NP-MRD: Showing NP-Card for methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate (NP0262579)

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Record Information

Version

2.0

Created at

2022-09-08 05:26:50 UTC

Updated at

2022-09-08 05:26:50 UTC

NP-MRD ID

NP0262579

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate

Description

Methyl 2-[(1S,2R)-2-[(3aR,4S,7R,7aR)-4-[(R)-(furan-3-yl)(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-octahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate is found in Khaya ivorensis. Based on a literature review very few articles have been published on methyl 2-[(1S,2R)-2-[(3aR,4S,7R,7aR)-4-[(R)-(furan-3-yl)(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-octahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082207262D          

 35 38  0  0  1  0            999 V2000
   -0.0191    2.1777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8054    2.1489    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1927    1.4204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7556    0.7208    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0172    1.3917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4544    2.0913    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0671    2.8197    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4170    2.3118    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4540    3.3718    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5043    3.5194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1170    4.2478    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.2789    2.0625    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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 33 34  1  0  0  0  0
 16 34  1  0  0  0  0
 28 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309082207262D          

 35 38  0  0  1  0            999 V2000
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  6 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  1  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  6  0  0  0
 19 21  1  1  0  0  0
 21 22  1  6  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 23 27  2  0  0  0  0
 19 28  1  0  0  0  0
 28 29  1  1  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 16 34  1  0  0  0  0
 28 34  1  0  0  0  0
 34 35  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0262579

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C[C@@H]1C(C)(C)C(=O)C=C[C@@]1(C)[C@H]1CC[C@@](C)([C@@H](O)C2=COC=C2)[C@]2(O)CC(=O)O[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C27H36O8/c1-23(2)18(13-20(29)33-6)24(3,10-8-19(23)28)17-7-11-25(4,22(31)16-9-12-34-15-16)27(32)14-21(30)35-26(17,27)5/h8-10,12,15,17-18,22,31-32H,7,11,13-14H2,1-6H3/t17-,18-,22+,24+,25+,26-,27-/m1/s1

> <INCHI_KEY>
AXPQVXURTHIQGM-IEKDFWFSSA-N

> <FORMULA>
C27H36O8

> <MOLECULAR_WEIGHT>
488.577

> <EXACT_MASS>
488.241018119

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
71

> <JCHEM_AVERAGE_POLARIZABILITY>
50.96462051965862

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
methyl 2-[(1S,2R)-2-[(3aR,4S,7R,7aR)-4-[(R)-(furan-3-yl)(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-octahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate

> <JCHEM_LOGP>
2.9177248316666646

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.727017009115674

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.862404259652116

> <JCHEM_PKA_STRONGEST_BASIC>
-2.88563705375984

> <JCHEM_POLAR_SURFACE_AREA>
123.27000000000002

> <JCHEM_REFRACTIVITY>
126.3886

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
methyl [(1S,2R)-2-[(3aR,4S,7R,7aR)-4-[(R)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.036   4.065   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.503   4.011   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.226   2.651   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       1.410   1.346   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.766   2.598   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.582   3.904   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.859   5.263   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.645   4.315   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.714   6.294   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.675   6.569   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       3.952   7.929   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.214   6.516   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.937   5.156   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.397   2.989   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.131  -1.950   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.111  -1.950   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.584  -3.397   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       8.627  -1.682   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.302  -0.298   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.827  -0.512   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      11.095  -2.029   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       9.735  -2.752   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.626  -1.532   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.417   0.770   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       0.877   0.770   0.000  0.00  0.00           O+0
HETATM   33  O   UNK     0       3.322   2.016   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.626   3.072   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7   14                                                  
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    6   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17   34                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21   28                                             
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   27                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   23                                                       
CONECT   28   19   29   30   34                                             
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   16   28   35                                             
CONECT   35   34                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-[(1S,2R)-2-[(3ar,4S,7R,7ar)-4-[(R)-(furan-3-yl)(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-octahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetic acid	Generator

Chemical Formula

C₂₇H₃₆O₈

Average Mass

488.5770 Da

Monoisotopic Mass

488.24102 Da

IUPAC Name

methyl 2-[(1S,2R)-2-[(3aR,4S,7R,7aR)-4-[(R)-(furan-3-yl)(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-octahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate

Traditional Name

methyl [(1S,2R)-2-[(3aR,4S,7R,7aR)-4-[(R)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate

CAS Registry Number

Not Available

SMILES

COC(=O)C[C@@H]1C(C)(C)C(=O)C=C[C@@]1(C)[C@H]1CC[C@@](C)([C@@H](O)C2=COC=C2)[C@]2(O)CC(=O)O[C@]12C

InChI Identifier

InChI=1S/C27H36O8/c1-23(2)18(13-20(29)33-6)24(3,10-8-19(23)28)17-7-11-25(4,22(31)16-9-12-34-15-16)27(32)14-21(30)35-26(17,27)5/h8-10,12,15,17-18,22,31-32H,7,11,13-14H2,1-6H3/t17-,18-,22+,24+,25+,26-,27-/m1/s1

InChI Key

AXPQVXURTHIQGM-IEKDFWFSSA-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
Khaya ivorensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as benzofurans. These are organic compounds containing a benzene ring fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzofurans

Sub Class

Not Available

Direct Parent

Benzofurans

Alternative Parents

Substituents

Benzofuran
Cyclohexenone
Gamma butyrolactone
Dicarboxylic acid or derivatives
Heteroaromatic compound
Methyl ester
Tetrahydrofuran
Tertiary alcohol
Furan
Cyclic alcohol
Cyclic ketone
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Aromatic alcohol
Organooxygen compound
Carbonyl group
Alcohol
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	2.92	ChemAxon
pKa (Strongest Acidic)	12.86	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	123.27 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	126.39 m³·mol⁻¹	ChemAxon
Polarizability	50.96 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

162913129

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate (NP0262579)

MOL for NP0262579 (methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate)

3D MOL for NP0262579 (methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate)

3D SDF for NP0262579 (methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate)

3D-SDF for NP0262579 (methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate)

PDB for NP0262579 (methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate)

3D PDB for NP0262579 (methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate)

SMILES for NP0262579 (methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate)

INCHI for NP0262579 (methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate)

Structure for NP0262579 (methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate)

3D Structure for NP0262579 (methyl 2-[(1s,2r)-2-[(3ar,4s,7r,7ar)-4-[(s)-furan-3-yl(hydroxy)methyl]-3a-hydroxy-4,7a-dimethyl-2-oxo-tetrahydro-1-benzofuran-7-yl]-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]acetate)