NP-MRD: Showing NP-Card for Asparaginylisoleucine (NP0136373)

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Record Information

Version

2.0

Created at

2022-05-12 15:12:53 UTC

Updated at

2022-05-12 15:12:53 UTC

NP-MRD ID

NP0136373

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Asparaginylisoleucine

Description

Asparaginylisoleucine, also known as N-I or H-L-asn-L-ile-OH, 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. Asparaginylisoleucine is a very strong basic compound (based on its pKa). It is an incomplete breakdown product of protein digestion or protein catabolism.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 35  0  0  0  0  0  0  0  0999 V2000
   -3.8836    0.8370   -1.1109 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4993    0.9004   -0.4997 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2097   -0.4487    0.1166 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.2544   -0.7253    1.1752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8569   -0.4806    0.7949 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2104   -0.1886   -0.1642 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0800    0.9170   -0.0072 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9129    1.6590    0.9948 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1462    1.2069   -0.9672 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8914    2.4034   -0.5640 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1474    0.1015   -1.1117 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8277   -0.1986    0.1775 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8173   -1.2089    0.2871 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4944    0.4801    1.1820 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6455   -1.8535    1.2904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3043   -2.5489    0.8809 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5131   -2.3769    2.2231 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6477    1.3067   -0.4546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1780   -0.1974   -1.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9241    1.4228   -2.0713 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4372    1.7226    0.2097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7895    1.0311   -1.3606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2370   -1.2405   -0.6308 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4866   -1.8082    1.1401 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2027   -0.1823    0.9677 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8929   -0.5074    2.2052 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8485    0.2748    1.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3505   -0.7992   -0.9916 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6729    1.3951   -1.9521 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2389    2.8208   -1.4692 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2510    3.0649   -0.0511 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7244   -0.8182   -1.5724 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9395    0.4594   -1.8138 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8444   -2.0615   -0.2936 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5691   -1.0623    1.0173 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9159   -3.2963    2.1982 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
  3  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  1  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
  5 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  0
  2 22  1  0
  3 23  1  6
  4 24  1  0
  4 25  1  0
  4 26  1  0
  5 27  1  1
  6 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


  Mrv1652304062013262D          

 17 16  0  0  0  0            999 V2000
 2498.1130 2497.1292    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 2498.1130 2497.9534    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 2498.8250 2498.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2499.5387 2497.9534    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2498.8250 2499.1891    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2498.1130 2499.6023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2497.3989 2499.1891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2496.6544 2499.6186    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 2497.3989 2498.3646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2499.5387 2499.6023    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 2497.3989 2496.7157    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 2496.6850 2497.1292    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2495.9692 2496.7157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2497.3989 2495.8914    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2498.8269 2496.7157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 2499.5408 2497.1292    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 2498.8269 2495.8914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  6  0  0  0
  1 11  1  0  0  0  0
  1 15  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  3  1  6  0  0  0
  5  6  1  0  0  0  0
  5 10  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
 11 12  1  0  0  0  0
 11 14  1  1  0  0  0
 12 13  1  0  0  0  0
 15 16  1  0  0  0  0
 15 17  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0136373

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C10H19N3O4/c1-3-5(2)8(10(16)17)13-9(15)6(11)4-7(12)14/h5-6,8H,3-4,11H2,1-2H3,(H2,12,14)(H,13,15)(H,16,17)/t5-,6-,8-/m0/s1

> <INCHI_KEY>
MQLZLIYPFDIDMZ-HAFWLYHUSA-N

> <FORMULA>
C10H19N3O4

> <MOLECULAR_WEIGHT>
245.279

> <EXACT_MASS>
245.137556104

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
24.89479664351972

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S)-2-[(2S)-2-amino-3-carbamoylpropanamido]-3-methylpentanoic acid

> <ALOGPS_LOGP>
-2.66

> <JCHEM_LOGP>
-3.4963257965746064

> <ALOGPS_LOGS>
-1.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.545220451958972

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.71363182408048

> <JCHEM_PKA_STRONGEST_BASIC>
7.346798017511727

> <JCHEM_POLAR_SURFACE_AREA>
135.51

> <JCHEM_REFRACTIVITY>
59.2489

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
7.56e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S)-2-[(2S)-2-amino-3-carbamoylpropanamido]-3-methylpentanoic 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    4663.1444661.308   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0    4663.1444662.846   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0    4664.4734663.614   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0    4665.8064662.846   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0    4664.4734665.153   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0    4663.1444665.924   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0    4661.8114665.153   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0    4660.4224665.955   0.000  0.00  0.00           N+0
HETATM    9  O   UNK     0    4661.8114663.614   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0    4665.8064665.924   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0    4661.8114660.536   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0    4660.4794661.308   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0    4659.1434660.536   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    4661.8114658.997   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0    4664.4774660.536   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0    4665.8094661.308   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0    4664.4774658.997   0.000  0.00  0.00           O+0
CONECT    1    2   11   15                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    5                                                            
CONECT   11    1   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12                                                            
CONECT   14   11                                                            
CONECT   15    1   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
(2S,3S)-2-{[(2S)-2,4-diamino-4-oxobutanoyl]amino}-3-methylpentanoic acid	ChEBI
Asparagine isoleucine dipeptide	ChEBI
Asparagine-isoleucine dipeptide	ChEBI
Asparaginyl-isoleucine	ChEBI
H-L-Asn-L-ile-OH	ChEBI
L-Asn-L-ile	ChEBI
N-I	ChEBI
N-I dipeptide	ChEBI
NI	ChEBI
NI dipeptide	ChEBI
(2S,3S)-2-{[(2S)-2,4-diamino-4-oxobutanoyl]amino}-3-methylpentanoate	Generator
(2S,3S)-2-{[(2S)-2-amino-1-hydroxy-3-(C-hydroxycarbonimidoyl)propylidene]amino}-3-methylpentanoate	HMDB
Asn-ile	HMDB
L-Asparaginyl-L-isoleucine	HMDB
Asparaginylisoleucine	ChEBI

Chemical Formula

C₁₀H₁₉N₃O₄

Average Mass

245.2790 Da

Monoisotopic Mass

245.13756 Da

IUPAC Name

(2S,3S)-2-[(2S)-2-amino-3-carbamoylpropanamido]-3-methylpentanoic acid

Traditional Name

(2S,3S)-2-[(2S)-2-amino-3-carbamoylpropanamido]-3-methylpentanoic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C10H19N3O4/c1-3-5(2)8(10(16)17)13-9(15)6(11)4-7(12)14/h5-6,8H,3-4,11H2,1-2H3,(H2,12,14)(H,13,15)(H,16,17)/t5-,6-,8-/m0/s1

InChI Key

MQLZLIYPFDIDMZ-HAFWLYHUSA-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
Isoleucine or derivatives
Asparagine or derivatives
N-acyl-alpha-amino acid
N-acyl-alpha amino acid or derivatives
N-acyl-l-alpha-amino acid
Alpha-amino acid amide
Alpha-amino acid or derivatives
Branched fatty acid
Methyl-branched fatty acid
N-acyl-amine
Fatty amide
Fatty acid
Fatty acyl
Primary carboxylic acid amide
Amino acid or derivatives
Secondary carboxylic acid amide
Carboxamide group
Amino acid
Carboxylic acid
Monocarboxylic acid or derivatives
Organic nitrogen compound
Organonitrogen compound
Primary aliphatic amine
Organooxygen compound
Primary amine
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organopnictogen compound
Amine
Organic oxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	-2.7	ALOGPS
logP	-3.5	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	3.71	ChemAxon
pKa (Strongest Basic)	7.35	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	59.25 m³·mol⁻¹	ChemAxon
Polarizability	24.89 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

HMDB0028734

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

56991460

PDB ID

Not Available

ChEBI ID

141421

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Asparaginylisoleucine (NP0136373)

MOL for NP0136373 (Asparaginylisoleucine)

3D MOL for NP0136373 (Asparaginylisoleucine)

3D SDF for NP0136373 (Asparaginylisoleucine)

3D-SDF for NP0136373 (Asparaginylisoleucine)

PDB for NP0136373 (Asparaginylisoleucine)

3D PDB for NP0136373 (Asparaginylisoleucine)

SMILES for NP0136373 (Asparaginylisoleucine)

INCHI for NP0136373 (Asparaginylisoleucine)

Structure for NP0136373 (Asparaginylisoleucine)

3D Structure for NP0136373 (Asparaginylisoleucine)