NP-MRD: Showing NP-Card for (2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid (NP0262927)

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Record Information

Version

2.0

Created at

2022-09-08 05:56:48 UTC

Updated at

2022-09-08 05:56:48 UTC

NP-MRD ID

NP0262927

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid

Description

QCHFHXZDZVJVJC-IFWYRXGASA- belongs to the class of organic compounds known as o-glucuronides. These are glucuronides in which the aglycone is linked to the carbohydrate unit through an O-glycosidic bond. (2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid is found in Prunus avium and Saccharum officinarum. Based on a literature review very few articles have been published on QCHFHXZDZVJVJC-IFWYRXGASA-.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 44  0  0  0  0  0  0  0  0999 V2000
    4.8643   -1.4310    0.6673 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4954   -1.2727    0.4733 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1582    0.0512    0.2020 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.2171    0.5056    1.3075 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0144    1.9664    1.3089 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8665    2.4277    1.3659 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1217    2.7924    1.2459 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0548   -0.2184    1.3705 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3662   -0.2513    0.1764 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8064   -0.9706    0.2799 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9320   -0.2387   -0.0650 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.7950   -0.1525    1.1857 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0592    0.3064    2.2744 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0051    0.7380    0.9468 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.1702    0.1137    1.4097 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1526    0.8511   -0.5670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0973   -0.4605   -1.0573 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7604   -0.8941   -1.1335 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.3286   -0.6112   -2.4183 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2259   -0.9083   -0.9143 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7123   -2.1330   -0.4867 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3990    0.0633   -1.1042 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8080    1.3353   -1.2173 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2601   -0.8377    1.5066 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0407   -2.4998    0.9005 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3684   -1.2181   -0.2928 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0230    0.7214    0.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7781    0.2788    2.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0684    3.6289    0.6524 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2152    0.7891   -0.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6010    0.7965   -0.3541 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1712   -1.1787    1.3765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1836   -0.2422    3.0735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8823    1.7200    1.4292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6453   -0.3425    0.6835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1556    1.2742   -0.8193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4014    1.5019   -1.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7566   -1.9957   -0.9240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5124   -1.4395   -2.9644 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6131   -0.9975   -1.8117 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1560   -2.8996   -0.7939 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0109   -0.1909   -1.9655 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5786    1.5228   -2.1698 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 22  1  0
 22 23  1  0
 22 20  1  0
 20 21  1  0
 20  9  1  0
  9 10  1  0
 10 11  1  0
 11 18  1  0
 18 19  1  0
 18 17  1  0
 17 16  1  0
 16 14  1  0
 14 15  1  0
 14 12  1  0
 12 13  1  0
  9  8  1  0
  8  4  1  0
  4  5  1  0
  5  7  1  0
  5  6  2  0
  4  3  1  0
 12 11  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  6
 22 42  1  6
 23 43  1  0
 20 40  1  6
 21 41  1  0
  9 30  1  6
 11 31  1  6
 18 38  1  1
 19 39  1  0
 16 36  1  0
 16 37  1  0
 14 34  1  1
 15 35  1  0
 12 32  1  1
 13 33  1  0
  4 28  1  1
  7 29  1  0
M  END


  Mrv1652309082207562D          

 23 24  0  0  1  0            999 V2000
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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
    0.0000   -1.6500    0.0000 O   0  0  0  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
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  2  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
    1.4289   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7145   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  3  2  1  1  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  1  0  0  0
 11 10  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  1  1  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  1  0  0  0
  9 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
  3 22  1  0  0  0  0
 22 23  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0262927

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CO[C@H]1[C@H](O)[C@@H](O)[C@@H](O[C@H]2[C@H](O)OC[C@@H](O)[C@@H]2O)O[C@@H]1C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C12H20O11/c1-20-7-5(15)6(16)12(23-9(7)10(17)18)22-8-4(14)3(13)2-21-11(8)19/h3-9,11-16,19H,2H2,1H3,(H,17,18)/t3-,4+,5-,6-,7+,8-,9+,11-,12+/m1/s1

> <INCHI_KEY>
QCHFHXZDZVJVJC-IFWYRXGASA-N

> <FORMULA>
C12H20O11

> <MOLECULAR_WEIGHT>
340.281

> <EXACT_MASS>
340.100561464

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
30.872816207441147

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3S,4R,5R,6S)-4,5-dihydroxy-3-methoxy-6-{[(2R,3R,4S,5R)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid

> <JCHEM_LOGP>
-3.10963888

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.287016529844294

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.321639567618623

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5268686626569306

> <JCHEM_POLAR_SURFACE_AREA>
175.37

> <JCHEM_REFRACTIVITY>
66.9928

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3S,4R,5R,6S)-4,5-dihydroxy-3-methoxy-6-{[(2R,3R,4S,5R)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.001 -10.010   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       1.334 -11.550   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5    8                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5                                                            
CONECT    8    4    9                                                       
CONECT    9    8   10   20                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   11   19                                                  
CONECT   19   18                                                            
CONECT   20    9   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    3   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₂H₂₀O₁₁

Average Mass

340.2810 Da

Monoisotopic Mass

340.10056 Da

IUPAC Name

(2S,3S,4R,5R,6S)-4,5-dihydroxy-3-methoxy-6-{[(2R,3R,4S,5R)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid

Traditional Name

(2S,3S,4R,5R,6S)-4,5-dihydroxy-3-methoxy-6-{[(2R,3R,4S,5R)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid

CAS Registry Number

Not Available

SMILES

CO[C@H]1[C@H](O)[C@@H](O)[C@@H](O[C@H]2[C@H](O)OC[C@@H](O)[C@@H]2O)O[C@@H]1C(O)=O

InChI Identifier

InChI=1S/C12H20O11/c1-20-7-5(15)6(16)12(23-9(7)10(17)18)22-8-4(14)3(13)2-21-11(8)19/h3-9,11-16,19H,2H2,1H3,(H,17,18)/t3-,4+,5-,6-,7+,8-,9+,11-,12+/m1/s1

InChI Key

QCHFHXZDZVJVJC-IFWYRXGASA-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 avium	LOTUS Database	35616633
Saccharum officinarum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as o-glucuronides. These are glucuronides in which the aglycone is linked to the carbohydrate unit through an O-glycosidic bond.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

O-glucuronides

Alternative Parents

Substituents

1-o-glucuronide
O-glucuronide
Disaccharide
Glycosyl compound
O-glycosyl compound
Pyran
Oxane
Hemiacetal
Secondary alcohol
Acetal
Carboxylic acid derivative
Carboxylic acid
Dialkyl ether
Ether
Polyol
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Oxacycle
Hydrocarbon derivative
Carbonyl group
Organic oxide
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
logP	-3.1	ChemAxon
pKa (Strongest Acidic)	3.32	ChemAxon
pKa (Strongest Basic)	-3.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	175.37 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	66.99 m³·mol⁻¹	ChemAxon
Polarizability	30.87 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	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

10269501

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21635776

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid (NP0262927)

MOL for NP0262927 ((2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid)

3D MOL for NP0262927 ((2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid)

3D SDF for NP0262927 ((2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid)

3D-SDF for NP0262927 ((2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid)

PDB for NP0262927 ((2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid)

3D PDB for NP0262927 ((2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid)

SMILES for NP0262927 ((2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid)

INCHI for NP0262927 ((2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid)

Structure for NP0262927 ((2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid)

3D Structure for NP0262927 ((2s,3s,4r,5r,6s)-4,5-dihydroxy-3-methoxy-6-{[(2r,3r,4s,5r)-2,4,5-trihydroxyoxan-3-yl]oxy}oxane-2-carboxylic acid)