NP-MRD: Showing NP-Card for 5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one (NP0150733)

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Record Information

Version

2.0

Created at

2022-09-02 06:56:19 UTC

Updated at

2022-09-02 06:56:19 UTC

NP-MRD ID

NP0150733

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one

Description

5-Hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenyl-2H,8H-pyrano[2,3-f]chromen-2-one belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone. 5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one is found in Kielmeyera elata. 5-Hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenyl-2H,8H-pyrano[2,3-f]chromen-2-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652308221903142D          

 31 34  0  0  0  0            999 V2000
   -1.1270    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1715   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1715    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4105    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5855    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8230    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1730    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4105    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5855    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5855    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1730    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.1105    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9355    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9355    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5395    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5855   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    1.3480   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270    1.1270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  2  0  0  0  0
  6  4  1  0  0  0  0
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  8  6  2  0  0  0  0
 10  9  2  0  0  0  0
 14  1  1  0  0  0  0
 14 11  1  0  0  0  0
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 30 23  1  0  0  0  0
 31 24  1  0  0  0  0
 31 25  1  0  0  0  0
M  END

     RDKit          3D

 55 58  0  0  0  0  0  0  0  0999 V2000
   -3.0216   -2.3881    1.8540 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4950   -2.8306    0.5284 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.2655   -4.3198    0.4281 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0502   -2.7217   -1.9469 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5896   -1.3976   -1.9496 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8009    1.0845   -0.5321 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8971    0.0186   -0.2961 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3902   -1.2183   -0.3285 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3940    4.0820   -0.2539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6624    4.3033   -0.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
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 25 47  1  0
M  END


  Mrv1652308221903142D          

 31 34  0  0  0  0            999 V2000
   -1.1270    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1715   -0.1178    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1715    0.9428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4105    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5855    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8230    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1730    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4105    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1270   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5855    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1105    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  2  0  0  0  0
 10  9  2  0  0  0  0
 14  1  1  0  0  0  0
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 25  3  1  0  0  0  0
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 26 13  1  0  0  0  0
 27 18  2  0  0  0  0
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 31 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0150733

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CO)CC(=O)C1=C2OC(C)(C)C=CC2=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C25H24O6/c1-14(13-26)11-18(27)21-22(29)20-17(15-7-5-4-6-8-15)12-19(28)30-23(20)16-9-10-25(2,3)31-24(16)21/h4-10,12,14,26,29H,11,13H2,1-3H3

> <INCHI_KEY>
HRZGNXKXQGTISZ-UHFFFAOYSA-N

> <FORMULA>
C25H24O6

> <MOLECULAR_WEIGHT>
420.461

> <EXACT_MASS>
420.157288493

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
44.69308052240025

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenyl-2H,8H-pyrano[2,3-f]chromen-2-one

> <ALOGPS_LOGP>
4.05

> <JCHEM_LOGP>
4.094662513666666

> <ALOGPS_LOGS>
-4.79

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
15.362218546704753

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.381609941182517

> <JCHEM_PKA_STRONGEST_BASIC>
-2.5960645564257216

> <JCHEM_POLAR_SURFACE_AREA>
93.06

> <JCHEM_REFRACTIVITY>
127.50659999999995

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.84e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 22-AUG-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-AUG-19         0                                  
HETATM    1  C   UNK     0      -2.104   7.438   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.053  -0.220   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.053   1.760   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.366   6.105   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.826   6.105   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.136   4.771   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.056   4.771   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.366   3.437   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.564  -0.564   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.104  -0.564   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.206   6.105   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.826   0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.206   8.772   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.564   7.438   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.826   3.437   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.206   0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.056   2.104   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.564   4.771   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.056  -0.564   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.516   2.104   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.206   3.437   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.746   3.437   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.746   0.770   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.564   2.104   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -2.874   0.770   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -0.564  10.106   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -2.104   4.771   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       4.826  -1.897   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       2.516   4.771   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0       2.516  -0.564   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      -2.104   2.104   0.000  0.00  0.00           O+0
CONECT    1   14                                                            
CONECT    2   25                                                            
CONECT    3   25                                                            
CONECT    4    5    6                                                       
CONECT    5    4    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5   15                                                       
CONECT    8    6   15                                                       
CONECT    9   10   16                                                       
CONECT   10    9   25                                                       
CONECT   11   14   18                                                       
CONECT   12   17   19                                                       
CONECT   13   14   26                                                       
CONECT   14    1   11   13                                                  
CONECT   15    7    8   17                                                  
CONECT   16    9   23   24                                                  
CONECT   17   12   15   20                                                  
CONECT   18   11   21   27                                                  
CONECT   19   12   28   30                                                  
CONECT   20   17   22   23                                                  
CONECT   21   18   22   24                                                  
CONECT   22   20   21   29                                                  
CONECT   23   16   20   30                                                  
CONECT   24   16   21   31                                                  
CONECT   25    2    3   10   31                                             
CONECT   26   13                                                            
CONECT   27   18                                                            
CONECT   28   19                                                            
CONECT   29   22                                                            
CONECT   30   19   23                                                       
CONECT   31   24   25                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₂₄O₆

Average Mass

420.4610 Da

Monoisotopic Mass

420.15729 Da

IUPAC Name

5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenyl-2H,8H-pyrano[2,3-f]chromen-2-one

Traditional Name

5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one

CAS Registry Number

Not Available

SMILES

CC(CO)CC(=O)C1=C2OC(C)(C)C=CC2=C2OC(=O)C=C(C3=CC=CC=C3)C2=C1O

InChI Identifier

InChI=1S/C25H24O6/c1-14(13-26)11-18(27)21-22(29)20-17(15-7-5-4-6-8-15)12-19(28)30-23(20)16-9-10-25(2,3)31-24(16)21/h4-10,12,14,26,29H,11,13H2,1-3H3

InChI Key

HRZGNXKXQGTISZ-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
Kielmeyera elata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as prenylated neoflavonoids. These are neoflavonoids that features a C5-isoprenoid substituent at any position of the A, B, or C ring. Neoflavonoids are compounds with a structure based on the 4-phenylchromene backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Neoflavonoids

Sub Class

Prenylated neoflavonoids

Direct Parent

Prenylated neoflavonoids

Alternative Parents

Substituents

Prenylated neoflavonoid
Pyranoneoflavonoid
4-phenylcoumarin
Pyranocoumarin
Angular pyranocoumarin
Pyranochromene
2,2-dimethyl-1-benzopyran
Butyrophenone
Coumarin
Benzopyran
1-benzopyran
Aryl alkyl ketone
Aryl ketone
Alkyl aryl ether
Pyranone
Benzenoid
Monocyclic benzene moiety
Pyran
Vinylogous acid
Heteroaromatic compound
Ketone
Lactone
Organoheterocyclic compound
Ether
Oxacycle
Alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Primary alcohol
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	4.05	ALOGPS
logP	4.09	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	7.38	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	127.51 m³·mol⁻¹	ChemAxon
Polarizability	44.69 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

HMDB0131611

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB089584

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

15478944

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-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one (NP0150733)

MOL for NP0150733 (5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one)

3D MOL for NP0150733 (5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one)

3D SDF for NP0150733 (5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one)

3D-SDF for NP0150733 (5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one)

PDB for NP0150733 (5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one)

3D PDB for NP0150733 (5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one)

SMILES for NP0150733 (5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one)

INCHI for NP0150733 (5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one)

Structure for NP0150733 (5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one)

3D Structure for NP0150733 (5-hydroxy-6-(4-hydroxy-3-methylbutanoyl)-8,8-dimethyl-4-phenylpyrano[2,3-f]chromen-2-one)