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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 21:03:33 UTC

Update Date

2021-09-14 15:19:02 UTC

HMDB ID

HMDB0029066

Secondary Accession Numbers

HMDB29066

Metabolite Identification

Common Name

Threonyllysine

Description

Threonyllysine is a dipeptide composed of threonine and lysine. 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

HMDB0029066
     RDKit          3D
Threonyllysine
 38 37  0  0  0  0  0  0  0  0999 V2000
   -5.4070   -0.7577   -0.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9280   -0.9505    0.0052 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3550   -1.9027   -0.8093 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1828    0.3562    0.0356 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0708    0.9907   -1.2373 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8967    0.2299    0.7464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8498   -0.3110    1.8775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7199    0.7250    0.1392 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5614    0.6017    0.8456 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4903   -0.2488    0.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8167   -0.4395    0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6858   -1.3276   -0.2264 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9006   -0.7091   -1.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5508    0.5765   -1.4236 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1050    1.9539    1.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4507    2.9485    0.6268 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2546    2.2668    1.7568 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7744   -1.6138   -0.8670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0048   -0.7752    0.6825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6224    0.2067   -0.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8618   -1.3627    1.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0038   -2.4233   -1.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8139    1.0436    0.6753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4689    0.4878   -1.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6331    1.9272   -1.0872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7310    1.1760   -0.7955 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3526    0.1107    1.8065 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9671   -1.2284   -0.1600 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6280    0.2712   -0.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3245    0.4976    0.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7222   -0.9979    1.6224 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041   -2.3112   -0.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6863   -1.4242    0.2480 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5472   -1.4144   -2.1737 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9773   -0.6143   -2.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0947    0.8756   -2.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0489    0.6481   -0.5243 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9552    2.9183    1.4417 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
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
  9 15  1  0
 15 16  2  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  1
  3 22  1  0
  4 23  1  1
  5 24  1  0
  5 25  1  0
  8 26  1  0
  9 27  1  1
 10 28  1  0
 10 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 14 37  1  0
 17 38  1  0
M  END


  Mrv1652304062014152D          

 17 16  0  0  0  0            999 V2000
10048.289210048.4602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10049.006310048.8722    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10049.720810048.4602    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10050.435210048.8722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10051.149710048.4602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10050.435210049.6970    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10047.575810048.8722    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10046.860310048.4602    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10046.146910048.8722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10046.860310047.6352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10047.575810049.6970    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10048.289210047.6352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10049.720810047.6352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10050.437010047.2217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10051.869610047.2217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10051.153310047.6352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10052.585710047.6352    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  7  1  0  0  0  0
  1 12  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  7  8  1  0  0  0  0
  7 11  1  6  0  0  0
  8  9  1  0  0  0  0
  3 13  1  6  0  0  0
 13 14  1  0  0  0  0
 16 14  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
  8 10  1  6  0  0  0
M  END
> <DATABASE_ID>
HMDB0029066

> <DATABASE_NAME>
hmdb

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

> <INCHI_IDENTIFIER>
InChI=1S/C10H21N3O4/c1-6(14)8(12)9(15)13-7(10(16)17)4-2-3-5-11/h6-8,14H,2-5,11-12H2,1H3,(H,13,15)(H,16,17)/t6-,7+,8+/m1/s1

> <INCHI_KEY>
YKRQRPFODDJQTC-CSMHCCOUSA-N

> <FORMULA>
C10H21N3O4

> <MOLECULAR_WEIGHT>
247.295

> <EXACT_MASS>
247.153206168

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
25.6929245304723

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-6-amino-2-[(2S,3R)-2-amino-3-hydroxybutanamido]hexanoic acid

> <ALOGPS_LOGP>
-3.34

> <JCHEM_LOGP>
-4.197438573952751

> <ALOGPS_LOGS>
-1.05

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
1

> <JCHEM_PKA>
13.66518731152361

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.7446204183899368

> <JCHEM_PKA_STRONGEST_BASIC>
10.20743327868809

> <JCHEM_POLAR_SURFACE_AREA>
138.67000000000002

> <JCHEM_REFRACTIVITY>
61.06940000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.21e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-6-amino-2-[(2S,3R)-2-amino-3-hydroxybutanamido]hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029066
     RDKit          3D
Threonyllysine
 38 37  0  0  0  0  0  0  0  0999 V2000
   -5.4070   -0.7577   -0.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9280   -0.9505    0.0052 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3550   -1.9027   -0.8093 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1828    0.3562    0.0356 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0708    0.9907   -1.2373 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8967    0.2299    0.7464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8498   -0.3110    1.8775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7199    0.7250    0.1392 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5614    0.6017    0.8456 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4903   -0.2488    0.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8167   -0.4395    0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6858   -1.3276   -0.2264 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9006   -0.7091   -1.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5508    0.5765   -1.4236 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1050    1.9539    1.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4507    2.9485    0.6268 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2546    2.2668    1.7568 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7744   -1.6138   -0.8670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0048   -0.7752    0.6825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6224    0.2067   -0.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8618   -1.3627    1.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0038   -2.4233   -1.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8139    1.0436    0.6753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4689    0.4878   -1.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6331    1.9272   -1.0872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7310    1.1760   -0.7955 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3526    0.1107    1.8065 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9671   -1.2284   -0.1600 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6280    0.2712   -0.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3245    0.4976    0.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7222   -0.9979    1.6224 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041   -2.3112   -0.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6863   -1.4242    0.2480 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5472   -1.4144   -2.1737 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9773   -0.6143   -2.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0947    0.8756   -2.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0489    0.6481   -0.5243 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9552    2.9183    1.4417 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
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
  9 15  1  0
 15 16  2  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  1
  3 22  1  0
  4 23  1  1
  5 24  1  0
  5 25  1  0
  8 26  1  0
  9 27  1  1
 10 28  1  0
 10 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 14 37  1  0
 17 38  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    8756.8078757.126   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0    8758.1458757.895   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0    8759.4798757.126   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8760.8128757.895   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0    8762.1468757.126   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0    8760.8128759.434   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0    8755.4758757.895   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8754.1398757.126   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8752.8088757.895   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0    8754.1398755.586   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0    8755.4758759.434   0.000  0.00  0.00           N+0
HETATM   12  O   UNK     0    8756.8078755.586   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0    8759.4798755.586   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8760.8168754.814   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8763.4908754.814   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8762.1538755.586   0.000  0.00  0.00           C+0
HETATM   17  N   UNK     0    8764.8278755.586   0.000  0.00  0.00           N+0
CONECT    1    2    7   12                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4                                                            
CONECT    7    1    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7                                                            
CONECT   12    1                                                            
CONECT   13    3   14                                                       
CONECT   14   13   16                                                       
CONECT   15   16   17                                                       
CONECT   16   14   15                                                       
CONECT   17   15                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   32    0
END

COMPND    HMDB0029066
HETATM    1  C1  UNL     1      -5.407  -0.758  -0.264  1.00  0.00           C  
HETATM    2  C2  UNL     1      -3.928  -0.951   0.005  1.00  0.00           C  
HETATM    3  O1  UNL     1      -3.355  -1.903  -0.809  1.00  0.00           O  
HETATM    4  C3  UNL     1      -3.183   0.356   0.036  1.00  0.00           C  
HETATM    5  N1  UNL     1      -3.071   0.991  -1.237  1.00  0.00           N  
HETATM    6  C4  UNL     1      -1.897   0.230   0.746  1.00  0.00           C  
HETATM    7  O2  UNL     1      -1.850  -0.311   1.878  1.00  0.00           O  
HETATM    8  N2  UNL     1      -0.720   0.725   0.139  1.00  0.00           N  
HETATM    9  C5  UNL     1       0.561   0.602   0.846  1.00  0.00           C  
HETATM   10  C6  UNL     1       1.490  -0.249   0.012  1.00  0.00           C  
HETATM   11  C7  UNL     1       2.817  -0.439   0.658  1.00  0.00           C  
HETATM   12  C8  UNL     1       3.686  -1.328  -0.226  1.00  0.00           C  
HETATM   13  C9  UNL     1       3.901  -0.709  -1.586  1.00  0.00           C  
HETATM   14  N3  UNL     1       4.551   0.577  -1.424  1.00  0.00           N  
HETATM   15  C10 UNL     1       1.105   1.954   1.084  1.00  0.00           C  
HETATM   16  O3  UNL     1       0.451   2.949   0.627  1.00  0.00           O  
HETATM   17  O4  UNL     1       2.255   2.267   1.757  1.00  0.00           O  
HETATM   18  H1  UNL     1      -5.774  -1.614  -0.867  1.00  0.00           H  
HETATM   19  H2  UNL     1      -6.005  -0.775   0.683  1.00  0.00           H  
HETATM   20  H3  UNL     1      -5.622   0.207  -0.755  1.00  0.00           H  
HETATM   21  H4  UNL     1      -3.862  -1.363   1.057  1.00  0.00           H  
HETATM   22  H5  UNL     1      -4.004  -2.423  -1.339  1.00  0.00           H  
HETATM   23  H6  UNL     1      -3.814   1.044   0.675  1.00  0.00           H  
HETATM   24  H7  UNL     1      -2.469   0.488  -1.916  1.00  0.00           H  
HETATM   25  H8  UNL     1      -2.633   1.927  -1.087  1.00  0.00           H  
HETATM   26  H9  UNL     1      -0.731   1.176  -0.796  1.00  0.00           H  
HETATM   27  H10 UNL     1       0.353   0.111   1.806  1.00  0.00           H  
HETATM   28  H11 UNL     1       0.967  -1.228  -0.160  1.00  0.00           H  
HETATM   29  H12 UNL     1       1.628   0.271  -0.980  1.00  0.00           H  
HETATM   30  H13 UNL     1       3.325   0.498   0.887  1.00  0.00           H  
HETATM   31  H14 UNL     1       2.722  -0.998   1.622  1.00  0.00           H  
HETATM   32  H15 UNL     1       3.204  -2.311  -0.282  1.00  0.00           H  
HETATM   33  H16 UNL     1       4.686  -1.424   0.248  1.00  0.00           H  
HETATM   34  H17 UNL     1       4.547  -1.414  -2.174  1.00  0.00           H  
HETATM   35  H18 UNL     1       2.977  -0.614  -2.185  1.00  0.00           H  
HETATM   36  H19 UNL     1       5.095   0.876  -2.249  1.00  0.00           H  
HETATM   37  H20 UNL     1       5.049   0.648  -0.524  1.00  0.00           H  
HETATM   38  H21 UNL     1       2.955   2.918   1.442  1.00  0.00           H  
CONECT    1    2   18   19   20
CONECT    2    3    4   21
CONECT    3   22
CONECT    4    5    6   23
CONECT    5   24   25
CONECT    6    7    7    8
CONECT    8    9   26
CONECT    9   10   15   27
CONECT   10   11   28   29
CONECT   11   12   30   31
CONECT   12   13   32   33
CONECT   13   14   34   35
CONECT   14   36   37
CONECT   15   16   16   17
CONECT   17   38
END

HMDB0029066
     RDKit          3D
Threonyllysine
 38 37  0  0  0  0  0  0  0  0999 V2000
   -5.4070   -0.7577   -0.2637 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9280   -0.9505    0.0052 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3550   -1.9027   -0.8093 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1828    0.3562    0.0356 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0708    0.9907   -1.2373 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8967    0.2299    0.7464 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8498   -0.3110    1.8775 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7199    0.7250    0.1392 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5614    0.6017    0.8456 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4903   -0.2488    0.0118 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8167   -0.4395    0.6577 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6858   -1.3276   -0.2264 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9006   -0.7091   -1.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5508    0.5765   -1.4236 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1050    1.9539    1.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4507    2.9485    0.6268 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2546    2.2668    1.7568 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7744   -1.6138   -0.8670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0048   -0.7752    0.6825 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6224    0.2067   -0.7548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8618   -1.3627    1.0570 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0038   -2.4233   -1.3388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8139    1.0436    0.6753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4689    0.4878   -1.9159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6331    1.9272   -1.0872 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7310    1.1760   -0.7955 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3526    0.1107    1.8065 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9671   -1.2284   -0.1600 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6280    0.2712   -0.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3245    0.4976    0.8871 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7222   -0.9979    1.6224 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2041   -2.3112   -0.2818 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6863   -1.4242    0.2480 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5472   -1.4144   -2.1737 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9773   -0.6143   -2.1855 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0947    0.8756   -2.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0489    0.6481   -0.5243 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9552    2.9183    1.4417 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
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
  9 15  1  0
 15 16  2  0
 15 17  1  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  1
  3 22  1  0
  4 23  1  1
  5 24  1  0
  5 25  1  0
  8 26  1  0
  9 27  1  1
 10 28  1  0
 10 29  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 12 33  1  0
 13 34  1  0
 13 35  1  0
 14 36  1  0
 14 37  1  0
 17 38  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
(2S)-6-Amino-2-[[(2S,3R)-2-amino-3-hydroxybutanoyl]amino]hexanoic acid	ChEBI
H-THR-Lys-OH	ChEBI
L-THR-L-Lys	ChEBI
T-K	ChEBI
T-K Dipeptide	ChEBI
TK	ChEBI
TK Dipeptide	ChEBI
(2S)-6-Amino-2-[[(2S,3R)-2-amino-3-hydroxybutanoyl]amino]hexanoate	Generator
L-Threoninyl-L-lysine	HMDB
L-Threonyl-L-lysine	HMDB
N2-L-Threoninyl-L-lysine	HMDB
N2-L-Threonyl-L-lysine	HMDB
N2-Threoninyllysine	HMDB
N2-Threonyllysine	HMDB
THR-Lys	HMDB
Threonine lysine dipeptide	HMDB
Threonine-lysine dipeptide	HMDB
Threoninyl-lysine	HMDB
Threoninyllysine	HMDB
Threonyl-lysine	HMDB
Threonyllysine	HMDB

Chemical Formula

C₁₀H₂₁N₃O₄

Average Molecular Weight

247.295

Monoisotopic Molecular Weight

247.153206168

IUPAC Name

(2S)-6-amino-2-[(2S,3R)-2-amino-3-hydroxybutanamido]hexanoic acid

Traditional Name

(2S)-6-amino-2-[(2S,3R)-2-amino-3-hydroxybutanamido]hexanoic acid

CAS Registry Number

23161-31-1

SMILES

C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN)C(O)=O

InChI Identifier

InChI=1S/C10H21N3O4/c1-6(14)8(12)9(15)13-7(10(16)17)4-2-3-5-11/h6-8,14H,2-5,11-12H2,1H3,(H,13,15)(H,16,17)/t6-,7+,8+/m1/s1

InChI Key

YKRQRPFODDJQTC-CSMHCCOUSA-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
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
Medium-chain fatty acid
Amino fatty acid
Hydroxy fatty acid
Fatty amide
N-acyl-amine
Fatty acyl
Fatty acid
Secondary carboxylic acid amide
Secondary alcohol
Amino acid or derivatives
Carboxamide group
Amino acid
Carboxylic acid
Monocarboxylic acid or derivatives
Alcohol
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organic nitrogen compound
Amine
Primary amine
Organonitrogen compound
Primary aliphatic amine
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Endogenous (HMDB: HMDB0029066)

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	-4.26	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	22.1 g/L	ALOGPS
logP	-3.3	ALOGPS
logP	-4.2	ChemAxon
logS	-1	ALOGPS
pKa (Strongest Acidic)	3.74	ChemAxon
pKa (Strongest Basic)	10.21	ChemAxon
Physiological Charge	1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	138.67 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	61.07 m³·mol⁻¹	ChemAxon
Polarizability	25.69 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	162.255	30932474
DeepCCS	[M-H]-	159.86	30932474
DeepCCS	[M-2H]-	192.744	30932474
DeepCCS	[M+Na]+	168.168	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.	1.37 minutes	32390414
Predicted by Siyang on May 30, 2022	9.6467 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	9.36 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	473.6 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	398.2 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	231.2 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	48.8 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	166.1 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	54.3 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	303.6 seconds	40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid	249.5 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	1004.1 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	574.2 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	44.4 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	596.6 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	167.3 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	227.9 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	935.7 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	752.0 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	431.5 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Threonyllysine	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN)C(O)=O	3355.3	Standard polar	33892256
Threonyllysine	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN)C(O)=O	2232.9	Standard non polar	33892256
Threonyllysine	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN)C(O)=O	2257.8	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Threonyllysine,1TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)O	2213.7	Semi standard non polar	33892256
Threonyllysine,1TMS,isomer #2	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C	2176.0	Semi standard non polar	33892256
Threonyllysine,1TMS,isomer #3	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)O	2234.7	Semi standard non polar	33892256
Threonyllysine,1TMS,isomer #4	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O	2332.1	Semi standard non polar	33892256
Threonyllysine,1TMS,isomer #5	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C	2165.6	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C	2226.6	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C	2225.4	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #11	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2278.4	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #12	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2477.7	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)O	2283.3	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O	2330.2	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C	2210.8	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #5	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C	2239.7	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #6	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C	2311.6	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #7	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2166.3	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #8	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O	2352.1	Semi standard non polar	33892256
Threonyllysine,2TMS,isomer #9	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2365.6	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C	2290.0	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C	2304.6	Standard non polar	33892256
Threonyllysine,3TMS,isomer #10	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2375.8	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #10	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2400.1	Standard non polar	33892256
Threonyllysine,3TMS,isomer #11	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2219.7	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #11	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2328.9	Standard non polar	33892256
Threonyllysine,3TMS,isomer #12	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2265.1	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #12	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2399.2	Standard non polar	33892256
Threonyllysine,3TMS,isomer #13	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2470.3	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #13	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2390.9	Standard non polar	33892256
Threonyllysine,3TMS,isomer #14	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2483.4	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #14	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2469.7	Standard non polar	33892256
Threonyllysine,3TMS,isomer #15	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2320.7	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #15	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2416.4	Standard non polar	33892256
Threonyllysine,3TMS,isomer #16	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2486.4	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #16	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2449.3	Standard non polar	33892256
Threonyllysine,3TMS,isomer #17	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2359.0	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #17	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2408.3	Standard non polar	33892256
Threonyllysine,3TMS,isomer #18	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2433.5	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #18	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2462.0	Standard non polar	33892256
Threonyllysine,3TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C	2353.0	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C	2337.1	Standard non polar	33892256
Threonyllysine,3TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2229.6	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2305.0	Standard non polar	33892256
Threonyllysine,3TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O	2377.5	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O	2406.6	Standard non polar	33892256
Threonyllysine,3TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2422.5	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2388.1	Standard non polar	33892256
Threonyllysine,3TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C	2255.9	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C	2331.4	Standard non polar	33892256
Threonyllysine,3TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2304.7	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2407.4	Standard non polar	33892256
Threonyllysine,3TMS,isomer #8	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2480.8	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #8	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2426.2	Standard non polar	33892256
Threonyllysine,3TMS,isomer #9	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C	2356.4	Semi standard non polar	33892256
Threonyllysine,3TMS,isomer #9	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C	2383.0	Standard non polar	33892256
Threonyllysine,4TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C	2382.6	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C	2428.1	Standard non polar	33892256
Threonyllysine,4TMS,isomer #10	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2469.7	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #10	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2511.4	Standard non polar	33892256
Threonyllysine,4TMS,isomer #11	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2438.4	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #11	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2512.0	Standard non polar	33892256
Threonyllysine,4TMS,isomer #12	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2294.6	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #12	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2449.3	Standard non polar	33892256
Threonyllysine,4TMS,isomer #13	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2485.4	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #13	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2467.5	Standard non polar	33892256
Threonyllysine,4TMS,isomer #14	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2398.7	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #14	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2478.5	Standard non polar	33892256
Threonyllysine,4TMS,isomer #15	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2440.8	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #15	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2512.8	Standard non polar	33892256
Threonyllysine,4TMS,isomer #16	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2418.1	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #16	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2548.6	Standard non polar	33892256
Threonyllysine,4TMS,isomer #17	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2646.2	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #17	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2569.8	Standard non polar	33892256
Threonyllysine,4TMS,isomer #18	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2465.9	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #18	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2500.1	Standard non polar	33892256
Threonyllysine,4TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2410.0	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2428.4	Standard non polar	33892256
Threonyllysine,4TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2252.4	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2369.3	Standard non polar	33892256
Threonyllysine,4TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2296.8	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2454.1	Standard non polar	33892256
Threonyllysine,4TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2495.2	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2451.4	Standard non polar	33892256
Threonyllysine,4TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2494.8	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2509.2	Standard non polar	33892256
Threonyllysine,4TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2334.6	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2461.4	Standard non polar	33892256
Threonyllysine,4TMS,isomer #8	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2504.9	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #8	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O	2486.8	Standard non polar	33892256
Threonyllysine,4TMS,isomer #9	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2431.5	Semi standard non polar	33892256
Threonyllysine,4TMS,isomer #9	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2462.9	Standard non polar	33892256
Threonyllysine,5TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2476.8	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2537.8	Standard non polar	33892256
Threonyllysine,5TMS,isomer #10	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2653.5	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #10	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2598.8	Standard non polar	33892256
Threonyllysine,5TMS,isomer #11	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2474.7	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #11	C[C@@H](O)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2526.6	Standard non polar	33892256
Threonyllysine,5TMS,isomer #12	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2649.5	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #12	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2638.7	Standard non polar	33892256
Threonyllysine,5TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2313.4	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2486.0	Standard non polar	33892256
Threonyllysine,5TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2521.6	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	2503.9	Standard non polar	33892256
Threonyllysine,5TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2463.5	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2509.0	Standard non polar	33892256
Threonyllysine,5TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2501.3	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #5	C[C@@H](O[Si](C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2553.0	Standard non polar	33892256
Threonyllysine,5TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2497.4	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #6	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2576.6	Standard non polar	33892256
Threonyllysine,5TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2690.4	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #7	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	2587.6	Standard non polar	33892256
Threonyllysine,5TMS,isomer #8	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2516.6	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #8	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	2538.9	Standard non polar	33892256
Threonyllysine,5TMS,isomer #9	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2438.4	Semi standard non polar	33892256
Threonyllysine,5TMS,isomer #9	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2579.8	Standard non polar	33892256
Threonyllysine,6TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2527.1	Semi standard non polar	33892256
Threonyllysine,6TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2608.2	Standard non polar	33892256
Threonyllysine,6TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2698.6	Semi standard non polar	33892256
Threonyllysine,6TMS,isomer #2	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2619.7	Standard non polar	33892256
Threonyllysine,6TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2533.6	Semi standard non polar	33892256
Threonyllysine,6TMS,isomer #3	C[C@@H](O[Si](C)(C)C)[C@H](N[Si](C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C	2569.5	Standard non polar	33892256
Threonyllysine,6TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2730.6	Semi standard non polar	33892256
Threonyllysine,6TMS,isomer #4	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2663.4	Standard non polar	33892256
Threonyllysine,6TMS,isomer #5	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2703.6	Semi standard non polar	33892256
Threonyllysine,6TMS,isomer #5	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2666.4	Standard non polar	33892256
Threonyllysine,7TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2772.1	Semi standard non polar	33892256
Threonyllysine,7TMS,isomer #1	C[C@@H](O[Si](C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	2700.0	Standard non polar	33892256
Threonyllysine,1TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)O	2455.7	Semi standard non polar	33892256
Threonyllysine,1TBDMS,isomer #2	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C	2446.1	Semi standard non polar	33892256
Threonyllysine,1TBDMS,isomer #3	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)O	2470.9	Semi standard non polar	33892256
Threonyllysine,1TBDMS,isomer #4	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O	2564.7	Semi standard non polar	33892256
Threonyllysine,1TBDMS,isomer #5	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C(C)(C)C	2419.6	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C	2705.7	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #10	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C(C)(C)C	2694.2	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #11	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2751.1	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #12	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2921.1	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)O	2715.7	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O	2799.9	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C(C)(C)C	2690.8	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #5	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C	2714.9	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #6	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2775.4	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #7	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2656.8	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #8	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O	2817.3	Semi standard non polar	33892256
Threonyllysine,2TBDMS,isomer #9	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2822.1	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C	2944.4	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C	2846.8	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #10	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3073.6	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #10	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2904.2	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #11	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2916.5	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #11	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2879.1	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #12	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2965.0	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #12	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2952.1	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #13	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3153.3	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #13	C[C@@H](O)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2936.3	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #14	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3179.6	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #14	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2961.8	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #15	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3014.0	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #15	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2913.9	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #16	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3168.4	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #16	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2960.3	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #17	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3033.5	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #17	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2926.7	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #18	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3085.2	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #18	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2984.5	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3007.8	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2897.6	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2932.7	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2870.8	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O	3050.1	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O	2920.0	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3099.8	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	2891.5	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C(C)(C)C	2950.5	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C(C)(C)C	2862.9	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2999.3	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	2939.1	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #8	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3176.9	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #8	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	2957.7	Standard non polar	33892256
Threonyllysine,3TBDMS,isomer #9	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3023.6	Semi standard non polar	33892256
Threonyllysine,3TBDMS,isomer #9	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	2906.2	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3236.1	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3071.0	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #10	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3335.5	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #10	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3171.1	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #11	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3395.3	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #11	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3147.4	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #12	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3198.2	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #12	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3097.5	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #13	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3386.9	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #13	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3133.9	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #14	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3262.5	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #14	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3148.3	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #15	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3313.6	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #15	C[C@@H](O)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3199.6	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #16	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3356.2	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #16	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3176.1	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #17	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3523.9	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #17	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3203.1	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #18	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3336.5	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #18	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3153.1	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3332.8	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3073.5	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3159.6	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3064.4	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3194.6	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3132.8	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3394.0	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3132.0	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3438.9	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3128.2	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3241.5	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3091.5	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #8	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3403.8	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #8	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3138.2	Standard non polar	33892256
Threonyllysine,4TBDMS,isomer #9	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3304.3	Semi standard non polar	33892256
Threonyllysine,4TBDMS,isomer #9	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3118.3	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3616.2	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #1	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3289.1	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #10	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3732.2	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #10	C[C@@H](O)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3372.2	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #11	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3551.5	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #11	C[C@@H](O)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3326.7	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #12	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3676.6	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #12	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3412.1	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3398.0	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #2	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3259.6	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3615.9	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #3	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3286.9	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3541.3	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #4	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3307.5	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3576.0	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #5	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3355.2	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3615.7	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #6	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3336.4	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3778.9	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #7	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](C(=O)N[C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3345.4	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #8	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3578.8	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #8	C[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N([C@@H](CCCCN([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C	3313.2	Standard non polar	33892256
Threonyllysine,5TBDMS,isomer #9	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3569.8	Semi standard non polar	33892256
Threonyllysine,5TBDMS,isomer #9	C[C@@H](O)[C@@H](C(=O)N([C@@H](CCCCN[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3363.0	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Threonyllysine GC-MS (TBDMS_2_10) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Threonyllysine GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Threonyllysine GC-MS ("Threonyllysine,2TBDMS,#10" TMS) - 70eV, Positive	Not Available	2021-10-14	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 - Threonyllysine 10V, Positive-QTOF	splash10-000t-2960000000-5a3ed781be9628b848e0	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonyllysine 20V, Positive-QTOF	splash10-001i-8900000000-c63b8ee206d35c4fe9a9	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonyllysine 40V, Positive-QTOF	splash10-0pc0-9400000000-1b09d7382d00954a84ea	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonyllysine 10V, Negative-QTOF	splash10-0002-0390000000-eb2443aa02982d8b42bd	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonyllysine 20V, Negative-QTOF	splash10-0002-0900000000-cbc5a0583e2c04daceae	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Threonyllysine 40V, Negative-QTOF	splash10-0006-9600000000-83002c4755b1e638f4fa	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

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

FDB112072

KNApSAcK ID

Not Available

Chemspider ID

8507670

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10332210

PDB ID

Not Available

ChEBI ID

157893

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

Gorbalenya AE, Donchenko AP, Blinov VM, Koonin EV: Cysteine proteases of positive strand RNA viruses and chymotrypsin-like serine proteases. A distinct protein superfamily with a common structural fold. FEBS Lett. 1989 Jan 30;243(2):103-14. [PubMed:2645167 ]

Showing metabocard for Threonyllysine (HMDB0029066)

MOL for HMDB0029066 (Threonyllysine)

3D MOL for HMDB0029066 (Threonyllysine)

3D SDF for HMDB0029066 (Threonyllysine)

3D-SDF for HMDB0029066 (Threonyllysine)

PDB for HMDB0029066 (Threonyllysine)

3D PDB for HMDB0029066 (Threonyllysine)

SMILES for HMDB0029066 (Threonyllysine)

INCHI for HMDB0029066 (Threonyllysine)

Structure for HMDB0029066 (Threonyllysine)

3D Structure for HMDB0029066 (Threonyllysine)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra