NP-MRD: Showing NP-Card for (3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one (NP0237550)

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Record Information

Version

2.0

Created at

2022-09-06 20:43:28 UTC

Updated at

2022-09-06 20:43:28 UTC

NP-MRD ID

NP0237550

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one

Description

DIHYDROVERMISTATIN belongs to the class of organic compounds known as benzofuranones. These are organic compounds containing a benzene ring fused to a furanone. (3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one is found in Penicillium simplicissimum. (3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one was first documented in 2012 (PMID: 22295871). Based on a literature review very few articles have been published on DIHYDROVERMISTATIN (PMID: 28202316).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    6.3398   -0.9278    1.4649 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0590   -0.8785    0.6913 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2647    0.3182    1.2240 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9988    0.3634    0.4565 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9691    1.0979   -0.7062 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7936    1.1468   -1.4302 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7332    1.8086   -2.4961 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6608    0.4646   -0.9895 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5748    0.5879   -1.8298 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.5575    1.9191   -2.2814 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3923    2.6622   -1.5007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5217    3.9329   -1.4471 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1783    1.7581   -0.6722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2507    1.9640    0.2030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9325    0.9154    0.7733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9944    1.0545    1.6417 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6327   -0.0849    2.1774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5050   -0.3457    0.4372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4560   -0.5917   -0.4160 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0758   -1.8768   -0.7207 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7633   -2.9666   -0.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7709    0.4888   -0.9838 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7701   -0.2386    0.1690 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9228   -0.2670    0.8479 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9005    0.0016    1.2460 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9220   -1.8289    1.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0829   -0.9256    2.5471 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4816   -1.8050    0.7095 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3133   -0.6061   -0.3695 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0911    0.2125    2.3145 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8557    1.2187    0.9848 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8497    1.6204   -1.0364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5644   -0.1467   -2.6601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5424    2.9703    0.4300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8749   -0.6711    2.7485 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9925   -0.7795    1.3745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4788    0.1516    2.8197 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0448   -1.1998    0.8860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8390   -2.9213   -0.3641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3603   -3.9218   -0.5082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6336   -2.8894    0.9482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0718   -0.7847    0.5607 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8 23  2  0
 23 24  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  2  0
 11 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 24  4  1  0
 22  9  1  0
 22 13  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  5 32  1  0
 23 42  1  0
  9 33  1  6
 14 34  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 18 38  1  0
 21 39  1  0
 21 40  1  0
 21 41  1  0
M  END


  Mrv1652309062222432D          

 24 26  0  0  1  0            999 V2000
    0.4161   -5.9016    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6710   -5.1170    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1190   -4.5039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3739   -3.7192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752   -1.7084    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838    0.7541    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    0.9521    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4358   -2.7631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1809   -3.5477    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
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  9  8  1  6  0  0  0
  9 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
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
 13 22  1  0  0  0  0
  9 22  1  0  0  0  0
  8 23  2  0  0  0  0
 23 24  1  0  0  0  0
  4 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0237550

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCC1=CC(=O)C(=CO1)[C@@H]1OC(=O)C2=CC(OC)=CC(OC)=C12

> <INCHI_IDENTIFIER>
InChI=1S/C18H18O6/c1-4-5-10-7-14(19)13(9-23-10)17-16-12(18(20)24-17)6-11(21-2)8-15(16)22-3/h6-9,17H,4-5H2,1-3H3/t17-/m0/s1

> <INCHI_KEY>
FLYWRXXEJAXBBG-KRWDZBQOSA-N

> <FORMULA>
C18H18O6

> <MOLECULAR_WEIGHT>
330.336

> <EXACT_MASS>
330.1103383

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
33.849995264740926

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R)-4,6-dimethoxy-3-(4-oxo-6-propyl-4H-pyran-3-yl)-1,3-dihydro-2-benzofuran-1-one

> <JCHEM_LOGP>
2.6660743486666663

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.463462084941083

> <JCHEM_PKA_STRONGEST_BASIC>
-4.4745181706832335

> <JCHEM_POLAR_SURFACE_AREA>
71.06000000000002

> <JCHEM_REFRACTIVITY>
87.9846

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3H-2-benzofuran-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-SEP-22         0                                  
HETATM    1  C   UNK     0       0.777 -11.016   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.253  -9.552   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.222  -8.407   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.698  -6.943   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.333  -5.798   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.143  -4.334   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -0.887  -3.189   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.220  -1.303   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.650   1.408   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.591   0.237   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       7.591   1.777   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       4.924  -4.383   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       3.590  -5.153   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.680  -5.158   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       2.204  -6.622   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   24                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   23                                                  
CONECT    9    8   10   22                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   22                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19                                                       
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   13    9                                                  
CONECT   23    8   24                                                       
CONECT   24   23    4                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₁₈O₆

Average Mass

330.3360 Da

Monoisotopic Mass

330.11034 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CCCC1=CC(=O)C(=CO1)[C@@H]1OC(=O)C2=CC(OC)=CC(OC)=C12

InChI Identifier

InChI=1S/C18H18O6/c1-4-5-10-7-14(19)13(9-23-10)17-16-12(18(20)24-17)6-11(21-2)8-15(16)22-3/h6-9,17H,4-5H2,1-3H3/t17-/m0/s1

InChI Key

FLYWRXXEJAXBBG-KRWDZBQOSA-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
Penicillium simplicissimum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzofuranones. These are organic compounds containing a benzene ring fused to a furanone.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Benzofuranones

Direct Parent

Benzofuranones

Alternative Parents

Substituents

Isobenzofuranone
Benzofuranone
Phthalide
Isocoumaran
Anisole
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Lactone
Carboxylic acid ester
Cyclic ketone
Oxacycle
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
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

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

9675667

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11500865

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Stierle AA, Stierle DB, Girtsman T: Caspase-1 inhibitors from an extremophilic fungus that target specific leukemia cell lines. J Nat Prod. 2012 Mar 23;75(3):344-50. doi: 10.1021/np200414c. Epub 2012 Feb 1. [PubMed:22295871 ]
Gubiani JR, Wijeratne EM, Shi T, Araujo AR, Arnold AE, Chapman E, Gunatilaka AA: An epigenetic modifier induces production of (10'S)-verruculide B, an inhibitor of protein tyrosine phosphatases by Phoma sp. nov. LG0217, a fungal endophyte of Parkinsonia microphylla. Bioorg Med Chem. 2017 Mar 15;25(6):1860-1866. doi: 10.1016/j.bmc.2017.01.048. Epub 2017 Feb 3. [PubMed:28202316 ]
LOTUS database [Link]

Showing NP-Card for (3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one (NP0237550)

MOL for NP0237550 ((3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one)

3D MOL for NP0237550 ((3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one)

3D SDF for NP0237550 ((3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one)

3D-SDF for NP0237550 ((3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one)

PDB for NP0237550 ((3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one)

3D PDB for NP0237550 ((3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one)

SMILES for NP0237550 ((3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one)

INCHI for NP0237550 ((3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one)

Structure for NP0237550 ((3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one)

3D Structure for NP0237550 ((3r)-4,6-dimethoxy-3-(4-oxo-6-propylpyran-3-yl)-3h-2-benzofuran-1-one)