NP-MRD: Showing NP-Card for (1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate (NP0316661)

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Record Information

Version

2.0

Created at

2022-09-11 15:59:58 UTC

Updated at

2022-09-11 15:59:59 UTC

NP-MRD ID

NP0316661

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate

Description

Violide M 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 Violide M.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112218002D          

 38 40  0  0  1  0            999 V2000
    2.7067    6.1725    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3537    5.2026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6225    4.8206    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3684    4.9060    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3337    4.0818    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0302    3.6396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7614    4.0216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7961    4.8459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4578    3.5794    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4231    2.7551    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0124    2.1778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6454    1.4389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0275    0.7077    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7232    1.5111    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7946    0.7353    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1935    1.0339    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.0046    1.9167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    4.2334    1.4063    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0469    1.5437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.6025    3.6997    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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  9 10  1  0  0  0  0
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 20 21  1  0  0  0  0
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 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  1  0  0  0
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  5 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309112218002D          

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  7  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  6  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  6  0  0  0
 14 16  1  1  0  0  0
 14 17  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  1  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  1  0  0  0
 25 27  1  6  0  0  0
 25 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 24 32  1  0  0  0  0
 32 33  1  1  0  0  0
 32 34  1  0  0  0  0
  5 34  1  0  0  0  0
 34 35  1  1  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0316661

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1C\C(C)=C/[C@@H]2OC(=O)[C@@](C)(O)[C@@]2(O)[C@H](OC(C)=O)[C@H]2[C@](C)(O)[C@H](O)C=C[C@]2(C)[C@H]1OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H36O12/c1-12-10-16(35-13(2)27)20(36-14(3)28)23(5)9-8-17(30)24(6,32)19(23)21(37-15(4)29)26(34)18(11-12)38-22(31)25(26,7)33/h8-9,11,16-21,30,32-34H,10H2,1-7H3/b12-11-/t16-,17-,18+,19-,20+,21-,23+,24-,25-,26+/m1/s1

> <INCHI_KEY>
QPNZJNODJNVMPM-LBOUFTSASA-N

> <FORMULA>
C26H36O12

> <MOLECULAR_WEIGHT>
540.562

> <EXACT_MASS>
540.220676599

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
74

> <JCHEM_AVERAGE_POLARIZABILITY>
53.61809300172115

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3S,4S,7S,8Z,11R,12R,13S,16R,17S)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadeca-8,14-dien-2-yl acetate

> <JCHEM_LOGP>
-0.9830396159999982

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.442422006392206

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.132547316923732

> <JCHEM_PKA_STRONGEST_BASIC>
-3.3865893428702663

> <JCHEM_POLAR_SURFACE_AREA>
186.11999999999998

> <JCHEM_REFRACTIVITY>
128.63960000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3S,4S,7S,8Z,11R,12R,13S,16R,17S)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadeca-8,14-dien-2-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       5.052  11.522   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.394   9.712   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.029   8.998   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       6.288   9.158   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       6.223   7.619   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.523   6.794   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.888   7.507   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.953   9.046   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.188   6.682   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.123   5.143   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      11.223   4.065   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.538   2.686   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      11.251   1.321   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       8.817   2.821   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.950   1.373   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       7.828   1.930   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       8.758   4.430   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.475   3.578   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.458   5.255   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       6.921   3.812   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.902   2.625   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       9.421   2.882   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.365   1.182   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.093   4.542   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.028   3.003   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.494   1.535   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.383   2.271   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       4.663   2.290   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       4.599   0.752   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       3.363   3.116   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.428   4.654   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.793   5.368   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.493   6.193   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.858   6.906   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       3.558   7.732   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       3.623   9.270   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.323  10.096   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       4.988   9.983   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   34                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16   17                                             
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   14   10   18   19                                             
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21                                                            
CONECT   24   19   25   32                                                  
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   24   33   34                                             
CONECT   33   32                                                            
CONECT   34   32    5   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₆H₃₆O₁₂

Average Mass

540.5620 Da

Monoisotopic Mass

540.22068 Da

IUPAC Name

(1S,2R,3S,4S,7S,8Z,11R,12R,13S,16R,17S)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadeca-8,14-dien-2-yl acetate

Traditional Name

(1S,2R,3S,4S,7S,8Z,11R,12R,13S,16R,17S)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0^{3,7}]heptadeca-8,14-dien-2-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1C\C(C)=C/[C@@H]2OC(=O)[C@@](C)(O)[C@@]2(O)[C@H](OC(C)=O)[C@H]2[C@](C)(O)[C@H](O)C=C[C@]2(C)[C@H]1OC(C)=O

InChI Identifier

InChI=1S/C26H36O12/c1-12-10-16(35-13(2)27)20(36-14(3)28)23(5)9-8-17(30)24(6,32)19(23)21(37-15(4)29)26(34)18(11-12)38-22(31)25(26,7)33/h8-9,11,16-21,30,32-34H,10H2,1-7H3/b12-11-/t16-,17-,18+,19-,20+,21-,23+,24-,25-,26+/m1/s1

InChI Key

QPNZJNODJNVMPM-LBOUFTSASA-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
Briarane diterpenoid
Tetracarboxylic acid or derivatives
Gamma butyrolactone
Tertiary alcohol
Tetrahydrofuran
Carboxylic acid ester
Lactone
Secondary alcohol
Polyol
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Organic oxide
Alcohol
Organic oxygen compound
Hydrocarbon derivative
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	-0.98	ChemAxon
pKa (Strongest Acidic)	11.13	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	186.12 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	128.64 m³·mol⁻¹	ChemAxon
Polarizability	53.62 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	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

8991588

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10816284

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate (NP0316661)

MOL for NP0316661 ((1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate)

3D MOL for NP0316661 ((1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate)

3D SDF for NP0316661 ((1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate)

3D-SDF for NP0316661 ((1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate)

PDB for NP0316661 ((1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate)

3D PDB for NP0316661 ((1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate)

SMILES for NP0316661 ((1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate)

INCHI for NP0316661 ((1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate)

Structure for NP0316661 ((1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate)

3D Structure for NP0316661 ((1s,2r,3s,4s,7s,8z,11r,12r,13s,16r,17s)-11,12-bis(acetyloxy)-3,4,16,17-tetrahydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.0³,⁷]heptadeca-8,14-dien-2-yl acetate)