NP-MRD: Showing NP-Card for (3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate (NP0171353)

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Record Information

Version

2.0

Created at

2022-09-03 07:50:16 UTC

Updated at

2022-09-03 07:50:16 UTC

NP-MRD ID

NP0171353

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate

Description

(3S,3aR,6S,6aS)-6-[(2E)-5-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-hexahydrofuro[3,2-b]furan-3-yl acetate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. Based on a literature review very few articles have been published on (3S,3aR,6S,6aS)-6-[(2E)-5-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-hexahydrofuro[3,2-b]furan-3-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309032209502D          

 35 38  0  0  1  0            999 V2000
   -4.5089   -6.9951    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7308   -6.7210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4664   -5.6035    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.9157   -4.8051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309032209502D          

 35 38  0  0  1  0            999 V2000
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    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  5  4  1  6  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  1  6  0  0  0
  8 10  1  0  0  0  0
  5 10  1  0  0  0  0
 10 11  1  1  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  1  0  0  0
 14 16  1  6  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 22 21  1  1  0  0  0
 22 23  1  6  0  0  0
 22 24  1  0  0  0  0
 24 25  1  6  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 30 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 35 34  1  6  0  0  0
 22 35  1  0  0  0  0
 28 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0171353

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@]2(C)[C@H](CCC=C2C)[C@@]1(C)CC\C(C)=C\C[C@@]1(O)C(=O)O[C@@H]2[C@H](CO[C@]12O)OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C28H42O7/c1-17(10-13-25(5)19(3)12-14-26(6)18(2)8-7-9-22(25)26)11-15-27(31)24(30)35-23-21(34-20(4)29)16-33-28(23,27)32/h8,11,19,21-23,31-32H,7,9-10,12-16H2,1-6H3/b17-11+/t19-,21+,22-,23-,25+,26+,27-,28+/m1/s1

> <INCHI_KEY>
UNRGCEXOJBFAII-LJCMEXSUSA-N

> <FORMULA>
C28H42O7

> <MOLECULAR_WEIGHT>
490.637

> <EXACT_MASS>
490.293053692

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
54.92895151255438

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(3S,3aR,6S,6aS)-6-[(2E)-5-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-hexahydrofuro[3,2-b]furan-3-yl acetate

> <ALOGPS_LOGP>
4.46

> <JCHEM_LOGP>
4.652444736000001

> <ALOGPS_LOGS>
-5.51

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.328420009870781

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.653557527150493

> <JCHEM_PKA_STRONGEST_BASIC>
-4.387370179884215

> <JCHEM_POLAR_SURFACE_AREA>
102.29

> <JCHEM_REFRACTIVITY>
131.47220000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.52e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(3S,3aR,6S,6aS)-6-[(2E)-5-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2H-furo[3,2-b]furan-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 03-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-SEP-22         0                                  
HETATM    1  C   UNK     0      -8.417 -13.057   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.964 -12.546   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -5.795 -13.548   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -6.681 -11.032   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -5.228 -10.521   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -3.961 -11.395   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -2.737 -10.460   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -3.249  -9.007   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -1.709  -8.970   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -4.788  -9.045   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -5.300  -7.592   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -4.076  -6.657   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -4.114  -5.117   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -2.809  -7.531   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      -1.794  -6.373   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.292  -7.799   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.302  -6.619   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.214  -6.887   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.741  -8.334   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.204  -5.707   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.677  -4.260   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.657  -4.260   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       4.001   0.770   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   10                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10   14                                             
CONECT    9    8                                                            
CONECT   10    8    5   11                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    8   15   16                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   35                                             
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30   35                                             
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   22   28                                                  
MASTER        0    0    0    0    0    0    0    0   35    0   76    0
END

View in JSmol

Synonyms

Value	Source
(3S,3AR,6S,6as)-6-[(2E)-5-[(1S,2R,4ar,8ar)-1,2,4a,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-hexahydrofuro[3,2-b]furan-3-yl acetic acid	Generator

Chemical Formula

C₂₈H₄₂O₇

Average Mass

490.6370 Da

Monoisotopic Mass

490.29305 Da

IUPAC Name

(3S,3aR,6S,6aS)-6-[(2E)-5-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-hexahydrofuro[3,2-b]furan-3-yl acetate

Traditional Name

(3S,3aR,6S,6aS)-6-[(2E)-5-[(1S,2R,4aR,8aR)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2H-furo[3,2-b]furan-3-yl acetate

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@]2(C)[C@H](CCC=C2C)[C@@]1(C)CC\C(C)=C\C[C@@]1(O)C(=O)O[C@@H]2[C@H](CO[C@]12O)OC(C)=O

InChI Identifier

InChI=1S/C28H42O7/c1-17(10-13-25(5)19(3)12-14-26(6)18(2)8-7-9-22(25)26)11-15-27(31)24(30)35-23-21(34-20(4)29)16-33-28(23,27)32/h8,11,19,21-23,31-32H,7,9-10,12-16H2,1-6H3/b17-11+/t19-,21+,22-,23-,25+,26+,27-,28+/m1/s1

InChI Key

UNRGCEXOJBFAII-LJCMEXSUSA-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 diterpene lactones. These are diterpenoids containing a lactone moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Diterpene lactones

Alternative Parents

Substituents

Diterpene lactone
Diterpenoid
Clerodane diterpenoid
Isosorbide
Furofuran
Dicarboxylic acid or derivatives
Gamma butyrolactone
Monosaccharide
Tertiary alcohol
Tetrahydrofuran
Lactone
Hemiacetal
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Alcohol
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	4.46	ALOGPS
logP	4.65	ChemAxon
logS	-5.5	ALOGPS
pKa (Strongest Acidic)	9.65	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	102.29 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	131.47 m³·mol⁻¹	ChemAxon
Polarizability	54.93 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

162907671

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate (NP0171353)

MOL for NP0171353 ((3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate)

3D MOL for NP0171353 ((3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate)

3D SDF for NP0171353 ((3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate)

3D-SDF for NP0171353 ((3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate)

PDB for NP0171353 ((3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate)

3D PDB for NP0171353 ((3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate)

SMILES for NP0171353 ((3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate)

INCHI for NP0171353 ((3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate)

Structure for NP0171353 ((3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate)

3D Structure for NP0171353 ((3s,3ar,6s,6as)-6-[(2e)-5-[(1s,2r,4ar,8ar)-1,2,4a,5-tetramethyl-2,3,4,7,8,8a-hexahydronaphthalen-1-yl]-3-methylpent-2-en-1-yl]-6,6a-dihydroxy-5-oxo-dihydro-2h-furo[3,2-b]furan-3-yl acetate)