NP-MRD: Showing NP-Card for (2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol (NP0250842)

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Record Information

Version

2.0

Created at

2022-09-07 13:48:57 UTC

Updated at

2022-09-07 13:48:57 UTC

NP-MRD ID

NP0250842

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol

Description

Epioritin-(4beta-6)-epioritin-(4beta-6)-epioritin-4alpha-ol belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''. (2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol is found in Senegalia galpinii. Based on a literature review very few articles have been published on Epioritin-(4beta-6)-epioritin-(4beta-6)-epioritin-4alpha-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072215482D          

 61 69  0  0  1  0            999 V2000
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  1  2  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309072215482D          

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M  END
> <DATABASE_ID>
NP0250842

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1[C@H](O)C2=C(O[C@@H]1C1=CC=C(O)C=C1)C(O)=C(O)C(=C2)[C@@H]1[C@@H](O)[C@H](OC2=C1C=C([C@@H]1[C@@H](O)[C@H](OC3=C1C=CC(O)=C3O)C1=CC=C(O)C=C1)C(O)=C2O)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C45H38O16/c46-20-7-1-17(2-8-20)40-35(54)29(23-13-14-28(49)34(53)43(23)59-40)24-15-26-30(36(55)41(18-3-9-21(47)10-4-18)60-44(26)38(57)31(24)50)25-16-27-33(52)37(56)42(19-5-11-22(48)12-6-19)61-45(27)39(58)32(25)51/h1-16,29-30,33,35-37,40-42,46-58H/t29-,30+,33-,35-,36-,37-,40-,41-,42-/m1/s1

> <INCHI_KEY>
TXWUPICCAPJKLS-ISMKCKKMSA-N

> <FORMULA>
C45H38O16

> <MOLECULAR_WEIGHT>
834.783

> <EXACT_MASS>
834.215985144

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
99

> <JCHEM_AVERAGE_POLARIZABILITY>
83.93705902792806

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3R,4R)-2-(4-hydroxyphenyl)-6-[(2R,3R,4S)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4S)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol

> <JCHEM_LOGP>
4.428082829999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.225931711231254

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.822864669414756

> <JCHEM_PKA_STRONGEST_BASIC>
-5.428126656757388

> <JCHEM_POLAR_SURFACE_AREA>
290.67999999999995

> <JCHEM_REFRACTIVITY>
214.28109999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3R,4R)-2-(4-hydroxyphenyl)-6-[(2R,3R,4S)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4S)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  O   UNK     0       8.002  -4.620   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.667  -9.240   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.000 -12.320   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -0.000 -13.860   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       1.334 -11.550   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.667 -12.320   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -5.335  -7.700   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.667  -9.240   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      -5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0     -10.669   0.000   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -8.002   0.000   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       0.000   1.540   0.000  0.00  0.00           O+0
HETATM   43  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   51  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   52  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   55  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   59  O   UNK     0       1.334  -5.390   0.000  0.00  0.00           O+0
HETATM   60  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   61                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   60                                                  
CONECT    6    5    7   58                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    8   15                                                  
CONECT   15   14                                                            
CONECT   16    9   17   58                                                  
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   36                                                  
CONECT   20   19   21   25                                                  
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   17   24                                                  
CONECT   24   23                                                            
CONECT   25   20   26                                                       
CONECT   26   25   27   34                                                  
CONECT   27   26   28   33                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   27                                                       
CONECT   34   26   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   19   37                                                  
CONECT   37   36   38   43                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40   56                                                  
CONECT   40   39   41   45                                                  
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41   37   44                                                  
CONECT   44   43                                                            
CONECT   45   40   46                                                       
CONECT   46   45   47   54                                                  
CONECT   47   46   48   53                                                  
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51   52                                                  
CONECT   51   50                                                            
CONECT   52   50   53                                                       
CONECT   53   52   47                                                       
CONECT   54   46   55   56                                                  
CONECT   55   54                                                            
CONECT   56   54   39   57                                                  
CONECT   57   56                                                            
CONECT   58   16    6   59                                                  
CONECT   59   58                                                            
CONECT   60    5   61                                                       
CONECT   61   60    2                                                       
MASTER        0    0    0    0    0    0    0    0   61    0  138    0
END

View in JSmol

Synonyms

Value	Source
Epioritin-(4b-6)-epioritin-(4b-6)-epioritin-4a-ol	Generator
Epioritin-(4β-6)-epioritin-(4β-6)-epioritin-4α-ol	Generator

Chemical Formula

C₄₅H₃₈O₁₆

Average Mass

834.7830 Da

Monoisotopic Mass

834.21599 Da

IUPAC Name

(2R,3R,4R)-2-(4-hydroxyphenyl)-6-[(2R,3R,4S)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4S)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,4,7,8-tetrol

Traditional Name

CAS Registry Number

Not Available

SMILES

O[C@@H]1[C@H](O)C2=C(O[C@@H]1C1=CC=C(O)C=C1)C(O)=C(O)C(=C2)[C@@H]1[C@@H](O)[C@H](OC2=C1C=C([C@@H]1[C@@H](O)[C@H](OC3=C1C=CC(O)=C3O)C1=CC=C(O)C=C1)C(O)=C2O)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C45H38O16/c46-20-7-1-17(2-8-20)40-35(54)29(23-13-14-28(49)34(53)43(23)59-40)24-15-26-30(36(55)41(18-3-9-21(47)10-4-18)60-44(26)38(57)31(24)50)25-16-27-33(52)37(56)42(19-5-11-22(48)12-6-19)61-45(27)39(58)32(25)51/h1-16,29-30,33,35-37,40-42,46-58H/t29-,30+,33-,35-,36-,37-,40-,41-,42-/m1/s1

InChI Key

TXWUPICCAPJKLS-ISMKCKKMSA-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
Acacia galpinii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Biflavonoids and polyflavonoids

Direct Parent

Biflavonoids and polyflavonoids

Alternative Parents

Substituents

B-type proanthocyanidin
Bi- and polyflavonoid skeleton
Leucoanthocyanidin-skeleton
Flavan-3-ol
Hydroxyflavonoid
8-hydroxyflavonoid
7-hydroxyflavonoid
4-hydroxyflavonoid
4'-hydroxyflavonoid
3-hydroxyflavonoid
Flavan
Chromane
1-benzopyran
Benzopyran
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Polyol
Organoheterocyclic compound
Oxacycle
Ether
Hydrocarbon derivative
Alcohol
Organic oxygen compound
Organooxygen compound
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	4.43	ChemAxon
pKa (Strongest Acidic)	8.82	ChemAxon
pKa (Strongest Basic)	-5.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	13	ChemAxon
Polar Surface Area	290.68 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	214.28 m³·mol⁻¹	ChemAxon
Polarizability	83.94 Å³	ChemAxon
Number of Rings	9	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

101333622

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol (NP0250842)

MOL for NP0250842 ((2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

3D MOL for NP0250842 ((2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

3D SDF for NP0250842 ((2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

3D-SDF for NP0250842 ((2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

PDB for NP0250842 ((2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

3D PDB for NP0250842 ((2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

SMILES for NP0250842 ((2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

INCHI for NP0250842 ((2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

Structure for NP0250842 ((2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)

3D Structure for NP0250842 ((2r,3r,4r)-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-6-[(2r,3r,4s)-3,7,8-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-4-yl]-3,4-dihydro-2h-1-benzopyran-3,4,7,8-tetrol)