NP-MRD: Showing NP-Card for Phenylalanylglutamic acid (NP0136594)

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Record Information

Version

2.0

Created at

2022-05-12 15:18:35 UTC

Updated at

2022-05-12 15:18:35 UTC

NP-MRD ID

NP0136594

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Phenylalanylglutamic acid

Description

Phe-Glu, also known as FE or L-phe-L-glu, 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. Phe-Glu is possibly neutral. A dipeptide formed from L-phenylalanine and L-glutamic acid residues.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 39  0  0  0  0  0  0  0  0999 V2000
   -1.0759   -0.9791   -1.4943 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3194    0.2902   -0.9167 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2096    0.1211    0.2974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5057   -0.4954   -0.0566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5484    0.3526   -0.4162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7842   -0.1796   -0.7567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9717   -1.5537   -0.7358 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9051   -2.3741   -0.3705 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6748   -1.8648   -0.0306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0770    0.9758   -0.4820 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1851    2.0901    0.0789 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2112    0.4338   -0.6703 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.4366    1.1144   -0.2384 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1259    0.2387    0.7274 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4023    0.7230    1.3086 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9932   -0.2333    2.2601 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5017   -0.3612    3.3949 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0835   -0.9890    1.9110 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2043    1.4859   -1.4425 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8733    1.2464   -2.6092 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4022    2.1640   -1.2537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7255   -1.7158   -0.8737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7305   -0.9944   -2.4618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8128    0.9434   -1.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6681   -0.5469    1.0072 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3645    1.0833    0.8280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4191    1.4251   -0.4373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6196    0.4459   -1.0427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9386   -1.9884   -1.0020 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0261   -3.4537   -0.3461 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8802   -2.5410    0.2455 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2911   -0.4951   -1.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1537    2.0619    0.2640 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3472   -0.7552    0.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4555   -0.0466    1.5801 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1715    1.6437    1.8878 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1589    0.9058    0.5170 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1697   -1.3414    0.9681 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4601    3.1637   -1.1347 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  2 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 18  1  0
 16 17  2  0
 13 19  1  0
 19 21  1  0
 19 20  2  0
  9  4  1  0
  1 22  1  0
  1 23  1  0
  2 24  1  6
  3 25  1  0
  3 26  1  0
  5 27  1  0
  6 28  1  0
  7 29  1  0
  8 30  1  0
  9 31  1  0
 12 32  1  0
 13 33  1  1
 14 34  1  0
 14 35  1  0
 15 36  1  0
 15 37  1  0
 18 38  1  0
 21 39  1  0
M  END


  Mrv1652304062014052D          

 21 21  0  0  0  0            999 V2000
10001.8001 9999.8034    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.085410000.2157    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10000.3730 9999.8034    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.659010000.2157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9455 9999.8034    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9998.230210000.2157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.9455 9998.9797    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.659010001.0394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.085410001.0394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.5187 9999.8043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.804210000.2167    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.0897 9999.8042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.0896 9998.9792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.8041 9998.5667    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.5187 9998.9793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10002.512010000.2149    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.800110001.4513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10000.373010001.4513    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.2264 9999.8024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.2264 9998.9774    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10003.940810000.2149    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  9  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  8  2  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  1  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 10  1  0  0  0  0
  6 10  1  0  0  0  0
  1 16  1  0  0  0  0
  9 17  1  0  0  0  0
  9 18  2  0  0  0  0
 16 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0136594

> <DATABASE_NAME>
NP-MRD

> <SMILES>
N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCC(O)=O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C14H18N2O5/c15-10(8-9-4-2-1-3-5-9)13(19)16-11(14(20)21)6-7-12(17)18/h1-5,10-11H,6-8,15H2,(H,16,19)(H,17,18)(H,20,21)/t10-,11-/m0/s1

> <INCHI_KEY>
JXWLMUIXUXLIJR-QWRGUYRKSA-N

> <FORMULA>
C14H18N2O5

> <MOLECULAR_WEIGHT>
294.307

> <EXACT_MASS>
294.121571688

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
29.06912660474311

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-2-[(2S)-2-amino-3-phenylpropanamido]pentanedioic acid

> <ALOGPS_LOGP>
-2.32

> <JCHEM_LOGP>
-2.3823920286556977

> <ALOGPS_LOGS>
-2.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
4.042640766608468

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.305693081007528

> <JCHEM_PKA_STRONGEST_BASIC>
8.009705260523113

> <JCHEM_POLAR_SURFACE_AREA>
129.71999999999997

> <JCHEM_REFRACTIVITY>
73.2041

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.92e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-2-[(2S)-2-amino-3-phenylpropanamido]pentanedioic 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    8670.0278666.300   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8668.6938667.069   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0    8667.3638666.300   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0    8666.0308667.069   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0    8664.6988666.300   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    8663.3638667.069   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0    8664.6988664.762   0.000  0.00  0.00           N+0
HETATM    8  O   UNK     0    8666.0308668.607   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0    8668.6938668.607   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0    8662.0358666.301   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0    8660.7018667.071   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    8659.3678666.301   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    8659.3678664.761   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8660.7018663.991   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    8662.0358664.761   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0    8671.3568667.068   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0    8670.0278669.376   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0    8667.3638669.376   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0    8672.6898666.298   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0    8672.6898664.758   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0    8674.0238667.068   0.000  0.00  0.00           O+0
CONECT    1    2   16                                                       
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5   10                                                       
CONECT    7    5                                                            
CONECT    8    4                                                            
CONECT    9    2   17   18                                                  
CONECT   10   11   15    6                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   10                                                       
CONECT   16    1   19                                                       
CONECT   17    9                                                            
CONECT   18    9                                                            
CONECT   19   16   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   42    0
END

View in JSmol

Synonyms

Value	Source
FE	ChEBI
L-Phe-L-glu	ChEBI
N-L-Phenylalanyl-L-glutamic acid	ChEBI
Phenylalanylglutamate	ChEBI
Phenylalanylglutamic acid	ChEBI
N-L-Phenylalanyl-L-glutamate	Generator
F-E dipeptide	HMDB
FE dipeptide	HMDB
L-Phenylalanyl-L-glutamate	HMDB
L-Phenylalanyl-L-glutamic acid	HMDB
L-alpha-Phenylalanyl-L-glutamic acid	HMDB
L-α-Phenylalanyl-L-glutamic acid	HMDB
N-(3-Phenyl-L-alanyl)-L-glutamic acid	HMDB
N-(3-Phenyl-L-alanyl)glutamic acid	HMDB
N-(3-Phenylalanyl)glutamic acid	HMDB
N-Phenylalanylglutamate	HMDB
N-Phenylalanylglutamic acid	HMDB
Phe-Glu	HMDB
Phenylalanine glutamate dipeptide	HMDB
Phenylalanine glutamic acid dipeptide	HMDB
Phenylalanine-glutamate dipeptide	HMDB
Phenylalanine-glutamic acid dipeptide	HMDB
Phenylalanyl-glutamate	HMDB
Phenylalanyl-glutamic acid	HMDB

Chemical Formula

C₁₄H₁₈N₂O₅

Average Mass

294.3070 Da

Monoisotopic Mass

294.12157 Da

IUPAC Name

(2S)-2-[(2S)-2-amino-3-phenylpropanamido]pentanedioic acid

Traditional Name

(2S)-2-[(2S)-2-amino-3-phenylpropanamido]pentanedioic acid

CAS Registry Number

Not Available

SMILES

N[C@@H](CC1=CC=CC=C1)C(=O)N[C@@H](CCC(O)=O)C(O)=O

InChI Identifier

InChI=1S/C14H18N2O5/c15-10(8-9-4-2-1-3-5-9)13(19)16-11(14(20)21)6-7-12(17)18/h1-5,10-11H,6-8,15H2,(H,16,19)(H,17,18)(H,20,21)/t10-,11-/m0/s1

InChI Key

JXWLMUIXUXLIJR-QWRGUYRKSA-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
Phenylalanine or derivatives
Glutamic acid or derivatives
N-acyl-l-alpha-amino acid
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
Alpha-amino acid amide
Alpha-amino acid or derivatives
Amphetamine or derivatives
Aralkylamine
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Fatty amide
Fatty acyl
Benzenoid
Amino acid or derivatives
Carboxamide group
Amino acid
Secondary carboxylic acid amide
Carboxylic acid
Primary aliphatic amine
Hydrocarbon derivative
Amine
Organic oxygen compound
Carbonyl group
Organic oxide
Organopnictogen compound
Organic nitrogen compound
Primary amine
Organonitrogen compound
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

dipeptide (CHEBI:74712 )

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	-2.3	ALOGPS
logP	-2.4	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	3.31	ChemAxon
pKa (Strongest Basic)	8.01	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	129.72 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	73.2 m³·mol⁻¹	ChemAxon
Polarizability	29.07 Å³	ChemAxon
Number of Rings	1	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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

133206

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

151134

PDB ID

Not Available

ChEBI ID

74712

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Phenylalanylglutamic acid (NP0136594)

MOL for NP0136594 (Phenylalanylglutamic acid)

3D MOL for NP0136594 (Phenylalanylglutamic acid)

3D SDF for NP0136594 (Phenylalanylglutamic acid)

3D-SDF for NP0136594 (Phenylalanylglutamic acid)

PDB for NP0136594 (Phenylalanylglutamic acid)

3D PDB for NP0136594 (Phenylalanylglutamic acid)

SMILES for NP0136594 (Phenylalanylglutamic acid)

INCHI for NP0136594 (Phenylalanylglutamic acid)

Structure for NP0136594 (Phenylalanylglutamic acid)

3D Structure for NP0136594 (Phenylalanylglutamic acid)