NP-MRD: Showing NP-Card for (2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol (NP0241564)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-07 01:41:01 UTC

Updated at

2022-09-07 01:41:01 UTC

NP-MRD ID

NP0241564

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol

Description

Bis-beta-D-fructofuranose 1,2':2,3'-Dianhydride, also known as difructose anhydride III, belongs to the class of organic compounds known as c-glycosyl compounds. These are glycoside in which a sugar group is bonded through one carbon to another group via a C-glycosidic bond. Bis-beta-D-fructofuranose 1,2':2,3'-Dianhydride is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. (2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol is found in Trypanosoma brucei. (2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol was first documented in 2005 (PMID: 16233782). Based on a literature review very few articles have been published on bis-beta-D-fructofuranose 1,2':2,3'-Dianhydride (PMID: 17444654).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    4.6508   -1.9245    1.1049 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4369   -0.6031    0.7099 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2143   -0.4710   -0.1813 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0860   -0.8881    0.4539 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9872   -0.2170   -0.1169 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3342   -1.2031   -1.0499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0168   -1.0473   -1.1778 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6550   -1.0852    0.0709 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5978   -2.4627    0.6793 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3173   -2.4539    1.8553 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9945   -0.7914   -0.1681 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2903    0.4105    0.4048 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.2296    1.2610   -0.4151 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6335    1.5202   -1.6699 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9572    1.1707    0.4655 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.9744    2.1803    1.3869 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0907   -0.0159    0.9197 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2138    0.2153    0.9024 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5450    0.9763   -0.8533 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9243    2.1639   -0.5221 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9591    1.0361   -0.3135 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8476    1.6341   -1.1683 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6707   -2.4616    0.2802 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3433   -0.3218    0.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4030    0.0973    1.5539 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3785   -0.8975   -1.1701 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5867   -2.2588   -0.7810 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7914   -1.0465   -2.0573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1411   -3.1433   -0.0400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5805   -2.8467    0.8036 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2844   -2.4043    1.6840 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6850    0.3173    1.4356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3639    2.2576    0.0511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1945    0.7775   -0.5957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3243    1.6886   -2.3581 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7357    1.4680   -0.5638 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0224    2.3273    1.6892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4269   -0.2010    1.9832 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5688    0.7918   -1.9467 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4369    2.4691   -1.3481 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9489    1.4974    0.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1884    2.4843   -0.7464 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 12  1  0
 12 11  1  0
 11  8  1  0
  8  9  1  1
  9 10  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  0
  5  4  1  1
  4  3  1  0
  3  2  1  0
  2  1  1  0
  3 21  1  0
 21 22  1  0
 21 19  1  0
 19 20  1  0
  5 18  1  0
 18 17  1  0
 17 15  1  0
 15 16  1  0
 15 12  1  0
 17  8  1  0
 19  5  1  0
 14 35  1  0
 13 33  1  0
 13 34  1  0
 12 32  1  1
  9 29  1  0
  9 30  1  0
 10 31  1  0
  6 27  1  0
  6 28  1  0
  3 26  1  6
  2 24  1  0
  2 25  1  0
  1 23  1  0
 21 41  1  1
 22 42  1  0
 19 39  1  6
 20 40  1  0
 17 38  1  1
 15 36  1  6
 16 37  1  0
M  END


  Mrv1652309072203412D          

 22 24  0  0  1  0            999 V2000
    6.1349    1.4468    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4819    0.9427    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7188    1.2562    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.0166    0.8232    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3877    1.3572    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1556    0.5655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3540    0.3706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7844    0.9674    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4709    0.2043    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6532    0.0943    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9597    0.9434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6821    1.7203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1096    1.9524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7064    1.3828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3352    2.2244    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3113    3.0491    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0164    1.7591    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8181    1.9540    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7012    2.1203    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.2682    2.8225    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5239    2.0579    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.0579    2.6867    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
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 12 15  1  0  0  0  0
 15 16  1  1  0  0  0
 15 17  1  0  0  0  0
  8 17  1  0  0  0  0
 17 18  1  6  0  0  0
  5 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  1  1  0  0  0
 19 21  1  0  0  0  0
  3 21  1  0  0  0  0
 21 22  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0241564

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1O[C@@]2(CO)OC[C@]3(O[C@H](CO)[C@@H](O)[C@@H]3O)O[C@H]2[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C12H20O10/c13-1-5-7(16)9(18)12(21-5)4-19-11(3-15)10(22-12)8(17)6(2-14)20-11/h5-10,13-18H,1-4H2/t5-,6-,7-,8-,9+,10+,11-,12+/m1/s1

> <INCHI_KEY>
KSRQDWNGXKYIDO-IYDDCBTQSA-N

> <FORMULA>
C12H20O10

> <MOLECULAR_WEIGHT>
324.282

> <EXACT_MASS>
324.105646844

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
29.986909896683485

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3'S,4'S,4aR,5'R,6R,7R,7aS)-4a,5',6-tris(hydroxymethyl)-tetrahydro-3H-spiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol

> <JCHEM_LOGP>
-3.1925914913333324

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.853786200610447

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.032320335543725

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9814328347506533

> <JCHEM_POLAR_SURFACE_AREA>
158.3

> <JCHEM_REFRACTIVITY>
65.7014

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3'S,4'S,4aR,5'R,6R,7R,7aS)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  O   UNK     0      11.452   2.701   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      10.233   1.760   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.808   2.345   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       7.498   1.537   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.324   2.533   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.891   1.056   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       4.394   0.692   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       3.331   1.806   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.746   0.381   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.219   0.176   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       1.792   1.761   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.273   3.211   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.205   3.644   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -1.319   2.581   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       2.492   4.152   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.448   5.692   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.764   3.284   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.260   3.647   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.909   3.958   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.101   5.269   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.445   3.841   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       9.441   5.015   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   18   19                                             
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   11   17                                             
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    8   12                                                       
CONECT   12   11   13   15                                                  
CONECT   13   12   14                                                       
CONECT   14   13                                                            
CONECT   15   12   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15    8   18                                                  
CONECT   18   17    5                                                       
CONECT   19    5   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19    3   22                                                  
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Value	Source
D-Fructofuranose 1,2':2,3'-dianhydride	ChEBI
Di-D-fructofuranose 1,2':2,3'-dianhydride	Kegg
Difructose anhydride III	Kegg
Bis-b-D-fructofuranose 1,2':2,3'-dianhydride	Generator
Bis-β-D-fructofuranose 1,2':2,3'-dianhydride	Generator

Chemical Formula

C₁₂H₂₀O₁₀

Average Mass

324.2820 Da

Monoisotopic Mass

324.10565 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@@]2(CO)OC[C@]3(O[C@H](CO)[C@@H](O)[C@@H]3O)O[C@H]2[C@@H]1O

InChI Identifier

InChI=1S/C12H20O10/c13-1-5-7(16)9(18)12(21-5)4-19-11(3-15)10(22-12)8(17)6(2-14)20-11/h5-10,13-18H,1-4H2/t5-,6-,7-,8-,9+,10+,11-,12+/m1/s1

InChI Key

KSRQDWNGXKYIDO-IYDDCBTQSA-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
Trypanosoma brucei	LOTUS Database	35616633

Chemical Taxonomy

Description

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

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

C-glycosyl compounds

Alternative Parents

Substituents

Disaccharide
C-glycosyl compound
Ketal
Para-dioxane
Tetrahydrofuran
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Hydrocarbon derivative
Primary alcohol
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

sugar dianhydride (CHEBI:4117 )

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

389299

KEGG Compound ID

C04420

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

440332

PDB ID

Not Available

ChEBI ID

4117

Good Scents ID

Not Available

References

General References

Matsumoto M, Matsukawa N, Chiji H, Hara H: Difructose anhydride III promotes absorption of the soluble flavonoid alphaG-rutin in rats. J Agric Food Chem. 2007 May 16;55(10):4202-8. doi: 10.1021/jf070049p. Epub 2007 Apr 20. [PubMed:17444654 ]
Minamida K, Shiga K, Sujaya IN, Sone T, Yokota A, Hara H, Asano K, Tomita F: Effects of difructose anhydride III (DFA III) administration on rat intestinal microbiota. J Biosci Bioeng. 2005 Mar;99(3):230-6. doi: 10.1263/jbb.99.230. [PubMed:16233782 ]
LOTUS database [Link]

Showing NP-Card for (2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol (NP0241564)

MOL for NP0241564 ((2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol)

3D MOL for NP0241564 ((2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol)

3D SDF for NP0241564 ((2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol)

3D-SDF for NP0241564 ((2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol)

PDB for NP0241564 ((2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol)

3D PDB for NP0241564 ((2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol)

SMILES for NP0241564 ((2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol)

INCHI for NP0241564 ((2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol)

Structure for NP0241564 ((2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol)

3D Structure for NP0241564 ((2s,3's,4's,4ar,5'r,6r,7r,7as)-4a,5',6-tris(hydroxymethyl)-tetrahydrospiro[furo[2,3-b][1,4]dioxine-2,2'-oxolane]-3',4',7-triol)