NP-MRD: Showing NP-Card for Valylglutamine (NP0136705)

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Record Information

Version

2.0

Created at

2022-05-12 15:21:23 UTC

Updated at

2022-05-12 15:21:23 UTC

NP-MRD ID

NP0136705

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Valylglutamine

Description

Val-Gln, also known as valyl-glutamine or L-val-L-GLN, 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. Val-Gln is a very strong basic compound (based on its pKa). A dipeptide formed from L-valine and L-glutamine residues.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 35  0  0  0  0  0  0  0  0999 V2000
   -4.4864    0.9398   -0.5913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0131    0.9870   -0.8474 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7838    1.5656   -2.2193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4722   -0.4254   -0.7180 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7511   -0.8831    0.6211 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0186   -0.4791   -0.9482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5489   -0.1304   -2.0374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1543   -0.9302    0.0767 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.2966   -1.0001   -0.1079 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.9780   -0.0200    0.8135 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4624    0.0032    0.7174 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9472    1.0379    1.7003 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3276    1.3005    1.8492 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1560    1.7003    2.4176 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7129   -2.3903    0.0519 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9012   -3.3115    0.3142 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0449   -2.7366   -0.0855 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9755    0.2400   -1.3008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7439    0.7202    0.4622 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9314    1.9484   -0.8028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5478    1.6329   -0.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1279    0.8281   -2.9716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7233    1.8664   -2.3729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4512    2.4714   -2.2889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0363   -1.0405   -1.4674 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7029   -1.2901    0.7299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5570   -0.1068    1.2891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5079   -1.2331    1.0086 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4970   -0.6447   -1.1456 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6037    0.9969    0.6036 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6977   -0.2740    1.8593 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8561    0.2981   -0.2549 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9556   -0.9407    1.0643 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9495    1.2459    1.0218 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7108    1.5419    2.7631 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4363   -3.4881    0.4884 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  4  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
  9 15  1  0
 15 17  1  0
 15 16  2  0
  1 18  1  0
  1 19  1  0
  1 20  1  0
  2 21  1  1
  3 22  1  0
  3 23  1  0
  3 24  1  0
  4 25  1  6
  5 26  1  0
  5 27  1  0
  8 28  1  0
  9 29  1  6
 10 30  1  0
 10 31  1  0
 11 32  1  0
 11 33  1  0
 13 34  1  0
 13 35  1  0
 17 36  1  0
M  END


  Mrv1652304062014252D          

 17 16  0  0  0  0            999 V2000
10023.927210024.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10024.644310024.5123    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10025.358710024.1004    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10026.073110024.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10026.787610024.1004    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10026.073110025.3371    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10023.213810024.5123    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10022.498410024.1004    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10021.784910024.5123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10022.498410023.2754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10023.213810025.3371    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10023.927210023.2754    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10025.358710023.2754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10026.074910022.8619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10026.074910022.0349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10025.358710021.6214    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10026.791110021.6214    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  7  1  0  0  0  0
  1 12  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  0  0  0  0
  7  8  1  0  0  0  0
  7 11  1  6  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  3 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0136705

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C10H19N3O4/c1-5(2)8(12)9(15)13-6(10(16)17)3-4-7(11)14/h5-6,8H,3-4,12H2,1-2H3,(H2,11,14)(H,13,15)(H,16,17)/t6-,8-/m0/s1

> <INCHI_KEY>
XXDVDTMEVBYRPK-XPUUQOCRSA-N

> <FORMULA>
C10H19N3O4

> <MOLECULAR_WEIGHT>
245.279

> <EXACT_MASS>
245.137556104

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
24.84550380558548

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-[(2S)-2-amino-3-methylbutanamido]-4-carbamoylbutanoic acid

> <ALOGPS_LOGP>
-2.94

> <JCHEM_LOGP>
-3.6522753476248138

> <ALOGPS_LOGS>
-1.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.640319980005692

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.7173694336519865

> <JCHEM_PKA_STRONGEST_BASIC>
8.514442273244482

> <JCHEM_POLAR_SURFACE_AREA>
135.51

> <JCHEM_REFRACTIVITY>
59.40290000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.37e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S)-2-amino-3-methylbutanamido]-4-carbamoylbutanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-APR-20         0                                  
HETATM    1  C   UNK     0    8711.3318711.654   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0    8712.6698712.423   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0    8714.0038711.654   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0    8715.3368712.423   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0    8716.6708711.654   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0    8715.3368713.963   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0    8709.9998712.423   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0    8708.6648711.654   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0    8707.3328712.423   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8708.6648710.114   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0    8709.9998713.963   0.000  0.00  0.00           N+0
HETATM   12  O   UNK     0    8711.3318710.114   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0    8714.0038710.114   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8715.3408709.342   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8715.3408707.798   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0    8714.0038707.027   0.000  0.00  0.00           O+0
HETATM   17  N   UNK     0    8716.6778707.027   0.000  0.00  0.00           N+0
CONECT    1    2    7   12                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   13                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4                                                            
CONECT    7    1    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7                                                            
CONECT   12    1                                                            
CONECT   13    3   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15                                                            
MASTER        0    0    0    0    0    0    0    0   17    0   32    0
END

View in JSmol

Synonyms

Value	Source
L-Val-L-GLN	ChEBI
Valyl-glutamine	ChEBI
Valylglutamine	ChEBI
VQ	ChEBI
L-Valyl-L-glutamine	HMDB
N2-L-Valyl-L-glutamine	HMDB
N2-Valylglutamine	HMDB
V-Q dipeptide	HMDB
VQ dipeptide	HMDB
Val-Gln	HMDB
Valine glutamine dipeptide	HMDB
Valine-glutamine dipeptide	HMDB

Chemical Formula

C₁₀H₁₉N₃O₄

Average Mass

245.2790 Da

Monoisotopic Mass

245.13756 Da

IUPAC Name

(2S)-2-[(2S)-2-amino-3-methylbutanamido]-4-carbamoylbutanoic acid

Traditional Name

(2S)-2-[(2S)-2-amino-3-methylbutanamido]-4-carbamoylbutanoic acid

CAS Registry Number

Not Available

SMILES

CC(C)[C@H](N)C(=O)N[C@@H](CCC(N)=O)C(O)=O

InChI Identifier

InChI=1S/C10H19N3O4/c1-5(2)8(12)9(15)13-6(10(16)17)3-4-7(11)14/h5-6,8H,3-4,12H2,1-2H3,(H2,11,14)(H,13,15)(H,16,17)/t6-,8-/m0/s1

InChI Key

XXDVDTMEVBYRPK-XPUUQOCRSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

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
Glutamine or derivatives
N-acyl-alpha amino acid or derivatives
Valine or derivatives
N-acyl-alpha-amino acid
N-acyl-l-alpha-amino acid
Alpha-amino acid amide
N-acyl-l-glutamine
Alpha-amino acid or derivatives
Branched fatty acid
N-acyl-amine
Fatty amide
Fatty acid
Fatty acyl
Amino acid
Secondary carboxylic acid amide
Carboxylic acid salt
Amino acid or derivatives
Primary carboxylic acid amide
Carboxamide group
Carboxylic acid
Monocarboxylic acid or derivatives
Primary amine
Organic nitrogen compound
Primary aliphatic amine
Organic zwitterion
Organic salt
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Amine
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

dipeptide (CHEBI:75010 )

Physical Properties

State

Not Available

Experimental 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

Predicted Properties

Property	Value	Source
logP	-2.9	ALOGPS
logP	-3.7	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	3.72	ChemAxon
pKa (Strongest Basic)	8.51	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	135.51 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	59.4 m³·mol⁻¹	ChemAxon
Polarizability	24.85 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

External Links

HMDB ID

HMDB0029125

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

5379066

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

7016044

PDB ID

Not Available

ChEBI ID

75010

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Valylglutamine (NP0136705)

MOL for NP0136705 (Valylglutamine)

3D MOL for NP0136705 (Valylglutamine)

3D SDF for NP0136705 (Valylglutamine)

3D-SDF for NP0136705 (Valylglutamine)

PDB for NP0136705 (Valylglutamine)

3D PDB for NP0136705 (Valylglutamine)

SMILES for NP0136705 (Valylglutamine)

INCHI for NP0136705 (Valylglutamine)

Structure for NP0136705 (Valylglutamine)

3D Structure for NP0136705 (Valylglutamine)