NP-MRD: Showing NP-Card for 1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate (NP0229657)

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Record Information

Version

2.0

Created at

2022-09-06 09:49:18 UTC

Updated at

2022-09-06 09:49:18 UTC

NP-MRD ID

NP0229657

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate

Description

8-Acetoxy-4'-methoxypinoresinol 4-glucoside belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones. 8-Acetoxy-4'-methoxypinoresinol 4-glucoside is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, 8-Acetoxy-4'-methoxypinoresinol 4-glucoside has been detected, but not quantified in, a few different foods, such as fats and oils, herbs and spices, and pomes. 1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate is found in Olea europaea. This could make 8-acetoxy-4'-methoxypinoresinol 4-glucoside a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061307022D          

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M  END

     RDKit          3D

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M  END


  Mrv0541 05061307022D          

 42 46  0  0  0  0            999 V2000
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    1.0989    5.5618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5469    4.9487    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8388   -0.9224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2695    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8018    4.1641    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    0.1576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5198    5.0472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7686    2.2201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4579    6.0034    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8440    6.3464    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2601    5.1202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8585   -4.0609    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9626   -2.8347    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8543    2.3248    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3237   -0.2549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2498    3.5510    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6088    3.9926    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542    0.9826    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  7  5  2  0  0  0  0
  8  6  2  0  0  0  0
 14  1  1  0  0  0  0
 15  5  1  0  0  0  0
 15  9  2  0  0  0  0
 16  6  1  0  0  0  0
 16 10  2  0  0  0  0
 17 12  1  0  0  0  0
 18  7  1  0  0  0  0
 19  8  1  0  0  0  0
 20  9  1  0  0  0  0
 20 18  2  0  0  0  0
 21 10  1  0  0  0  0
 21 19  2  0  0  0  0
 22 11  1  0  0  0  0
 23 22  1  0  0  0  0
 24 23  1  0  0  0  0
 25 24  1  0  0  0  0
 26 15  1  0  0  0  0
 26 17  1  0  0  0  0
 27 16  1  0  0  0  0
 28 25  1  0  0  0  0
 29 13  1  0  0  0  0
 29 17  1  0  0  0  0
 29 27  1  0  0  0  0
 30 11  1  0  0  0  0
 31 14  2  0  0  0  0
 32 23  1  0  0  0  0
 33 24  1  0  0  0  0
 34 25  1  0  0  0  0
 35  2  1  0  0  0  0
 35 18  1  0  0  0  0
 36  3  1  0  0  0  0
 36 20  1  0  0  0  0
 37  4  1  0  0  0  0
 37 21  1  0  0  0  0
 38 12  1  0  0  0  0
 38 27  1  0  0  0  0
 39 13  1  0  0  0  0
 39 26  1  0  0  0  0
 40 19  1  0  0  0  0
 40 28  1  0  0  0  0
 41 22  1  0  0  0  0
 41 28  1  0  0  0  0
 42 14  1  0  0  0  0
 42 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0229657

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C=C(C=C1)C1OCC2(OC(C)=O)C1COC2C1=CC(OC)=C(OC2OC(CO)C(O)C(O)C2O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C29H36O13/c1-14(31)42-29-13-39-26(15-5-7-18(35-2)20(9-15)36-3)17(29)12-38-27(29)16-6-8-19(21(10-16)37-4)40-28-25(34)24(33)23(32)22(11-30)41-28/h5-10,17,22-28,30,32-34H,11-13H2,1-4H3

> <INCHI_KEY>
ZKCRENDTQNGLGO-UHFFFAOYSA-N

> <FORMULA>
C29H36O13

> <MOLECULAR_WEIGHT>
592.5883

> <EXACT_MASS>
592.215591238

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_AVERAGE_POLARIZABILITY>
60.334719693646036

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-hexahydrofuro[3,4-c]furan-3a-yl acetate

> <ALOGPS_LOGP>
1.57

> <JCHEM_LOGP>
0.046702229333333026

> <ALOGPS_LOGS>
-3.23

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.196043729414267

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.200014899680406

> <JCHEM_PKA_STRONGEST_BASIC>
-2.981092354907191

> <JCHEM_POLAR_SURFACE_AREA>
171.82999999999998

> <JCHEM_REFRACTIVITY>
141.75949999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.52e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1H-furo[3,4-c]furan-3a-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       6.502   1.834   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.172  -8.725   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.739  -6.756   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.071   5.804   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.745  -4.331   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.924   3.379   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.220  -5.795   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.449   4.844   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.281  -3.507   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.388   2.555   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.540   8.277   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.370  -1.722   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.299   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.168   2.604   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.775  -3.186   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.894   2.235   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.835  -1.246   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.727  -6.116   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       0.942   5.164   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.757  -4.971   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.088   4.019   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.033   8.597   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.558  10.062   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.051  10.382   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.021   9.238   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.299  -1.722   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.370   0.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.497   7.773   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.835   0.294   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       6.570   9.421   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0       5.168   4.144   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       4.588  11.206   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       1.575  11.847   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      -0.486   9.558   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       7.203  -7.580   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       9.264  -5.291   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      -1.595   4.340   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       1.465  -0.476   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       6.204  -0.476   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0       0.466   6.629   0.000  0.00  0.00           O+0
HETATM   41  O   UNK     0       3.003   7.453   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0       3.835   1.834   0.000  0.00  0.00           O+0
CONECT    1   14                                                            
CONECT    2   35                                                            
CONECT    3   36                                                            
CONECT    4   37                                                            
CONECT    5    7   15                                                       
CONECT    6    8   16                                                       
CONECT    7    5   18                                                       
CONECT    8    6   19                                                       
CONECT    9   15   20                                                       
CONECT   10   16   21                                                       
CONECT   11   22   30                                                       
CONECT   12   17   38                                                       
CONECT   13   29   39                                                       
CONECT   14    1   31   42                                                  
CONECT   15    5    9   26                                                  
CONECT   16    6   10   27                                                  
CONECT   17   12   26   29                                                  
CONECT   18    7   20   35                                                  
CONECT   19    8   21   40                                                  
CONECT   20    9   18   36                                                  
CONECT   21   10   19   37                                                  
CONECT   22   11   23   41                                                  
CONECT   23   22   24   32                                                  
CONECT   24   23   25   33                                                  
CONECT   25   24   28   34                                                  
CONECT   26   15   17   39                                                  
CONECT   27   16   29   38                                                  
CONECT   28   25   40   41                                                  
CONECT   29   13   17   27   42                                             
CONECT   30   11                                                            
CONECT   31   14                                                            
CONECT   32   23                                                            
CONECT   33   24                                                            
CONECT   34   25                                                            
CONECT   35    2   18                                                       
CONECT   36    3   20                                                       
CONECT   37    4   21                                                       
CONECT   38   12   27                                                       
CONECT   39   13   26                                                       
CONECT   40   19   28                                                       
CONECT   41   22   28                                                       
CONECT   42   14   29                                                       
MASTER        0    0    0    0    0    0    0    0   42    0   92    0
END

View in JSmol

Synonyms

Value	Source
1-(3,4-Dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-hexahydrofuro[3,4-c]furan-3a-yl acetic acid	Generator

Chemical Formula

C₂₉H₃₆O₁₃

Average Mass

592.5883 Da

Monoisotopic Mass

592.21559 Da

IUPAC Name

1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-hexahydrofuro[3,4-c]furan-3a-yl acetate

Traditional Name

1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1H-furo[3,4-c]furan-3a-yl acetate

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C=C(C=C1)C1OCC2(OC(C)=O)C1COC2C1=CC(OC)=C(OC2OC(CO)C(O)C(O)C2O)C=C1

InChI Identifier

InChI=1S/C29H36O13/c1-14(31)42-29-13-39-26(15-5-7-18(35-2)20(9-15)36-3)17(29)12-38-27(29)16-6-8-19(21(10-16)37-4)40-28-25(34)24(33)23(32)22(11-30)41-28/h5-10,17,22-28,30,32-34H,11-13H2,1-4H3

InChI Key

ZKCRENDTQNGLGO-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
Olea europaea	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignan glycosides. These are aromatic polycyclic compounds containing a carbohydrate component glycosidically linked to a lignan moiety. They include 1-aryltetralin lactones.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Lignan glycosides

Sub Class

Not Available

Direct Parent

Lignan glycosides

Alternative Parents

Substituents

Lignan glycoside
Furanoid lignan
Furofuran lignan skeleton
Phenolic glycoside
Fatty acyl glycoside of mono- or disaccharide
Fatty acyl glycoside
Hexose monosaccharide
Alkyl glycoside
Glycosyl compound
O-glycosyl compound
O-dimethoxybenzene
Dimethoxybenzene
Phenoxy compound
Anisole
Furofuran
Methoxybenzene
Phenol ether
Alkyl aryl ether
Monosaccharide
Oxane
Monocyclic benzene moiety
Fatty acyl
Benzenoid
Tetrahydrofuran
Carboxylic acid ester
Secondary alcohol
Acetal
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Dialkyl ether
Ether
Polyol
Monocarboxylic acid or derivatives
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Alcohol
Organooxygen compound
Carbonyl group
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	1.57	ALOGPS
logP	0.047	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	12.2	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	171.83 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	141.76 m³·mol⁻¹	ChemAxon
Polarizability	60.33 Å³	ChemAxon
Number of Rings	5	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

HMDB0033278

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB011301

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

73830447

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate (NP0229657)

MOL for NP0229657 (1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate)

3D MOL for NP0229657 (1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate)

3D SDF for NP0229657 (1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate)

3D-SDF for NP0229657 (1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate)

PDB for NP0229657 (1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate)

3D PDB for NP0229657 (1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate)

SMILES for NP0229657 (1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate)

INCHI for NP0229657 (1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate)

Structure for NP0229657 (1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate)

3D Structure for NP0229657 (1-(3,4-dimethoxyphenyl)-4-(3-methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-tetrahydro-1h-furo[3,4-c]furan-3a-yl acetate)