NP-MRD: Showing NP-Card for (1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione (NP0254686)

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Record Information

Version

2.0

Created at

2022-09-07 18:55:36 UTC

Updated at

2022-09-07 18:55:36 UTC

NP-MRD ID

NP0254686

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione

Description

(1S,4R,9R,11R,13S,16S,17S,22S)-19-ethenyl-9,13-dihydroxy-5,5,15,15-tetramethyl-22-(propan-2-yl)-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]Docos-18-ene-12,21-dione belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. (1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione is found in Salvia bucharica. Based on a literature review very few articles have been published on (1S,4R,9R,11R,13S,16S,17S,22S)-19-ethenyl-9,13-dihydroxy-5,5,15,15-tetramethyl-22-(propan-2-yl)-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]Docos-18-ene-12,21-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072220552D          

 35 40  0  0  1  0            999 V2000
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 33 35  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309072220552D          

 35 40  0  0  1  0            999 V2000
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    1.6926    0.4727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0951   -0.2378    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9040   -0.6405    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2928    0.0777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2764    0.9400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3832   -0.5096    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9901    0.1592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9301   -0.1334    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0147    1.0357    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  7 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  2  0  0  0  0
 15 13  1  6  0  0  0
  5 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 17 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 15 28  1  0  0  0  0
 28 29  1  0  0  0  0
  3 29  1  0  0  0  0
 28 30  1  1  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
  6 32  1  0  0  0  0
 11 32  1  0  0  0  0
 32 33  1  1  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0254686

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)[C@@]12[C@@H]3[C@@H]4C=C(C[C@]5(CC[C@@H]6C(C)(C)CCC[C@@]6(O)C[C@@]45C(=O)[C@@]1(O)OC3(C)C)C2=O)C=C

> <INCHI_IDENTIFIER>
InChI=1S/C30H42O5/c1-8-18-14-19-21-25(6,7)35-30(34)23(32)28(19)16-27(33)12-9-11-24(4,5)20(27)10-13-26(28,15-18)22(31)29(21,30)17(2)3/h8,14,17,19-21,33-34H,1,9-13,15-16H2,2-7H3/t19-,20+,21+,26+,27+,28-,29-,30+/m0/s1

> <INCHI_KEY>
QXPZXEGAVVDUNB-RRYMYKPSSA-N

> <FORMULA>
C30H42O5

> <MOLECULAR_WEIGHT>
482.661

> <EXACT_MASS>
482.303224452

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
77

> <JCHEM_AVERAGE_POLARIZABILITY>
54.158317047139974

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4R,9R,11R,13S,16S,17S,22S)-19-ethenyl-9,13-dihydroxy-5,5,15,15-tetramethyl-22-(propan-2-yl)-14-oxahexacyclo[11.7.2.0^{1,11}.0^{4,9}.0^{11,17}.0^{16,22}]docos-18-ene-12,21-dione

> <JCHEM_LOGP>
5.417460915333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.498889174089314

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.775120678235957

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0180873336048055

> <JCHEM_POLAR_SURFACE_AREA>
83.83000000000001

> <JCHEM_REFRACTIVITY>
134.8082

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,9R,11R,13S,16S,17S,22S)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0^{1,11}.0^{4,9}.0^{11,17}.0^{16,22}]docos-18-ene-12,21-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       6.556  -5.578   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.554  -4.107   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.875  -2.955   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.531  -3.780   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.119  -3.040   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.686  -2.394   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.551  -2.426   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -3.299  -3.872   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.220  -2.374   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -2.239  -1.002   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -1.459  -2.708   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -2.182  -4.240   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       0.206  -3.431   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       0.043  -5.073   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       1.576  -1.846   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.065  -2.332   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.800  -2.016   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       4.503  -3.834   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.671  -3.286   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.206  -3.166   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.871  -1.777   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.000  -0.507   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.513   0.148   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.118   1.132   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.464  -0.626   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.719   0.705   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.159   0.882   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.044  -0.444   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       3.554  -1.196   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.546   0.145   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       0.516   1.755   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -0.715  -0.951   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.848   0.297   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -3.603  -0.249   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.894   1.933   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   29                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   15                                                  
CONECT    6    5    7   32                                                  
CONECT    7    6    8    9   10                                             
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    7   11                                                       
CONECT   11   10   12   13   32                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13    5   16   28                                             
CONECT   16   15   17                                                       
CONECT   17   16   18   19   25                                             
CONECT   18   17                                                            
CONECT   19   17   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   17   26                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   15   29   30                                             
CONECT   29   28    3                                                       
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30    6   11   33                                             
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   80    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₂O₅

Average Mass

482.6610 Da

Monoisotopic Mass

482.30322 Da

IUPAC Name

(1S,4R,9R,11R,13S,16S,17S,22S)-19-ethenyl-9,13-dihydroxy-5,5,15,15-tetramethyl-22-(propan-2-yl)-14-oxahexacyclo[11.7.2.0^{1,11}.0^{4,9}.0^{11,17}.0^{16,22}]docos-18-ene-12,21-dione

Traditional Name

(1S,4R,9R,11R,13S,16S,17S,22S)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0^{1,11}.0^{4,9}.0^{11,17}.0^{16,22}]docos-18-ene-12,21-dione

CAS Registry Number

Not Available

SMILES

CC(C)[C@@]12[C@@H]3[C@@H]4C=C(C[C@]5(CC[C@@H]6C(C)(C)CCC[C@@]6(O)C[C@@]45C(=O)[C@@]1(O)OC3(C)C)C2=O)C=C

InChI Identifier

InChI=1S/C30H42O5/c1-8-18-14-19-21-25(6,7)35-30(34)23(32)28(19)16-27(33)12-9-11-24(4,5)20(27)10-13-26(28,15-18)22(31)29(21,30)17(2)3/h8,14,17,19-21,33-34H,1,9-13,15-16H2,2-7H3/t19-,20+,21+,26+,27+,28-,29-,30+/m0/s1

InChI Key

QXPZXEGAVVDUNB-RRYMYKPSSA-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
Salvia bucharica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthofurans. Naphthofurans are compounds containing a furan ring fused to a naphthalene moiety. Furan is a 5 membered- ring aromatic ring with four carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthofurans

Sub Class

Not Available

Direct Parent

Naphthofurans

Alternative Parents

Substituents

Naphthofuran
Oxepane
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Ketone
Hemiacetal
Oxacycle
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	5.42	ChemAxon
pKa (Strongest Acidic)	9.78	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	134.81 m³·mol⁻¹	ChemAxon
Polarizability	54.16 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

162982004

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione (NP0254686)

MOL for NP0254686 ((1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione)

3D MOL for NP0254686 ((1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione)

3D SDF for NP0254686 ((1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione)

3D-SDF for NP0254686 ((1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione)

PDB for NP0254686 ((1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione)

3D PDB for NP0254686 ((1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione)

SMILES for NP0254686 ((1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione)

INCHI for NP0254686 ((1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione)

Structure for NP0254686 ((1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione)

3D Structure for NP0254686 ((1s,4r,9r,11r,13s,16s,17s,22s)-19-ethenyl-9,13-dihydroxy-22-isopropyl-5,5,15,15-tetramethyl-14-oxahexacyclo[11.7.2.0¹,¹¹.0⁴,⁹.0¹¹,¹⁷.0¹⁶,²²]docos-18-ene-12,21-dione)