MiMeDB: Showing metabocard for Leucyl-Glycine (MMDBc0000309)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-10-28 18:28:40 UTC

Update Date

2024-04-30 19:31:46 UTC

Metabolite ID

MMDBc0000309

Metabolite Identification

Common Name

Leucyl-Glycine

Description

Leucyl-Glycine is a dipeptide composed of leucine and glycine. 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

HMDB0028929
     RDKit          3D
Leucyl-Glycine
 29 28  0  0  0  0  0  0  0  0999 V2000
   -3.3846    0.0133    1.2480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0508   -0.3078    0.5853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3466   -1.3296   -0.4938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4715    0.9517    0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1907    0.8013   -0.6885 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1448    2.1445   -1.2426 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0181    0.4807    0.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3612    1.3663    0.9366 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6682   -0.7039    0.0212 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8437   -1.2467    0.6320 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0781   -0.5218    0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8912   -0.1631    1.0920 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2993   -0.2370   -1.0718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0959    0.3621    0.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3204    0.7512    2.0402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8023   -0.9788    1.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3918   -0.7383    1.3323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0082   -2.0897   -0.0330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9428   -0.8850   -1.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4375   -1.8406   -0.8538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1838    1.5602   -0.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2777    1.5923    0.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1977    0.1131   -1.5340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0575    2.1033   -1.7364 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1113    2.8495   -0.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2091   -1.4316   -0.7055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7372   -0.9835    1.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9845   -2.2892    0.5367 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6981    0.6572   -1.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  9 26  1  0
 10 27  1  0
 10 28  1  0
 13 29  1  0
M  END

HMDB0028929
     RDKit          3D
Leucyl-Glycine
 29 28  0  0  0  0  0  0  0  0999 V2000
   -3.3846    0.0133    1.2480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0508   -0.3078    0.5853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3466   -1.3296   -0.4938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4715    0.9517    0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1907    0.8013   -0.6885 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1448    2.1445   -1.2426 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0181    0.4807    0.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3612    1.3663    0.9366 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6682   -0.7039    0.0212 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8437   -1.2467    0.6320 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0781   -0.5218    0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8912   -0.1631    1.0920 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2993   -0.2370   -1.0718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0959    0.3621    0.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3204    0.7512    2.0402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8023   -0.9788    1.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3918   -0.7383    1.3323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0082   -2.0897   -0.0330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9428   -0.8850   -1.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4375   -1.8406   -0.8538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1838    1.5602   -0.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2777    1.5923    0.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1977    0.1131   -1.5340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0575    2.1033   -1.7364 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1113    2.8495   -0.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2091   -1.4316   -0.7055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7372   -0.9835    1.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9845   -2.2892    0.5367 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6981    0.6572   -1.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  9 26  1  0
 10 27  1  0
 10 28  1  0
 13 29  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      12.265   4.001   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0      10.931   4.771   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      10.931   6.311   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       9.597   4.001   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0       9.597   2.461   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0       8.264   4.771   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.596   4.771   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.930   2.461   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.598   4.771   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.932   4.001   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      16.266   4.771   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      14.932   2.461   0.000  0.00  0.00           O+0
CONECT    1    2   10                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    1   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
MASTER        0    0    0    0    0    0    0    0   13    0   24    0
END

COMPND    HMDB0028929
HETATM    1  C1  UNL     1      -3.385   0.013   1.248  1.00  0.00           C  
HETATM    2  C2  UNL     1      -2.051  -0.308   0.585  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.347  -1.330  -0.494  1.00  0.00           C  
HETATM    4  C4  UNL     1      -1.471   0.952   0.021  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.191   0.801  -0.688  1.00  0.00           C  
HETATM    6  N1  UNL     1       0.145   2.144  -1.243  1.00  0.00           N  
HETATM    7  C6  UNL     1       1.018   0.481   0.190  1.00  0.00           C  
HETATM    8  O1  UNL     1       1.361   1.366   0.937  1.00  0.00           O  
HETATM    9  N2  UNL     1       1.668  -0.704   0.021  1.00  0.00           N  
HETATM   10  C7  UNL     1       2.844  -1.247   0.632  1.00  0.00           C  
HETATM   11  C8  UNL     1       4.078  -0.522   0.253  1.00  0.00           C  
HETATM   12  O2  UNL     1       4.891  -0.163   1.092  1.00  0.00           O  
HETATM   13  O3  UNL     1       4.299  -0.237  -1.072  1.00  0.00           O  
HETATM   14  H1  UNL     1      -4.096   0.362   0.440  1.00  0.00           H  
HETATM   15  H2  UNL     1      -3.320   0.751   2.040  1.00  0.00           H  
HETATM   16  H3  UNL     1      -3.802  -0.979   1.578  1.00  0.00           H  
HETATM   17  H4  UNL     1      -1.392  -0.738   1.332  1.00  0.00           H  
HETATM   18  H5  UNL     1      -3.008  -2.090  -0.033  1.00  0.00           H  
HETATM   19  H6  UNL     1      -2.943  -0.885  -1.326  1.00  0.00           H  
HETATM   20  H7  UNL     1      -1.438  -1.841  -0.854  1.00  0.00           H  
HETATM   21  H8  UNL     1      -2.184   1.560  -0.562  1.00  0.00           H  
HETATM   22  H9  UNL     1      -1.278   1.592   0.941  1.00  0.00           H  
HETATM   23  H10 UNL     1      -0.198   0.113  -1.534  1.00  0.00           H  
HETATM   24  H11 UNL     1       1.057   2.103  -1.736  1.00  0.00           H  
HETATM   25  H12 UNL     1       0.111   2.850  -0.503  1.00  0.00           H  
HETATM   26  H13 UNL     1       1.209  -1.432  -0.706  1.00  0.00           H  
HETATM   27  H14 UNL     1       2.737  -0.984   1.764  1.00  0.00           H  
HETATM   28  H15 UNL     1       2.984  -2.289   0.537  1.00  0.00           H  
HETATM   29  H16 UNL     1       4.698   0.657  -1.344  1.00  0.00           H  
CONECT    1    2   14   15   16
CONECT    2    3    4   17
CONECT    3   18   19   20
CONECT    4    5   21   22
CONECT    5    6    7   23
CONECT    6   24   25
CONECT    7    8    8    9
CONECT    9   10   26
CONECT   10   11   27   28
CONECT   11   12   12   13
CONECT   13   29
END

HMDB0028929
     RDKit          3D
Leucyl-Glycine
 29 28  0  0  0  0  0  0  0  0999 V2000
   -3.3846    0.0133    1.2480 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0508   -0.3078    0.5853 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3466   -1.3296   -0.4938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4715    0.9517    0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1907    0.8013   -0.6885 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1448    2.1445   -1.2426 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0181    0.4807    0.1901 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3612    1.3663    0.9366 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6682   -0.7039    0.0212 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8437   -1.2467    0.6320 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0781   -0.5218    0.2527 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8912   -0.1631    1.0920 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2993   -0.2370   -1.0718 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0959    0.3621    0.4397 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3204    0.7512    2.0402 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8023   -0.9788    1.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3918   -0.7383    1.3323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0082   -2.0897   -0.0330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9428   -0.8850   -1.3263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4375   -1.8406   -0.8538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1838    1.5602   -0.5622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2777    1.5923    0.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1977    0.1131   -1.5340 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0575    2.1033   -1.7364 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1113    2.8495   -0.5030 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2091   -1.4316   -0.7055 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7372   -0.9835    1.7638 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9845   -2.2892    0.5367 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6981    0.6572   -1.3438 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
  1 14  1  0
  1 15  1  0
  1 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  5 23  1  0
  6 24  1  0
  6 25  1  0
  9 26  1  0
 10 27  1  0
 10 28  1  0
 13 29  1  0
M  END

Synonyms

Value	Source
L-g Dipeptide	HMDB
L-Leucyl-L-glycine	HMDB
Leu-gly	HMDB, MeSH
Leucine glycine dipeptide	HMDB
Leucine-glycine dipeptide	HMDB
Leucylglycine	HMDB, MeSH
LG Dipeptide	HMDB
Glycyl-L-leucine	MeSH, HMDB
Glycylleucine	MeSH, HMDB
Glycylleucine, (D)-isomer	MeSH, HMDB
Gly-leu	MeSH, HMDB
2-[(2-Amino-1-hydroxy-4-methylpentylidene)amino]acetate	Generator, HMDB

Molecular Formula

C₈H₁₆N₂O₃

Average Mass

188.2242

Monoisotopic Mass

188.116092388

IUPAC Name

2-(2-amino-4-methylpentanamido)acetic acid

Traditional Name

(2-amino-4-methylpentanamido)acetic acid

CAS Registry Number

Not Available

SMILES

CC(C)CC(N)C(=O)NCC(O)=O

InChI Identifier

InChI=1S/C8H16N2O3/c1-5(2)3-6(9)8(13)10-4-7(11)12/h5-6H,3-4,9H2,1-2H3,(H,10,13)(H,11,12)

InChI Key

LESXFEZIFXFIQR-UHFFFAOYSA-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
Leucine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Alpha-amino acid or derivatives
Fatty amide
N-acyl-amine
Fatty acyl
Amino acid or derivatives
Carboxamide group
Amino acid
Secondary carboxylic acid amide
Monocarboxylic acid or derivatives
Carboxylic acid
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Primary aliphatic amine
Organopnictogen compound
Organic nitrogen compound
Carbonyl group
Organonitrogen compound
Organooxygen compound
Primary amine
Amine
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	11.8 g/L	ALOGPS
logP	-1.8	ALOGPS
logP	-2.7	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	3.94	ChemAxon
pKa (Strongest Basic)	8.43	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	92.42 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	46.97 m³·mol⁻¹	ChemAxon
Polarizability	19.85 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

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-000f-9300000000-849662080baf057abff4	2017-09-01	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (1 TMS) - 70eV, Positive	splash10-00di-9110000000-61823aaef1dce714d003	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-11-04	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-11-04	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_1_1) - 70eV, Positive	Not Available	2021-11-04	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_1_2) - 70eV, Positive	Not Available	2021-11-04	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TBDMS_1_3) - 70eV, Positive	Not Available	2021-11-04	View Spectrum
LC-MS/MS	LC-MS/MS Spectrum - 6V, Positive	splash10-000i-9600000000-2a5feb5dc798e987848b	2021-09-20	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-000i-4900000000-52dc51f7498f286ecfc6	2017-09-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-05p9-9100000000-5e75d94c0b9833517075	2017-09-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0aor-9000000000-807eedfb971ea170f1a4	2017-09-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-000i-0900000000-556ee40e30169fde70f7	2017-09-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-00dr-5900000000-532ce77cf9de1544d6a3	2017-09-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-05fr-9200000000-94c9657911237839d995	2017-09-01	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-000i-9500000000-a18b1832f4ecb67ff5c4	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-014r-9000000000-188c347076776da83c2a	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0a4l-9000000000-1a9366990b8c2ba1a414	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-000i-1900000000-4169d8f6d9d59766e193	2021-09-24	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-00ri-7900000000-ba307a0a4b308c6a1323	2021-09-24	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0600-9000000000-87ffb4e2796df6b6260b	2021-09-24	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		2021-09-16	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		2021-09-16	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Verrucomicrobia	1	Human feces; Human stool; Human ; Human urine	Indirect association between microbiota composition and metabolites measured in host biospecimen
Bacteria	Firmicutes	2	Human feces; Human stool; Human ; Human urine; Human sputum	Indirect association between microbiota composition and metabolites measured in host biospecimen

Exposure Sources

Host Biospecimen and Location

Host and Biospecimen	Status	Age	Sex	Health Condition	Data Source	Reference
Human Feces	Detected but not Quantified				HMDB
Human Feces	Detected but not Quantified	Adult (>18 years old)	Both	Normal	HMDB	27543620
Human Feces	Detected but not Quantified	Adult (>18 years old)	Both	Normal	HMDB	25037050
Human Feces	Detected but not Quantified	Adult (>18 years old)	Both	Normal	HMDB	29808030

External Links

HMDB ID

HMDB0254027

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB111956

KNApSAcK ID

Not Available

Chemspider ID

71402

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

79070

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Nethery A, O'Grady RL: Interstitial collagenase from rat mammary carcinoma cells: interaction with substrates and inhibitors. Invasion Metastasis. 1991;11(5):241-8. [PubMed:1666066 ]
Xia T, Akers K, Eisen AZ, Seltzer JL: Comparison of cleavage site specificity of gelatinases A and B using collagenous peptides. Biochim Biophys Acta. 1996 Apr 16;1293(2):259-66. doi: 10.1016/0167-4838(95)00259-6. [PubMed:8620038 ]
Suzuki H, Kamatani S, Kumagai H: Purification and characterization of aminopeptidase B from Escherichia coli K-12. Biosci Biotechnol Biochem. 2001 Jul;65(7):1549-58. doi: 10.1271/bbb.65.1549. [PubMed:11515538 ]
Fujii Y, Kiss T, Gajda T, Tan XS, Sato T, Nakano Y, Hayashi Y, Yashiro M: Copper(II)- cis, cis-1,3,5-triaminocyclohexane complex-promoted hydrolysis of dipeptides: kinetic, speciation and structural studies. J Biol Inorg Chem. 2002 Sep;7(7-8):843-51. doi: 10.1007/s00775-002-0368-9. Epub 2002 Apr 30. [PubMed:12203021 ]
Yoshino AH, Okabayashi HF, Kanbe HH, Suzuki K, O'Connor CJ: Folded structures of L-leucylglycine oligopeptides and their aggregational behavior in aqueous solution: Raman scattering spectra and proton NMR spin-lattice relaxation studies. J Phys Chem B. 2008 May 8;112(18):5824-33. doi: 10.1021/jp074732q. Epub 2008 Apr 12. [PubMed:18407703 ]
Kiyotani T, Sugawara Y: L-Leucylglycine 0.67-hydrate and [(4S)-2,2-dimethyl-4-(2-methylpropyl)-5-oxoimidazolidin-3-ium-1-yl]acetate. Acta Crystallogr C. 2012 Dec;68(Pt 12):o498-501. doi: 10.1107/S010827011204810X. Epub 2012 Nov 28. [PubMed:23221255 ]

Showing metabocard for Leucyl-Glycine (MMDBc0000309)

MOL for #<Metabolite:0x00007fdb4c23af58>

3D MOL for #<Metabolite:0x00007fdb4c23af58>

3D SDF for #<Metabolite:0x00007fdb4c23af58>

3D-SDF for #<Metabolite:0x00007fdb4c23af58>

PDB for #<Metabolite:0x00007fdb4c23af58>

3D PDB for #<Metabolite:0x00007fdb4c23af58>

SMILES for #<Metabolite:0x00007fdb4c23af58>

INCHI for #<Metabolite:0x00007fdb4c23af58>

Structure for #<Metabolite:0x00007fdb4c23af58>

3D Structure for #<Metabolite:0x00007fdb4c23af58>