NP-MRD: Showing NP-Card for 8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol (NP0287037)

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Record Information

Version

2.0

Created at

2022-09-09 15:54:27 UTC

Updated at

2022-09-09 15:54:27 UTC

NP-MRD ID

NP0287037

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol

Description

8-(3,4-Dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]Dodeca-2,4,6-triene-4,5,8-triol belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position. 8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol is found in Curculigo sinensis. 8-(3,4-Dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]Dodeca-2,4,6-triene-4,5,8-triol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 42  0  0  0  0  0  0  0  0999 V2000
    5.1403   -1.2479    0.9653 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8971   -0.7441    0.5974 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6313   -0.3882   -0.7085 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3835    0.1101   -1.0405 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4279    0.2423   -0.0607 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0717    0.7770   -0.3778 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0229    1.0103   -1.7756 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9758   -0.2453   -0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7744   -1.5635   -0.5661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7445   -2.5054   -0.3451 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5802   -3.8235   -0.7565 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9128   -2.1088    0.3090 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8895   -3.0576    0.5314 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0995   -0.8263    0.7224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1268    0.1226    0.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2922    1.5217    0.9354 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.4523    2.4560   -0.2447 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0681    3.0311   -0.4213 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2240    2.0326    0.3817 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0367    1.8581    1.4977 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7146   -0.1220    1.2511 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9464   -0.6198    1.6068 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2518   -0.9862    2.8958 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8526   -1.3541    0.2772 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3630   -0.4815   -1.4941 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1232    0.4034   -2.0484 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5946    1.7406   -2.0597 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1475   -1.8140   -1.0666 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7226   -4.0742   -1.2272 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7900   -4.0281    0.2382 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9990   -0.4659    1.2396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1063    1.6673    1.6661 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7976    1.9124   -1.1365 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1360    3.2780    0.0532 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9446    3.9975    0.1226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7515    3.1333   -1.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7071    2.5372    0.7459 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9794   -0.0277    2.0407 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1695   -1.3474    3.1137 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5 21  1  0
 21 22  2  0
 22 23  1  0
  5  6  1  0
  6  7  1  6
  6 19  1  0
 19 18  1  0
 18 17  1  0
 17 16  1  0
 16 20  1  0
 16 15  1  0
 15 14  2  0
 14 12  1  0
 12 13  1  0
 12 10  2  0
 10 11  1  0
 10  9  1  0
  9  8  2  0
 22  2  1  0
  8  6  1  0
 20 19  1  0
  8 15  1  0
  1 24  1  0
  3 25  1  0
  4 26  1  0
 21 38  1  0
 23 39  1  0
  7 27  1  0
 19 37  1  1
 18 35  1  0
 18 36  1  0
 17 33  1  0
 17 34  1  0
 16 32  1  1
 14 31  1  0
 13 30  1  0
 11 29  1  0
  9 28  1  0
M  END


  Mrv1533004201503582D          

 23 26  0  0  0  0            999 V2000
    2.2254   -2.5410    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9508   -1.7630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1398   -1.6118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8652   -0.8339    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4017   -0.2071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2127   -0.3583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4873   -1.1363    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2983   -1.2875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1271    0.5709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4297    0.1301    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9466    0.6655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3837    1.3652    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1091    2.1431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3297    2.4135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8567    1.6166    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6323    1.9727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0328    2.4608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7881    2.1289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4532    2.6170    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8782    1.3088    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6335    0.9769    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2131    0.8207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5421    1.1527    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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 11 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
  9 23  1  0  0  0  0
 16 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287037

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1O)C1(O)C2CCC(O2)C2=CC(O)=C(O)C=C12

> <INCHI_IDENTIFIER>
InChI=1S/C17H16O6/c18-11-2-1-8(5-12(11)19)17(22)10-7-14(21)13(20)6-9(10)15-3-4-16(17)23-15/h1-2,5-7,15-16,18-22H,3-4H2

> <INCHI_KEY>
YKWUBZBBRYXVKO-UHFFFAOYSA-N

> <FORMULA>
C17H16O6

> <MOLECULAR_WEIGHT>
316.309

> <EXACT_MASS>
316.094688235

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
30.958627276324894

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol

> <ALOGPS_LOGP>
1.10

> <JCHEM_LOGP>
1.7905074573333328

> <ALOGPS_LOGS>
-2.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.434002002178156

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.824218246960971

> <JCHEM_PKA_STRONGEST_BASIC>
-3.94164193207848

> <JCHEM_POLAR_SURFACE_AREA>
110.38000000000001

> <JCHEM_REFRACTIVITY>
81.65039999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.84e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  O   UNK     0       4.154  -4.743   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       3.641  -3.291   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.128  -3.009   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.615  -1.557   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.616  -0.387   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.130  -0.669   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.643  -2.121   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.157  -2.403   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.104   1.066   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       0.802   0.243   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.634   1.242   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.450   2.548   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.937   4.001   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.482   4.505   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.466   3.018   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.180   3.682   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.061   4.594   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -1.471   3.974   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -2.713   4.885   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.639   2.443   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -3.049   1.824   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.398   1.532   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.012   2.152   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7                                                            
CONECT    9    5   10   11   23                                             
CONECT   10    9                                                            
CONECT   11    9   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14   11                                                       
CONECT   16   14   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22    9   16                                                  
MASTER        0    0    0    0    0    0    0    0   23    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₆O₆

Average Mass

316.3090 Da

Monoisotopic Mass

316.09469 Da

IUPAC Name

8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol

Traditional Name

8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1O)C1(O)C2CCC(O2)C2=CC(O)=C(O)C=C12

InChI Identifier

InChI=1S/C17H16O6/c18-11-2-1-8(5-12(11)19)17(22)10-7-14(21)13(20)6-9(10)15-3-4-16(17)23-15/h1-2,5-7,15-16,18-22H,3-4H2

InChI Key

YKWUBZBBRYXVKO-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
Curculigo sinensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-benzopyrans. These are organic aromatic compounds that 1-benzopyran, a bicyclic compound made up of a benzene ring fused to a pyran, so that the oxygen atom is at the 2-position.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

2-benzopyrans

Direct Parent

2-benzopyrans

Alternative Parents

Substituents

2-benzopyran
Catechol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Tetrahydrofuran
Tertiary alcohol
Dialkyl ether
Ether
Oxacycle
Polyol
Alcohol
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
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	1.1	ALOGPS
logP	1.79	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	8.82	ChemAxon
pKa (Strongest Basic)	-3.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	110.38 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	81.65 m³·mol⁻¹	ChemAxon
Polarizability	30.96 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

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HMDB ID

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Showing NP-Card for 8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol (NP0287037)

MOL for NP0287037 (8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol)

3D MOL for NP0287037 (8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol)

3D SDF for NP0287037 (8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol)

3D-SDF for NP0287037 (8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol)

PDB for NP0287037 (8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol)

3D PDB for NP0287037 (8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol)

SMILES for NP0287037 (8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol)

INCHI for NP0287037 (8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol)

Structure for NP0287037 (8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol)

3D Structure for NP0287037 (8-(3,4-dihydroxyphenyl)-12-oxatricyclo[7.2.1.0²,⁷]dodeca-2,4,6-triene-4,5,8-triol)