NP-MRD: Showing NP-Card for (2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate (NP0154701)

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Record Information

Version

2.0

Created at

2022-09-02 11:39:03 UTC

Updated at

2022-09-02 11:39:03 UTC

NP-MRD ID

NP0154701

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate

Description

2'-O-acetylsalicin belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. (2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate was first documented in 2013 (PMID: 23154841). Based on a literature review very few articles have been published on 2'-O-acetylsalicin (PMID: 34681798).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 43 44  0  0  0  0  0  0  0  0999 V2000
   -0.3978    2.0243    3.4634 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5917    1.9593    1.9958 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2805    2.9073    1.2641 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1257    0.8224    1.4589 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3614    0.6403    0.0529 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.4170   -0.4423   -0.3914 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.8419    0.1186   -0.5632 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9985   -0.1190    0.1065 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1844   -1.0034    1.1438 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4054   -1.1861    1.7758 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4851   -0.4559    1.3549 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3380    0.4277    0.3321 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1298    0.6034   -0.2876 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0323    1.5820   -1.3970 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2555    2.1616   -1.6018 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8664   -1.1468   -1.5028 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0805   -1.7459   -1.1075 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3999   -2.9476   -1.9594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5250   -2.6354   -3.2920 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1120   -0.6537   -1.2188 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4114   -1.1178   -1.0426 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7907    0.4027   -0.2215 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3715    1.6038   -0.6921 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3713    1.8937    4.0069 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2941    1.2293    3.8173 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0422    2.9835    3.8024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0226    1.5845   -0.4210 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3620   -1.1798    0.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3358   -1.5820    1.4797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5485   -1.8802    2.5890 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4698   -0.5619    1.8191 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1993    1.0106   -0.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3176    2.3788   -1.0751 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5900    1.1319   -2.3086 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3599    2.9120   -0.9837 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0374   -2.0623   -0.0456 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5947   -3.6926   -1.7696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3298   -3.3925   -1.5399 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4536   -3.4491   -3.8466 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0436   -0.2688   -2.2765 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9289   -0.5716   -0.4084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3779    0.1663    0.7139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5746    1.5506   -1.6577 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5 22  1  0
 22 23  1  0
 22 20  1  0
 20 21  1  0
 20 17  1  0
 17 18  1  0
 18 19  1  0
 17 16  1  0
 16  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
  6  5  1  0
 13  8  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  5 27  1  6
 22 42  1  1
 23 43  1  0
 20 40  1  6
 21 41  1  0
 17 36  1  1
 18 37  1  0
 18 38  1  0
 19 39  1  0
  6 28  1  1
  9 29  1  0
 10 30  1  0
 11 31  1  0
 12 32  1  0
 14 33  1  0
 14 34  1  0
 15 35  1  0
M  END


  Mrv1652309022213392D          

 23 24  0  0  1  0            999 V2000
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   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
   -0.7145   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -1.2375    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -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  0  0  0  0  0  0  0  0  0  0
   -3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    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
   -0.7145   -2.8875    0.0000 C   0  0  2  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
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    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
    0.0000   -1.6500    0.0000 C   0  0  2  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
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
  5 22  1  0  0  0  0
 22 23  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0154701

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC=CC=C1CO

> <INCHI_IDENTIFIER>
InChI=1S/C15H20O8/c1-8(18)21-14-13(20)12(19)11(7-17)23-15(14)22-10-5-3-2-4-9(10)6-16/h2-5,11-17,19-20H,6-7H2,1H3/t11-,12-,13+,14-,15-/m1/s1

> <INCHI_KEY>
RRRGZNGWWIEOLB-UXXRCYHCSA-N

> <FORMULA>
C15H20O8

> <MOLECULAR_WEIGHT>
328.317

> <EXACT_MASS>
328.115817604

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
32.000765042452294

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate

> <ALOGPS_LOGP>
-0.46

> <JCHEM_LOGP>
-0.9246119560000001

> <ALOGPS_LOGS>
-1.50

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.937324975031082

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.690819453134417

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9361037052741548

> <JCHEM_POLAR_SURFACE_AREA>
125.68000000000002

> <JCHEM_REFRACTIVITY>
76.15070000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.03e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7   16                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12    8   14                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16    6   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20    5   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

C₁₅H₂₀O₈

Average Mass

328.3170 Da

Monoisotopic Mass

328.11582 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=CC=CC=C1CO

InChI Identifier

InChI=1S/C15H20O8/c1-8(18)21-14-13(20)12(19)11(7-17)23-15(14)22-10-5-3-2-4-9(10)6-16/h2-5,11-17,19-20H,6-7H2,1H3/t11-,12-,13+,14-,15-/m1/s1

InChI Key

RRRGZNGWWIEOLB-UXXRCYHCSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Phenolic glycosides

Alternative Parents

Substituents

Phenolic glycoside
O-glycosyl compound
Phenoxy compound
Benzyl alcohol
Phenol ether
Monocyclic benzene moiety
Monosaccharide
Oxane
Benzenoid
Carboxylic acid ester
Secondary alcohol
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Acetal
Organoheterocyclic compound
Primary alcohol
Hydrocarbon derivative
Alcohol
Carbonyl group
Organic oxide
Aromatic 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

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

137333735

PDB ID

Not Available

ChEBI ID

137481

Good Scents ID

Not Available

References

General References

Yang H, Lee SH, Sung SH, Kim J, Kim YC: Neuroprotective compounds from Salix pseudo-lasiogyne twigs and their anti-amnesic effects on scopolamine-induced memory deficit in mice. Planta Med. 2013 Jan;79(1):78-82. doi: 10.1055/s-0032-1327949. Epub 2012 Nov 15. [PubMed:23154841 ]
Antoniadou K, Herz C, Le NPK, Mittermeier-Klessinger VK, Forster N, Zander M, Ulrichs C, Mewis I, Hofmann T, Dawid C, Lamy E: Identification of Salicylates in Willow Bark (Salix Cortex) for Targeting Peripheral Inflammation. Int J Mol Sci. 2021 Oct 15;22(20):11138. doi: 10.3390/ijms222011138. [PubMed:34681798 ]
LOTUS database [Link]

Showing NP-Card for (2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate (NP0154701)

MOL for NP0154701 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate)

3D MOL for NP0154701 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate)

3D SDF for NP0154701 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate)

3D-SDF for NP0154701 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate)

PDB for NP0154701 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate)

3D PDB for NP0154701 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate)

SMILES for NP0154701 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate)

INCHI for NP0154701 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate)

Structure for NP0154701 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate)

3D Structure for NP0154701 ((2s,3r,4s,5s,6r)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl acetate)