NP-MRD: Showing NP-Card for Tryptophyl-Valine (NP0136679)

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Record Information

Version

2.0

Created at

2022-05-12 15:20:44 UTC

Updated at

2022-05-12 15:20:44 UTC

NP-MRD ID

NP0136679

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Tryptophyl-Valine

Description

Tryptophyl-Valine, also known as W-V dipeptide or TRP-val, 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. Tryptophyl-Valine is a very strong basic compound (based on its pKa). 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. Tryptophyl-Valine is a dipeptide composed of tryptophan and valine. 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 PDB SMILES InChI

     RDKit          3D

 43 44  0  0  0  0  0  0  0  0999 V2000
   -3.2084   -1.1924   -1.6423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7216   -1.2199   -0.2034 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.2325   -1.2444   -0.2981 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2073   -0.0021    0.4999 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7636   -0.0223    0.4811 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0115    0.9867   -0.1802 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6626    1.9048   -0.7516 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4505    1.0132   -0.2300 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9039    2.1646   -0.9528 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.1044    0.8702    1.1285 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5662    0.9198    0.8987 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3863    1.9898    1.1573 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6451    1.6660    0.8215 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.6878    0.4130    0.3473 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7587   -0.3187   -0.1089 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5233   -1.6051   -0.5486 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2332   -2.1040   -0.5139 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1684   -1.3440   -0.0479 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3950   -0.0622    0.3913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6704    0.1069    1.8947 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9064    0.1724    2.8864 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0467    0.1395    2.1369 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2399   -1.7408   -1.7326 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9609   -1.6285   -2.3245 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0036   -0.1553   -1.9810 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3817   -2.1641    0.2341 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4720   -2.0590   -1.0356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5877   -0.2960   -0.7510 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7325   -1.5164    0.6364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5493    0.8923   -0.0718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2288   -0.7907    0.9606 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7724    0.1044   -0.8055 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0230    2.9438   -0.2488 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1225    2.4539   -1.5981 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7854   -0.1134    1.5390 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8284    1.6676    1.8303 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1254    2.9652    1.5650 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4875    2.3015    0.9142 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7663    0.0672   -0.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3076   -2.2293   -0.9154 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0273   -3.1098   -0.8541 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1588   -1.7310   -0.0188 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6400    0.9066    1.7950 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
  6  7  2  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 14 19  2  0
 19 18  1  0
 18 17  2  0
 17 16  1  0
 16 15  2  0
  4 20  1  0
 20 22  1  0
 20 21  2  0
 19 11  1  0
 15 14  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
  2 26  1  1
  3 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  6
  5 31  1  0
  8 32  1  6
  9 33  1  0
  9 34  1  0
 10 35  1  0
 10 36  1  0
 12 37  1  0
 13 38  1  0
 18 42  1  0
 17 41  1  0
 16 40  1  0
 15 39  1  0
 22 43  1  0
M  END


  Mrv1652304062014202D          

 22 23  0  0  0  0            999 V2000
    1.3279    0.4353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5029    0.4353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0904    1.1498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0904   -0.2791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7346   -0.2791    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1471   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7346   -1.7081    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9721   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3846   -0.2791    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3846   -1.7081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2096   -1.7081    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6945   -1.0406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4791   -1.2956    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4791   -2.1206    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6945   -2.3755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5230   -3.1825    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1361   -3.7345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9207   -3.4796    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0922   -2.6726    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5029   -0.9936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3279   -0.9936    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0904   -1.7081    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
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 14 19  1  0  0  0  0
  4 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0136679

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C16H21N3O3/c1-9(2)14(16(21)22)19-15(20)12(17)7-10-8-18-13-6-4-3-5-11(10)13/h3-6,8-9,12,14,18H,7,17H2,1-2H3,(H,19,20)(H,21,22)

> <INCHI_KEY>
LWFWZRANSFAJDR-UHFFFAOYSA-N

> <FORMULA>
C16H21N3O3

> <MOLECULAR_WEIGHT>
303.3562

> <EXACT_MASS>
303.158291553

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
32.41973172571316

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <ALOGPS_LOGP>
-0.56

> <JCHEM_LOGP>
-0.7362635347196758

> <ALOGPS_LOGS>
-2.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.79468617555359

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.8321246138333174

> <JCHEM_PKA_STRONGEST_BASIC>
7.959216654384908

> <JCHEM_POLAR_SURFACE_AREA>
108.21000000000001

> <JCHEM_REFRACTIVITY>
82.4958

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.35e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[2-amino-3-(1H-indol-3-yl)propanamido]-3-methylbutanoic 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       2.479   0.813   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.939   0.813   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.169   2.146   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.169  -0.521   0.000  0.00  0.00           C+0
HETATM    5  N   UNK     0      -1.371  -0.521   0.000  0.00  0.00           N+0
HETATM    6  C   UNK     0      -2.141  -1.855   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.371  -3.188   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.681  -1.855   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -4.451  -0.521   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -4.451  -3.188   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -5.991  -3.188   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.896  -1.942   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      -8.361  -2.418   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      -8.361  -3.958   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -6.896  -4.434   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -6.576  -5.941   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -7.721  -6.971   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -9.185  -6.495   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -9.505  -4.989   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.939  -1.855   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.479  -1.855   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.169  -3.188   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5   20                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   19                                                  
CONECT   15   14   11   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   14                                                       
CONECT   20    4   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
L-Tryptophyl-L-valine	HMDB
TRP-Val	HMDB
Tryptophan valine dipeptide	HMDB
Tryptophan-valine dipeptide	HMDB
Tryptophylvaline	HMDB
W-V Dipeptide	HMDB
WV Dipeptide	HMDB
2-{[2-amino-1-hydroxy-3-(1H-indol-3-yl)propylidene]amino}-3-methylbutanoate	Generator

Chemical Formula

C₁₆H₂₁N₃O₃

Average Mass

303.3562 Da

Monoisotopic Mass

303.15829 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C16H21N3O3/c1-9(2)14(16(21)22)19-15(20)12(17)7-10-8-18-13-6-4-3-5-11(10)13/h3-6,8-9,12,14,18H,7,17H2,1-2H3,(H,19,20)(H,21,22)

InChI Key

LWFWZRANSFAJDR-UHFFFAOYSA-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
Valine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Triptan
Alpha-amino acid or derivatives
3-alkylindole
Indole
Indole or derivatives
Aralkylamine
Fatty amide
Substituted pyrrole
Fatty acyl
Benzenoid
Heteroaromatic compound
Pyrrole
Secondary carboxylic acid amide
Amino acid or derivatives
Carboxamide group
Amino acid
Organoheterocyclic compound
Azacycle
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxygen compound
Primary aliphatic amine
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Organonitrogen compound
Carbonyl group
Organooxygen compound
Amine
Primary amine
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

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	-0.56	ALOGPS
logP	-0.74	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Acidic)	3.83	ChemAxon
pKa (Strongest Basic)	7.96	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	108.21 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	82.5 m³·mol⁻¹	ChemAxon
Polarizability	32.42 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

External Links

HMDB ID

HMDB0029096

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB 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

19816756

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Tryptophyl-Valine (NP0136679)

MOL for NP0136679 (Tryptophyl-Valine)

3D MOL for NP0136679 (Tryptophyl-Valine)

3D SDF for NP0136679 (Tryptophyl-Valine)

3D-SDF for NP0136679 (Tryptophyl-Valine)

PDB for NP0136679 (Tryptophyl-Valine)

3D PDB for NP0136679 (Tryptophyl-Valine)

SMILES for NP0136679 (Tryptophyl-Valine)

INCHI for NP0136679 (Tryptophyl-Valine)

Structure for NP0136679 (Tryptophyl-Valine)

3D Structure for NP0136679 (Tryptophyl-Valine)