NP-MRD: Showing NP-Card for (2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol (NP0258377)

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Record Information

Version

2.0

Created at

2022-09-07 23:48:17 UTC

Updated at

2022-09-07 23:48:17 UTC

NP-MRD ID

NP0258377

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol

Description

18997-54-1 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. (2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol is found in Artemisia santolinifolia, Aster koraiensis, Breynia fruticosa, Buddleja officinalis, Carica papaya, Citrus reticulata, Crocus sativus, Epimedium grandiflorum, Epimedium sagittatum, Equisetum ramosissimum, Foeniculum vulgare, Glehnia littoralis, Hydrangea macrophylla, Hylocereus undatus, Hypericum sikokumontanum, Ipomoea nil, Isatis tinctoria, Mentha spicata, Mikania hirsutissima, Moricandia arvensis, Pluchea indica, Rhodiola crenulata, Rhodiola rosea, Rhodiola sachalinensis, Rhodiola sacra, Rosa damascena, Rosa gallica, Rosa rugosa, Saussurea medusa, Sedum sarmentosum and Ziziphora clinopodioides. Based on a literature review very few articles have been published on 18997-54-1.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 41  0  0  0  0  0  0  0  0999 V2000
   -3.8340   -1.2150   -2.4629 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5976   -1.0507   -1.8834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6831   -1.2477   -0.3902 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4875   -1.0987    0.2531 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9288    0.1524    0.1946 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1696    0.2515   -0.9433 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1777    0.4171   -0.7473 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8508   -0.6872    0.0061 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2952   -0.3410    0.1227 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7922    0.3830    1.1837 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1093    0.7056    1.3011 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9802    0.2938    0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5133   -0.4301   -0.7473 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1752   -0.7457   -0.8461 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9163    1.2786    0.3150 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3529    2.3175    1.0544 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1633    0.8017    0.9797 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.1103    1.8242    0.9044 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7253   -0.4061    0.2643 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.4043   -1.1578    1.2237 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1100   -0.4806   -3.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1072   -0.1300   -2.1927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9510   -1.8927   -2.2717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9851   -2.3290   -0.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2474    0.2338    1.0932 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6534    0.4610   -1.7557 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3890    1.3901   -0.2276 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7892   -1.6050   -0.6166 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4822   -0.8383    1.0293 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1113    0.6990    1.9381 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4592    1.2728    2.1454 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0354    0.5501    0.4140 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2436   -0.7338   -1.4969 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8635   -1.3206   -1.7156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1991    1.7159   -0.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0023    3.0540    1.1803 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9896    0.6105    2.0651 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0084    1.4620    1.1132 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5032   -0.0669   -0.4649 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4444   -2.0976    0.9120 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  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
  5 15  1  0
 15 16  1  0
 15 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19  3  1  0
 14  9  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  6
  5 25  1  1
  7 26  1  0
  7 27  1  0
  8 28  1  0
  8 29  1  0
 10 30  1  0
 11 31  1  0
 12 32  1  0
 13 33  1  0
 14 34  1  0
 15 35  1  6
 16 36  1  0
 17 37  1  1
 18 38  1  0
 19 39  1  6
 20 40  1  0
M  END


  Mrv1652309082201482D          

 20 21  0  0  1  0            999 V2000
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   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  1  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    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
    1.4289   -2.4750    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  0  0  0  0
  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
  5 15  1  0  0  0  0
 15 16  1  6  0  0  0
 15 17  1  0  0  0  0
 17 18  1  1  0  0  0
 17 19  1  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0258377

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC[C@H]1O[C@@H](OCCC2=CC=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C14H20O6/c15-8-10-11(16)12(17)13(18)14(20-10)19-7-6-9-4-2-1-3-5-9/h1-5,10-18H,6-8H2/t10-,11-,12+,13-,14-/m1/s1

> <INCHI_KEY>
MLRIJUWUQTVDQE-RKQHYHRCSA-N

> <FORMULA>
C14H20O6

> <MOLECULAR_WEIGHT>
284.308

> <EXACT_MASS>
284.125988364

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
29.26893331594109

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol

> <JCHEM_LOGP>
-0.27627839200000043

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.200250835140363

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.21097236237618

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981083411880946

> <JCHEM_POLAR_SURFACE_AREA>
99.38000000000001

> <JCHEM_REFRACTIVITY>
70.0422

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol

> <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  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.669 -12.320   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.669 -13.860   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336 -14.630   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667  -7.700   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15    5   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    3   20                                                  
CONECT   20   19                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   42    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₄H₂₀O₆

Average Mass

284.3080 Da

Monoisotopic Mass

284.12599 Da

IUPAC Name

(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol

Traditional Name

(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol

CAS Registry Number

Not Available

SMILES

OC[C@H]1O[C@@H](OCCC2=CC=CC=C2)[C@H](O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C14H20O6/c15-8-10-11(16)12(17)13(18)14(20-10)19-7-6-9-4-2-1-3-5-9/h1-5,10-18H,6-8H2/t10-,11-,12+,13-,14-/m1/s1

InChI Key

MLRIJUWUQTVDQE-RKQHYHRCSA-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
Artemisia santolinifolia	LOTUS Database	35616633
Aster koraiensis	LOTUS Database	35616633
Breynia fruticosa	LOTUS Database	35616633
Buddleja officinalis	LOTUS Database	35616633
Carica papaya	LOTUS Database	35616633
Citrus reticulata	LOTUS Database	35616633
Crocus sativus	LOTUS Database	35616633
Epimedium grandiflorum	LOTUS Database	35616633
Epimedium sagittatum	LOTUS Database	35616633
Equisetum ramosissimum	LOTUS Database	35616633
Foeniculum vulgare	LOTUS Database	35616633
Glehnia littoralis	LOTUS Database	35616633
Hydrangea macrophylla	LOTUS Database	35616633
Hylocereus undatus	LOTUS Database	35616633
Hypericum sikokumontanum	LOTUS Database	35616633
Ipomoea nil	LOTUS Database	35616633
Isatis tinctoria	LOTUS Database	35616633
Mentha spicata	LOTUS Database	35616633
Mikania hirsutissima	LOTUS Database	35616633
Moricandia arvensis	LOTUS Database	35616633
Pluchea indica	LOTUS Database	35616633
Rhodiola crenulata	LOTUS Database	35616633
Rhodiola rosea	LOTUS Database	35616633
Rhodiola sachalinensis	LOTUS Database	35616633
Rhodiola sacra	LOTUS Database	35616633
Rosa damascena	LOTUS Database	35616633
Rosa gallica	LOTUS Database	35616633
Rosa rugosa	LOTUS Database	35616633
Saussurea medusa	LOTUS Database	35616633
Sedum sarmentosum	LOTUS Database	35616633
Ziziphora clinopodioides	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
Benzenoid
Oxane
Monosaccharide
Monocyclic benzene moiety
Secondary alcohol
Oxacycle
Organoheterocyclic compound
Polyol
Acetal
Hydrocarbon derivative
Primary alcohol
Alcohol
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	-0.28	ChemAxon
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	99.38 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	70.04 m³·mol⁻¹	ChemAxon
Polarizability	29.27 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

C00029468

Chemspider ID

9464086

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11289099

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol (NP0258377)

MOL for NP0258377 ((2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol)

3D MOL for NP0258377 ((2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol)

3D SDF for NP0258377 ((2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol)

3D-SDF for NP0258377 ((2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol)

PDB for NP0258377 ((2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol)

3D PDB for NP0258377 ((2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol)

SMILES for NP0258377 ((2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol)

INCHI for NP0258377 ((2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol)

Structure for NP0258377 ((2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol)

3D Structure for NP0258377 ((2r,3s,4s,5r,6r)-2-(hydroxymethyl)-6-(2-phenylethoxy)oxane-3,4,5-triol)