NP-MRD: Showing NP-Card for 8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate (NP0246639)

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Record Information

Version

2.0

Created at

2022-09-07 08:10:52 UTC

Updated at

2022-09-07 08:10:52 UTC

NP-MRD ID

NP0246639

Secondary Accession Numbers

None

Natural Product Identification

Common Name

8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate

Description

8-{4-[5-(Acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2,5-dihydrofuran-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate belongs to the class of organic compounds known as diterpene lactones. These are diterpenoids containing a lactone moiety. 8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate is found in Melampodium leucanthum. 8-{4-[5-(Acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2,5-dihydrofuran-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004181502042D          

 32 32  0  0  0  0            999 V2000
    4.8546    7.7143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    7.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    7.7143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    6.4768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    5.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    4.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9967    5.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    4.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9967    3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9967    2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    2.3518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8697    3.0663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6947    1.6373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3297   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1501   -0.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6351   -1.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4555   -1.3177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7911   -0.5640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9405   -1.9851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6049   -2.7388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0898   -3.4062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7543   -4.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9103   -3.3200    0.0000 C   0  0  0  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
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  4  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END


  Mrv1533004181502042D          

 32 32  0  0  0  0            999 V2000
    4.8546    7.7143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    7.3018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    7.7143    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1401    6.4768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    6.0643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4256    5.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    4.8268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9967    5.2393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    4.0018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9967    3.5893    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9967    2.7643    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7112    2.3518    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2822    2.3518    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8697    3.0663    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6947    1.6373    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.9393    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5678    1.1143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2352    0.6294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9803   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4652   -0.8227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1553   -0.1553    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0997    0.6294    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3297   -0.8227    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1501   -0.7365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6351   -1.4039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4555   -1.3177    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7911   -0.5640    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9405   -1.9851    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6049   -2.7388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0898   -3.4062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7543   -4.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9103   -3.3200    0.0000 C   0  0  0  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
  4  5  1  0  0  0  0
  6  5  1  4  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 17 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  4  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0246639

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OCC=C(C)CCC(O)C(C)(O)CC1OC(=O)C(CCC=C(C)COC(C)=O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H36O8/c1-16(11-12-30-18(3)25)9-10-22(27)24(5,29)14-21-13-20(23(28)32-21)8-6-7-17(2)15-31-19(4)26/h7,11,13,21-22,27,29H,6,8-10,12,14-15H2,1-5H3

> <INCHI_KEY>
PYHNWCDPXQSNQA-UHFFFAOYSA-N

> <FORMULA>
C24H36O8

> <MOLECULAR_WEIGHT>
452.544

> <EXACT_MASS>
452.241018119

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
49.95780850979388

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2,5-dihydrofuran-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate

> <ALOGPS_LOGP>
2.45

> <JCHEM_LOGP>
2.1466984133333327

> <ALOGPS_LOGS>
-4.69

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.881053813112022

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.522142040881935

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2375926752214603

> <JCHEM_POLAR_SURFACE_AREA>
119.36000000000001

> <JCHEM_REFRACTIVITY>
120.83249999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.21e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2H-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0       9.062  14.400   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       7.728  13.630   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       6.395  14.400   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       7.728  12.090   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.395  11.320   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.395   9.780   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.061   9.010   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.727   9.780   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.061   7.470   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.727   6.700   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.727   5.160   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.061   4.390   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.393   4.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.623   5.724   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       3.163   3.056   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.060   3.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.060   2.080   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.306   1.175   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.830  -0.290   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.735  -1.536   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.290  -0.290   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.186   1.175   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.615  -1.536   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -2.147  -1.375   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.052  -2.621   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -4.584  -2.460   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.210  -1.053   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.489  -3.706   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -4.863  -5.112   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -5.768  -6.358   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -5.141  -7.765   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -7.299  -6.197   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                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   23                                                  
CONECT   22   21   17                                                       
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   64    0
END

View in JSmol

Synonyms

Value	Source
8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2,5-dihydrofuran-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₆O₈

Average Mass

452.5440 Da

Monoisotopic Mass

452.24102 Da

IUPAC Name

8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2,5-dihydrofuran-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate

Traditional Name

8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2H-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OCC=C(C)CCC(O)C(C)(O)CC1OC(=O)C(CCC=C(C)COC(C)=O)=C1

InChI Identifier

InChI=1S/C24H36O8/c1-16(11-12-30-18(3)25)9-10-22(27)24(5,29)14-21-13-20(23(28)32-21)8-6-7-17(2)15-31-19(4)26/h7,11,13,21-22,27,29H,6,8-10,12,14-15H2,1-5H3

InChI Key

PYHNWCDPXQSNQA-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Melampodium leucanthum	LOTUS Database	35616633

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
Fatty alcohol ester
Tricarboxylic acid or derivatives
Fatty alcohol
2-furanone
Fatty acyl
Dihydrofuran
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tertiary alcohol
1,2-diol
Carboxylic acid ester
Secondary alcohol
Lactone
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organic oxygen compound
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	2.45	ALOGPS
logP	2.15	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	12.52	ChemAxon
pKa (Strongest Basic)	-3.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	119.36 Å²	ChemAxon
Rotatable Bond Count	15	ChemAxon
Refractivity	120.83 m³·mol⁻¹	ChemAxon
Polarizability	49.96 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

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 8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate (NP0246639)

MOL for NP0246639 (8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate)

3D MOL for NP0246639 (8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate)

3D SDF for NP0246639 (8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate)

3D-SDF for NP0246639 (8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate)

PDB for NP0246639 (8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate)

3D PDB for NP0246639 (8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate)

SMILES for NP0246639 (8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate)

INCHI for NP0246639 (8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate)

Structure for NP0246639 (8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate)

3D Structure for NP0246639 (8-{4-[5-(acetyloxy)-4-methylpent-3-en-1-yl]-5-oxo-2h-furan-2-yl}-6,7-dihydroxy-3,7-dimethyloct-2-en-1-yl acetate)