NP-MRD: Showing NP-Card for (3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid (NP0321946)

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Record Information

Version

2.0

Created at

2022-09-12 00:25:49 UTC

Updated at

2022-09-12 00:25:49 UTC

NP-MRD ID

NP0321946

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid

Description

(3R)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-2H-spiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid belongs to the class of organic compounds known as salicylic acid and derivatives. Salicylic acid and derivatives are compounds containing a 2-hydroxybenzoic acid moiety or a derivative thereof. (3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid is found in Lepra truncata. Based on a literature review very few articles have been published on (3R)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-2H-spiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309122202252D          

 34 36  0  0  1  0            999 V2000
   -0.4333    4.7303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3019    5.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0108    4.6442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8554    4.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7221    4.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6533    4.8333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5994    4.6442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6008    4.8640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6226    5.6887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3476    6.0823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7869    6.8195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0510    5.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0292    4.8264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6909    4.3341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4498    4.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3041    4.4328    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9586    3.9305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9218    3.7726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6830    3.1529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8583    3.1746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2903    2.5763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4881    2.7690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0699    2.0277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2540    3.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3878    3.3247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1472    4.1605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7323    2.7385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8220    4.1584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9988    5.2044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3837    6.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1350    6.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3275    7.8269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7247    8.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6242    3.9657    0.0000 C   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  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
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 28 34  2  0  0  0  0
 20 34  1  0  0  0  0
 16 34  1  0  0  0  0
M  END


  Mrv1652309122202252D          

 34 36  0  0  1  0            999 V2000
   -0.4333    4.7303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3019    5.1047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0108    4.6442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8554    4.7036    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7221    4.5872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6533    4.8333    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5994    4.6442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6008    4.8640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6226    5.6887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3476    6.0823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7869    6.8195    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0510    5.6511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0292    4.8264    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6909    4.3341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4498    4.7239    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3041    4.4328    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9586    3.9305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9218    3.7726    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.6830    3.1529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8583    3.1746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2903    2.5763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4881    2.7690    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0699    2.0277    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2540    3.5601    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3878    3.3247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1472    4.1605    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7323    2.7385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8220    4.1584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9988    5.2044    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3837    6.1263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1350    6.9960    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3275    7.8269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7247    8.3900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6242    3.9657    0.0000 C   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  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
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  1  0  0  0  0
  8 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 28 34  2  0  0  0  0
 20 34  1  0  0  0  0
 16 34  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0321946

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCC1=CC(=O)C=C(OC)[C@@]11C(=O)OC2=CC(O)=C(C(O)=O)C(CCCCC)=C12

> <INCHI_IDENTIFIER>
InChI=1S/C27H34O7/c1-4-6-8-9-11-12-17-14-18(28)15-22(33-3)27(17)24-19(13-10-7-5-2)23(25(30)31)20(29)16-21(24)34-26(27)32/h14-16,29H,4-13H2,1-3H3,(H,30,31)/t27-/m0/s1

> <INCHI_KEY>
LTZCIJKZYQDMTE-MHZLTWQESA-N

> <FORMULA>
C27H34O7

> <MOLECULAR_WEIGHT>
470.562

> <EXACT_MASS>
470.230453435

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
51.39168856029325

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3R)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-2H-spiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid

> <JCHEM_LOGP>
6.8754781083333345

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.15819362036319

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.750532114099374

> <JCHEM_PKA_STRONGEST_BASIC>
-4.817704895245987

> <JCHEM_POLAR_SURFACE_AREA>
110.13000000000001

> <JCHEM_REFRACTIVITY>
130.97239999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(3R)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.809   8.830   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.563   9.529   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.887   8.669   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.463   8.780   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.081   8.563   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.819   9.022   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.585   8.669   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      10.455   9.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.495  10.619   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.849  11.354   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      12.669  12.730   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      13.162  10.549   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.121   9.009   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      14.356   8.090   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      15.773   8.818   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.768   8.275   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      12.989   7.337   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      14.787   7.042   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      12.475   5.885   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.936   5.926   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.875   4.809   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.378   5.169   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.597   3.785   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.941   6.646   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.324   6.206   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.875   7.766   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       5.100   5.112   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       9.001   7.762   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.331   9.715   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      10.050  11.436   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.585  13.059   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       9.945  14.610   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       8.819  15.661   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.498   7.403   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   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13    8   17   34                                             
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21   34                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   28                                                  
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   24   29   34                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   28   20   16                                                  
MASTER        0    0    0    0    0    0    0    0   34    0   72    0
END

View in JSmol

Synonyms

Value	Source
(3R)-6'-Heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-2H-spiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylate	Generator

Chemical Formula

C₂₇H₃₄O₇

Average Mass

470.5620 Da

Monoisotopic Mass

470.23045 Da

IUPAC Name

(3R)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentyl-2H-spiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid

Traditional Name

(3R)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCC1=CC(=O)C=C(OC)[C@@]11C(=O)OC2=CC(O)=C(C(O)=O)C(CCCCC)=C12

InChI Identifier

InChI=1S/C27H34O7/c1-4-6-8-9-11-12-17-14-18(28)15-22(33-3)27(17)24-19(13-10-7-5-2)23(25(30)31)20(29)16-21(24)34-26(27)32/h14-16,29H,4-13H2,1-3H3,(H,30,31)/t27-/m0/s1

InChI Key

LTZCIJKZYQDMTE-MHZLTWQESA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Lepra truncata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as salicylic acid and derivatives. Salicylic acid and derivatives are compounds containing a 2-hydroxybenzoic acid moiety or a derivative thereof.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Salicylic acid and derivatives

Alternative Parents

Substituents

Salicylic acid or derivatives
Benzofuran
Coumaran
1-hydroxy-2-unsubstituted benzenoid
Dicarboxylic acid or derivatives
Vinylogous ester
Vinylogous acid
Carboxylic acid ester
Ketone
Lactone
Cyclic ketone
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Carbonyl group
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	6.88	ChemAxon
pKa (Strongest Acidic)	2.75	ChemAxon
pKa (Strongest Basic)	-4.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	110.13 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	130.97 m³·mol⁻¹	ChemAxon
Polarizability	51.39 Å³	ChemAxon
Number of Rings	3	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

163043522

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid (NP0321946)

MOL for NP0321946 ((3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

3D MOL for NP0321946 ((3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

3D SDF for NP0321946 ((3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

3D-SDF for NP0321946 ((3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

PDB for NP0321946 ((3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

3D PDB for NP0321946 ((3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

SMILES for NP0321946 ((3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

INCHI for NP0321946 ((3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

Structure for NP0321946 ((3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)

3D Structure for NP0321946 ((3r)-6'-heptyl-6-hydroxy-2'-methoxy-2,4'-dioxo-4-pentylspiro[1-benzofuran-3,1'-cyclohexane]-2',5'-diene-5-carboxylic acid)