MiMeDB: Showing metabocard for N2,N6-Diacetyllysine (MMDBc0000727)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-12-10 18:53:39 UTC

Update Date

2022-08-31 06:11:39 UTC

Metabolite ID

MMDBc0000727

Metabolite Identification

Common Name

N2,N6-Diacetyllysine

Description

AC-LYS(AC)-OH belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom. AC-LYS(AC)-OH is a very strong basic compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652304021923592D          

 17 16  0  0  1  0            999 V2000
   -1.2375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    4.2868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0625    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    2.8579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8250    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    2.8579    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7125    2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125    3.5724    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5375    2.1434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3000    1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    2.1434    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  1  1  0  0  0  0
  8  2  1  4  0  0  0
  9  5  1  0  0  0  0
 10  9  1  0  0  0  0
 11  6  1  4  0  0  0
 11  7  2  0  0  0  0
 12  8  2  0  0  0  0
  9 12  1  1  0  0  0
 13  7  1  0  0  0  0
 14  8  1  0  0  0  0
 15 10  2  0  0  0  0
 16 10  1  0  0  0  0
  9 17  1  1  0  0  0
M  END
> <DATABASE_ID>
MMDBc0000727

> <DATABASE_NAME>
MIME

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

> <INCHI_IDENTIFIER>
InChI=1S/C10H18N2O4/c1-7(13)11-6-4-3-5-9(10(15)16)12-8(2)14/h9H,3-6H2,1-2H3,(H,11,13)(H,12,14)(H,15,16)/t9-/m0/s1

> <INCHI_KEY>
ZHZUEHHBTYJTKY-VIFPVBQESA-N

> <FORMULA>
C10H18N2O4

> <MOLECULAR_WEIGHT>
230.2609

> <EXACT_MASS>
230.126657074

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
24.111472734372274

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2,6-bis[(1-hydroxyethylidene)amino]hexanoic acid

> <ALOGPS_LOGP>
0.21

> <JCHEM_LOGP>
-0.8875884166605946

> <ALOGPS_LOGS>
-2.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
4.5422031288658395

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.776407912348697

> <JCHEM_PKA_STRONGEST_BASIC>
6.65373791730633

> <JCHEM_POLAR_SURFACE_AREA>
102.48

> <JCHEM_REFRACTIVITY>
57.74050000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.30e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2,6-bis[(1-hydroxyethylidene)amino]hexanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-APR-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-APR-19         0                                  
HETATM    1  C   UNK     0      -2.310   4.001   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.240   8.002   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.850   4.001   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.310   4.001   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.620   5.335   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.540   2.667   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -0.770   4.001   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.470   6.668   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.160   5.335   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.930   4.001   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       0.000   2.667   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0       6.930   6.668   0.000  0.00  0.00           N+0
HETATM   13  O   UNK     0       0.000   5.335   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       9.240   5.335   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       8.470   4.001   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       6.160   2.667   0.000  0.00  0.00           O+0
HETATM   17  H   UNK     0       5.390   4.001   0.000  0.00  0.00           H+0
CONECT    1    7                                                            
CONECT    2    8                                                            
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3    9                                                       
CONECT    6    4   11                                                       
CONECT    7    1   11   13                                                  
CONECT    8    2   12   14                                                  
CONECT    9    5   10   12   17                                             
CONECT   10    9   15   16                                                  
CONECT   11    6    7                                                       
CONECT   12    8    9                                                       
CONECT   13    7                                                            
CONECT   14    8                                                            
CONECT   15   10                                                            
CONECT   16   10                                                            
CONECT   17    9                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   32    0
END

Synonyms

Value	Source
(S)-26-Diacetamidohexanoic acid	ChEMBL
(S)-26-Diacetamidohexanoate	Generator
(2S)-2,6-Bis[(1-hydroxyethylidene)amino]hexanoate	Generator

Molecular Formula

C₁₀H₁₈N₂O₄

Average Mass

230.2609

Monoisotopic Mass

230.126657074

IUPAC Name

(2S)-2,6-bis[(1-hydroxyethylidene)amino]hexanoic acid

Traditional Name

(2S)-2,6-bis[(1-hydroxyethylidene)amino]hexanoic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C10H18N2O4/c1-7(13)11-6-4-3-5-9(10(15)16)12-8(2)14/h9H,3-6H2,1-2H3,(H,11,13)(H,12,14)(H,15,16)/t9-/m0/s1

InChI Key

ZHZUEHHBTYJTKY-VIFPVBQESA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as n-acyl-l-alpha-amino acids. These are n-acylated alpha amino acids which have the L-configuration of the alpha-carbon atom.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

N-acyl-L-alpha-amino acids

Alternative Parents

Substituents

N-acyl-l-alpha-amino acid
Medium-chain fatty acid
Amino fatty acid
Fatty acyl
Fatty acid
Acetamide
Secondary carboxylic acid amide
Carboxamide group
Monocarboxylic acid or derivatives
Carboxylic acid
Organic oxide
Hydrocarbon derivative
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Carbonyl group
Organic oxygen compound
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	0.63 g/L	ALOGPS
logP	0.21	ALOGPS
logP	-0.89	ChemAxon
logS	-2.6	ALOGPS
pKa (Strongest Acidic)	3.78	ChemAxon
pKa (Strongest Basic)	6.65	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	102.48 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	57.74 m³·mol⁻¹	ChemAxon
Polarizability	24.11 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

Not Available

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

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/Eubacteria	Actinobacteria	1	Human ; Human feces	Indirect association between microbiota composition and metabolites measured in host biospecimen
Bacteria/Eubacteria	Firmicutes	1	Human feces	Indirect association between microbiota composition and metabolites measured in host biospecimen
Bacteria/Eubacteria	Bacteroidetes	1	Human ; Human feces; Human urine	Indirect association between microbiota composition and metabolites measured in host biospecimen

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

HMDB0240320

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

7019608

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Showing metabocard for N2,N6-Diacetyllysine (MMDBc0000727)

MOL for #<Metabolite:0x00007f9252447ca8>

3D MOL for #<Metabolite:0x00007f9252447ca8>

3D SDF for #<Metabolite:0x00007f9252447ca8>

3D-SDF for #<Metabolite:0x00007f9252447ca8>

PDB for #<Metabolite:0x00007f9252447ca8>

3D PDB for #<Metabolite:0x00007f9252447ca8>

SMILES for #<Metabolite:0x00007f9252447ca8>

INCHI for #<Metabolite:0x00007f9252447ca8>

Structure for #<Metabolite:0x00007f9252447ca8>

3D Structure for #<Metabolite:0x00007f9252447ca8>