)C)C(=O)O	2484.4	Semi standard non polar	33892256
Histidylvaline,2TMS,isomer #5	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N[Si](C)(C)C)C(=O)O	2317.2	Standard non polar	33892256
Histidylvaline,2TMS,isomer #6	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2494.7	Semi standard non polar	33892256
Histidylvaline,2TMS,isomer #6	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2421.2	Standard non polar	33892256
Histidylvaline,2TMS,isomer #7	CC(C)[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)[Si](C)(C)C	2386.8	Semi standard non polar	33892256
Histidylvaline,2TMS,isomer #7	CC(C)[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)[Si](C)(C)C	2301.3	Standard non polar	33892256
Histidylvaline,3TMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C)[Si](C)(C)C	2319.2	Semi standard non polar	33892256
Histidylvaline,3TMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C)[Si](C)(C)C	2372.3	Standard non polar	33892256
Histidylvaline,3TMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2487.2	Semi standard non polar	33892256
Histidylvaline,3TMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2335.2	Standard non polar	33892256
Histidylvaline,3TMS,isomer #3	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2442.5	Semi standard non polar	33892256
Histidylvaline,3TMS,isomer #3	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2431.1	Standard non polar	33892256
Histidylvaline,3TMS,isomer #4	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)[Si](C)(C)C	2395.6	Semi standard non polar	33892256
Histidylvaline,3TMS,isomer #4	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)[Si](C)(C)C	2334.2	Standard non polar	33892256
Histidylvaline,3TMS,isomer #5	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N[Si](C)(C)C)[Si](C)(C)C	2425.2	Semi standard non polar	33892256
Histidylvaline,3TMS,isomer #5	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N[Si](C)(C)C)[Si](C)(C)C	2391.5	Standard non polar	33892256
Histidylvaline,3TMS,isomer #6	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2418.0	Semi standard non polar	33892256
Histidylvaline,3TMS,isomer #6	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2484.6	Standard non polar	33892256
Histidylvaline,3TMS,isomer #7	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2624.2	Semi standard non polar	33892256
Histidylvaline,3TMS,isomer #7	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2458.9	Standard non polar	33892256
Histidylvaline,4TMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N[Si](C)(C)C)[Si](C)(C)C	2442.6	Semi standard non polar	33892256
Histidylvaline,4TMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N[Si](C)(C)C)[Si](C)(C)C	2428.1	Standard non polar	33892256
Histidylvaline,4TMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2467.6	Semi standard non polar	33892256
Histidylvaline,4TMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2495.5	Standard non polar	33892256
Histidylvaline,4TMS,isomer #3	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2597.4	Semi standard non polar	33892256
Histidylvaline,4TMS,isomer #3	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2485.6	Standard non polar	33892256
Histidylvaline,4TMS,isomer #4	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2549.9	Semi standard non polar	33892256
Histidylvaline,4TMS,isomer #4	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2547.7	Standard non polar	33892256
Histidylvaline,5TMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2618.7	Semi standard non polar	33892256
Histidylvaline,5TMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2576.6	Standard non polar	33892256
Histidylvaline,1TBDMS,isomer #1	CC(C)[C@H](NC(=O)[C@@H](N)CC1=C[NH]C=N1)C(=O)O[Si](C)(C)C(C)(C)C	2585.5	Semi standard non polar	33892256
Histidylvaline,1TBDMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C(C)(C)C)C(=O)O	2600.3	Semi standard non polar	33892256
Histidylvaline,1TBDMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[Si](C)(C)C(C)(C)C	2502.4	Semi standard non polar	33892256
Histidylvaline,1TBDMS,isomer #4	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)O	2704.8	Semi standard non polar	33892256
Histidylvaline,2TBDMS,isomer #1	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2816.9	Semi standard non polar	33892256
Histidylvaline,2TBDMS,isomer #1	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2739.4	Standard non polar	33892256
Histidylvaline,2TBDMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[Si](C)(C)C(C)(C)C	2761.0	Semi standard non polar	33892256
Histidylvaline,2TBDMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[Si](C)(C)C(C)(C)C	2670.9	Standard non polar	33892256
Histidylvaline,2TBDMS,isomer #3	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)O[Si](C)(C)C(C)(C)C	2923.4	Semi standard non polar	33892256
Histidylvaline,2TBDMS,isomer #3	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)O[Si](C)(C)C(C)(C)C	2622.3	Standard non polar	33892256
Histidylvaline,2TBDMS,isomer #4	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2759.5	Semi standard non polar	33892256
Histidylvaline,2TBDMS,isomer #4	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2757.3	Standard non polar	33892256
Histidylvaline,2TBDMS,isomer #5	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N[Si](C)(C)C(C)(C)C)C(=O)O	2948.7	Semi standard non polar	33892256
Histidylvaline,2TBDMS,isomer #5	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N[Si](C)(C)C(C)(C)C)C(=O)O	2691.8	Standard non polar	33892256
Histidylvaline,2TBDMS,isomer #6	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2908.4	Semi standard non polar	33892256
Histidylvaline,2TBDMS,isomer #6	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2808.3	Standard non polar	33892256
Histidylvaline,2TBDMS,isomer #7	CC(C)[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1)[Si](C)(C)C(C)(C)C	2850.0	Semi standard non polar	33892256
Histidylvaline,2TBDMS,isomer #7	CC(C)[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1)[Si](C)(C)C(C)(C)C	2659.8	Standard non polar	33892256
Histidylvaline,3TBDMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2986.6	Semi standard non polar	33892256
Histidylvaline,3TBDMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=C[NH]C=N1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2918.7	Standard non polar	33892256
Histidylvaline,3TBDMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3120.1	Semi standard non polar	33892256
Histidylvaline,3TBDMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2899.9	Standard non polar	33892256
Histidylvaline,3TBDMS,isomer #3	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3137.4	Semi standard non polar	33892256
Histidylvaline,3TBDMS,isomer #3	CC(C)[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2967.2	Standard non polar	33892256
Histidylvaline,3TBDMS,isomer #4	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1)[Si](C)(C)C(C)(C)C	3055.8	Semi standard non polar	33892256
Histidylvaline,3TBDMS,isomer #4	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1)[Si](C)(C)C(C)(C)C	2875.1	Standard non polar	33892256
Histidylvaline,3TBDMS,isomer #5	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3102.0	Semi standard non polar	33892256
Histidylvaline,3TBDMS,isomer #5	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2937.1	Standard non polar	33892256
Histidylvaline,3TBDMS,isomer #6	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3082.3	Semi standard non polar	33892256
Histidylvaline,3TBDMS,isomer #6	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3016.4	Standard non polar	33892256
Histidylvaline,3TBDMS,isomer #7	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3282.2	Semi standard non polar	33892256
Histidylvaline,3TBDMS,isomer #7	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2980.0	Standard non polar	33892256
Histidylvaline,4TBDMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3283.1	Semi standard non polar	33892256
Histidylvaline,4TBDMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3129.8	Standard non polar	33892256
Histidylvaline,4TBDMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3328.9	Semi standard non polar	33892256
Histidylvaline,4TBDMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3163.5	Standard non polar	33892256
Histidylvaline,4TBDMS,isomer #3	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3454.7	Semi standard non polar	33892256
Histidylvaline,4TBDMS,isomer #3	CC(C)[C@H](NC(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3175.5	Standard non polar	33892256
Histidylvaline,4TBDMS,isomer #4	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3440.0	Semi standard non polar	33892256
Histidylvaline,4TBDMS,isomer #4	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3205.3	Standard non polar	33892256
Histidylvaline,5TBDMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3646.0	Semi standard non polar	33892256
Histidylvaline,5TBDMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3412.9	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Histidylvaline GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylvaline 10V, Negative-QTOF	splash10-0udi-0190000000-8bf9ff39c58c497d35fe	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylvaline 20V, Negative-QTOF	splash10-014i-4920000000-e60123d830c30d022936	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylvaline 40V, Negative-QTOF	splash10-00kf-9100000000-a79d3cced8d3e5dab7cc	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylvaline 10V, Positive-QTOF	splash10-08g0-0940000000-102d3931ebb3be5b89fc	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylvaline 20V, Positive-QTOF	splash10-03di-3900000000-7dbc163af9a44079a6fa	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylvaline 40V, Positive-QTOF	splash10-03di-9800000000-a0e7246046297ca4c781	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-29	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Normal	25037050	details

Abnormal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal Cancer	27275383	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal cancer	27015276	details
Feces	Detected but not Quantified	Not Quantified	Adult (>18 years old)	Both	Colorectal cancer	25037050	details

Associated Disorders and Diseases

Disease References

Colorectal cancer

Brown DG, Rao S, Weir TL, O'Malia J, Bazan M, Brown RJ, Ryan EP: Metabolomics and metabolic pathway networks from human colorectal cancers, adjacent mucosa, and stool. Cancer Metab. 2016 Jun 6;4:11. doi: 10.1186/s40170-016-0151-y. eCollection 2016. [PubMed:27275383 ]
Sinha R, Ahn J, Sampson JN, Shi J, Yu G, Xiong X, Hayes RB, Goedert JJ: Fecal Microbiota, Fecal Metabolome, and Colorectal Cancer Interrelations. PLoS One. 2016 Mar 25;11(3):e0152126. doi: 10.1371/journal.pone.0152126. eCollection 2016. [PubMed:27015276 ]
Goedert JJ, Sampson JN, Moore SC, Xiao Q, Xiong X, Hayes RB, Ahn J, Shi J, Sinha R: Fecal metabolomics: assay performance and association with colorectal cancer. Carcinogenesis. 2014 Sep;35(9):2089-96. doi: 10.1093/carcin/bgu131. Epub 2014 Jul 18. [PubMed:25037050 ]

Associated OMIM IDs

114500 (Colorectal cancer)

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB111927

KNApSAcK ID

Not Available

Chemspider ID

5384763

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

7021870

PDB ID

Not Available

ChEBI ID

74060

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

Not Available

Showing metabocard for Histidylvaline (HMDB0028898)

MOL for HMDB0028898 (Histidylvaline)

3D MOL for HMDB0028898 (Histidylvaline)

3D SDF for HMDB0028898 (Histidylvaline)

3D-SDF for HMDB0028898 (Histidylvaline)

PDB for HMDB0028898 (Histidylvaline)

3D PDB for HMDB0028898 (Histidylvaline)

SMILES for HMDB0028898 (Histidylvaline)

INCHI for HMDB0028898 (Histidylvaline)

Structure for HMDB0028898 (Histidylvaline)

3D Structure for HMDB0028898 (Histidylvaline)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra