NP-MRD: Showing NP-Card for 3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol (NP0213933)

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Record Information

Version

2.0

Created at

2022-09-05 13:05:01 UTC

Updated at

2022-09-05 13:05:01 UTC

NP-MRD ID

NP0213933

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol

Description

3-[4-(2-{4-[2-(3,5-Dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol belongs to the class of organic compounds known as tannins. These are naturally occurring polyphenols which be categorized into four main classes: Hydrolyzable tannin (based on ellagic acid or gallic acid), condensed tannins (made of oligomeric or polymeric proanthocyanidins), complex tannins (made of a catechin bound to a gallotannin or elagitannin), and phlorotannins (oligomers of phloroglucinol). 3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol is found in Cystoseira granulata and Himanthalia elongata. Based on a literature review very few articles have been published on 3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052215052D          

 63 69  0  0  0  0            999 V2000
    2.1434  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.5724  -15.2625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4289  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0000  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.2881  -22.6875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.4289  -14.0250    0.0000 C   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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  4  6  2  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  2  0  0  0  0
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 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
  9 16  1  0  0  0  0
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 61 62  1  0  0  0  0
  7 63  2  0  0  0  0
  2 63  1  0  0  0  0
M  END

     RDKit          3D

 93 99  0  0  0  0  0  0  0  0999 V2000
   -4.7031    5.7430   -2.8848 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309052215052D          

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M  END
> <DATABASE_ID>
NP0213933

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC(O)=C(C(O)=C1)C1=C(O)C(OC2=CC(O)=C(OC3=CC(O)=CC(O)=C3OC3=CC(O)=C(OC4=CC(O)=CC(O)=C4OC4=CC(O)=CC(O)=C4)C(O)=C3)C(O)=C2)=C(O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C42H30O21/c43-15-1-16(44)3-20(2-15)59-40-26(51)6-18(46)8-33(40)62-38-28(53)10-21(11-29(38)54)60-41-27(52)7-19(47)9-34(41)63-39-30(55)12-22(13-31(39)56)61-42-32(57)14-25(50)36(37(42)58)35-23(48)4-17(45)5-24(35)49/h1-14,43-58H

> <INCHI_KEY>
SWSXKCWLFMARQN-UHFFFAOYSA-N

> <FORMULA>
C42H30O21

> <MOLECULAR_WEIGHT>
870.681

> <EXACT_MASS>
870.127957986

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
93

> <JCHEM_AVERAGE_POLARIZABILITY>
82.06662879442864

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
16

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol

> <JCHEM_LOGP>
6.264861946333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-5

> <JCHEM_PKA>
6.282494633542073

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.804956327150198

> <JCHEM_PKA_STRONGEST_BASIC>
-5.747759448792967

> <JCHEM_POLAR_SURFACE_AREA>
369.83000000000004

> <JCHEM_REFRACTIVITY>
214.0926

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  O   UNK     0       4.001 -23.870   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.001 -25.410   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335 -26.180   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335 -27.720   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       6.668 -28.490   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.001 -28.490   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667 -27.720   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.334 -28.490   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       0.000 -27.720   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000 -26.180   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.334 -25.410   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -1.334 -25.410   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667 -26.180   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -4.001 -25.410   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -2.667 -27.720   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.334 -28.490   0.000  0.00  0.00           C+0
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HETATM   18  C   UNK     0      -2.667 -30.800   0.000  0.00  0.00           C+0
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HETATM   21  C   UNK     0      -4.001 -33.110   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -5.335 -32.340   0.000  0.00  0.00           C+0
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HETATM   26  O   UNK     0      -4.001 -34.650   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -5.335 -36.960   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.668 -37.730   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -6.668 -39.270   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -8.002 -36.960   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -8.002 -35.420   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -9.336 -34.650   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0     -10.669 -35.420   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -10.669 -36.960   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -9.336 -37.730   0.000  0.00  0.00           O+0
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HETATM   37  C   UNK     0     -13.337 -36.960   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0     -14.670 -37.730   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0     -14.670 -39.270   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -13.337 -40.040   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0     -12.003 -39.270   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0     -13.337 -41.580   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0     -14.670 -42.350   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0     -14.670 -43.890   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0     -16.004 -41.580   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -17.338 -42.350   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0     -17.338 -43.890   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0     -16.004 -44.660   0.000  0.00  0.00           O+0
HETATM   49  C   UNK     0     -18.672 -44.660   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0     -20.005 -43.890   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0     -21.339 -44.660   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0     -20.005 -42.350   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0     -18.672 -41.580   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0     -18.672 -40.040   0.000  0.00  0.00           O+0
HETATM   55  C   UNK     0     -16.004 -40.040   0.000  0.00  0.00           C+0
HETATM   56  O   UNK     0     -17.338 -39.270   0.000  0.00  0.00           O+0
HETATM   57  C   UNK     0     -13.337 -35.420   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0     -12.003 -34.650   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0     -12.003 -33.110   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0      -5.335 -30.800   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0      -4.001 -30.030   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      -4.001 -28.490   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0       2.667 -26.180   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   63                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8   63                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   16                                                  
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15    9   17                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   61                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23   60                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   31                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   24   32                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34   58                                                  
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38   57                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   55                                                  
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42   44   45                                                  
CONECT   44   43                                                            
CONECT   45   43   46   55                                                  
CONECT   46   45   47   53                                                  
CONECT   47   46   48   49                                                  
CONECT   48   47                                                            
CONECT   49   47   50                                                       
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50   53                                                       
CONECT   53   52   46   54                                                  
CONECT   54   53                                                            
CONECT   55   45   39   56                                                  
CONECT   56   55                                                            
CONECT   57   37   58                                                       
CONECT   58   57   33   59                                                  
CONECT   59   58                                                            
CONECT   60   22   61                                                       
CONECT   61   60   18   62                                                  
CONECT   62   61                                                            
CONECT   63    7    2                                                       
MASTER        0    0    0    0    0    0    0    0   63    0  138    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₂H₃₀O₂₁

Average Mass

870.6810 Da

Monoisotopic Mass

870.12796 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC1=CC(O)=C(C(O)=C1)C1=C(O)C(OC2=CC(O)=C(OC3=CC(O)=CC(O)=C3OC3=CC(O)=C(OC4=CC(O)=CC(O)=C4OC4=CC(O)=CC(O)=C4)C(O)=C3)C(O)=C2)=C(O)C=C1O

InChI Identifier

InChI=1S/C42H30O21/c43-15-1-16(44)3-20(2-15)59-40-26(51)6-18(46)8-33(40)62-38-28(53)10-21(11-29(38)54)60-41-27(52)7-19(47)9-34(41)63-39-30(55)12-22(13-31(39)56)61-42-32(57)14-25(50)36(37(42)58)35-23(48)4-17(45)5-24(35)49/h1-14,43-58H

InChI Key

SWSXKCWLFMARQN-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
Cystoseira granulata	LOTUS Database	35616633
Himanthalia elongata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tannins. These are naturally occurring polyphenols which be categorized into four main classes: Hydrolyzable tannin (based on ellagic acid or gallic acid), condensed tannins (made of oligomeric or polymeric proanthocyanidins), complex tannins (made of a catechin bound to a gallotannin or elagitannin), and phlorotannins (oligomers of phloroglucinol).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Not Available

Direct Parent

Tannins

Alternative Parents

Substituents

Tannin
Biphenol
Diphenylether
Biphenyl
Diaryl ether
Benzenetriol
Phloroglucinol derivative
Resorcinol
Phenol ether
Phenoxy compound
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Monocyclic benzene moiety
Benzenoid
Polyol
Ether
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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

162854566

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol (NP0213933)

MOL for NP0213933 (3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol)

3D MOL for NP0213933 (3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol)

3D SDF for NP0213933 (3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol)

3D-SDF for NP0213933 (3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol)

PDB for NP0213933 (3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol)

3D PDB for NP0213933 (3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol)

SMILES for NP0213933 (3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol)

INCHI for NP0213933 (3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol)

Structure for NP0213933 (3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol)

3D Structure for NP0213933 (3-[4-(2-{4-[2-(3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-3,5-dihydroxyphenoxy}-3,5-dihydroxyphenoxy)-3,5-dihydroxyphenoxy]-[1,1'-biphenyl]-2,2',4,4',6,6'-hexol)