NP-MRD: Showing NP-Card for 5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one (NP0325064)

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Record Information

Version

2.0

Created at

2022-09-12 05:32:12 UTC

Updated at

2022-09-12 05:32:12 UTC

NP-MRD ID

NP0325064

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one

Description

5-Hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3,4-dihydro-2H-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety. 5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one is found in Monodictys putredinis. 5-Hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3,4-dihydro-2H-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241516312D          

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M  END

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  Mrv1533004241516312D          

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    2.8579   -2.4750    0.0000 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3848   -0.5558    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9783    0.0173    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7067   -0.3700    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4482   -0.0083    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5634   -1.1824    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7465   -1.2973    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3592   -2.0257    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 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  2  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
  8 20  1  0  0  0  0
 16 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 25 32  1  0  0  0  0
 32 33  2  0  0  0  0
 21 33  1  0  0  0  0
 33 34  1  0  0  0  0
 27 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 37 39  1  0  0  0  0
 39 40  1  0  0  0  0
 35 40  1  0  0  0  0
 40 41  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0325064

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC(=O)OC1C1(C)CC(=O)C2=C(O)C(=CC=C2O1)C1=C(C)C=C2OC(C)(CC(=O)C2=C1O)C1OC(=O)CC1O

> <INCHI_IDENTIFIER>
InChI=1S/C30H30O11/c1-12-7-19-24(17(33)11-30(4,41-19)28-15(31)9-21(35)39-28)26(37)22(12)14-5-6-18-23(25(14)36)16(32)10-29(3,40-18)27-13(2)8-20(34)38-27/h5-7,13,15,27-28,31,36-37H,8-11H2,1-4H3

> <INCHI_KEY>
YSURVZRGQKOUAG-UHFFFAOYSA-N

> <FORMULA>
C30H30O11

> <MOLECULAR_WEIGHT>
566.559

> <EXACT_MASS>
566.178811786

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
56.867210233230544

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3,4-dihydro-2H-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
2.99

> <JCHEM_LOGP>
3.705648968666666

> <ALOGPS_LOGS>
-3.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.891615800511662

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.050537514205532

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3162725100681865

> <JCHEM_POLAR_SURFACE_AREA>
165.89000000000001

> <JCHEM_REFRACTIVITY>
140.5243

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.36e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3H-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3H-1-benzopyran-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -7.745  -6.947   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -7.959  -5.422   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -9.319  -4.699   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -9.051  -3.183   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0     -10.121  -2.075   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      -7.526  -2.968   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -6.851  -4.353   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -5.861  -6.067   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000  -4.620   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  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.195   0.677   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       8.185  -1.037   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       9.293   0.032   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      10.653  -0.691   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0      12.037  -0.016   0.000  0.00  0.00           O+0
HETATM   39  C   UNK     0      10.385  -2.207   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       8.860  -2.422   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       8.137  -3.781   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9   10   20                                             
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   19                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   13   20                                                  
CONECT   20   19    8                                                       
CONECT   21   16   22   33                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   32                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29   35                                             
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   25   33                                                  
CONECT   33   32   21   34                                                  
CONECT   34   33                                                            
CONECT   35   27   36   40                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37   40                                                       
CONECT   40   39   35   41                                                  
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   92    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₀O₁₁

Average Mass

566.5590 Da

Monoisotopic Mass

566.17881 Da

IUPAC Name

5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3,4-dihydro-2H-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3H-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3H-1-benzopyran-4-one

CAS Registry Number

Not Available

SMILES

CC1CC(=O)OC1C1(C)CC(=O)C2=C(O)C(=CC=C2O1)C1=C(C)C=C2OC(C)(CC(=O)C2=C1O)C1OC(=O)CC1O

InChI Identifier

InChI=1S/C30H30O11/c1-12-7-19-24(17(33)11-30(4,41-19)28-15(31)9-21(35)39-28)26(37)22(12)14-5-6-18-23(25(14)36)16(32)10-29(3,40-18)27-13(2)8-20(34)38-27/h5-7,13,15,27-28,31,36-37H,8-11H2,1-4H3

InChI Key

YSURVZRGQKOUAG-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
Monodictys putredinis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Chromones

Alternative Parents

Substituents

Chromone
Aryl ketone
Aryl alkyl ketone
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Dicarboxylic acid or derivatives
Gamma butyrolactone
Benzenoid
Vinylogous acid
Oxolane
Carboxylic acid ester
Ketone
Lactone
Secondary alcohol
Ether
Oxacycle
Carboxylic acid derivative
Alcohol
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organooxygen compound
Carbonyl group
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	2.99	ALOGPS
logP	3.71	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	8.05	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	165.89 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	140.52 m³·mol⁻¹	ChemAxon
Polarizability	56.87 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one (NP0325064)

MOL for NP0325064 (5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one)

3D MOL for NP0325064 (5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one)

3D SDF for NP0325064 (5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one)

3D-SDF for NP0325064 (5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one)

PDB for NP0325064 (5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one)

3D PDB for NP0325064 (5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one)

SMILES for NP0325064 (5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one)

INCHI for NP0325064 (5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one)

Structure for NP0325064 (5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one)

3D Structure for NP0325064 (5-hydroxy-6-[5-hydroxy-2-methyl-2-(3-methyl-5-oxooxolan-2-yl)-4-oxo-3h-1-benzopyran-6-yl]-2-(3-hydroxy-5-oxooxolan-2-yl)-2,7-dimethyl-3h-1-benzopyran-4-one)