NP-MRD: Showing NP-Card for (2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid (NP0214552)

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Record Information

Version

2.0

Created at

2022-09-05 13:53:08 UTC

Updated at

2022-09-05 13:53:08 UTC

NP-MRD ID

NP0214552

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid

Description

2-Amino-2-deoxy-alpha-l-altropyranuronic acid belongs to the class of organic compounds known as pyranoid amino acids and derivatives. Pyranoid amino acids and derivatives are compounds containing a (hydro)pyran ring bearing unprotected amino and carboxylic acid functionalities. (2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid is found in Shigella sonnei. Based on a literature review very few articles have been published on 2-amino-2-deoxy-alpha-l-altropyranuronic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052215532D          

 13 13  0  0  1  0            999 V2000
    0.7145    2.0625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  6  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  2  0  0  0  0
  7  9  1  0  0  0  0
  6 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
  2 12  1  0  0  0  0
 12 13  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0214552

> <DATABASE_NAME>
NP-MRD

> <SMILES>
N[C@H]1[C@H](O)O[C@H]([C@H](O)[C@@H]1O)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C6H11NO6/c7-1-2(8)3(9)4(5(10)11)13-6(1)12/h1-4,6,8-9,12H,7H2,(H,10,11)/t1-,2-,3-,4-,6-/m1/s1

> <INCHI_KEY>
CRIPFXSBMSGPKB-YBSDWZGDSA-N

> <FORMULA>
C6H11NO6

> <MOLECULAR_WEIGHT>
193.155

> <EXACT_MASS>
193.058637078

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
24

> <JCHEM_AVERAGE_POLARIZABILITY>
16.67837157868775

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4R,5R,6R)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid

> <JCHEM_LOGP>
-4.984005965454803

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.742888085332483

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.09388076793223

> <JCHEM_PKA_STRONGEST_BASIC>
8.23121683748413

> <JCHEM_POLAR_SURFACE_AREA>
133.24

> <JCHEM_REFRACTIVITY>
37.448299999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4R,5R,6R)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  N   UNK     0       1.334   3.850   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      -0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   12                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   10                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    6   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10    2   13                                                  
CONECT   13   12                                                            
MASTER        0    0    0    0    0    0    0    0   13    0   26    0
END

View in JSmol

Synonyms

Value	Source
2-Amino-2-deoxy-a-L-altropyranuronate	Generator
2-Amino-2-deoxy-a-L-altropyranuronic acid	Generator
2-Amino-2-deoxy-alpha-L-altropyranuronate	Generator
2-Amino-2-deoxy-α-L-altropyranuronate	Generator
2-Amino-2-deoxy-α-L-altropyranuronic acid	Generator

Chemical Formula

C₆H₁₁NO₆

Average Mass

193.1550 Da

Monoisotopic Mass

193.05864 Da

IUPAC Name

(2R,3R,4R,5R,6R)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid

Traditional Name

(2R,3R,4R,5R,6R)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

N[C@H]1[C@H](O)O[C@H]([C@H](O)[C@@H]1O)C(O)=O

InChI Identifier

InChI=1S/C6H11NO6/c7-1-2(8)3(9)4(5(10)11)13-6(1)12/h1-4,6,8-9,12H,7H2,(H,10,11)/t1-,2-,3-,4-,6-/m1/s1

InChI Key

CRIPFXSBMSGPKB-YBSDWZGDSA-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, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Shigella sonnei	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranoid amino acids and derivatives. Pyranoid amino acids and derivatives are compounds containing a (hydro)pyran ring bearing unprotected amino and carboxylic acid functionalities.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Pyranoid amino acids and derivatives

Alternative Parents

Substituents

Pyranoid amino acid
Delta amino acid or derivatives
Hexose monosaccharide
Beta-hydroxy acid
Amino saccharide
Hydroxy acid
Monosaccharide
Oxane
Pyran
Secondary alcohol
Amino acid or derivatives
Hemiacetal
1,2-aminoalcohol
1,2-diol
Amino acid
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Polyol
Oxacycle
Carboxylic acid derivative
Carboxylic acid
Amine
Organopnictogen compound
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic nitrogen compound
Organonitrogen compound
Alcohol
Primary aliphatic amine
Primary amine
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	-5	ChemAxon
pKa (Strongest Acidic)	3.09	ChemAxon
pKa (Strongest Basic)	8.23	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	133.24 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	37.45 m³·mol⁻¹	ChemAxon
Polarizability	16.68 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

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

157010738

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid (NP0214552)

MOL for NP0214552 ((2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid)

3D MOL for NP0214552 ((2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid)

3D SDF for NP0214552 ((2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid)

3D-SDF for NP0214552 ((2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid)

PDB for NP0214552 ((2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid)

3D PDB for NP0214552 ((2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid)

SMILES for NP0214552 ((2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid)

INCHI for NP0214552 ((2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid)

Structure for NP0214552 ((2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid)

3D Structure for NP0214552 ((2r,3r,4r,5r,6r)-5-amino-3,4,6-trihydroxyoxane-2-carboxylic acid)