NP-MRD: Showing NP-Card for (1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one (NP0282069)

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Record Information

Version

2.0

Created at

2022-09-09 08:45:48 UTC

Updated at

2022-09-09 08:45:49 UTC

NP-MRD ID

NP0282069

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one

Description

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092210452D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309092210452D          

 44 51  0  0  1  0            999 V2000
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   -3.2271    0.4529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0488    0.3791    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8801    1.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0584    1.2751    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7114    2.0236    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7537    2.2449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5754    2.3186    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9223    3.0671    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0501    1.6439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8789    1.6832    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1419    2.5020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5835    3.1093    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
  5 11  1  0  0  0  0
 11 12  1  0  0  0  0
  2 12  1  0  0  0  0
  4 13  1  0  0  0  0
 13 14  1  1  0  0  0
 14 15  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 16 22  1  0  0  0  0
 22 23  1  0  0  0  0
 15 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 35 36  2  0  0  0  0
 30 36  1  0  0  0  0
 36 37  1  0  0  0  0
 27 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 39 41  2  0  0  0  0
 25 41  1  0  0  0  0
 42 41  1  1  0  0  0
 13 42  1  0  0  0  0
 42 43  1  0  0  0  0
  2 43  1  0  0  0  0
 43 44  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0282069

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@]12C[C@@H](C3=CC=C(O)C=C3O1)[C@]13O[C@]1(OC1=CC(\C=C\C4=CC=C(O)C=C4O)=CC(O)=C1[C@H]3C2=O)C1=CC=C(O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C34H26O10/c1-32-15-23(21-8-6-20(37)14-27(21)42-32)33-30(31(32)41)29-26(40)10-16(2-3-17-4-5-18(35)12-24(17)38)11-28(29)43-34(33,44-33)22-9-7-19(36)13-25(22)39/h2-14,23,30,35-40H,15H2,1H3/b3-2+/t23?,30-,32-,33+,34+/m0/s1

> <INCHI_KEY>
HEAKAXOVOXEHND-VBDFEGCBSA-N

> <FORMULA>
C34H26O10

> <MOLECULAR_WEIGHT>
594.572

> <EXACT_MASS>
594.152597037

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
60.7432675361873

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,4S,12R,14S)-4-(2,4-dihydroxyphenyl)-8-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0^{2,4}.0^{2,12}.0^{6,11}.0^{16,21}]docosa-6,8,10,16,18,20-hexaen-13-one

> <JCHEM_LOGP>
6.224837343999999

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.46469325157707

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.073818944677

> <JCHEM_PKA_STRONGEST_BASIC>
-4.479282754296007

> <JCHEM_POLAR_SURFACE_AREA>
169.44

> <JCHEM_REFRACTIVITY>
157.37040000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,4S,12R,14S)-4-(2,4-dihydroxyphenyl)-8-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0^{2,4}.0^{2,12}.0^{6,11}.0^{16,21}]docosa-6,8,10,16,18,20-hexaen-13-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0       7.143   6.546   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.456   5.038   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.720   3.724   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       8.022   2.356   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.614   2.693   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.581   1.494   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.102   1.732   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.657   3.169   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      14.178   3.407   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      11.690   4.367   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.168   4.130   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       9.071   5.336   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.413   1.892   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       7.148   0.468   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.627   0.522   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.657  -1.018   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.006  -1.762   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.036  -3.301   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.717  -4.097   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       5.747  -5.637   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       4.369  -3.353   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.339  -1.814   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.990  -1.070   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       4.072   0.405   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       3.179   1.671   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.645   1.534   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.759   2.793   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.775   2.656   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.422   1.258   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.956   1.121   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -3.604  -0.276   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.138  -0.414   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -6.024   0.845   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -7.558   0.708   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0      -5.376   2.243   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -3.842   2.380   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -3.195   3.777   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       1.407   4.190   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       2.941   4.328   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       3.588   5.725   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0       3.827   3.069   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.374   3.142   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.865   4.670   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       4.822   5.804   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   12   43                                             
CONECT    3    2    4                                                       
CONECT    4    3    5   13                                                  
CONECT    5    4    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10    5   12                                                  
CONECT   12   11    2                                                       
CONECT   13    4   14   15   42                                             
CONECT   14   13   15                                                       
CONECT   15   14   13   16   24                                             
CONECT   16   15   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   16   23                                                  
CONECT   23   22                                                            
CONECT   24   15   25                                                       
CONECT   25   24   26   41                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   38                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   36                                                  
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33   36                                                       
CONECT   36   35   30   37                                                  
CONECT   37   36                                                            
CONECT   38   27   39                                                       
CONECT   39   38   40   41                                                  
CONECT   40   39                                                            
CONECT   41   39   25   42                                                  
CONECT   42   41   13   43                                                  
CONECT   43   42    2   44                                                  
CONECT   44   43                                                            
MASTER        0    0    0    0    0    0    0    0   44    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₄H₂₆O₁₀

Average Mass

594.5720 Da

Monoisotopic Mass

594.15260 Da

IUPAC Name

(1S,2R,4S,12R,14S)-4-(2,4-dihydroxyphenyl)-8-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0^{2,4}.0^{2,12}.0^{6,11}.0^{16,21}]docosa-6,8,10,16,18,20-hexaen-13-one

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@]12C[C@@H](C3=CC=C(O)C=C3O1)[C@]13O[C@]1(OC1=CC(\C=C\C4=CC=C(O)C=C4O)=CC(O)=C1[C@H]3C2=O)C1=CC=C(O)C=C1O

InChI Identifier

InChI=1S/C34H26O10/c1-32-15-23(21-8-6-20(37)14-27(21)42-32)33-30(31(32)41)29-26(40)10-16(2-3-17-4-5-18(35)12-24(17)38)11-28(29)43-34(33,44-33)22-9-7-19(36)13-25(22)39/h2-14,23,30,35-40H,15H2,1H3/b3-2+/t23?,30-,32-,33+,34+/m0/s1

InChI Key

HEAKAXOVOXEHND-VBDFEGCBSA-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
Morus alba	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	6.22	ChemAxon
pKa (Strongest Acidic)	6.07	ChemAxon
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	169.44 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	157.37 m³·mol⁻¹	ChemAxon
Polarizability	60.74 Å³	ChemAxon
Number of Rings	8	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

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one (NP0282069)

MOL for NP0282069 ((1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one)

3D MOL for NP0282069 ((1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one)

3D SDF for NP0282069 ((1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one)

3D-SDF for NP0282069 ((1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one)

PDB for NP0282069 ((1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one)

3D PDB for NP0282069 ((1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one)

SMILES for NP0282069 ((1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one)

INCHI for NP0282069 ((1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one)

Structure for NP0282069 ((1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one)

3D Structure for NP0282069 ((1s,2r,4s,12r,14s)-4-(2,4-dihydroxyphenyl)-8-[(1e)-2-(2,4-dihydroxyphenyl)ethenyl]-10,18-dihydroxy-14-methyl-3,5,15-trioxahexacyclo[12.7.1.0²,⁴.0²,¹².0⁶,¹¹.0¹⁶,²¹]docosa-6,8,10,16,18,20-hexaen-13-one)