NP-MRD: Showing NP-Card for 3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid (NP0294425)

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Record Information

Version

2.0

Created at

2022-09-10 02:57:24 UTC

Updated at

2022-09-10 02:57:24 UTC

NP-MRD ID

NP0294425

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid

Description

3-[2-(Furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-4,5,6,7-tetrahydro-1-benzofuran-2-yl]-3-methyl-6-oxo-3,6-dihydro-2H-pyran-3-yl]propanoic acid belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups. 3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid is found in Xylocarpus granatum. 3-[2-(Furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-4,5,6,7-tetrahydro-1-benzofuran-2-yl]-3-methyl-6-oxo-3,6-dihydro-2H-pyran-3-yl]propanoic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171521172D          

 42 45  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004171521172D          

 42 45  0  0  0  0            999 V2000
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    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    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
    2.2534   -0.0288    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8661   -0.6996    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0945    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5070   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3320   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7445   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7445    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3320    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7445    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5650    1.9277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7366    2.7346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0221    3.1471    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4090    2.5951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5070    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4783    1.9515    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8074    1.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8362    2.3887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1366    2.8258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4081    2.4385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1653    3.6503    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
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  9 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 16 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 11 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 31 35  1  0  0  0  0
 30 36  1  0  0  0  0
 25 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
 40 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0294425

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCC(C)C(=O)OC1C2=C(OC(=C2)C2=CC(=O)OC(C3=COC=C3)C2(C)CCC(O)=O)C(C)C(CC(=O)OC)C1(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C32H40O10/c1-8-17(2)30(37)42-29-20-13-23(40-27(20)18(3)21(31(29,4)5)14-25(35)38-7)22-15-26(36)41-28(19-10-12-39-16-19)32(22,6)11-9-24(33)34/h10,12-13,15-18,21,28-29H,8-9,11,14H2,1-7H3,(H,33,34)

> <INCHI_KEY>
SUDQSSBJBLXQMO-UHFFFAOYSA-N

> <FORMULA>
C32H40O10

> <MOLECULAR_WEIGHT>
584.662

> <EXACT_MASS>
584.262147488

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
82

> <JCHEM_AVERAGE_POLARIZABILITY>
62.50105815253054

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-4,5,6,7-tetrahydro-1-benzofuran-2-yl]-3-methyl-6-oxo-3,6-dihydro-2H-pyran-3-yl]propanoic acid

> <ALOGPS_LOGP>
5.18

> <JCHEM_LOGP>
5.417716522666669

> <ALOGPS_LOGS>
-4.79

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.951925220609124

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6119243647624897

> <JCHEM_POLAR_SURFACE_AREA>
142.48

> <JCHEM_REFRACTIVITY>
150.21210000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.59e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4H-1-benzofuran-2-yl]-3-methyl-6-oxo-2H-pyran-3-yl]propanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -2.370   0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -1.465   2.016   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.000   1.540   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  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       6.668   2.310   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.206  -0.054   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.483  -1.306   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.910   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.680  -0.564   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -6.220  -0.564   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      -6.990  -1.897   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      -6.990   0.770   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -6.220   2.104   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -6.990   3.437   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -8.521   3.598   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -8.842   5.105   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0      -7.508   5.875   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -6.363   4.844   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -4.680   2.104   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -4.626   3.643   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -3.374   2.920   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -3.428   4.459   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      -2.122   5.275   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0      -0.762   4.552   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      -2.175   6.814   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   22                                                  
CONECT    9    8   10   13                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   25                                                  
CONECT   12   11   13                                                       
CONECT   13   12    9   14                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   22                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   16    8   23   24                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   11   26   36                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30                                                       
CONECT   30   29   31   36                                                  
CONECT   31   30   32   35                                                  
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   31                                                       
CONECT   36   30   25   37   38                                             
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

View in JSmol

Synonyms

Value	Source
3-[2-(Furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-4,5,6,7-tetrahydro-1-benzofuran-2-yl]-3-methyl-6-oxo-3,6-dihydro-2H-pyran-3-yl]propanoate	Generator

Chemical Formula

C₃₂H₄₀O₁₀

Average Mass

584.6620 Da

Monoisotopic Mass

584.26215 Da

IUPAC Name

3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-4,5,6,7-tetrahydro-1-benzofuran-2-yl]-3-methyl-6-oxo-3,6-dihydro-2H-pyran-3-yl]propanoic acid

Traditional Name

3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4H-1-benzofuran-2-yl]-3-methyl-6-oxo-2H-pyran-3-yl]propanoic acid

CAS Registry Number

Not Available

SMILES

CCC(C)C(=O)OC1C2=C(OC(=C2)C2=CC(=O)OC(C3=COC=C3)C2(C)CCC(O)=O)C(C)C(CC(=O)OC)C1(C)C

InChI Identifier

InChI=1S/C32H40O10/c1-8-17(2)30(37)42-29-20-13-23(40-27(20)18(3)21(31(29,4)5)14-25(35)38-7)22-15-26(36)41-28(19-10-12-39-16-19)32(22,6)11-9-24(33)34/h10,12-13,15-18,21,28-29H,8-9,11,14H2,1-7H3,(H,33,34)

InChI Key

SUDQSSBJBLXQMO-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
Xylocarpus granatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tetracarboxylic acids and derivatives

Direct Parent

Tetracarboxylic acids and derivatives

Alternative Parents

Substituents

Tetracarboxylic acid or derivatives
Benzofuran
Dihydropyranone
Fatty acid ester
Fatty acyl
Pyran
Heteroaromatic compound
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Furan
Carboxylic acid ester
Lactone
Oxacycle
Organoheterocyclic compound
Carboxylic acid
Carbonyl group
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
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	5.18	ALOGPS
logP	5.42	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	3.95	ChemAxon
pKa (Strongest Basic)	-2.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	142.48 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	150.21 m³·mol⁻¹	ChemAxon
Polarizability	62.5 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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 3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid (NP0294425)

MOL for NP0294425 (3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid)

3D MOL for NP0294425 (3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid)

3D SDF for NP0294425 (3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid)

3D-SDF for NP0294425 (3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid)

PDB for NP0294425 (3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid)

3D PDB for NP0294425 (3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid)

SMILES for NP0294425 (3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid)

INCHI for NP0294425 (3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid)

Structure for NP0294425 (3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid)

3D Structure for NP0294425 (3-[2-(furan-3-yl)-4-[6-(2-methoxy-2-oxoethyl)-5,5,7-trimethyl-4-[(2-methylbutanoyl)oxy]-6,7-dihydro-4h-1-benzofuran-2-yl]-3-methyl-6-oxo-2h-pyran-3-yl]propanoic acid)