NP-MRD: Showing NP-Card for 2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate (NP0217708)

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Record Information

Version

2.0

Created at

2022-09-05 18:08:21 UTC

Updated at

2022-09-05 18:08:21 UTC

NP-MRD ID

NP0217708

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate

Description

2-{[3-(Acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate belongs to the class of organic compounds known as scalarane sesterterpenoids. These are sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions. 2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate is found in Prunus maximowiczii. 2-{[3-(Acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191523252D          

 43 45  0  0  0  0            999 V2000
   -3.7378   -6.1445    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 29 42  1  0  0  0  0
  6 42  1  0  0  0  0
 42 43  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004191523252D          

 43 45  0  0  0  0            999 V2000
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   -3.4325   -2.8294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9845   -2.2163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6255   -2.6578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3706   -1.8732    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9226   -1.2601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7296   -1.4316    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6677   -0.4755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0470   -4.1974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7376   -3.9425    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3507   -4.4945    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1792   -5.3015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1353   -4.2396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7484   -4.7916    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5330   -4.5367    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7045   -3.7297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4892   -3.4748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1023   -4.0268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8869   -3.7719    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9307   -4.8338    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1461   -5.0887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020   -4.9820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1830   -5.6495    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
  4  5  1  0  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  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 33 31  1  4  0  0  0
 33 34  2  0  0  0  0
 34 35  1  0  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 38 40  1  0  0  0  0
 40 41  2  0  0  0  0
 35 41  1  0  0  0  0
 29 42  1  0  0  0  0
  6 42  1  0  0  0  0
 42 43  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0217708

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC1OC(COC(C)=O)(OC2OC(CO)C(O)C(O)C2OC(C)=O)C(OC(=O)C=CC2=CC=C(O)C=C2)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O16/c1-13(29)37-11-19-22(35)25(41-20(33)9-6-16-4-7-17(32)8-5-16)27(42-19,12-38-14(2)30)43-26-24(39-15(3)31)23(36)21(34)18(10-28)40-26/h4-9,18-19,21-26,28,32,34-36H,10-12H2,1-3H3

> <INCHI_KEY>
XAEXDDRZTSBTMR-UHFFFAOYSA-N

> <FORMULA>
C27H34O16

> <MOLECULAR_WEIGHT>
614.553

> <EXACT_MASS>
614.184685015

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
58.522681415922

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate

> <ALOGPS_LOGP>
0.35

> <JCHEM_LOGP>
-0.4751333363333336

> <ALOGPS_LOGS>
-2.42

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.498429803838434

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.398220184721431

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810855582710714

> <JCHEM_POLAR_SURFACE_AREA>
234.03999999999996

> <JCHEM_REFRACTIVITY>
137.7772

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.33e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      -6.977 -11.470   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.446 -11.631   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.819 -13.037   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -4.540 -10.385   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -3.009 -10.546   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.104  -9.300   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.580  -7.835   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.303  -5.786   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -0.779  -4.321   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.285  -4.001   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -3.316  -5.145   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.761  -2.536   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -2.364  -5.786   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -3.870  -6.106   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -4.346  -7.570   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -5.853  -7.891   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -6.329  -9.355   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -7.835  -9.675   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -6.883  -6.746   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -8.390  -7.066   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -6.407  -5.281   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -7.438  -4.137   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.901  -4.961   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -4.425  -3.497   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -5.456  -2.352   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -6.962  -2.672   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -4.980  -0.888   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.088  -7.835   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.377  -7.359   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       2.521  -8.390   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.201  -9.896   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       3.986  -7.914   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.130  -8.944   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.595  -8.468   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       6.915  -6.962   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.380  -6.486   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.524  -7.517   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      10.989  -7.041   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       9.204  -9.023   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.739  -9.499   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -0.564  -9.300   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0       0.342 -10.546   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                                                       
CONECT    6    5    7   42                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14   29                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    8   15                                                       
CONECT   15   14   16   24                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   15   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
CONECT   29    8   30   42                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   41                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   35                                                       
CONECT   42   29    6   43                                                  
CONECT   43   42                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   90    0
END

View in JSmol

Synonyms

Value	Source
2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoic acid	Generator

Chemical Formula

C₂₇H₃₄O₁₆

Average Mass

614.5530 Da

Monoisotopic Mass

614.18469 Da

IUPAC Name

2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate

Traditional Name

2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC1OC(COC(C)=O)(OC2OC(CO)C(O)C(O)C2OC(C)=O)C(OC(=O)C=CC2=CC=C(O)C=C2)C1O

InChI Identifier

InChI=1S/C27H34O16/c1-13(29)37-11-19-22(35)25(41-20(33)9-6-16-4-7-17(32)8-5-16)27(42-19,12-38-14(2)30)43-26-24(39-15(3)31)23(36)21(34)18(10-28)40-26/h4-9,18-19,21-26,28,32,34-36H,10-12H2,1-3H3

InChI Key

XAEXDDRZTSBTMR-UHFFFAOYSA-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 maximowiczii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as scalarane sesterterpenoids. These are sesterterpenoids with a structure based on the scalarane backbone. Scalarane is a tetracyclic compound, which is similar the homoandrostane with five methyl groups at the 4-, 4-, 8-, 17-, 17a-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesterterpenoids

Direct Parent

Scalarane sesterterpenoids

Alternative Parents

Substituents

Scalarane sesterterpenoid
Fluorene
Arylsulfate
Indane
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Sulfuric acid monoester
Sulfate-ester
Sulfuric acid ester
Organic sulfuric acid or derivatives
Hydrocarbon derivative
Organooxygen compound
Organic oxygen compound
Organic oxide
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	0.35	ALOGPS
logP	-0.48	ChemAxon
logS	-2.4	ALOGPS
pKa (Strongest Acidic)	9.4	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	234.04 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	137.78 m³·mol⁻¹	ChemAxon
Polarizability	58.52 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate (NP0217708)

MOL for NP0217708 (2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate)

3D MOL for NP0217708 (2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate)

3D SDF for NP0217708 (2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate)

3D-SDF for NP0217708 (2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate)

PDB for NP0217708 (2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate)

3D PDB for NP0217708 (2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate)

SMILES for NP0217708 (2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate)

INCHI for NP0217708 (2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate)

Structure for NP0217708 (2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate)

3D Structure for NP0217708 (2-{[3-(acetyloxy)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-2,5-bis[(acetyloxy)methyl]-4-hydroxyoxolan-3-yl 3-(4-hydroxyphenyl)prop-2-enoate)