NP-MRD: Showing NP-Card for (2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid (NP0290828)

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Record Information

Version

2.0

Created at

2022-09-09 21:41:28 UTC

Updated at

2022-09-09 21:41:28 UTC

NP-MRD ID

NP0290828

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

(2S,3S,4R,5R,6R)-4,5,6-trihydroxy-3-{[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid belongs to the class of organic compounds known as glucuronic acid derivatives. Glucuronic acid derivatives are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid. (2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid is found in Anadenanthera colubrina. Based on a literature review very few articles have been published on (2S,3S,4R,5R,6R)-4,5,6-trihydroxy-3-{[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
   -2.5243   -1.3338    1.3790 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5586   -1.4127   -0.1251 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3350   -1.2525   -0.7146 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6854   -0.0715   -0.3525 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5747   -0.1582   -0.9452 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5898   -0.3149   -0.0493 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6116    0.7702   -0.2464 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0822    2.0819   -0.5942 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4261    2.2295   -1.6518 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2840    3.1852    0.2182 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3569    0.7688    0.9333 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1900   -0.3136    0.9442 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7282   -0.4015    2.2507 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6738   -1.6084    0.4737 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6243   -2.2730   -0.3356 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3537   -1.6189   -0.2377 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5682   -2.7152    0.1206 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4558    1.1510   -0.6516 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0601    2.2229    0.1825 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9391    1.0223   -0.6019 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5919    1.8675   -1.7051 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3780    1.6207    0.6043 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4958   -0.3482   -0.6294 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.8402   -0.6947   -1.9431 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6172   -1.7554    1.8186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3914   -1.9011    1.8067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6520   -0.2874    1.7427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9443   -2.4117   -0.4148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5169   -0.1446    0.7486 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1567   -0.2922    0.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3405    0.4144   -1.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3223    3.0188    1.2167 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0847   -0.0393    0.3086 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7341    0.4680    2.6981 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5601   -2.2793    1.3745 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5255   -3.2471   -0.2906 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5245   -1.7094   -1.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8000   -3.5287   -0.3880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2041    1.4895   -1.6911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2040    1.9290    1.1111 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2764    2.9235   -1.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6861    1.8518   -1.5212 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4135    1.4110   -2.6869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1473    2.5743    0.6408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4385   -0.4483   -0.0352 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7562   -0.4390   -2.1641 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6 16  1  0
 16 17  1  0
 16 14  1  0
 14 15  1  0
 14 12  1  0
 12 13  1  0
 12 11  1  0
 11  7  1  0
  7  8  1  0
  8 10  1  0
  8  9  2  0
  4 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 20 22  1  1
 20 23  1  0
 23 24  1  0
 23  2  1  0
  7  6  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  1
  4 29  1  1
  6 30  1  1
 16 37  1  6
 17 38  1  0
 14 35  1  1
 15 36  1  0
 12 33  1  6
 13 34  1  0
  7 31  1  6
 10 32  1  0
 18 39  1  6
 19 40  1  0
 21 41  1  0
 21 42  1  0
 21 43  1  0
 22 44  1  0
 23 45  1  1
 24 46  1  0
M  END


  Mrv1652309092223412D          

 24 25  0  0  1  0            999 V2000
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1434   -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  1  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
    3.5724   -3.7125    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  2  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
    2.8579   -4.1250    0.0000 C   0  0  1  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
    2.8579   -1.6500    0.0000 C   0  0  2  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
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6737   -0.6055    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6131   -0.6055    0.0000 O   0  0  0  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 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  6  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  7 11  1  0  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
  6 16  1  0  0  0  0
 16 17  1  1  0  0  0
  4 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  1  0  0  0
 20 23  1  0  0  0  0
  2 23  1  0  0  0  0
 23 24  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0290828

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C13H22O11/c1-3-8(16)13(2,21)9(17)12(22-3)24-6-4(14)5(15)11(20)23-7(6)10(18)19/h3-9,11-12,14-17,20-21H,1-2H3,(H,18,19)/t3-,4+,5+,6-,7-,8-,9-,11+,12-,13+/m0/s1

> <INCHI_KEY>
OXOBFAFRCBEQTM-OZZDBJGTSA-N

> <FORMULA>
C13H22O11

> <MOLECULAR_WEIGHT>
354.308

> <EXACT_MASS>
354.116211528

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
32.072935334280935

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

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

> <JCHEM_LOGP>
-3.055613690666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.247209376435723

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3914316361090306

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6777076685228334

> <JCHEM_POLAR_SURFACE_AREA>
186.37

> <JCHEM_REFRACTIVITY>
71.29860000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       8.002  -9.240   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.668 -11.550   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.001 -10.010   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.991  -1.130   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.011  -1.130   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   18                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   16                                                  
CONECT    7    6    8   11                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    7   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    6   17                                                  
CONECT   17   16                                                            
CONECT   18    4   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20    2   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
(2S,3S,4R,5R,6R)-4,5,6-Trihydroxy-3-{[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylate	Generator

Chemical Formula

C₁₃H₂₂O₁₁

Average Mass

354.3080 Da

Monoisotopic Mass

354.11621 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C13H22O11/c1-3-8(16)13(2,21)9(17)12(22-3)24-6-4(14)5(15)11(20)23-7(6)10(18)19/h3-9,11-12,14-17,20-21H,1-2H3,(H,18,19)/t3-,4+,5+,6-,7-,8-,9-,11+,12-,13+/m0/s1

InChI Key

OXOBFAFRCBEQTM-OZZDBJGTSA-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
Anadenanthera colubrina	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as glucuronic acid derivatives. Glucuronic acid derivatives are compounds containing a glucuronic acid moiety (or a derivative), which consists of a glucose moiety with the C6 carbon oxidized to a carboxylic acid.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Glucuronic acid derivatives

Alternative Parents

Substituents

Glucuronic acid or derivatives
Disaccharide
Glycosyl compound
O-glycosyl compound
Pyran
Oxane
Tertiary alcohol
Hemiacetal
Secondary alcohol
Acetal
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Polyol
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Carbonyl group
Alcohol
Organic oxide
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)	3.39	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	186.37 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	71.3 m³·mol⁻¹	ChemAxon
Polarizability	32.07 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

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

162917686

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,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid (NP0290828)

MOL for NP0290828 ((2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid)

3D MOL for NP0290828 ((2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid)

3D SDF for NP0290828 ((2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid)

3D-SDF for NP0290828 ((2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid)

PDB for NP0290828 ((2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid)

3D PDB for NP0290828 ((2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid)

SMILES for NP0290828 ((2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid)

INCHI for NP0290828 ((2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid)

Structure for NP0290828 ((2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid)

3D Structure for NP0290828 ((2s,3s,4r,5r,6r)-4,5,6-trihydroxy-3-{[(2s,3r,4r,5s,6s)-3,4,5-trihydroxy-4,6-dimethyloxan-2-yl]oxy}oxane-2-carboxylic acid)