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Record Information

Version

5.0

Status

Detected but not Quantified

Creation Date

2022-09-09 19:26:43 UTC

Update Date

2022-09-22 18:35:04 UTC

HMDB ID

HMDB0341164

Secondary Accession Numbers

None

Metabolite Identification

Common Name

His-Glu-Lys

Description

His-Glu-Lys belongs to the class of organic compounds known as peptides. Peptides are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another. Based on a literature review very few articles have been published on His-Glu-Lys.

Structure

MOL SDF PDB SMILES InChI

  Mrv1652309092222052D          

 32 32  0  0  1  0            999 V2000
    3.8547  -10.6443    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0297  -10.6443    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4422   -9.9299    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4422  -11.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2672  -11.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7521  -10.6914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5367  -10.9463    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5367  -11.7713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7521  -12.0263    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2047  -10.6443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7922  -11.3588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7922   -9.9299    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9672   -9.9299    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3797  -10.6443    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5547  -10.6443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2703  -10.6443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828  -11.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2703  -12.0733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5078  -11.3588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5547   -9.2154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2703   -9.2154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9672   -8.5009    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5547   -7.7865    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1422   -8.5009    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2703   -7.7865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828   -7.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5078   -7.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9203   -6.3575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7453   -6.3575    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9672   -7.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5547   -6.3575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7922   -7.0720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  5  9  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  4  0  0  0
 10 12  2  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  4  0  0  0
 20 22  2  0  0  0  0
 23 22  1  1  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
M  END

  Mrv1652309092222052D          

 32 32  0  0  1  0            999 V2000
    3.8547  -10.6443    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0297  -10.6443    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4422   -9.9299    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4422  -11.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2672  -11.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7521  -10.6914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5367  -10.9463    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.5367  -11.7713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7521  -12.0263    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2047  -10.6443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7922  -11.3588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7922   -9.9299    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9672   -9.9299    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3797  -10.6443    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5547  -10.6443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2703  -10.6443    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828  -11.3588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2703  -12.0733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5078  -11.3588    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5547   -9.2154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2703   -9.2154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9672   -8.5009    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.5547   -7.7865    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1422   -8.5009    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2703   -7.7865    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6828   -7.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5078   -7.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9203   -6.3575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7453   -6.3575    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.9672   -7.0720    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5547   -6.3575    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7922   -7.0720    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  1  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  5  9  1  0  0  0  0
  2 10  1  0  0  0  0
 10 11  1  4  0  0  0
 10 12  2  0  0  0  0
 13 12  1  1  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 13 20  1  0  0  0  0
 20 21  1  4  0  0  0
 20 22  2  0  0  0  0
 23 22  1  1  0  0  0
 23 24  1  6  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 23 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0341164

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@](N)(CC1=CN=CN1)C(O)=N[C@@]([H])(CCC(O)=O)C(O)=N[C@@]([H])(CCCCN)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H28N6O6/c18-6-2-1-3-13(17(28)29)23-16(27)12(4-5-14(24)25)22-15(26)11(19)7-10-8-20-9-21-10/h8-9,11-13H,1-7,18-19H2,(H,20,21)(H,22,26)(H,23,27)(H,24,25)(H,28,29)/t11-,12-,13-/m0/s1

> <INCHI_KEY>
JCOSMKPAOYDKRO-AVGNSLFASA-N

> <FORMULA>
C17H28N6O6

> <MOLECULAR_WEIGHT>
412.447

> <EXACT_MASS>
412.207032646

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
42.29738189100287

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-6-amino-2-{[(2S)-2-{[(2S)-2-amino-1-hydroxy-3-(1H-imidazol-5-yl)propylidene]amino}-4-carboxy-1-hydroxybutylidene]amino}hexanoic acid

> <JCHEM_LOGP>
-6.820105394878763

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
3.4139989175872425

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.8469874779130717

> <JCHEM_PKA_STRONGEST_BASIC>
10.287054427264287

> <JCHEM_POLAR_SURFACE_AREA>
220.5

> <JCHEM_REFRACTIVITY>
101.79979999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-6-amino-2-{[(2S)-2-{[(2S)-2-amino-1-hydroxy-3-(3H-imidazol-4-yl)propylidene]amino}-4-carboxy-1-hydroxybutylidene]amino}hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  H   UNK     0       7.195 -19.869   0.000  0.00  0.00           H+0
HETATM    2  C   UNK     0       5.655 -19.869   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0       6.425 -18.536   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0       6.425 -21.203   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.965 -21.203   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.871 -19.957   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      10.335 -20.433   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      10.335 -21.973   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       8.871 -22.449   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       4.115 -19.869   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.345 -21.203   0.000  0.00  0.00           O+0
HETATM   12  N   UNK     0       3.345 -18.536   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       1.805 -18.536   0.000  0.00  0.00           C+0
HETATM   14  H   UNK     0       2.575 -19.869   0.000  0.00  0.00           H+0
HETATM   15  C   UNK     0       1.035 -19.869   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.505 -19.869   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.275 -21.203   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -0.505 -22.537   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -2.815 -21.203   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.035 -17.202   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.505 -17.202   0.000  0.00  0.00           O+0
HETATM   22  N   UNK     0       1.805 -15.868   0.000  0.00  0.00           N+0
HETATM   23  C   UNK     0       1.035 -14.535   0.000  0.00  0.00           C+0
HETATM   24  H   UNK     0       0.265 -15.868   0.000  0.00  0.00           H+0
HETATM   25  C   UNK     0      -0.505 -14.535   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.275 -13.201   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.815 -13.201   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.585 -11.867   0.000  0.00  0.00           C+0
HETATM   29  N   UNK     0      -5.125 -11.867   0.000  0.00  0.00           N+0
HETATM   30  C   UNK     0       1.805 -13.201   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       1.035 -11.867   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       3.345 -13.201   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4   10                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    5                                                       
CONECT   10    2   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15   20                                             
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   13   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25   30                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28                                                            
CONECT   30   23   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   64    0
END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₁₇H₂₈N₆O₆

Average Molecular Weight

412.447

Monoisotopic Molecular Weight

412.207032646

IUPAC Name

(2S)-6-amino-2-{[(2S)-2-{[(2S)-2-amino-1-hydroxy-3-(1H-imidazol-5-yl)propylidene]amino}-4-carboxy-1-hydroxybutylidene]amino}hexanoic acid

Traditional Name

(2S)-6-amino-2-{[(2S)-2-{[(2S)-2-amino-1-hydroxy-3-(3H-imidazol-4-yl)propylidene]amino}-4-carboxy-1-hydroxybutylidene]amino}hexanoic acid

CAS Registry Number

Not Available

SMILES

[H][C@](N)(CC1=CN=CN1)C(O)=N[C@@]([H])(CCC(O)=O)C(O)=N[C@@]([H])(CCCCN)C(O)=O

InChI Identifier

InChI=1S/C17H28N6O6/c18-6-2-1-3-13(17(28)29)23-16(27)12(4-5-14(24)25)22-15(26)11(19)7-10-8-20-9-21-10/h8-9,11-13H,1-7,18-19H2,(H,20,21)(H,22,26)(H,23,27)(H,24,25)(H,28,29)/t11-,12-,13-/m0/s1

InChI Key

JCOSMKPAOYDKRO-AVGNSLFASA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as peptides. Peptides are compounds containing an amide derived from two or more amino carboxylic acid molecules (the same or different) by formation of a covalent bond from the carbonyl carbon of one to the nitrogen atom of another.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Peptides

Alternative Parents

Substituents

Alpha peptide
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
Alpha-amino acid or derivatives
Medium-chain fatty acid
Imidazolyl carboxylic acid derivative
Aralkylamine
Heterocyclic fatty acid
Amino fatty acid
Fatty acyl
Fatty acid
Dicarboxylic acid or derivatives
Heteroaromatic compound
Imidazole
Azole
Amino acid
Amino acid or derivatives
Azacycle
Organoheterocyclic compound
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboxylic acid
Carboximidic acid derivative
Carboximidic acid
Organic nitrogen compound
Organic oxygen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary amine
Organooxygen compound
Organonitrogen compound
Primary aliphatic amine
Carbonyl group
Amine
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Physical Properties

State

Not Available

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	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
logP	-6.8	ChemAxon
pKa (Strongest Acidic)	2.85	ChemAxon
pKa (Strongest Basic)	10.29	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	220.5 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	101.8 m³·mol⁻¹	ChemAxon
Polarizability	42.3 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Kovats Retention Indices

Not Available

Spectra

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Blood
Urine

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Biospecimen	Status	Value	Age	Sex	Condition	Reference	Details
Blood	Expected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	34436864	details
Urine	Detected but not Quantified	Not Quantified	Not Specified	Not Specified	Normal	34436864	details

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

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

145455836

PDB ID

Not Available

ChEBI ID

164450

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

Neto FC, Raftery D: Expanding Urinary Metabolite Annotation through Integrated Mass Spectral Similarity Networking. Anal Chem. 2021 Sep 7;93(35):12001-12010. doi: 10.1021/acs.analchem.1c02041. Epub 2021 Aug 26. [PubMed:34436864 ]

Showing metabocard for His-Glu-Lys (HMDB0341164)

MOL for HMDB0341164 (His-Glu-Lys)

3D MOL for HMDB0341164 (His-Glu-Lys)

3D SDF for HMDB0341164 (His-Glu-Lys)

3D-SDF for HMDB0341164 (His-Glu-Lys)

PDB for HMDB0341164 (His-Glu-Lys)

3D PDB for HMDB0341164 (His-Glu-Lys)

SMILES for HMDB0341164 (His-Glu-Lys)

INCHI for HMDB0341164 (His-Glu-Lys)

Structure for HMDB0341164 (His-Glu-Lys)

3D Structure for HMDB0341164 (His-Glu-Lys)

Predicted Kovats Retention Indices