NP-MRD: Showing NP-Card for 4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one (NP0230454)

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Record Information

Version

2.0

Created at

2022-09-06 10:54:27 UTC

Updated at

2022-09-06 10:54:28 UTC

NP-MRD ID

NP0230454

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one

Description

SCHEMBL22043215 belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond. 4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one is found in Crocus sativus. Based on a literature review very few articles have been published on SCHEMBL22043215.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 34 35  0  0  0  0  0  0  0  0999 V2000
    5.3039    0.6203    1.7889 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3366    0.7471    1.0003 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9384    0.3248    1.3084 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3203    0.1008   -0.0786 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9972    0.4177    0.0050 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1047   -0.5908   -0.3204 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.6117   -0.3839   -1.4483 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7503    0.3308   -1.2861 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6299    1.7864   -1.0110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9516    2.0770    0.1567 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7199   -0.3037   -0.3028 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8370   -0.7512   -0.9925 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0500   -1.5409    0.2863 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8535   -2.0835    1.2612 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7062   -1.0945    0.8063 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1079   -2.1490    1.5000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0568    1.1604   -0.8757 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3425    1.2807   -0.2723 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8821   -0.5627    1.9352 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4319    1.2087    1.7285 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5556   -0.9142   -0.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8124   -1.4688   -0.5865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2855    0.2732   -2.3000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6168    2.2973   -0.9348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1119    2.2425   -1.8984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8806    3.0607    0.2271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0625    0.3980    0.4765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5998   -0.9357   -0.3889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8579   -2.2294   -0.5607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8044   -3.0644    1.1800 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9407   -0.2692    1.5436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4383   -3.0113    1.0971 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5298    2.1262   -0.7295 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2042    0.9006   -1.9216 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  0
  4 17  1  0
 17 18  1  0
 18  2  1  0
  2  1  2  0
  2  3  1  0
  6 15  1  0
 15 16  1  0
 15 13  1  0
 13 14  1  0
 13 11  1  0
 11 12  1  0
 11  8  1  0
  3  4  1  0
 10 26  1  0
  9 24  1  0
  9 25  1  0
  8 23  1  6
  6 22  1  6
  4 21  1  6
 17 33  1  0
 17 34  1  0
  3 19  1  0
  3 20  1  0
 15 31  1  1
 16 32  1  0
 13 29  1  6
 14 30  1  0
 11 27  1  1
 12 28  1  0
M  END


  Mrv1652309062212542D          

 18 19  0  0  1  0            999 V2000
    2.0367   -0.4741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9341   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5986   -3.9898    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0835   -4.6572    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7479   -5.4109    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2329   -6.0783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0533   -5.9921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9275   -5.4971    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5919   -6.2508    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4425   -4.8297    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6221   -4.9159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7781   -4.0760    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2932   -3.4086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  6  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  1  0  0  0
 11 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  1  0  0  0
  4 17  1  0  0  0  0
 17 18  1  0  0  0  0
  2 18  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0230454

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1O[C@@H](OC2COC(=O)C2)[C@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C10H16O8/c11-2-5-7(13)8(14)9(15)10(18-5)17-4-1-6(12)16-3-4/h4-5,7-11,13-15H,1-3H2/t4?,5-,7-,8+,9-,10-/m1/s1

> <INCHI_KEY>
MQEPWBMWFIVRPS-WQPQPNDESA-N

> <FORMULA>
C10H16O8

> <MOLECULAR_WEIGHT>
264.23

> <EXACT_MASS>
264.084517475

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
34

> <JCHEM_AVERAGE_POLARIZABILITY>
24.366951243896708

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one

> <JCHEM_LOGP>
-2.540280487

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.20004389003082

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.210442440063574

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083553403314

> <JCHEM_POLAR_SURFACE_AREA>
125.68000000000002

> <JCHEM_REFRACTIVITY>
53.92889999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-{[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  O   UNK     0       3.802  -0.885   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.802  -2.425   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.048  -3.330   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.572  -4.795   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.477  -6.041   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.851  -7.448   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.756  -8.693   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.129 -10.100   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.035 -11.346   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       7.566 -11.185   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.598 -10.261   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.972 -11.668   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.693  -9.015   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.161  -9.176   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       3.319  -7.609   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.414  -6.363   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.032  -4.795   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.556  -3.330   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   18                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   17                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   11                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    6   16                                                  
CONECT   16   15                                                            
CONECT   17    4   18                                                       
CONECT   18   17    2                                                       
MASTER        0    0    0    0    0    0    0    0   18    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₀H₁₆O₈

Average Mass

264.2300 Da

Monoisotopic Mass

264.08452 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@@H](OC2COC(=O)C2)[C@H](O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C10H16O8/c11-2-5-7(13)8(14)9(15)10(18-5)17-4-1-6(12)16-3-4/h4-5,7-11,13-15H,1-3H2/t4?,5-,7-,8+,9-,10-/m1/s1

InChI Key

MQEPWBMWFIVRPS-WQPQPNDESA-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
Crocus sativus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glycosyl compounds

Alternative Parents

Substituents

O-glycosyl compound
Oxane
Monosaccharide
Gamma butyrolactone
Tetrahydrofuran
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organic oxide
Hydrocarbon derivative
Primary alcohol
Carbonyl group
Alcohol
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

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

146636843

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one (NP0230454)

MOL for NP0230454 (4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one)

3D MOL for NP0230454 (4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one)

3D SDF for NP0230454 (4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one)

3D-SDF for NP0230454 (4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one)

PDB for NP0230454 (4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one)

3D PDB for NP0230454 (4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one)

SMILES for NP0230454 (4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one)

INCHI for NP0230454 (4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one)

Structure for NP0230454 (4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one)

3D Structure for NP0230454 (4-{[(2r,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}oxolan-2-one)