NP-MRD: Showing NP-Card for 4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol (NP0158196)

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Record Information

Version

2.0

Created at

2022-09-02 15:44:16 UTC

Updated at

2022-09-02 15:44:16 UTC

NP-MRD ID

NP0158196

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol

Description

4-[(8R)-6,8-dihydroxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol belongs to the class of organic compounds known as hydroxyisoflavonoids. These are organic compounds containing an isoflavonoid skeleton carrying one or more hydroxyl groups. 4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol is found in Bolusanthus speciosus. Based on a literature review very few articles have been published on 4-[(8R)-6,8-dihydroxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 36 39  0  0  0  0  0  0  0  0999 V2000
   -1.0254   -0.4059   -2.5532 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1514   -0.2460   -1.4752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6441   -0.1466   -0.2216 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0782   -0.2991   -0.1222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6723   -1.3861   -0.7817 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0366   -1.5721   -0.7418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8416   -0.6966   -0.0545 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2201   -0.8384    0.0183 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2726    0.4002    0.6147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0883    1.2718    1.3006 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8880    0.5656    0.5574 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2982    1.6295    1.1982 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2910    0.0279    0.8948 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1052    1.2495    1.5983 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7027    0.0567    0.5019 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6787    0.2066    1.4635 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0241    0.2514    1.1464 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4115    0.1418   -0.1871 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4463   -0.0091   -1.1633 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1009   -0.0487   -0.7932 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1852   -0.2005   -1.7900 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7973    0.2205   -0.1879 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3067    0.0729    1.1224 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1755    0.3914    1.9097 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8234    0.0059   -3.4678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0210   -2.0656   -1.3084 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5054   -2.4178   -1.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6454   -1.6177   -0.4556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7410    2.0606    1.7903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8331    2.2895    1.7086 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1620   -0.8158    1.6428 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4328    1.9568    0.9906 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4247    0.2967    2.5201 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7714   -0.0905   -2.1822 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6109   -0.9904    1.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1590    0.7516    1.3185 H   0  0  0  0  0  0  0  0  0  0  0  0
 14 13  1  0
 13 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 22  1  0
 22 23  1  0
 23 24  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21  2  1  0
  2  1  1  0
  2  3  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  7  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
  3 13  1  0
 11  4  1  0
 20 15  1  0
 24 17  1  0
 14 32  1  0
 13 31  1  1
 16 33  1  0
 23 35  1  0
 23 36  1  0
 19 34  1  0
  1 25  1  0
  5 26  1  0
  6 27  1  0
  8 28  1  0
 10 29  1  0
 12 30  1  0
M  END


  Mrv1652309022217442D          

 24 27  0  0  1  0            999 V2000
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -1.4924    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8419   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3570   -0.1576    0.0000 O   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
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  2  0  0  0  0
  4 11  1  0  0  0  0
 11 12  1  0  0  0  0
  3 13  1  0  0  0  0
 13 14  1  6  0  0  0
 13 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 20 21  1  0  0  0  0
  2 21  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 17 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0158196

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@@H]1C2=CC3=C(OCO3)C=C2OC(O)=C1C1=CC=C(O)C(O)=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C16H12O8/c17-8-2-1-6(14(19)15(8)20)12-13(18)7-3-10-11(23-5-22-10)4-9(7)24-16(12)21/h1-4,13,17-21H,5H2/t13-/m1/s1

> <INCHI_KEY>
IPQKKNLEQHEZTA-CYBMUJFWSA-N

> <FORMULA>
C16H12O8

> <MOLECULAR_WEIGHT>
332.264

> <EXACT_MASS>
332.053217346

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
36

> <JCHEM_AVERAGE_POLARIZABILITY>
31.535010649438448

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(8R)-6,8-dihydroxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol

> <ALOGPS_LOGP>
0.92

> <JCHEM_LOGP>
1.7436248073333336

> <ALOGPS_LOGS>
-2.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
9.234917988185112

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.9357791867861165

> <JCHEM_PKA_STRONGEST_BASIC>
-3.5776849409509444

> <JCHEM_POLAR_SURFACE_AREA>
128.84

> <JCHEM_REFRACTIVITY>
89.25150000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.32e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4-[(8R)-6,8-dihydroxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -1.334   3.850   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       8.133  -2.786   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       9.038  -1.540   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       8.133  -0.294   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   21                                                  
CONECT    3    2    4   13                                                  
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9    4   12                                                  
CONECT   12   11                                                            
CONECT   13    3   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   24                                                  
CONECT   18   17   19   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   15   21                                                  
CONECT   21   20    2                                                       
CONECT   22   18   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   17                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₂O₈

Average Mass

332.2640 Da

Monoisotopic Mass

332.05322 Da

IUPAC Name

4-[(8R)-6,8-dihydroxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol

Traditional Name

4-[(8R)-6,8-dihydroxy-2H,8H-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol

CAS Registry Number

Not Available

SMILES

O[C@@H]1C2=CC3=C(OCO3)C=C2OC(O)=C1C1=CC=C(O)C(O)=C1O

InChI Identifier

InChI=1S/C16H12O8/c17-8-2-1-6(14(19)15(8)20)12-13(18)7-3-10-11(23-5-22-10)4-9(7)24-16(12)21/h1-4,13,17-21H,5H2/t13-/m1/s1

InChI Key

IPQKKNLEQHEZTA-CYBMUJFWSA-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
Bolusanthus speciosus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydroxyisoflavonoids. These are organic compounds containing an isoflavonoid skeleton carrying one or more hydroxyl groups.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

Hydroxyisoflavonoids

Direct Parent

Hydroxyisoflavonoids

Alternative Parents

Substituents

Hydroxyisoflavonoid
Isoflav-2-ene skeleton
Benzopyran
1-benzopyran
Benzenetriol
Benzodioxole
5-unsubstituted pyrrogallol
Pyrogallol derivative
1-hydroxy-2-unsubstituted benzenoid
Phenol
1-hydroxy-4-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Secondary alcohol
Ketene acetal or derivatives
Polyol
Acetal
Organoheterocyclic compound
Oxacycle
Organooxygen compound
Alcohol
Hydrocarbon derivative
Organic oxygen 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	0.92	ALOGPS
logP	1.74	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	4.94	ChemAxon
pKa (Strongest Basic)	-3.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	128.84 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	89.25 m³·mol⁻¹	ChemAxon
Polarizability	31.54 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

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

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FoodDB ID

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KNApSAcK ID

Not Available

Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

Not Available

PubChem Compound

163031601

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for 4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol (NP0158196)

MOL for NP0158196 (4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol)

3D MOL for NP0158196 (4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol)

3D SDF for NP0158196 (4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol)

3D-SDF for NP0158196 (4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol)

PDB for NP0158196 (4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol)

3D PDB for NP0158196 (4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol)

SMILES for NP0158196 (4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol)

INCHI for NP0158196 (4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol)

Structure for NP0158196 (4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol)

3D Structure for NP0158196 (4-[(8r)-6,8-dihydroxy-2h,8h-[1,3]dioxolo[4,5-g]chromen-7-yl]benzene-1,2,3-triol)