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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-06 21:03:41 UTC

Update Date

2021-09-14 15:29:57 UTC

HMDB ID

HMDB0029097

Secondary Accession Numbers

HMDB29097

Metabolite Identification

Common Name

Tryptophyl-Gamma-glutamate

Description

Tryptophyl-Gamma-glutamate is a dipeptide composed of tryptophan and gamma-glutamate. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an 'Expected' metabolite.

Structure

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

HMDB0029097
     RDKit          3D
Tryptophyl-Gamma-glutamate
 44 45  0  0  0  0  0  0  0  0999 V2000
   -5.5327    1.9848   -0.4064 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4718    1.0187   -0.7317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3971    1.2000    0.2908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1974    0.3184    0.1724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4321    0.4994   -1.0688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9319    1.3634   -1.8815 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2611   -0.1369   -1.4668 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5430   -1.0670   -0.8015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5403   -1.5420   -1.4860 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3758   -1.5511    0.5714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0551   -2.8726    0.6505 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0919   -0.6485    1.5696 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5476   -0.5649    1.3347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4952   -1.3609    1.9759 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6989   -1.0424    1.4884 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5748   -0.0720    0.5574 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4761    0.6148   -0.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0630    1.5942   -1.1140 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7263    1.9175   -1.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8269    1.2285   -0.4408 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2201    0.2436    0.4471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1023   -0.3269   -0.7038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4526   -1.3786   -1.0011 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4144   -0.4683   -0.3530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4304    1.5311   -0.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2429    2.6702    0.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1264    1.2178   -1.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1226    2.2894    0.2837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8635    1.0509    1.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5824    0.4587    1.0781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5960   -0.7449    0.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0926    0.1234   -2.4671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6607   -1.7453    0.8153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6741   -3.4441    1.4112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -3.3680   -0.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9064   -1.1332    2.5733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6319    0.3512    1.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2375   -2.0891    2.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6205   -1.4769    1.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5253    0.3501   -0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7768    2.1346   -1.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3985    2.6939   -1.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7723    1.4699   -0.4991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9707   -1.2906   -0.4800 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  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
  2 22  1  0
 22 23  2  0
 22 24  1  0
 21 13  1  0
 21 16  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  7 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 14 38  1  0
 15 39  1  0
 17 40  1  0
 18 41  1  0
 19 42  1  0
 20 43  1  0
 24 44  1  0
M  END


  Mrv1652304062014202D          

 24 25  0  0  0  0            999 V2000
    3.5812    0.8570    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5812    0.0320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8668   -0.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1523    0.0320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4378   -0.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4378   -1.2055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7233    0.0320    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0089   -0.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0089   -1.2055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7056    0.0320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7056    0.8570    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4201   -0.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1345    0.0320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2208    0.8525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0277    1.0240    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4402    0.3095    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8882   -0.3036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1432   -1.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9501   -1.2597    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5022   -0.6466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2472    0.1380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2957   -0.3805    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0102    0.0320    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2957   -1.2055    0.0000 O   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 13 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0029097

> <DATABASE_NAME>
hmdb

> <SMILES>
NC(CCC(=O)NC(=O)C(N)CC1=CNC2=C1C=CC=C2)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H20N4O4/c17-11(16(23)24)5-6-14(21)20-15(22)12(18)7-9-8-19-13-4-2-1-3-10(9)13/h1-4,8,11-12,19H,5-7,17-18H2,(H,23,24)(H,20,21,22)

> <INCHI_KEY>
FNGTUNXVLUYBPN-UHFFFAOYSA-N

> <FORMULA>
C16H20N4O4

> <MOLECULAR_WEIGHT>
332.3544

> <EXACT_MASS>
332.148455148

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
34.06494416078731

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-amino-5-[2-amino-3-(1H-indol-3-yl)propanamido]-5-oxopentanoic acid

> <ALOGPS_LOGP>
-1.29

> <JCHEM_LOGP>
-2.635761367037638

> <ALOGPS_LOGS>
-2.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.621897093313363

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.9691943870451345

> <JCHEM_PKA_STRONGEST_BASIC>
9.409674702973675

> <JCHEM_POLAR_SURFACE_AREA>
151.29999999999998

> <JCHEM_REFRACTIVITY>
86.2349

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.69e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-amino-5-[2-amino-3-(1H-indol-3-yl)propanamido]-5-oxopentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0029097
     RDKit          3D
Tryptophyl-Gamma-glutamate
 44 45  0  0  0  0  0  0  0  0999 V2000
   -5.5327    1.9848   -0.4064 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4718    1.0187   -0.7317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3971    1.2000    0.2908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1974    0.3184    0.1724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4321    0.4994   -1.0688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9319    1.3634   -1.8815 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2611   -0.1369   -1.4668 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5430   -1.0670   -0.8015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5403   -1.5420   -1.4860 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3758   -1.5511    0.5714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0551   -2.8726    0.6505 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0919   -0.6485    1.5696 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5476   -0.5649    1.3347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4952   -1.3609    1.9759 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6989   -1.0424    1.4884 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5748   -0.0720    0.5574 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4761    0.6148   -0.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0630    1.5942   -1.1140 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7263    1.9175   -1.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8269    1.2285   -0.4408 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2201    0.2436    0.4471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1023   -0.3269   -0.7038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4526   -1.3786   -1.0011 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4144   -0.4683   -0.3530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4304    1.5311   -0.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2429    2.6702    0.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1264    1.2178   -1.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1226    2.2894    0.2837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8635    1.0509    1.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5824    0.4587    1.0781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5960   -0.7449    0.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0926    0.1234   -2.4671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6607   -1.7453    0.8153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6741   -3.4441    1.4112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -3.3680   -0.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9064   -1.1332    2.5733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6319    0.3512    1.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2375   -2.0891    2.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6205   -1.4769    1.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5253    0.3501   -0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7768    2.1346   -1.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3985    2.6939   -1.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7723    1.4699   -0.4991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9707   -1.2906   -0.4800 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  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
  2 22  1  0
 22 23  2  0
 22 24  1  0
 21 13  1  0
 21 16  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  7 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 14 38  1  0
 15 39  1  0
 17 40  1  0
 18 41  1  0
 19 42  1  0
 20 43  1  0
 24 44  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  N   UNK     0       6.685   1.600   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       6.685   0.060   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.351  -0.710   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.018   0.060   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.684  -0.710   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       2.684  -2.250   0.000  0.00  0.00           O+0
HETATM    7  N   UNK     0       1.350   0.060   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0       0.017  -0.710   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.017  -2.250   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.317   0.060   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0      -1.317   1.600   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -2.651  -0.710   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.984   0.060   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.145   1.591   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      -5.652   1.911   0.000  0.00  0.00           N+0
HETATM   16  C   UNK     0      -6.422   0.578   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.391  -0.567   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.867  -2.031   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -7.374  -2.351   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -8.404  -1.207   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -7.928   0.258   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.019  -0.710   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.352   0.060   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       8.019  -2.250   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   22                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   21                                                  
CONECT   17   16   13   18                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22    2   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

COMPND    HMDB0029097
HETATM    1  N1  UNL     1      -5.533   1.985  -0.406  1.00  0.00           N  
HETATM    2  C1  UNL     1      -4.472   1.019  -0.732  1.00  0.00           C  
HETATM    3  C2  UNL     1      -3.397   1.200   0.291  1.00  0.00           C  
HETATM    4  C3  UNL     1      -2.197   0.318   0.172  1.00  0.00           C  
HETATM    5  C4  UNL     1      -1.432   0.499  -1.069  1.00  0.00           C  
HETATM    6  O1  UNL     1      -1.932   1.363  -1.882  1.00  0.00           O  
HETATM    7  N2  UNL     1      -0.261  -0.137  -1.467  1.00  0.00           N  
HETATM    8  C5  UNL     1       0.543  -1.067  -0.802  1.00  0.00           C  
HETATM    9  O2  UNL     1       1.540  -1.542  -1.486  1.00  0.00           O  
HETATM   10  C6  UNL     1       0.376  -1.551   0.571  1.00  0.00           C  
HETATM   11  N3  UNL     1       1.055  -2.873   0.651  1.00  0.00           N  
HETATM   12  C7  UNL     1       1.092  -0.649   1.570  1.00  0.00           C  
HETATM   13  C8  UNL     1       2.548  -0.565   1.335  1.00  0.00           C  
HETATM   14  C9  UNL     1       3.495  -1.361   1.976  1.00  0.00           C  
HETATM   15  N4  UNL     1       4.699  -1.042   1.488  1.00  0.00           N  
HETATM   16  C10 UNL     1       4.575  -0.072   0.557  1.00  0.00           C  
HETATM   17  C11 UNL     1       5.476   0.615  -0.232  1.00  0.00           C  
HETATM   18  C12 UNL     1       5.063   1.594  -1.114  1.00  0.00           C  
HETATM   19  C13 UNL     1       3.726   1.917  -1.232  1.00  0.00           C  
HETATM   20  C14 UNL     1       2.827   1.228  -0.441  1.00  0.00           C  
HETATM   21  C15 UNL     1       3.220   0.244   0.447  1.00  0.00           C  
HETATM   22  C16 UNL     1      -5.102  -0.327  -0.704  1.00  0.00           C  
HETATM   23  O3  UNL     1      -4.453  -1.379  -1.001  1.00  0.00           O  
HETATM   24  O4  UNL     1      -6.414  -0.468  -0.353  1.00  0.00           O  
HETATM   25  H1  UNL     1      -6.430   1.531  -0.206  1.00  0.00           H  
HETATM   26  H2  UNL     1      -5.243   2.670   0.299  1.00  0.00           H  
HETATM   27  H3  UNL     1      -4.126   1.218  -1.756  1.00  0.00           H  
HETATM   28  H4  UNL     1      -3.123   2.289   0.284  1.00  0.00           H  
HETATM   29  H5  UNL     1      -3.863   1.051   1.300  1.00  0.00           H  
HETATM   30  H6  UNL     1      -1.582   0.459   1.078  1.00  0.00           H  
HETATM   31  H7  UNL     1      -2.596  -0.745   0.203  1.00  0.00           H  
HETATM   32  H8  UNL     1       0.093   0.123  -2.467  1.00  0.00           H  
HETATM   33  H9  UNL     1      -0.661  -1.745   0.815  1.00  0.00           H  
HETATM   34  H10 UNL     1       0.674  -3.444   1.411  1.00  0.00           H  
HETATM   35  H11 UNL     1       0.918  -3.368  -0.273  1.00  0.00           H  
HETATM   36  H12 UNL     1       0.906  -1.133   2.573  1.00  0.00           H  
HETATM   37  H13 UNL     1       0.632   0.351   1.650  1.00  0.00           H  
HETATM   38  H14 UNL     1       3.237  -2.089   2.727  1.00  0.00           H  
HETATM   39  H15 UNL     1       5.621  -1.477   1.779  1.00  0.00           H  
HETATM   40  H16 UNL     1       6.525   0.350  -0.129  1.00  0.00           H  
HETATM   41  H17 UNL     1       5.777   2.135  -1.736  1.00  0.00           H  
HETATM   42  H18 UNL     1       3.399   2.694  -1.930  1.00  0.00           H  
HETATM   43  H19 UNL     1       1.772   1.470  -0.499  1.00  0.00           H  
HETATM   44  H20 UNL     1      -6.971  -1.291  -0.480  1.00  0.00           H  
CONECT    1    2   25   26
CONECT    2    3   22   27
CONECT    3    4   28   29
CONECT    4    5   30   31
CONECT    5    6    6    7
CONECT    7    8   32
CONECT    8    9    9   10
CONECT   10   11   12   33
CONECT   11   34   35
CONECT   12   13   36   37
CONECT   13   14   14   21
CONECT   14   15   38
CONECT   15   16   39
CONECT   16   17   17   21
CONECT   17   18   40
CONECT   18   19   19   41
CONECT   19   20   42
CONECT   20   21   21   43
CONECT   22   23   23   24
CONECT   24   44
END

HMDB0029097
     RDKit          3D
Tryptophyl-Gamma-glutamate
 44 45  0  0  0  0  0  0  0  0999 V2000
   -5.5327    1.9848   -0.4064 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4718    1.0187   -0.7317 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3971    1.2000    0.2908 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1974    0.3184    0.1724 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4321    0.4994   -1.0688 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9319    1.3634   -1.8815 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2611   -0.1369   -1.4668 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5430   -1.0670   -0.8015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5403   -1.5420   -1.4860 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3758   -1.5511    0.5714 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0551   -2.8726    0.6505 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0919   -0.6485    1.5696 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5476   -0.5649    1.3347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4952   -1.3609    1.9759 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6989   -1.0424    1.4884 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.5748   -0.0720    0.5574 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4761    0.6148   -0.2323 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0630    1.5942   -1.1140 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7263    1.9175   -1.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8269    1.2285   -0.4408 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2201    0.2436    0.4471 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1023   -0.3269   -0.7038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4526   -1.3786   -1.0011 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4144   -0.4683   -0.3530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4304    1.5311   -0.2064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2429    2.6702    0.2987 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1264    1.2178   -1.7564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1226    2.2894    0.2837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8635    1.0509    1.2998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5824    0.4587    1.0781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5960   -0.7449    0.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0926    0.1234   -2.4671 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6607   -1.7453    0.8153 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6741   -3.4441    1.4112 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9177   -3.3680   -0.2731 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9064   -1.1332    2.5733 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6319    0.3512    1.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2375   -2.0891    2.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6205   -1.4769    1.7786 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5253    0.3501   -0.1290 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7768    2.1346   -1.7363 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3985    2.6939   -1.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7723    1.4699   -0.4991 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9707   -1.2906   -0.4800 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  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
  2 22  1  0
 22 23  2  0
 22 24  1  0
 21 13  1  0
 21 16  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  7 32  1  0
 10 33  1  0
 11 34  1  0
 11 35  1  0
 12 36  1  0
 12 37  1  0
 14 38  1  0
 15 39  1  0
 17 40  1  0
 18 41  1  0
 19 42  1  0
 20 43  1  0
 24 44  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Tryptophyl-g-glutamate	Generator
Tryptophyl-g-glutamic acid	Generator
Tryptophyl-gamma-glutamic acid	Generator
Tryptophyl-γ-glutamate	Generator
Tryptophyl-γ-glutamic acid	Generator
L-Tryptophyl-L-gamma-glutamate	HMDB
TRP-GGlu	HMDB
Tryptophan gamma-glutamate dipeptide	HMDB
Tryptophan-gamma-glutamate dipeptide	HMDB
Tryptophylgamma-glutamate	HMDB
W-GE dipeptide	HMDB
WGE dipeptide	HMDB
2-Amino-4-{[2-amino-3-(1H-indol-3-yl)propanoyl]-C-hydroxycarbonimidoyl}butanoate	HMDB

Chemical Formula

C₁₆H₂₀N₄O₄

Average Molecular Weight

332.3544

Monoisotopic Molecular Weight

332.148455148

IUPAC Name

2-amino-5-[2-amino-3-(1H-indol-3-yl)propanamido]-5-oxopentanoic acid

Traditional Name

2-amino-5-[2-amino-3-(1H-indol-3-yl)propanamido]-5-oxopentanoic acid

CAS Registry Number

Not Available

SMILES

NC(CCC(=O)NC(=O)C(N)CC1=CNC2=C1C=CC=C2)C(O)=O

InChI Identifier

InChI=1S/C16H20N4O4/c17-11(16(23)24)5-6-14(21)20-15(22)12(18)7-9-8-19-13-4-2-1-3-10(9)13/h1-4,8,11-12,19H,5-7,17-18H2,(H,23,24)(H,20,21,22)

InChI Key

FNGTUNXVLUYBPN-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glutamine and derivatives. Glutamine and derivatives are compounds containing glutamine or a derivative thereof resulting from reaction of glutamine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Glutamine and derivatives

Alternative Parents

Substituents

Glutamine or derivatives
Alpha-amino acid amide
Triptan
Alpha-amino acid
3-alkylindole
Indole
Indole or derivatives
Aralkylamine
N-acyl-amine
Benzenoid
Substituted pyrrole
Heteroaromatic compound
Pyrrole
Carboxylic acid imide, n-unsubstituted
Carboxylic acid imide
Dicarboximide
Amino acid
Carboxylic acid
Azacycle
Monocarboxylic acid or derivatives
Organoheterocyclic compound
Amine
Primary aliphatic amine
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organic nitrogen compound
Organopnictogen compound
Carbonyl group
Primary amine
Organonitrogen compound
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Endogenous (HMDB: HMDB0029097)

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	-2.74	Extrapolated

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.57 g/L	ALOGPS
logP	-1.3	ALOGPS
logP	-2.6	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	1.97	ChemAxon
pKa (Strongest Basic)	9.41	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	151.3 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	86.23 m³·mol⁻¹	ChemAxon
Polarizability	34.06 Å³	ChemAxon
Number of Rings	2	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
DarkChem	[M+H]+	178.679	31661259
DarkChem	[M-H]-	172.728	31661259
DeepCCS	[M+H]+	176.774	30932474
DeepCCS	[M-H]-	174.416	30932474
DeepCCS	[M-2H]-	207.302	30932474
DeepCCS	[M+Na]+	182.867	30932474
AllCCS	[M+H]+	176.4	32859911
AllCCS	[M+H-H2O]+	173.6	32859911
AllCCS	[M+NH4]+	179.0	32859911
AllCCS	[M+Na]+	179.8	32859911
AllCCS	[M-H]-	178.1	32859911
AllCCS	[M+Na-2H]-	178.3	32859911
AllCCS	[M+HCOO]-	178.5	32859911

Predicted Retention Times

Underivatized

Chromatographic Method	Retention Time	Reference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.	2.71 minutes	32390414
Predicted by Siyang on May 30, 2022	9.936 minutes	33406817
Predicted by Siyang using ReTip algorithm on June 8, 2022	8.74 minutes	32390414
AjsUoB = Accucore 150 Amide HILIC with 10mM Ammonium Formate, 0.1% Formic Acid	324.8 seconds	40023050
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid	716.2 seconds	40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid	205.4 seconds	40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid	95.5 seconds	40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid	168.5 seconds	40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	96.7 seconds	40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid	287.1 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	290.1 seconds	40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)	853.9 seconds	40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid	627.2 seconds	40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid	197.1 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	742.3 seconds	40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	193.9 seconds	40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid	221.4 seconds	40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate	533.0 seconds	40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA	483.0 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	355.3 seconds	40023050

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
Tryptophyl-Gamma-glutamate	NC(CCC(=O)NC(=O)C(N)CC1=CNC2=C1C=CC=C2)C(O)=O	4451.3	Standard polar	33892256
Tryptophyl-Gamma-glutamate	NC(CCC(=O)NC(=O)C(N)CC1=CNC2=C1C=CC=C2)C(O)=O	2649.3	Standard non polar	33892256
Tryptophyl-Gamma-glutamate	NC(CCC(=O)NC(=O)C(N)CC1=CNC2=C1C=CC=C2)C(O)=O	3510.6	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
Tryptophyl-Gamma-glutamate,1TMS,isomer #1	C[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12	3316.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,1TMS,isomer #2	C[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)C(=O)O	3417.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,1TMS,isomer #3	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O	3388.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,1TMS,isomer #4	C[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(N)CC1=C[NH]C2=CC=CC=C12	3316.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,1TMS,isomer #5	C[Si](C)(C)N1C=C(CC(N)C(=O)NC(=O)CCC(N)C(=O)O)C2=CC=CC=C21	3370.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #1	C[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)C(=O)O[Si](C)(C)C	3322.7	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #1	C[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)C(=O)O[Si](C)(C)C	3035.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #10	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O	3364.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #10	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O	3143.0	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #11	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O)[Si](C)(C)C	3290.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #11	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O)[Si](C)(C)C	3122.1	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #12	C[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12	3275.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #12	C[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12	3102.1	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #2	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O[Si](C)(C)C	3309.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #2	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O[Si](C)(C)C	3099.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #3	C[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C	3225.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #3	C[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C	3047.0	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #4	C[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12	3276.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #4	C[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12	3035.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #5	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N[Si](C)(C)C)C(=O)O	3364.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #5	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N[Si](C)(C)C)C(=O)O	3131.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #6	C[Si](C)(C)N(C(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)C(=O)O)[Si](C)(C)C	3486.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #6	C[Si](C)(C)N(C(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)C(=O)O)[Si](C)(C)C	3144.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #7	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C)C(=O)O	3319.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #7	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C)C(=O)O	3109.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #8	C[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)O	3368.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #8	C[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)O	3101.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #9	C[Si](C)(C)N(C(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O)[Si](C)(C)C	3408.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TMS,isomer #9	C[Si](C)(C)N(C(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O)[Si](C)(C)C	3189.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #1	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C	3293.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #1	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C	3150.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #10	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	3276.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #10	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	3204.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #11	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N[Si](C)(C)C)C(=O)O	3354.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #11	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N[Si](C)(C)C)C(=O)O	3179.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #12	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3394.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #12	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3265.3	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #13	C[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)C(N)CC1=C[NH]C2=CC=CC=C12	3411.7	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #13	C[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)C(N)CC1=C[NH]C2=CC=CC=C12	3233.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #14	C[Si](C)(C)N(C(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)O)[Si](C)(C)C	3440.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #14	C[Si](C)(C)N(C(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)O)[Si](C)(C)C	3210.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #15	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C)C(=O)O	3277.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #15	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C)C(=O)O	3153.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #16	C[Si](C)(C)N(C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O)[Si](C)(C)C	3411.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #16	C[Si](C)(C)N(C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O)[Si](C)(C)C	3275.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #17	C[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3372.7	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #17	C[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3258.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #18	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O)[Si](C)(C)C	3258.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #18	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O)[Si](C)(C)C	3193.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #2	C[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3418.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #2	C[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3148.9	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #3	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3236.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #3	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3116.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #4	C[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)O[Si](C)(C)C	3272.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #4	C[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)O[Si](C)(C)C	3075.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #5	C[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3334.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #5	C[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3240.3	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #6	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O[Si](C)(C)C	3259.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #6	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O[Si](C)(C)C	3123.9	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #7	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3221.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #7	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3155.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #8	C[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C	3178.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #8	C[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C	3082.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #9	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	3441.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TMS,isomer #9	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	3244.0	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #1	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3343.1	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #1	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3273.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #10	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3188.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #10	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O[Si](C)(C)C)[Si](C)(C)C	3170.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #11	C[Si](C)(C)N(C(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3515.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #11	C[Si](C)(C)N(C(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3373.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #12	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	3424.1	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #12	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C	3284.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #13	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3382.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #13	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3317.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #14	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	3264.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #14	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O	3226.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #15	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	3359.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #15	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	3319.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #16	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3414.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #16	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O	3298.0	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #17	C[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12	3391.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #17	C[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12	3267.1	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #18	C[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3376.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #18	C[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3326.1	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #2	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C	3276.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #2	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N[Si](C)(C)C)C(=O)O[Si](C)(C)C	3159.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #3	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3217.7	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #3	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3209.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #4	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3381.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #4	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3244.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #5	C[Si](C)(C)OC(=O)C(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3368.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #5	C[Si](C)(C)OC(=O)C(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3226.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #6	C[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3407.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #6	C[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3189.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #7	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3200.1	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #7	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3135.3	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #8	C[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3311.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #8	C[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3283.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #9	C[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3325.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TMS,isomer #9	C[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3251.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #1	C[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3512.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #1	C[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3364.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #10	C[Si](C)(C)N(C(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3544.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #10	C[Si](C)(C)N(C(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O)[Si](C)(C)C	3396.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #11	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3391.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #11	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3338.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #12	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	3378.1	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #12	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O	3347.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #2	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3326.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #2	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3331.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #3	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3360.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #3	C[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3281.9	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #4	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3213.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #4	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3224.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #5	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3403.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #5	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3252.1	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #6	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3382.1	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #6	C[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3314.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #7	C[Si](C)(C)OC(=O)C(CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3372.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #7	C[Si](C)(C)OC(=O)C(CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C)C2=CC=CC=C12)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3243.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #8	C[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3322.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #8	C[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3296.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #9	C[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3531.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,5TMS,isomer #9	C[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3443.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,6TMS,isomer #1	C[Si](C)(C)OC(=O)C(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3553.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,6TMS,isomer #1	C[Si](C)(C)OC(=O)C(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3437.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,6TMS,isomer #2	C[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3552.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,6TMS,isomer #2	C[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3373.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,6TMS,isomer #3	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3351.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,6TMS,isomer #3	C[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C	3345.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,6TMS,isomer #4	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3393.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,6TMS,isomer #4	C[Si](C)(C)NC(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C	3329.9	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,6TMS,isomer #5	C[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3574.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,6TMS,isomer #5	C[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C	3455.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,7TMS,isomer #1	C[Si](C)(C)OC(=O)C(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3602.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,7TMS,isomer #1	C[Si](C)(C)OC(=O)C(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C	3448.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,1TBDMS,isomer #1	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12	3638.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,1TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)C(=O)O	3696.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,1TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O	3647.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,1TBDMS,isomer #4	CC(C)(C)[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(N)CC1=C[NH]C2=CC=CC=C12	3562.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,1TBDMS,isomer #5	CC(C)(C)[Si](C)(C)N1C=C(CC(N)C(=O)NC(=O)CCC(N)C(=O)O)C2=CC=CC=C21	3631.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)C(=O)O[Si](C)(C)C(C)(C)C	3854.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)C(=O)O[Si](C)(C)C(C)(C)C	3458.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O	3827.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O	3540.0	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O)[Si](C)(C)C(C)(C)C	3788.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O)[Si](C)(C)C(C)(C)C	3536.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12	3746.1	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #12	CC(C)(C)[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12	3488.0	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O[Si](C)(C)C(C)(C)C	3835.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O[Si](C)(C)C(C)(C)C	3527.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3754.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #3	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3457.3	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12	3790.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #4	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12	3452.3	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N[Si](C)(C)C(C)(C)C)C(=O)O	3869.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #5	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N[Si](C)(C)C(C)(C)C)C(=O)O	3547.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)C(=O)O)[Si](C)(C)C(C)(C)C	4028.7	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #6	CC(C)(C)[Si](C)(C)N(C(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)C(=O)O)[Si](C)(C)C(C)(C)C	3526.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C)C(=O)O	3807.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C)C(=O)O	3514.1	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)O	3845.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #8	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)O	3491.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N(C(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O)[Si](C)(C)C(C)(C)C	3933.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,2TBDMS,isomer #9	CC(C)(C)[Si](C)(C)N(C(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O)[Si](C)(C)C(C)(C)C	3579.3	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4018.9	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3730.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4009.1	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3762.9	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N[Si](C)(C)C(C)(C)C)C(=O)O	4018.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #11	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N[Si](C)(C)C(C)(C)C)C(=O)O	3726.1	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4140.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3801.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)C(N)CC1=C[NH]C2=CC=CC=C12	4130.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #13	CC(C)(C)[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)C(N)CC1=C[NH]C2=CC=CC=C12	3725.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N(C(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)O)[Si](C)(C)C(C)(C)C	4167.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #14	CC(C)(C)[Si](C)(C)N(C(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)O)[Si](C)(C)C(C)(C)C	3707.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C)C(=O)O	3944.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #15	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C)C(=O)O	3677.1	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N(C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O)[Si](C)(C)C(C)(C)C	4118.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #16	CC(C)(C)[Si](C)(C)N(C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O)[Si](C)(C)C(C)(C)C	3777.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4076.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3794.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O)[Si](C)(C)C(C)(C)C	3916.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #18	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O)[Si](C)(C)C(C)(C)C	3733.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4181.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #2	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(N)CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3715.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3952.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3673.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)O[Si](C)(C)C(C)(C)C	3964.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)O[Si](C)(C)C(C)(C)C	3637.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4102.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3766.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O[Si](C)(C)C(C)(C)C	3950.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #6	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N)C(=O)O[Si](C)(C)C(C)(C)C	3678.0	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3948.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3723.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3852.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C	3618.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4189.3	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,3TBDMS,isomer #9	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3783.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)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	4290.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #1	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)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	3949.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4003.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #10	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)N(C(=O)CCC(N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3834.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(C(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)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	4480.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #11	CC(C)(C)[Si](C)(C)N(C(CCC(=O)NC(=O)C(CC1=C[NH]C2=CC=CC=C12)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	3993.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4333.0	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #12	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3900.7	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4295.1	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #13	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3965.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4077.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #14	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3882.4	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4273.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #15	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3990.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	4311.2	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #16	CC(C)(C)[Si](C)(C)NC(CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O	3930.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12	4261.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #17	CC(C)(C)[Si](C)(C)N(C(=O)CCC(C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12	3855.0	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4230.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #18	CC(C)(C)[Si](C)(C)N(C(=O)CCC(N)C(=O)O)C(=O)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3947.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4101.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #2	CC(C)(C)[Si](C)(C)NC(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)C(=O)NC(=O)CCC(N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3831.6	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)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	4079.4	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #3	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)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	3902.1	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(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	4333.5	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #4	CC(C)(C)[Si](C)(C)NC(CC1=C[NH]C2=CC=CC=C12)C(=O)NC(=O)CCC(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	3935.5	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4273.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #5	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)N(C(=O)C(N)CC1=C[NH]C2=CC=CC=C12)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3873.2	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4281.6	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #6	CC(C)(C)[Si](C)(C)OC(=O)C(CCC(=O)NC(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3845.3	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	4014.1	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #7	CC(C)(C)[Si](C)(C)NC(CCC(=O)N(C(=O)C(N)CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C	3789.0	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4219.8	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #8	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)N(C(=O)C(CC1=C[NH]C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3940.8	Standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	4235.1	Semi standard non polar	33892256
Tryptophyl-Gamma-glutamate,4TBDMS,isomer #9	CC(C)(C)[Si](C)(C)OC(=O)C(N)CCC(=O)NC(=O)C(CC1=CN([Si](C)(C)C(C)(C)C)C2=CC=CC=C12)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C	3877.7	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - Tryptophyl-Gamma-glutamate GC-MS (Non-derivatized) - 70eV, Positive	splash10-0a4i-4920000000-8fa0366133db654419df	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tryptophyl-Gamma-glutamate GC-MS (1 TMS) - 70eV, Positive	splash10-0kh9-9858000000-495a975d871dc83307a8	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - Tryptophyl-Gamma-glutamate 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 - Tryptophyl-Gamma-glutamate 10V, Positive-QTOF	splash10-0kui-0955000000-9611cd22edfd4716f7a6	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 20V, Positive-QTOF	splash10-0pbl-1920000000-8c7fb123b4a2724f797c	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 40V, Positive-QTOF	splash10-053r-4900000000-e37551fdb4100043d7e1	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 10V, Negative-QTOF	splash10-001i-0119000000-8abecf4766e8381851ca	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 20V, Negative-QTOF	splash10-0w5j-3976000000-aab41da57d74876e5d3a	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 40V, Negative-QTOF	splash10-00du-9710000000-5c8d97ae0322de0e0039	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 10V, Negative-QTOF	splash10-01q9-0209000000-0914b83258c055bd588c	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 20V, Negative-QTOF	splash10-0203-5941000000-92ae0d0ac270bda94d0b	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 40V, Negative-QTOF	splash10-00kf-5900000000-21fbc70d42fa5f834399	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 10V, Positive-QTOF	splash10-01c0-0279000000-362cc82feaf766290070	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 20V, Positive-QTOF	splash10-05gr-0950000000-afc516e5f01f4989dfe7	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - Tryptophyl-Gamma-glutamate 40V, Positive-QTOF	splash10-0536-2900000000-c04277e302372f531d9b	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

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

FDB112101

KNApSAcK ID

Not Available

Chemspider ID

35032828

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

131750788

PDB ID

Not Available

ChEBI ID

175248

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for Tryptophyl-Gamma-glutamate (HMDB0029097)

MOL for HMDB0029097 (Tryptophyl-Gamma-glutamate)

3D MOL for HMDB0029097 (Tryptophyl-Gamma-glutamate)

3D SDF for HMDB0029097 (Tryptophyl-Gamma-glutamate)

3D-SDF for HMDB0029097 (Tryptophyl-Gamma-glutamate)

PDB for HMDB0029097 (Tryptophyl-Gamma-glutamate)

3D PDB for HMDB0029097 (Tryptophyl-Gamma-glutamate)

SMILES for HMDB0029097 (Tryptophyl-Gamma-glutamate)

INCHI for HMDB0029097 (Tryptophyl-Gamma-glutamate)

Structure for HMDB0029097 (Tryptophyl-Gamma-glutamate)

3D Structure for HMDB0029097 (Tryptophyl-Gamma-glutamate)

Predicted Collision Cross Sections

Predicted Retention Times

Underivatized

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra