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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 21:02:51 UTC

Update Date

2021-09-14 15:37:01 UTC

HMDB ID

HMDB0028881

Secondary Accession Numbers

HMDB28881

Metabolite Identification

Common Name

Histidylaspartic acid

Description

Histidylaspartic acid is a dipeptide composed of histidine and aspartic acid. 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

HMDB0028881
     RDKit          3D
Histidylaspartic acid
 33 33  0  0  0  0  0  0  0  0999 V2000
    2.1484    1.3334   -2.1501 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2265    0.3250   -1.6857 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8861   -0.7932   -0.9560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6224   -0.4039    0.2408 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8308    0.8172    0.8399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5863    0.6489    1.9346 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8542   -0.6734    2.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2770   -1.3262    1.0074 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0735    0.9150   -0.9623 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0257    2.1646   -0.8175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9275    0.0520   -0.4637 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0950    0.5109    0.2550 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3140    0.1483   -0.6008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4206   -1.3008   -0.8352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7065   -1.8328   -1.7134 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2897   -2.0696   -0.1050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1849   -0.1554    1.5779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2977   -0.9815    1.8986 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2015    0.0861    2.4842 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9292    2.2863   -1.8482 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1447    1.0556   -2.0934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7802   -0.1267   -2.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5797   -1.3038   -1.6535 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1072   -1.5237   -0.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4237    1.7295    0.4428 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8831    1.4194    2.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4467   -1.1354    2.8078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8430   -0.9660   -0.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1017    1.6035    0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2517    0.4993   -0.1255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1778    0.6776   -1.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0459   -2.3931    0.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    0.7128    2.2111 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
  5  6  1  0
  6  7  1  0
  7  8  2  0
  2  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 12 17  1  0
 17 18  2  0
 17 19  1  0
  8  4  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  6
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
 11 28  1  0
 12 29  1  1
 13 30  1  0
 13 31  1  0
 16 32  1  0
 19 33  1  0
M  END


  Mrv1652304062013472D          

 19 19  0  0  0  0            999 V2000
 9999.289410000.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.004010000.3519    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10000.718410000.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.433210000.3519    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10002.147210000.7644    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10002.861410000.3519    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.575410000.7644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10004.291610000.3519    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.575410001.5900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.147210001.5900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.861410002.0028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.433210002.0028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.718410001.5900    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.0040 9999.5269    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9997.903410000.8462    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9997.236110000.3612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.4910 9999.5765    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9998.3160 9999.5765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.571010000.3612    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 14  1  1  0  0  0
  3  4  1  0  0  0  0
  3 13  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5 10  1  6  0  0  0
  6  7  1  0  0  0  0
  7  9  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
 18 19  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 15 16  2  0  0  0  0
 15 19  1  0  0  0  0
  1 19  1  0  0  0  0
  7  8  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0028881

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C10H14N4O5/c11-6(1-5-3-12-4-13-5)9(17)14-7(10(18)19)2-8(15)16/h3-4,6-7H,1-2,11H2,(H,12,13)(H,14,17)(H,15,16)(H,18,19)/t6-,7-/m0/s1

> <INCHI_KEY>
MDCTVRUPVLZSPG-BQBZGAKWSA-N

> <FORMULA>
C10H14N4O5

> <MOLECULAR_WEIGHT>
270.245

> <EXACT_MASS>
270.096419567

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
25.10916807901133

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-3.10

> <JCHEM_LOGP>
-5.551323358153725

> <ALOGPS_LOGS>
-1.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
4.848226837747603

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.1192219689779477

> <JCHEM_PKA_STRONGEST_BASIC>
7.838975275848857

> <JCHEM_POLAR_SURFACE_AREA>
158.4

> <JCHEM_REFRACTIVITY>
60.8261

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.91e+00 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0028881
     RDKit          3D
Histidylaspartic acid
 33 33  0  0  0  0  0  0  0  0999 V2000
    2.1484    1.3334   -2.1501 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2265    0.3250   -1.6857 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8861   -0.7932   -0.9560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6224   -0.4039    0.2408 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8308    0.8172    0.8399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5863    0.6489    1.9346 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8542   -0.6734    2.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2770   -1.3262    1.0074 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0735    0.9150   -0.9623 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0257    2.1646   -0.8175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9275    0.0520   -0.4637 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0950    0.5109    0.2550 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3140    0.1483   -0.6008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4206   -1.3008   -0.8352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7065   -1.8328   -1.7134 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2897   -2.0696   -0.1050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1849   -0.1554    1.5779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2977   -0.9815    1.8986 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2015    0.0861    2.4842 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9292    2.2863   -1.8482 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1447    1.0556   -2.0934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7802   -0.1267   -2.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5797   -1.3038   -1.6535 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1072   -1.5237   -0.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4237    1.7295    0.4428 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8831    1.4194    2.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4467   -1.1354    2.8078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8430   -0.9660   -0.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1017    1.6035    0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2517    0.4993   -0.1255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1778    0.6776   -1.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0459   -2.3931    0.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    0.7128    2.2111 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
  5  6  1  0
  6  7  1  0
  7  8  2  0
  2  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 12 17  1  0
 17 18  2  0
 17 19  1  0
  8  4  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  6
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
 11 28  1  0
 12 29  1  1
 13 30  1  0
 13 31  1  0
 16 32  1  0
 19 33  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    8665.3408668.094   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8666.6748667.324   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8668.0088668.094   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0    8669.3428667.324   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0    8670.6758668.094   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8672.0088667.324   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    8673.3418668.094   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0    8674.6788667.324   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0    8673.3418669.635   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0    8670.6758669.635   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0    8672.0088670.405   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0    8669.3428670.405   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0    8668.0088669.635   0.000  0.00  0.00           O+0
HETATM   14  N   UNK     0    8666.6748665.784   0.000  0.00  0.00           N+0
HETATM   15  N   UNK     0    8662.7538668.246   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0    8661.5078667.341   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0    8661.9838665.876   0.000  0.00  0.00           N+0
HETATM   18  C   UNK     0    8663.5238665.876   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0    8663.9998667.341   0.000  0.00  0.00           C+0
CONECT    1    2   19                                                       
CONECT    2    1    3   14                                                  
CONECT    3    2    4   13                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    9    8                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    5   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    3                                                            
CONECT   14    2                                                            
CONECT   15   16   19                                                       
CONECT   16   17   15                                                       
CONECT   17   16   18                                                       
CONECT   18   19   17                                                       
CONECT   19   18   15    1                                                  
MASTER        0    0    0    0    0    0    0    0   19    0   38    0
END

COMPND    HMDB0028881
HETATM    1  N1  UNL     1       2.148   1.333  -2.150  1.00  0.00           N  
HETATM    2  C1  UNL     1       1.226   0.325  -1.686  1.00  0.00           C  
HETATM    3  C2  UNL     1       1.886  -0.793  -0.956  1.00  0.00           C  
HETATM    4  C3  UNL     1       2.622  -0.404   0.241  1.00  0.00           C  
HETATM    5  C4  UNL     1       2.831   0.817   0.840  1.00  0.00           C  
HETATM    6  N2  UNL     1       3.586   0.649   1.935  1.00  0.00           N  
HETATM    7  C5  UNL     1       3.854  -0.673   2.027  1.00  0.00           C  
HETATM    8  N3  UNL     1       3.277  -1.326   1.007  1.00  0.00           N  
HETATM    9  C6  UNL     1       0.073   0.915  -0.962  1.00  0.00           C  
HETATM   10  O1  UNL     1       0.026   2.165  -0.817  1.00  0.00           O  
HETATM   11  N4  UNL     1      -0.927   0.052  -0.464  1.00  0.00           N  
HETATM   12  C7  UNL     1      -2.095   0.511   0.255  1.00  0.00           C  
HETATM   13  C8  UNL     1      -3.314   0.148  -0.601  1.00  0.00           C  
HETATM   14  C9  UNL     1      -3.421  -1.301  -0.835  1.00  0.00           C  
HETATM   15  O2  UNL     1      -2.707  -1.833  -1.713  1.00  0.00           O  
HETATM   16  O3  UNL     1      -4.290  -2.070  -0.105  1.00  0.00           O  
HETATM   17  C10 UNL     1      -2.185  -0.155   1.578  1.00  0.00           C  
HETATM   18  O4  UNL     1      -1.298  -0.981   1.899  1.00  0.00           O  
HETATM   19  O5  UNL     1      -3.201   0.086   2.484  1.00  0.00           O  
HETATM   20  H1  UNL     1       1.929   2.286  -1.848  1.00  0.00           H  
HETATM   21  H2  UNL     1       3.145   1.056  -2.093  1.00  0.00           H  
HETATM   22  H3  UNL     1       0.780  -0.127  -2.624  1.00  0.00           H  
HETATM   23  H4  UNL     1       2.580  -1.304  -1.654  1.00  0.00           H  
HETATM   24  H5  UNL     1       1.107  -1.524  -0.658  1.00  0.00           H  
HETATM   25  H6  UNL     1       2.424   1.729   0.443  1.00  0.00           H  
HETATM   26  H7  UNL     1       3.883   1.419   2.561  1.00  0.00           H  
HETATM   27  H8  UNL     1       4.447  -1.135   2.808  1.00  0.00           H  
HETATM   28  H9  UNL     1      -0.843  -0.966  -0.609  1.00  0.00           H  
HETATM   29  H10 UNL     1      -2.102   1.604   0.365  1.00  0.00           H  
HETATM   30  H11 UNL     1      -4.252   0.499  -0.126  1.00  0.00           H  
HETATM   31  H12 UNL     1      -3.178   0.678  -1.579  1.00  0.00           H  
HETATM   32  H13 UNL     1      -4.046  -2.393   0.826  1.00  0.00           H  
HETATM   33  H14 UNL     1      -3.968   0.713   2.211  1.00  0.00           H  
CONECT    1    2   20   21
CONECT    2    3    9   22
CONECT    3    4   23   24
CONECT    4    5    5    8
CONECT    5    6   25
CONECT    6    7   26
CONECT    7    8    8   27
CONECT    9   10   10   11
CONECT   11   12   28
CONECT   12   13   17   29
CONECT   13   14   30   31
CONECT   14   15   15   16
CONECT   16   32
CONECT   17   18   18   19
CONECT   19   33
END

HMDB0028881
     RDKit          3D
Histidylaspartic acid
 33 33  0  0  0  0  0  0  0  0999 V2000
    2.1484    1.3334   -2.1501 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2265    0.3250   -1.6857 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8861   -0.7932   -0.9560 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6224   -0.4039    0.2408 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8308    0.8172    0.8399 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5863    0.6489    1.9346 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8542   -0.6734    2.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2770   -1.3262    1.0074 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0735    0.9150   -0.9623 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0257    2.1646   -0.8175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9275    0.0520   -0.4637 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0950    0.5109    0.2550 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3140    0.1483   -0.6008 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4206   -1.3008   -0.8352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7065   -1.8328   -1.7134 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2897   -2.0696   -0.1050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1849   -0.1554    1.5779 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2977   -0.9815    1.8986 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2015    0.0861    2.4842 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9292    2.2863   -1.8482 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1447    1.0556   -2.0934 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7802   -0.1267   -2.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5797   -1.3038   -1.6535 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1072   -1.5237   -0.6579 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4237    1.7295    0.4428 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8831    1.4194    2.5609 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4467   -1.1354    2.8078 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8430   -0.9660   -0.6086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1017    1.6035    0.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2517    0.4993   -0.1255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1778    0.6776   -1.5791 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0459   -2.3931    0.8265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9680    0.7128    2.2111 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
  5  6  1  0
  6  7  1  0
  7  8  2  0
  2  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 14 16  1  0
 12 17  1  0
 17 18  2  0
 17 19  1  0
  8  4  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  6
  3 23  1  0
  3 24  1  0
  5 25  1  0
  6 26  1  0
  7 27  1  0
 11 28  1  0
 12 29  1  1
 13 30  1  0
 13 31  1  0
 16 32  1  0
 19 33  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
HD	ChEBI
Histidinyl-aspartate	ChEBI
Histidylaspartate	ChEBI
L-His-L-asp	ChEBI
Histidinyl-aspartic acid	Generator
H-D Dipeptide	HMDB
HD Dipeptide	HMDB
His-asp	HMDB
Histidine aspartate dipeptide	HMDB
Histidine aspartic acid dipeptide	HMDB
Histidine-aspartate dipeptide	HMDB
Histidine-aspartic acid dipeptide	HMDB
Histidinylaspartate	HMDB
Histidinylaspartic acid	HMDB
Histidyl-aspartate	HMDB
Histidyl-aspartic acid	HMDB
L-Histidinyl-L-aspartate	HMDB
L-Histidinyl-L-aspartic acid	HMDB
L-Histidyl-L-aspartate	HMDB
L-Histidyl-L-aspartic acid	HMDB
N-Histidinylaspartate	HMDB
N-Histidinylaspartic acid	HMDB
N-Histidylaspartate	HMDB
N-Histidylaspartic acid	HMDB
N-L-Histidinyl-L-aspartate	HMDB
N-L-Histidinyl-L-aspartic acid	HMDB
N-L-Histidyl-L-aspartate	HMDB
N-L-Histidyl-L-aspartic acid	HMDB
Histidylaspartic acid	ChEBI

Chemical Formula

C₁₀H₁₄N₄O₅

Average Molecular Weight

270.245

Monoisotopic Molecular Weight

270.096419567

IUPAC Name

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

Traditional Name

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

CAS Registry Number

41658-60-0

SMILES

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

InChI Identifier

InChI=1S/C10H14N4O5/c11-6(1-5-3-12-4-13-5)9(17)14-7(10(18)19)2-8(15)16/h3-4,6-7H,1-2,11H2,(H,12,13)(H,14,17)(H,15,16)(H,18,19)/t6-,7-/m0/s1

InChI Key

MDCTVRUPVLZSPG-BQBZGAKWSA-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
Aspartic acid or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Acyl-homoserine
N-acyl-l-alpha-amino acid
Acyl-l-homoserine
Alpha-amino acid amide
Alpha-amino acid or derivatives
Imidazolyl carboxylic acid derivative
Aralkylamine
Dicarboxylic acid or derivatives
Fatty amide
Fatty acyl
Azole
Imidazole
Heteroaromatic compound
Secondary carboxylic acid amide
Amino acid or derivatives
Amino acid
Carboxamide group
Organoheterocyclic compound
Carboxylic acid
Azacycle
Primary amine
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Primary aliphatic amine
Organic oxide
Carbonyl group
Amine
Organonitrogen compound
Organooxygen compound
Hydrocarbon derivative
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

dipeptide (CHEBI:73925 )

Ontology

Not Available

Endogenous (HMDB: HMDB0028881)

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	-6.79	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	5.82 g/L	ALOGPS
logP	-3.1	ALOGPS
logP	-5.6	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	3.12	ChemAxon
pKa (Strongest Basic)	7.84	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	158.4 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	60.83 m³·mol⁻¹	ChemAxon
Polarizability	25.11 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]+	158.226	30932474
DeepCCS	[M-H]-	155.868	30932474
DeepCCS	[M-2H]-	188.837	30932474
DeepCCS	[M+Na]+	164.319	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.	1.96 minutes	32390414
Predicted by Siyang on May 30, 2022	9.9887 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	9.64 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	480.2 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	378.2 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	273.8 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	30.3 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	164.7 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	73.9 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	326.9 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	233.7 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	1067.1 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	562.5 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	50.4 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	696.1 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	194.8 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	369.4 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	707.4 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	726.8 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	506.9 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Histidylaspartic acid	N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC(O)=O)C(O)=O	3613.4	Standard polar	33892256
Histidylaspartic acid	N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC(O)=O)C(O)=O	2188.7	Standard non polar	33892256
Histidylaspartic acid	N[C@@H](CC1=CNC=N1)C(=O)N[C@@H](CC(O)=O)C(O)=O	2864.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Histidylaspartic acid,1TMS,isomer #1	C[Si](C)(C)OC(=O)C[C@H](NC(=O)[C@@H](N)CC1=C[NH]C=N1)C(=O)O	2676.0	Semi standard non polar	33892256
Histidylaspartic acid,1TMS,isomer #2	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](N)CC1=C[NH]C=N1	2615.9	Semi standard non polar	33892256
Histidylaspartic acid,1TMS,isomer #3	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O	2658.8	Semi standard non polar	33892256
Histidylaspartic acid,1TMS,isomer #4	C[Si](C)(C)N1C=NC(C[C@H](N)C(=O)N[C@@H](CC(=O)O)C(=O)O)=C1	2741.1	Semi standard non polar	33892256
Histidylaspartic acid,1TMS,isomer #5	C[Si](C)(C)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[C@@H](CC(=O)O)C(=O)O	2559.8	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #1	C[Si](C)(C)OC(=O)C[C@H](NC(=O)[C@@H](N)CC1=C[NH]C=N1)C(=O)O[Si](C)(C)C	2629.6	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #10	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2602.1	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #11	C[Si](C)(C)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)[C@@H](CC(=O)O)C(=O)O	2690.9	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #2	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O	2697.0	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #3	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[Si](C)(C)C	2558.1	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #4	C[Si](C)(C)OC(=O)C[C@H](NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)C(=O)O	2765.8	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #5	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C	2662.8	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #6	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[Si](C)(C)C	2569.5	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #7	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1	2715.2	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #8	C[Si](C)(C)N([C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2737.9	Semi standard non polar	33892256
Histidylaspartic acid,2TMS,isomer #9	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O	2762.0	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #1	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2658.5	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #1	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2539.0	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #10	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2595.4	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #10	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2576.9	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)[Si](C)(C)C	2669.5	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #11	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)[Si](C)(C)C	2531.1	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #12	C[Si](C)(C)N([C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2877.9	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #12	C[Si](C)(C)N([C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2716.9	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #13	C[Si](C)(C)N(C(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CC(=O)O)C(=O)O	2691.4	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #13	C[Si](C)(C)N(C(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CC(=O)O)C(=O)O	2696.7	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #14	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2726.8	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #14	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C	2639.1	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #2	C[Si](C)(C)OC(=O)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	2551.8	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #2	C[Si](C)(C)OC(=O)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	2477.6	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #3	C[Si](C)(C)OC(=O)C[C@H](NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)C(=O)O[Si](C)(C)C	2738.6	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #3	C[Si](C)(C)OC(=O)C[C@H](NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)C(=O)O[Si](C)(C)C	2479.2	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #4	C[Si](C)(C)OC(=O)C[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2751.3	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #4	C[Si](C)(C)OC(=O)C[C@H](NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2675.5	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #5	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O	2777.2	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #5	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O	2592.1	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #6	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2586.4	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #6	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2615.3	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #7	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)[Si](C)(C)C	2665.5	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #7	C[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C)C=N1)[Si](C)(C)C	2564.2	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C	2719.5	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C)[Si](C)(C)C	2641.8	Standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #9	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C	2763.3	Semi standard non polar	33892256
Histidylaspartic acid,3TMS,isomer #9	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C	2560.3	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)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	2691.0	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #1	C[Si](C)(C)OC(=O)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	2642.1	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #10	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2710.9	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #10	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2624.7	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #11	C[Si](C)(C)N(C(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CC(=O)O)C(=O)O	2824.8	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #11	C[Si](C)(C)N(C(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CC(=O)O)C(=O)O	2774.4	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #2	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2763.0	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #2	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C	2568.5	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #3	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2588.3	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #3	C[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2599.5	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #4	C[Si](C)(C)OC(=O)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	2658.4	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #4	C[Si](C)(C)OC(=O)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	2556.5	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #5	C[Si](C)(C)OC(=O)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	2690.3	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #5	C[Si](C)(C)OC(=O)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	2716.5	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #6	C[Si](C)(C)OC(=O)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	2885.8	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #6	C[Si](C)(C)OC(=O)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	2719.3	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #7	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2704.8	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #7	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2650.8	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H](CC(=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	2714.7	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #8	C[Si](C)(C)OC(=O)[C@H](CC(=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	2687.0	Standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #9	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C	2873.6	Semi standard non polar	33892256
Histidylaspartic acid,4TMS,isomer #9	C[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC1=CN([Si](C)(C)C)C=N1)N([Si](C)(C)C)[Si](C)(C)C	2699.7	Standard non polar	33892256
Histidylaspartic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)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	2752.4	Semi standard non polar	33892256
Histidylaspartic acid,5TMS,isomer #1	C[Si](C)(C)OC(=O)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	2694.9	Standard non polar	33892256
Histidylaspartic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)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	2851.8	Semi standard non polar	33892256
Histidylaspartic acid,5TMS,isomer #2	C[Si](C)(C)OC(=O)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	2704.9	Standard non polar	33892256
Histidylaspartic acid,5TMS,isomer #3	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2721.8	Semi standard non polar	33892256
Histidylaspartic acid,5TMS,isomer #3	C[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2641.5	Standard non polar	33892256
Histidylaspartic acid,5TMS,isomer #4	C[Si](C)(C)OC(=O)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	2829.9	Semi standard non polar	33892256
Histidylaspartic acid,5TMS,isomer #4	C[Si](C)(C)OC(=O)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	2781.9	Standard non polar	33892256
Histidylaspartic acid,5TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H](CC(=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	2847.6	Semi standard non polar	33892256
Histidylaspartic acid,5TMS,isomer #5	C[Si](C)(C)OC(=O)[C@H](CC(=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	2757.2	Standard non polar	33892256
Histidylaspartic acid,6TMS,isomer #1	C[Si](C)(C)OC(=O)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	2886.7	Semi standard non polar	33892256
Histidylaspartic acid,6TMS,isomer #1	C[Si](C)(C)OC(=O)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	2772.0	Standard non polar	33892256
Histidylaspartic acid,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)[C@@H](N)CC1=C[NH]C=N1)C(=O)O	2916.9	Semi standard non polar	33892256
Histidylaspartic acid,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](N)CC1=C[NH]C=N1	2852.4	Semi standard non polar	33892256
Histidylaspartic acid,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O	2851.3	Semi standard non polar	33892256
Histidylaspartic acid,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N1C=NC(C[C@H](N)C(=O)N[C@@H](CC(=O)O)C(=O)O)=C1	2986.4	Semi standard non polar	33892256
Histidylaspartic acid,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[C@@H](CC(=O)O)C(=O)O	2827.8	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)[C@@H](N)CC1=C[NH]C=N1)C(=O)O[Si](C)(C)C(C)(C)C	3105.5	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	3051.3	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(C(=O)[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1)[C@@H](CC(=O)O)C(=O)O	3174.0	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	3124.2	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)C[C@@H](C(=O)O)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[Si](C)(C)C(C)(C)C	3049.2	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C[C@H](NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)O	3249.2	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	3079.3	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)N(C(=O)[C@@H](N)CC1=C[NH]C=N1)[Si](C)(C)C(C)(C)C	3037.8	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)[C@@H](N)CC1=CN([Si](C)(C)C(C)(C)C)C=N1	3195.0	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)N([C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	3159.5	Semi standard non polar	33892256
Histidylaspartic acid,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O	3207.6	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3317.9	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3088.0	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3270.0	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3096.6	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=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	3370.2	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=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	3054.2	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N([C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	3552.5	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N([C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	3212.9	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #13	CC(C)(C)[Si](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)[C@@H](CC(=O)O)C(=O)O	3361.8	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #13	CC(C)(C)[Si](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)[C@@H](CC(=O)O)C(=O)O	3196.3	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	3409.2	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O)[Si](C)(C)C(C)(C)C	3128.2	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)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	3257.4	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)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	3028.3	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)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	3419.6	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)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	3025.2	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)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	3432.8	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)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	3187.3	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	3452.9	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O	3123.8	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3273.5	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3124.8	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)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	3375.8	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)OC(=O)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	3075.9	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3398.1	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CC1=C[NH]C=N1)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3160.1	Standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	3425.8	Semi standard non polar	33892256
Histidylaspartic acid,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C	3098.1	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)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	3631.7	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)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	3285.5	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3593.0	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3280.3	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #11	CC(C)(C)[Si](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)[C@@H](CC(=O)O)C(=O)O	3731.3	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #11	CC(C)(C)[Si](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)[C@@H](CC(=O)O)C(=O)O	3386.6	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3608.8	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N[C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3249.1	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3457.5	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N[C@@H](CC1=C[NH]C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3241.1	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)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	3551.3	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)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	3223.5	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)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	3587.7	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)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	3339.8	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)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	3771.7	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)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	3372.0	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3587.9	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3298.1	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=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	3586.4	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=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	3317.3	Standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)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	3744.2	Semi standard non polar	33892256
Histidylaspartic acid,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=O)O)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	3345.4	Standard non polar	33892256
Histidylaspartic acid,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)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	3802.2	Semi standard non polar	33892256
Histidylaspartic acid,5TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)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	3456.0	Standard non polar	33892256
Histidylaspartic acid,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)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	3935.0	Semi standard non polar	33892256
Histidylaspartic acid,5TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)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	3487.3	Standard non polar	33892256
Histidylaspartic acid,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3750.0	Semi standard non polar	33892256
Histidylaspartic acid,5TBDMS,isomer #3	CC(C)(C)[Si](C)(C)N[C@@H](CC1=CN([Si](C)(C)C(C)(C)C)C=N1)C(=O)N([C@@H](CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3436.2	Standard non polar	33892256
Histidylaspartic acid,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)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	3914.8	Semi standard non polar	33892256
Histidylaspartic acid,5TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)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	3546.3	Standard non polar	33892256
Histidylaspartic acid,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=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	3911.3	Semi standard non polar	33892256
Histidylaspartic acid,5TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)[C@H](CC(=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	3533.7	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Histidylaspartic acid 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 - Histidylaspartic acid 10V, Positive-QTOF	splash10-03k9-0980000000-2c1988fe162abd50705f	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylaspartic acid 20V, Positive-QTOF	splash10-03di-5900000000-74ee74164a572dcff684	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylaspartic acid 40V, Positive-QTOF	splash10-03ec-9500000000-6d020f6c09fc7aeb3118	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylaspartic acid 10V, Negative-QTOF	splash10-0uxr-0590000000-c87be6d6e9ff89ada2c6	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylaspartic acid 20V, Negative-QTOF	splash10-000i-9820000000-5d109018e037084c6815	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Histidylaspartic acid 40V, Negative-QTOF	splash10-0006-9100000000-065fe186ea7654949e87	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
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, 1000 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, 200 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, 300 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, 400 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, 500 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, 600 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, 700 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, 800 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, 900 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

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB111910

KNApSAcK ID

Not Available

Chemspider ID

5383051

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

7020094

PDB ID

Not Available

ChEBI ID

73925

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

Pischke MS, Jones LG, Otsuga D, Fernandez DE, Drews GN, Sussman MR: An Arabidopsis histidine kinase is essential for megagametogenesis. Proc Natl Acad Sci U S A. 2002 Nov 26;99(24):15800-5. Epub 2002 Nov 8. [PubMed:12426401 ]

Showing metabocard for Histidylaspartic acid (HMDB0028881)

MOL for HMDB0028881 (Histidylaspartic acid)

3D MOL for HMDB0028881 (Histidylaspartic acid)

3D SDF for HMDB0028881 (Histidylaspartic acid)

3D-SDF for HMDB0028881 (Histidylaspartic acid)

PDB for HMDB0028881 (Histidylaspartic acid)

3D PDB for HMDB0028881 (Histidylaspartic acid)

SMILES for HMDB0028881 (Histidylaspartic acid)

INCHI for HMDB0028881 (Histidylaspartic acid)

Structure for HMDB0028881 (Histidylaspartic acid)

3D Structure for HMDB0028881 (Histidylaspartic acid)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra