NP-MRD: Showing NP-Card for n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid (NP0172226)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-03 09:05:03 UTC

Updated at

2022-09-03 09:05:03 UTC

NP-MRD ID

NP0172226

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid

Description

Glcnac6P belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphated group linked to the carbohydrate unit. Based on a literature review very few articles have been published on Glcnac6P.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 34  0  0  0  0  0  0  0  0999 V2000
    5.0035    0.3335    0.5733 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8516    1.0835   -0.0934 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0408    2.4995   -0.0664 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9132    0.5770   -0.5784 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.0164   -0.3414   -1.0182 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.7277   -1.7902   -0.9050 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1252   -2.7490   -1.1505 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7524   -0.5762   -0.3781 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.8189   -1.1234    0.9127 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1530    0.6714   -0.2712 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3326    1.3279    0.9029 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4823    0.1438   -0.1548 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9782   -0.4174   -1.3667 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6692    0.8341    0.5066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3882   -0.2695    1.0755 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9195   -0.3508    0.4850 P   0  0  0  0  0  5  0  0  0  0  0  0
   -5.7841   -1.2327    1.3843 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7291   -1.3373   -0.9515 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6408    1.0732    0.1634 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6351    1.0410    1.1362 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5747   -0.4665    1.2184 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5748   -0.0684   -0.2790 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3327    3.0044    0.5325 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9154   -0.3287   -2.1532 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7451   -1.7590   -0.6039 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1469   -1.3237   -0.9925 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2163   -1.9033    0.9710 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0601    1.3667   -1.0863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0622    0.7792    1.6813 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3827   -0.8515    0.5406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3801   -0.9544   -1.8490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3581    1.5100    1.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2674    1.2988   -0.2480 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3581   -1.2159   -1.6256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2308    1.5155   -0.6281 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  5  8  1  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 18  1  0
 16 19  1  0
 16 17  2  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  3 23  1  0
  5 24  1  6
  6 25  1  0
  8 26  1  6
  9 27  1  0
 10 28  1  6
 11 29  1  0
 12 30  1  1
 13 31  1  0
 14 32  1  0
 14 33  1  0
 18 34  1  0
 19 35  1  0
M  END


  Mrv1652309032211052D          

 19 18  0  0  1  0            999 V2000
    1.2375   -2.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6500   -1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2375   -0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750   -1.4289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875   -0.7145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4750    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8875    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7125   -0.7145    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.1250   -1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1250    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7125    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.3625    0.7145    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3625   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9500   -1.4289    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3625   -2.1434    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    5.7750   -2.8579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6480   -2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0770   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  6  0  0  0
  8 10  1  0  0  0  0
 10 11  1  6  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 16 19  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0172226

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C8H16NO9P/c1-4(11)9-5(2-10)7(13)8(14)6(12)3-18-19(15,16)17/h2,5-8,12-14H,3H2,1H3,(H,9,11)(H2,15,16,17)/t5-,6+,7+,8+/m0/s1

> <INCHI_KEY>
QDSLHWJDSQGPEE-LXGUWJNJSA-N

> <FORMULA>
C8H16NO9P

> <MOLECULAR_WEIGHT>
301.188

> <EXACT_MASS>
301.056268097

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
24.914804084548827

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[(2R,3R,4S,5R)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid

> <ALOGPS_LOGP>
-2.10

> <JCHEM_LOGP>
-3.6750140554101627

> <ALOGPS_LOGS>
-1.28

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.621617329782305

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.6657339368125545

> <JCHEM_PKA_STRONGEST_BASIC>
1.0095423100869674

> <JCHEM_POLAR_SURFACE_AREA>
177.10999999999999

> <JCHEM_REFRACTIVITY>
59.841499999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.60e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[(2R,3R,4S,5R)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0       2.310  -4.001   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.080  -2.667   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.310  -1.334   0.000  0.00  0.00           O+0
HETATM    4  N   UNK     0       4.620  -2.667   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0       5.390  -1.334   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.620   0.000   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.390   1.334   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       6.930  -1.334   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.700  -2.667   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.700   0.000   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.930   1.334   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.240   0.000   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.010   1.334   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      10.010  -1.334   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       9.240  -2.667   0.000  0.00  0.00           O+0
HETATM   16  P   UNK     0      10.010  -4.001   0.000  0.00  0.00           P+0
HETATM   17  O   UNK     0      10.780  -5.335   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       8.676  -4.771   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      11.344  -3.231   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   36    0
END

View in JSmol

Synonyms

Value	Source
N-Acetylglucosamine 6-phosphate	MeSH

Chemical Formula

C₈H₁₆NO₉P

Average Mass

301.1880 Da

Monoisotopic Mass

301.05627 Da

IUPAC Name

N-[(2R,3R,4S,5R)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid

Traditional Name

N-[(2R,3R,4S,5R)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C8H16NO9P/c1-4(11)9-5(2-10)7(13)8(14)6(12)3-18-19(15,16)17/h2,5-8,12-14H,3H2,1H3,(H,9,11)(H2,15,16,17)/t5-,6+,7+,8+/m0/s1

InChI Key

QDSLHWJDSQGPEE-LXGUWJNJSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monosaccharide phosphates. These are monosaccharides comprising a phosphated group linked to the carbohydrate unit.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Monosaccharide phosphates

Alternative Parents

Substituents

Monosaccharide phosphate
Monoalkyl phosphate
Amino saccharide
Alkyl phosphate
Phosphoric acid ester
Organic phosphoric acid derivative
Beta-hydroxy aldehyde
Acetamide
Secondary carboxylic acid amide
Secondary alcohol
Carboxamide group
Polyol
Carboxylic acid derivative
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Organonitrogen compound
Carbonyl group
Aldehyde
Alcohol
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	-2.1	ALOGPS
logP	-3.7	ChemAxon
logS	-1.3	ALOGPS
pKa (Strongest Acidic)	1.67	ChemAxon
pKa (Strongest Basic)	1.01	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	177.11 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	59.84 m³·mol⁻¹	ChemAxon
Polarizability	24.91 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

133037

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

150941

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid (NP0172226)

MOL for NP0172226 (n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid)

3D MOL for NP0172226 (n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid)

3D SDF for NP0172226 (n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid)

3D-SDF for NP0172226 (n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid)

PDB for NP0172226 (n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid)

3D PDB for NP0172226 (n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid)

SMILES for NP0172226 (n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid)

INCHI for NP0172226 (n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid)

Structure for NP0172226 (n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid)

3D Structure for NP0172226 (n-[(2r,3r,4s,5r)-3,4,5-trihydroxy-1-oxo-6-(phosphonooxy)hexan-2-yl]ethanimidic acid)