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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2012-09-06 21:03:20 UTC

Update Date

2021-09-14 15:45:45 UTC

HMDB ID

HMDB0029008

Secondary Accession Numbers

HMDB29008

Metabolite Identification

Common Name

Phenylalanylvaline

Description

Phenylalanylvaline is a dipeptide composed of phenylalanine 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

HMDB0029008
     RDKit          3D
Phenylalanylvaline
 39 39  0  0  0  0  0  0  0  0999 V2000
   -3.0858   -0.3959    1.7654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2630   -0.4008    0.2818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6704   -0.6312   -0.1711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6498    0.8559   -0.3272 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2371    0.8224    0.0271 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2954    0.7589   -1.0101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6248    0.7303   -2.2196 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1501    0.7234   -0.6874 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3556    0.7639    0.7485 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6800   -0.6146   -1.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1306   -0.7687   -0.9324 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0690   -0.3441   -1.8477 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3883   -0.5053   -1.5621 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8016   -1.0833   -0.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8594   -1.5048    0.5303 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5156   -1.3457    0.2500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2271    2.0882    0.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5422    2.8984    0.9017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5666    2.3536    0.0449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3749   -1.1640    2.1243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0306   -0.5486    2.3244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7222    0.6235    2.0808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6428   -1.2553   -0.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7601   -1.5305   -0.8401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3218   -0.8165    0.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0338    0.2189   -0.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8094    0.8260   -1.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9207    0.8443    1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6286    1.5661   -1.2014 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0479   -0.0917    1.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0609    1.6447    1.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4548   -0.7090   -2.2868 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1291   -1.4051   -0.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7398    0.1066   -2.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1340   -0.1791   -2.2660 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8596   -1.2021   -0.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2028   -1.9558    1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8202   -1.6934    0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2494    2.3205    0.7837 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  2  0
 14 15  1  0
 15 16  2  0
  4 17  1  0
 17 18  2  0
 17 19  1  0
 16 11  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  6
  5 28  1  0
  8 29  1  6
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 12 34  1  0
 13 35  1  0
 14 36  1  0
 15 37  1  0
 16 38  1  0
 19 39  1  0
M  END


  Mrv1652304062014072D          

 19 19  0  0  0  0            999 V2000
10001.8001 9999.8034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.085510000.2157    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.3730 9999.8034    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.659010000.2157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9456 9999.8034    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.230210000.2157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9456 9998.9797    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.659010001.0394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.085510001.0394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.5187 9999.8043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.804210000.2167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.0897 9999.8042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.0896 9998.9792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.8041 9998.5667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.5187 9998.9793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.512010000.2149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.800110001.4513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.373010001.4513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.8005 9998.9784    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  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  8  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  1  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 10  1  0  0  0  0
  6 10  1  0  0  0  0
  1 16  1  0  0  0  0
  9 17  1  0  0  0  0
  9 18  2  0  0  0  0
  1 19  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0029008

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(C)[C@H](NC(=O)[C@@H](N)CC1=CC=CC=C1)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H20N2O3/c1-9(2)12(14(18)19)16-13(17)11(15)8-10-6-4-3-5-7-10/h3-7,9,11-12H,8,15H2,1-2H3,(H,16,17)(H,18,19)/t11-,12-/m0/s1

> <INCHI_KEY>
IEHDJWSAXBGJIP-RYUDHWBXSA-N

> <FORMULA>
C14H20N2O3

> <MOLECULAR_WEIGHT>
264.325

> <EXACT_MASS>
264.147392512

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
28.18009293053641

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-[(2S)-2-amino-3-phenylpropanamido]-3-methylbutanoic acid

> <ALOGPS_LOGP>
-0.87

> <JCHEM_LOGP>
-0.8351253569843071

> <ALOGPS_LOGS>
-2.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.74742377179405

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8403219152610286

> <JCHEM_PKA_STRONGEST_BASIC>
8.009689579850892

> <JCHEM_POLAR_SURFACE_AREA>
92.41999999999999

> <JCHEM_REFRACTIVITY>
71.4093

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.20e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S)-2-amino-3-phenylpropanamido]-3-methylbutanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029008
     RDKit          3D
Phenylalanylvaline
 39 39  0  0  0  0  0  0  0  0999 V2000
   -3.0858   -0.3959    1.7654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2630   -0.4008    0.2818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6704   -0.6312   -0.1711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6498    0.8559   -0.3272 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2371    0.8224    0.0271 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2954    0.7589   -1.0101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6248    0.7303   -2.2196 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1501    0.7234   -0.6874 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3556    0.7639    0.7485 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6800   -0.6146   -1.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1306   -0.7687   -0.9324 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0690   -0.3441   -1.8477 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3883   -0.5053   -1.5621 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8016   -1.0833   -0.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8594   -1.5048    0.5303 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5156   -1.3457    0.2500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2271    2.0882    0.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5422    2.8984    0.9017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5666    2.3536    0.0449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3749   -1.1640    2.1243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0306   -0.5486    2.3244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7222    0.6235    2.0808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6428   -1.2553   -0.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7601   -1.5305   -0.8401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3218   -0.8165    0.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0338    0.2189   -0.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8094    0.8260   -1.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9207    0.8443    1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6286    1.5661   -1.2014 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0479   -0.0917    1.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0609    1.6447    1.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4548   -0.7090   -2.2868 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1291   -1.4051   -0.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7398    0.1066   -2.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1340   -0.1791   -2.2660 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8596   -1.2021   -0.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2028   -1.9558    1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8202   -1.6934    0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2494    2.3205    0.7837 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  2  0
 14 15  1  0
 15 16  2  0
  4 17  1  0
 17 18  2  0
 17 19  1  0
 16 11  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  6
  5 28  1  0
  8 29  1  6
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 12 34  1  0
 13 35  1  0
 14 36  1  0
 15 37  1  0
 16 38  1  0
 19 39  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    8670.0278666.300   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8668.6938667.069   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0    8667.3638666.300   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0    8666.0308667.069   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0    8664.6988666.300   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8663.3638667.069   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0    8664.6988664.762   0.000  0.00  0.00           N+0
HETATM    8  O   UNK     0    8666.0308668.607   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0    8668.6938668.607   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8662.0358666.301   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8660.7018667.071   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8659.3678666.301   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8659.3678664.761   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8660.7018663.991   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8662.0358664.761   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8671.3568667.068   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0    8670.0278669.376   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0    8667.3638669.376   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0    8670.0288664.760   0.000  0.00  0.00           C+0
CONECT    1    2   16   19                                                  
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   10                                                       
CONECT    7    5                                                            
CONECT    8    4                                                            
CONECT    9    2   17   18                                                  
CONECT   10   11   15    6                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16    1                                                            
CONECT   17    9                                                            
CONECT   18    9                                                            
CONECT   19    1                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   38    0
END

COMPND    HMDB0029008
HETATM    1  C1  UNL     1      -3.086  -0.396   1.765  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.263  -0.401   0.282  1.00  0.00           C  
HETATM    3  C3  UNL     1      -4.670  -0.631  -0.171  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.650   0.856  -0.327  1.00  0.00           C  
HETATM    5  N1  UNL     1      -1.237   0.822   0.027  1.00  0.00           N  
HETATM    6  C5  UNL     1      -0.295   0.759  -1.010  1.00  0.00           C  
HETATM    7  O1  UNL     1      -0.625   0.730  -2.220  1.00  0.00           O  
HETATM    8  C6  UNL     1       1.150   0.723  -0.687  1.00  0.00           C  
HETATM    9  N2  UNL     1       1.356   0.764   0.748  1.00  0.00           N  
HETATM   10  C7  UNL     1       1.680  -0.615  -1.200  1.00  0.00           C  
HETATM   11  C8  UNL     1       3.131  -0.769  -0.932  1.00  0.00           C  
HETATM   12  C9  UNL     1       4.069  -0.344  -1.848  1.00  0.00           C  
HETATM   13  C10 UNL     1       5.388  -0.505  -1.562  1.00  0.00           C  
HETATM   14  C11 UNL     1       5.802  -1.083  -0.379  1.00  0.00           C  
HETATM   15  C12 UNL     1       4.859  -1.505   0.530  1.00  0.00           C  
HETATM   16  C13 UNL     1       3.516  -1.346   0.250  1.00  0.00           C  
HETATM   17  C14 UNL     1      -3.227   2.088   0.244  1.00  0.00           C  
HETATM   18  O2  UNL     1      -2.542   2.898   0.902  1.00  0.00           O  
HETATM   19  O3  UNL     1      -4.567   2.354   0.045  1.00  0.00           O  
HETATM   20  H1  UNL     1      -2.375  -1.164   2.124  1.00  0.00           H  
HETATM   21  H2  UNL     1      -4.031  -0.549   2.324  1.00  0.00           H  
HETATM   22  H3  UNL     1      -2.722   0.623   2.081  1.00  0.00           H  
HETATM   23  H4  UNL     1      -2.643  -1.255  -0.116  1.00  0.00           H  
HETATM   24  H5  UNL     1      -4.760  -1.531  -0.840  1.00  0.00           H  
HETATM   25  H6  UNL     1      -5.322  -0.817   0.722  1.00  0.00           H  
HETATM   26  H7  UNL     1      -5.034   0.219  -0.784  1.00  0.00           H  
HETATM   27  H8  UNL     1      -2.809   0.826  -1.407  1.00  0.00           H  
HETATM   28  H9  UNL     1      -0.921   0.844   1.016  1.00  0.00           H  
HETATM   29  H10 UNL     1       1.629   1.566  -1.201  1.00  0.00           H  
HETATM   30  H11 UNL     1       1.048  -0.092   1.217  1.00  0.00           H  
HETATM   31  H12 UNL     1       1.061   1.645   1.178  1.00  0.00           H  
HETATM   32  H13 UNL     1       1.455  -0.709  -2.287  1.00  0.00           H  
HETATM   33  H14 UNL     1       1.129  -1.405  -0.663  1.00  0.00           H  
HETATM   34  H15 UNL     1       3.740   0.107  -2.770  1.00  0.00           H  
HETATM   35  H16 UNL     1       6.134  -0.179  -2.266  1.00  0.00           H  
HETATM   36  H17 UNL     1       6.860  -1.202  -0.172  1.00  0.00           H  
HETATM   37  H18 UNL     1       5.203  -1.956   1.453  1.00  0.00           H  
HETATM   38  H19 UNL     1       2.820  -1.693   0.997  1.00  0.00           H  
HETATM   39  H20 UNL     1      -5.249   2.320   0.784  1.00  0.00           H  
CONECT    1    2   20   21   22
CONECT    2    3    4   23
CONECT    3   24   25   26
CONECT    4    5   17   27
CONECT    5    6   28
CONECT    6    7    7    8
CONECT    8    9   10   29
CONECT    9   30   31
CONECT   10   11   32   33
CONECT   11   12   12   16
CONECT   12   13   34
CONECT   13   14   14   35
CONECT   14   15   36
CONECT   15   16   16   37
CONECT   16   38
CONECT   17   18   18   19
CONECT   19   39
END

HMDB0029008
     RDKit          3D
Phenylalanylvaline
 39 39  0  0  0  0  0  0  0  0999 V2000
   -3.0858   -0.3959    1.7654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2630   -0.4008    0.2818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6704   -0.6312   -0.1711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6498    0.8559   -0.3272 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2371    0.8224    0.0271 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2954    0.7589   -1.0101 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6248    0.7303   -2.2196 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1501    0.7234   -0.6874 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3556    0.7639    0.7485 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.6800   -0.6146   -1.1997 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1306   -0.7687   -0.9324 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0690   -0.3441   -1.8477 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3883   -0.5053   -1.5621 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8016   -1.0833   -0.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8594   -1.5048    0.5303 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5156   -1.3457    0.2500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2271    2.0882    0.2440 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5422    2.8984    0.9017 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5666    2.3536    0.0449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3749   -1.1640    2.1243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0306   -0.5486    2.3244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7222    0.6235    2.0808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6428   -1.2553   -0.1163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7601   -1.5305   -0.8401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3218   -0.8165    0.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0338    0.2189   -0.7844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8094    0.8260   -1.4073 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9207    0.8443    1.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6286    1.5661   -1.2014 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0479   -0.0917    1.2175 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0609    1.6447    1.1779 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4548   -0.7090   -2.2868 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1291   -1.4051   -0.6631 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7398    0.1066   -2.7702 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1340   -0.1791   -2.2660 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8596   -1.2021   -0.1716 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2028   -1.9558    1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8202   -1.6934    0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2494    2.3205    0.7837 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  2  0
 14 15  1  0
 15 16  2  0
  4 17  1  0
 17 18  2  0
 17 19  1  0
 16 11  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  6
  5 28  1  0
  8 29  1  6
  9 30  1  0
  9 31  1  0
 10 32  1  0
 10 33  1  0
 12 34  1  0
 13 35  1  0
 14 36  1  0
 15 37  1  0
 16 38  1  0
 19 39  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
F-V	ChEBI
FV	ChEBI
L-Phe-L-val	ChEBI
F-V Dipeptide	HMDB
FV Dipeptide	HMDB
L-Phenylalanyl-L-valine	HMDB
N-L-Phenylalanyl-L-valine	HMDB
N-Phenylalanylvaline	HMDB
Phe-val	HMDB
Phenylalanine valine dipeptide	HMDB
Phenylalanine-valine dipeptide	HMDB
Phenylalanyl-valine	HMDB
Phenylalanylvaline	ChEBI

Chemical Formula

C₁₄H₂₀N₂O₃

Average Molecular Weight

264.325

Monoisotopic Molecular Weight

264.147392512

IUPAC Name

(2S)-2-[(2S)-2-amino-3-phenylpropanamido]-3-methylbutanoic acid

Traditional Name

(2S)-2-[(2S)-2-amino-3-phenylpropanamido]-3-methylbutanoic acid

CAS Registry Number

3918-90-9

SMILES

CC(C)[C@H](NC(=O)[C@@H](N)CC1=CC=CC=C1)C(O)=O

InChI Identifier

InChI=1S/C14H20N2O3/c1-9(2)12(14(18)19)16-13(17)11(15)8-10-6-4-3-5-7-10/h3-7,9,11-12H,8,15H2,1-2H3,(H,16,17)(H,18,19)/t11-,12-/m0/s1

InChI Key

IEHDJWSAXBGJIP-RYUDHWBXSA-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
Phenylalanine or derivatives
Valine or derivatives
N-acyl-alpha-amino acid
N-acyl-l-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Alpha-amino acid or derivatives
Amphetamine or derivatives
Aralkylamine
Monocyclic benzene moiety
Fatty amide
Fatty acyl
Benzenoid
Amino acid or derivatives
Carboxamide group
Carboxylic acid salt
Amino acid
Secondary carboxylic acid amide
Monocarboxylic acid or derivatives
Carboxylic acid
Organic salt
Hydrocarbon derivative
Primary aliphatic amine
Organic nitrogen compound
Amine
Organic oxygen compound
Carbonyl group
Organic oxide
Organonitrogen compound
Organooxygen compound
Primary amine
Organopnictogen compound
Organic zwitterion
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

dipeptide (CHEBI:73638 )

Ontology

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	-0.84	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	1.2 g/L	ALOGPS
logP	-0.87	ALOGPS
logP	-0.84	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	3.84	ChemAxon
pKa (Strongest Basic)	8.01	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	92.42 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	71.41 m³·mol⁻¹	ChemAxon
Polarizability	28.18 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]+	165.661	30932474
DeepCCS	[M-H]-	163.303	30932474
DeepCCS	[M-2H]-	196.189	30932474
DeepCCS	[M+Na]+	171.754	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.	2.61 minutes	32390414
Predicted by Siyang on May 30, 2022	10.7797 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	6.18 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	150.6 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	1341.7 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	236.3 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	118.8 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	162.1 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	88.2 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	329.7 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	357.3 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	265.0 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	804.2 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	375.3 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	1015.5 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	212.7 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	268.7 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	301.0 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	319.2 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	65.0 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Phenylalanylvaline	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CC=CC=C1)C(O)=O	3485.4	Standard polar	33892256
Phenylalanylvaline	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CC=CC=C1)C(O)=O	2010.8	Standard non polar	33892256
Phenylalanylvaline	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CC=CC=C1)C(O)=O	2212.7	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Phenylalanylvaline,1TMS,isomer #1	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CC=CC=C1)C(=O)O[Si](C)(C)C	2159.8	Semi standard non polar	33892256
Phenylalanylvaline,1TMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C)C(=O)O	2212.8	Semi standard non polar	33892256
Phenylalanylvaline,1TMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=CC=CC=C1)[Si](C)(C)C	2135.7	Semi standard non polar	33892256
Phenylalanylvaline,2TMS,isomer #1	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2199.0	Semi standard non polar	33892256
Phenylalanylvaline,2TMS,isomer #1	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C)C(=O)O[Si](C)(C)C	2201.3	Standard non polar	33892256
Phenylalanylvaline,2TMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@@H](N)CC1=CC=CC=C1)[Si](C)(C)C	2117.9	Semi standard non polar	33892256
Phenylalanylvaline,2TMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@@H](N)CC1=CC=CC=C1)[Si](C)(C)C	2188.4	Standard non polar	33892256
Phenylalanylvaline,2TMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C)[Si](C)(C)C	2188.2	Semi standard non polar	33892256
Phenylalanylvaline,2TMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C)[Si](C)(C)C	2227.1	Standard non polar	33892256
Phenylalanylvaline,2TMS,isomer #4	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2357.9	Semi standard non polar	33892256
Phenylalanylvaline,2TMS,isomer #4	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2257.3	Standard non polar	33892256
Phenylalanylvaline,3TMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C)[Si](C)(C)C	2180.2	Semi standard non polar	33892256
Phenylalanylvaline,3TMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C)[Si](C)(C)C	2283.1	Standard non polar	33892256
Phenylalanylvaline,3TMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2324.6	Semi standard non polar	33892256
Phenylalanylvaline,3TMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2324.2	Standard non polar	33892256
Phenylalanylvaline,3TMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2315.7	Semi standard non polar	33892256
Phenylalanylvaline,3TMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2362.3	Standard non polar	33892256
Phenylalanylvaline,4TMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2360.6	Semi standard non polar	33892256
Phenylalanylvaline,4TMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	2418.7	Standard non polar	33892256
Phenylalanylvaline,1TBDMS,isomer #1	CC(C)[C@H](NC(=O)[C@@H](N)CC1=CC=CC=C1)C(=O)O[Si](C)(C)C(C)(C)C	2419.1	Semi standard non polar	33892256
Phenylalanylvaline,1TBDMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C(C)(C)C)C(=O)O	2426.5	Semi standard non polar	33892256
Phenylalanylvaline,1TBDMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=CC=CC=C1)[Si](C)(C)C(C)(C)C	2381.6	Semi standard non polar	33892256
Phenylalanylvaline,2TBDMS,isomer #1	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2635.0	Semi standard non polar	33892256
Phenylalanylvaline,2TBDMS,isomer #1	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2590.2	Standard non polar	33892256
Phenylalanylvaline,2TBDMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@@H](N)CC1=CC=CC=C1)[Si](C)(C)C(C)(C)C	2615.5	Semi standard non polar	33892256
Phenylalanylvaline,2TBDMS,isomer #2	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@@H](N)CC1=CC=CC=C1)[Si](C)(C)C(C)(C)C	2579.5	Standard non polar	33892256
Phenylalanylvaline,2TBDMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2647.7	Semi standard non polar	33892256
Phenylalanylvaline,2TBDMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2604.3	Standard non polar	33892256
Phenylalanylvaline,2TBDMS,isomer #4	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2786.7	Semi standard non polar	33892256
Phenylalanylvaline,2TBDMS,isomer #4	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2622.1	Standard non polar	33892256
Phenylalanylvaline,3TBDMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2849.0	Semi standard non polar	33892256
Phenylalanylvaline,3TBDMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2826.8	Standard non polar	33892256
Phenylalanylvaline,3TBDMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)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	3006.8	Semi standard non polar	33892256
Phenylalanylvaline,3TBDMS,isomer #2	CC(C)[C@H](NC(=O)[C@H](CC1=CC=CC=C1)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	2850.3	Standard non polar	33892256
Phenylalanylvaline,3TBDMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3005.9	Semi standard non polar	33892256
Phenylalanylvaline,3TBDMS,isomer #3	CC(C)[C@@H](C(=O)O)N(C(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2880.2	Standard non polar	33892256
Phenylalanylvaline,4TBDMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3219.0	Semi standard non polar	33892256
Phenylalanylvaline,4TBDMS,isomer #1	CC(C)[C@@H](C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)[C@H](CC1=CC=CC=C1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3092.8	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Phenylalanylvaline 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 - Phenylalanylvaline 10V, Positive-QTOF	splash10-01b9-1980000000-412d0ec298d1b6026d3e	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenylalanylvaline 20V, Positive-QTOF	splash10-006x-8900000000-6a75d317cfa9fa572cd1	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenylalanylvaline 40V, Positive-QTOF	splash10-0096-9600000000-cf06cfa15e9e25136a41	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenylalanylvaline 10V, Negative-QTOF	splash10-03di-0090000000-b7c71fa74fc8ffccaeab	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenylalanylvaline 20V, Negative-QTOF	splash10-00kf-7970000000-0c0785aee2bc8add13b9	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Phenylalanylvaline 40V, Negative-QTOF	splash10-002f-9400000000-568179886d37f352ae6c	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	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	Not Specified	Both	Normal	25486321	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

FDB112024

KNApSAcK ID

Not Available

Chemspider ID

5685589

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

7359121

PDB ID

Not Available

ChEBI ID

73638

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

Demeshkina N, Repkova M, Ven'yaminova A, Graifer D, Karpova G: Nucleotides of 18S rRNA surrounding mRNA codons at the human ribosomal A, P, and E sites: a crosslinking study with mRNA analogs carrying an aryl azide group at either the uracil or the guanine residue. RNA. 2000 Dec;6(12):1727-36. [PubMed:11142373 ]

Showing metabocard for Phenylalanylvaline (HMDB0029008)

MOL for HMDB0029008 (Phenylalanylvaline)

3D MOL for HMDB0029008 (Phenylalanylvaline)

3D SDF for HMDB0029008 (Phenylalanylvaline)

3D-SDF for HMDB0029008 (Phenylalanylvaline)

PDB for HMDB0029008 (Phenylalanylvaline)

3D PDB for HMDB0029008 (Phenylalanylvaline)

SMILES for HMDB0029008 (Phenylalanylvaline)

INCHI for HMDB0029008 (Phenylalanylvaline)

Structure for HMDB0029008 (Phenylalanylvaline)

3D Structure for HMDB0029008 (Phenylalanylvaline)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra