NP-MRD: Showing NP-Card for phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid (NP0319108)

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Record Information

Version

2.0

Created at

2022-09-11 19:58:17 UTC

Updated at

2022-09-11 19:58:18 UTC

NP-MRD ID

NP0319108

Secondary Accession Numbers

None

Natural Product Identification

Common Name

phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid

Description

(S)-Mandelic acid O-beta-D-Glucopyranoside, also known as (S)-mandelate O-b-D-glucopyranoside, 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 (S)-Mandelic acid O-beta-D-Glucopyranoside is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, (S)-Mandelic acid O-beta-D-Glucopyranoside has been detected, but not quantified in, fruits. phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid is found in Prunus persica, Prunus zippeliana and Sambucus nigra. This could make (S)-mandelic acid O-beta-D-glucopyranoside a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 41  0  0  0  0  0  0  0  0999 V2000
    0.4140    2.3652   -2.3981 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2609    1.4422   -2.2860 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3351    1.4866   -3.1661 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1044    0.3968   -1.2838 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0174    0.4631   -0.4831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8962   -0.5710   -0.5372 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.0086    0.0101   -1.1304 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9329    0.5534   -0.2979 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2654    1.5403    0.6263 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6789    2.5446   -0.1330 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5262   -0.5560    0.5242 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6283   -0.1724    1.2490 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4420   -1.1228    1.3904 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9502   -2.3395    1.9102 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1209   -1.2687    0.7444 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9092   -2.6649    0.6138 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3934    0.2409   -0.5578 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3602   -0.6532   -0.9656 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5565   -0.8480   -0.3525 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8352   -0.0826    0.7846 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8916    0.8232    1.2233 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6834    0.9955    0.5741 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1531    0.8901   -3.0515 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9940   -0.5772   -1.8577 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5771   -1.3580   -1.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7704    1.0348   -0.8468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5122    1.0996    1.2778 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0055    2.0460    1.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9922    2.5212   -1.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8791   -1.3365   -0.2092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3020    0.1596    2.1302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3502   -0.4615    2.2815 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2470   -2.8733    1.1491 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2984   -0.9551    1.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0797   -2.9025   -0.3171 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1354   -1.2398   -1.8448 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3082   -1.5398   -0.6657 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7852   -0.2017    1.3152 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1521    1.3987    2.1148 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9927    1.7128    0.9618 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  2  1  0
  2  3  1  0
  2  1  2  0
  4 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  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
 22 17  1  0
 10 29  1  0
  9 27  1  0
  9 28  1  0
  8 26  1  6
  6 25  1  6
  4 24  1  6
  3 23  1  0
 18 36  1  0
 19 37  1  0
 20 38  1  0
 21 39  1  0
 22 40  1  0
 15 34  1  1
 16 35  1  0
 13 32  1  1
 14 33  1  0
 11 30  1  6
 12 31  1  0
M  END


  Mrv0541 05061310232D          

 22 23  0  0  0  0            999 V2000
   -1.4289    0.8250    0.0000 C   0  0  0  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
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    2.0625    0.0000 C   0  0  0  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    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  2  0  0  0  0
  7  4  2  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 12  7  1  0  0  0  0
 13 12  1  0  0  0  0
 14 11  1  0  0  0  0
 15  6  1  0  0  0  0
 16  9  1  0  0  0  0
 17 10  1  0  0  0  0
 18 11  1  0  0  0  0
 19 13  2  0  0  0  0
 20 13  1  0  0  0  0
 21  8  1  0  0  0  0
 21 14  1  0  0  0  0
 22 12  1  0  0  0  0
 22 14  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0319108

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC1OC(OC(C(O)=O)C2=CC=CC=C2)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C14H18O8/c15-6-8-9(16)10(17)11(18)14(21-8)22-12(13(19)20)7-4-2-1-3-5-7/h1-5,8-12,14-18H,6H2,(H,19,20)

> <INCHI_KEY>
PRBPGFIPERGSFI-UHFFFAOYSA-N

> <FORMULA>
C14H18O8

> <MOLECULAR_WEIGHT>
314.2879

> <EXACT_MASS>
314.100167552

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_AVERAGE_POLARIZABILITY>
29.8945948337328

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-phenyl-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}acetic acid

> <ALOGPS_LOGP>
-1.39

> <JCHEM_LOGP>
-0.8750000009999999

> <ALOGPS_LOGS>
-1.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.210616942695719

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.489545108649686

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810838951428513

> <JCHEM_POLAR_SURFACE_AREA>
136.68

> <JCHEM_REFRACTIVITY>
71.11710000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.57e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -4.001   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   6.160   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334   6.930   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       4.001   3.850   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.001   6.930   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       1.334   8.470   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -4.001   8.470   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -5.335   6.160   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       0.000   4.620   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -1.334   6.930   0.000  0.00  0.00           O+0
CONECT    1    2    3                                                       
CONECT    2    1    4                                                       
CONECT    3    1    5                                                       
CONECT    4    2    7                                                       
CONECT    5    3    7                                                       
CONECT    6    8   15                                                       
CONECT    7    4    5   12                                                  
CONECT    8    6    9   21                                                  
CONECT    9    8   10   16                                                  
CONECT   10    9   11   17                                                  
CONECT   11   10   14   18                                                  
CONECT   12    7   13   22                                                  
CONECT   13   12   19   20                                                  
CONECT   14   11   21   22                                                  
CONECT   15    6                                                            
CONECT   16    9                                                            
CONECT   17   10                                                            
CONECT   18   11                                                            
CONECT   19   13                                                            
CONECT   20   13                                                            
CONECT   21    8   14                                                       
CONECT   22   12   14                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Value	Source
(S)-Mandelate O-b-D-glucopyranoside	Generator
(S)-Mandelate O-beta-D-glucopyranoside	Generator
(S)-Mandelate O-β-D-glucopyranoside	Generator
(S)-Mandelic acid O-b-D-glucopyranoside	Generator
(S)-Mandelic acid O-β-D-glucopyranoside	Generator
2-Phenyl-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}acetate	Generator

Chemical Formula

C₁₄H₁₈O₈

Average Mass

314.2879 Da

Monoisotopic Mass

314.10017 Da

IUPAC Name

2-phenyl-2-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}acetic acid

Traditional Name

phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid

CAS Registry Number

Not Available

SMILES

OCC1OC(OC(C(O)=O)C2=CC=CC=C2)C(O)C(O)C1O

InChI Identifier

InChI=1S/C14H18O8/c15-6-8-9(16)10(17)11(18)14(21-8)22-12(13(19)20)7-4-2-1-3-5-7/h1-5,8-12,14-18H,6H2,(H,19,20)

InChI Key

PRBPGFIPERGSFI-UHFFFAOYSA-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
Prunus persica	LOTUS Database	35616633
Prunus zippeliana	LOTUS Database	35616633
Sambucus nigra	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

Hexose monosaccharide
O-glycosyl compound
Monocyclic benzene moiety
Monosaccharide
Oxane
Benzenoid
Secondary alcohol
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Acetal
Organoheterocyclic compound
Oxacycle
Primary alcohol
Hydrocarbon derivative
Alcohol
Organic oxide
Carbonyl group
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic 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	-1.4	ALOGPS
logP	-0.88	ChemAxon
logS	-1.1	ALOGPS
pKa (Strongest Acidic)	3.49	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	136.68 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	71.12 m³·mol⁻¹	ChemAxon
Polarizability	29.89 Å³	ChemAxon
Number of Rings	2	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

HMDB0038335

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB017670

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

73229629

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid (NP0319108)

MOL for NP0319108 (phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid)

3D MOL for NP0319108 (phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid)

3D SDF for NP0319108 (phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid)

3D-SDF for NP0319108 (phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid)

PDB for NP0319108 (phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid)

3D PDB for NP0319108 (phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid)

SMILES for NP0319108 (phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid)

INCHI for NP0319108 (phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid)

Structure for NP0319108 (phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid)

3D Structure for NP0319108 (phenyl({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})acetic acid)