NP-MRD: Showing NP-Card for (3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione (NP0218031)

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Record Information

Version

2.0

Created at

2022-09-05 18:33:42 UTC

Updated at

2022-09-05 18:33:42 UTC

NP-MRD ID

NP0218031

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione

Description

(3R,3aR,7aS)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-2,3,3a,4,7,7a-hexahydro-1-benzofuran-2,7-dione belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain. Based on a literature review very few articles have been published on (3R,3aR,7aS)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-2,3,3a,4,7,7a-hexahydro-1-benzofuran-2,7-dione.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309052220332D          

 28 29  0  0  1  0            999 V2000
    6.2116   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9260   -1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6405   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3550   -1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0694   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7839   -1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4984   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2128   -1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2128   -2.5302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9273   -1.2927    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.0136   -0.4722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4005    0.0798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8205   -0.3007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2330   -1.0152    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.7179   -0.3477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0400   -1.1867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5920   -0.5736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2949   -1.9713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1019   -2.1428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7429   -2.5844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9978   -3.3690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8048   -3.5406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0598   -4.3252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3568   -2.9275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1638   -3.0990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7159   -2.4859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9359   -2.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6810   -1.6283    0.0000 C   0  0  2  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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
 10  8  1  6  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  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 20 27  1  0  0  0  0
 28 27  1  6  0  0  0
 10 28  1  0  0  0  0
 14 28  1  0  0  0  0
M  END


  Mrv1652309052220332D          

 28 29  0  0  1  0            999 V2000
    6.2116   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9260   -1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6405   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3550   -1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0694   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7839   -1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4984   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2128   -1.7052    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2128   -2.5302    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9273   -1.2927    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.0136   -0.4722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4005    0.0798    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.8205   -0.3007    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2330   -1.0152    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.7179   -0.3477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0400   -1.1867    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5920   -0.5736    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.2949   -1.9713    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.1019   -2.1428    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7429   -2.5844    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9978   -3.3690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8048   -3.5406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0598   -4.3252    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.3568   -2.9275    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1638   -3.0990    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.7159   -2.4859    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9359   -2.4129    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6810   -1.6283    0.0000 C   0  0  2  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  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
 10  8  1  6  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  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 20 27  1  0  0  0  0
 28 27  1  6  0  0  0
 10 28  1  0  0  0  0
 14 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0218031

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC(=O)[C@H]1[C@H]2CC(CC(=O)CCC)=C(C)C(=O)[C@@]2(C)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O5/c1-5-7-8-9-10-12-19(25)20-18-14-16(13-17(24)11-6-2)15(3)21(26)23(18,4)28-22(20)27/h18,20H,5-14H2,1-4H3/t18-,20-,23+/m1/s1

> <INCHI_KEY>
RXZCDZQEPIRHQP-XQFWAAQXSA-N

> <FORMULA>
C23H34O5

> <MOLECULAR_WEIGHT>
390.52

> <EXACT_MASS>
390.240624195

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.04822637113537

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(3R,3aR,7aS)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-2,3,3a,4,7,7a-hexahydro-1-benzofuran-2,7-dione

> <JCHEM_LOGP>
5.427140838333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.353386609182778

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.046774951622009

> <JCHEM_PKA_STRONGEST_BASIC>
-5.859408767227804

> <JCHEM_POLAR_SURFACE_AREA>
77.51

> <JCHEM_REFRACTIVITY>
107.9512

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R,3aR,7aS)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3H-1-benzofuran-2,7-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      11.595  -2.413   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.929  -3.183   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      14.262  -2.413   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.596  -3.183   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      16.930  -2.413   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.263  -3.183   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      19.597  -2.413   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      20.931  -3.183   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      20.931  -4.723   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      22.264  -2.413   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.425  -0.881   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      21.281   0.149   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      23.932  -0.561   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      24.702  -1.895   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      25.607  -0.649   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      26.208  -2.215   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      27.238  -1.071   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      26.684  -3.680   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      28.190  -4.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      25.653  -4.824   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      26.129  -6.289   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      27.636  -6.609   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      28.112  -8.074   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      28.666  -5.465   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      30.172  -5.785   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      31.203  -4.640   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      24.147  -4.504   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      23.671  -3.039   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   28                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16   28                                             
CONECT   15   14                                                            
CONECT   16   14   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   27                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25                                                            
CONECT   27   20   28                                                       
CONECT   28   27   10   14                                                  
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₃₄O₅

Average Mass

390.5200 Da

Monoisotopic Mass

390.24062 Da

IUPAC Name

(3R,3aR,7aS)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-2,3,3a,4,7,7a-hexahydro-1-benzofuran-2,7-dione

Traditional Name

(3R,3aR,7aS)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3H-1-benzofuran-2,7-dione

CAS Registry Number

Not Available

SMILES

CCCCCCCC(=O)[C@H]1[C@H]2CC(CC(=O)CCC)=C(C)C(=O)[C@@]2(C)OC1=O

InChI Identifier

InChI=1S/C23H34O5/c1-5-7-8-9-10-12-19(25)20-18-14-16(13-17(24)11-6-2)15(3)21(26)23(18,4)28-22(20)27/h18,20H,5-14H2,1-4H3/t18-,20-,23+/m1/s1

InChI Key

RXZCDZQEPIRHQP-XQFWAAQXSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as annonaceous acetogenins. These are waxy derivatives of fatty acids (usually C32 or C34), containing a terminal carboxylic acid combined with a 2-propanol unit at the C-2 position to form a methyl- substituted alpha,beta-unsaturated-gamma-lactone. One of their interesting structural features is a single, adjacent, or nonadjacent tetrahydrofuran (THF) or tetrahydropyran (THP) system with one or two flanking hydroxyl group(s) at the center of a long hydrocarbon chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Annonaceous acetogenins

Alternative Parents

Substituents

Annonaceae acetogenin skeleton
Benzofuran
Cyclohexenone
Alpha-acyloxy ketone
Gamma butyrolactone
1,3-dicarbonyl compound
Tetrahydrofuran
Carboxylic acid ester
Ketone
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Organooxygen compound
Carbonyl group
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic 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	5.43	ChemAxon
pKa (Strongest Acidic)	10.05	ChemAxon
pKa (Strongest Basic)	-5.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	77.51 Å²	ChemAxon
Rotatable Bond Count	11	ChemAxon
Refractivity	107.95 m³·mol⁻¹	ChemAxon
Polarizability	44.05 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	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

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

162928905

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione (NP0218031)

MOL for NP0218031 ((3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione)

3D MOL for NP0218031 ((3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione)

3D SDF for NP0218031 ((3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione)

3D-SDF for NP0218031 ((3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione)

PDB for NP0218031 ((3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione)

3D PDB for NP0218031 ((3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione)

SMILES for NP0218031 ((3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione)

INCHI for NP0218031 ((3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione)

Structure for NP0218031 ((3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione)

3D Structure for NP0218031 ((3r,3ar,7as)-6,7a-dimethyl-3-octanoyl-5-(2-oxopentyl)-3a,4-dihydro-3h-1-benzofuran-2,7-dione)