NP-MRD: Showing NP-Card for 1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one (NP0222438)

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Record Information

Version

2.0

Created at

2022-09-06 00:16:30 UTC

Updated at

2022-09-06 00:16:30 UTC

NP-MRD ID

NP0222438

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one

Description

1,11-Dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]Icosa-5,16-dien-7-one belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring. 1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one is found in Kadsura ananosma. 1,11-Dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]Icosa-5,16-dien-7-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004241501432D          

 37 42  0  0  0  0            999 V2000
    8.4938    2.3637    0.0000 C   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


  Mrv1533004241501432D          

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    0.6317    1.3174    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8774    1.9499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6951    2.0596    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2906    1.4887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2424    2.3122    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9797    1.9422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8964    1.9508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1169    2.7457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
  3 10  1  0  0  0  0
  2 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 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
 18 20  1  0  0  0  0
 14 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 29 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 18 35  1  0  0  0  0
 33 35  1  0  0  0  0
 16 36  1  0  0  0  0
 11 36  1  0  0  0  0
 36 37  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0222438

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C1CC=C(C)C(=O)O1)C1=CCC2(C)C(CC3(O)C4OC44C=CC(=O)OC(C)(C)C4C(O)CC23)C1=C

> <INCHI_IDENTIFIER>
InChI=1S/C30H38O7/c1-15-7-8-21(35-25(15)33)17(3)18-9-11-28(6)19(16(18)2)14-29(34)22(28)13-20(31)24-27(4,5)36-23(32)10-12-30(24)26(29)37-30/h7,9-10,12,17,19-22,24,26,31,34H,2,8,11,13-14H2,1,3-6H3

> <INCHI_KEY>
COACAZUXJVRXJK-UHFFFAOYSA-N

> <FORMULA>
C30H38O7

> <MOLECULAR_WEIGHT>
510.627

> <EXACT_MASS>
510.261753564

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
55.5991163355347

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one

> <ALOGPS_LOGP>
4.96

> <JCHEM_LOGP>
3.2541730346666666

> <ALOGPS_LOGS>
-4.73

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.767637468779345

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.458973773936183

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9135222371946954

> <JCHEM_POLAR_SURFACE_AREA>
105.59

> <JCHEM_REFRACTIVITY>
137.9304

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.59e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      15.855   4.412   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      15.443   2.928   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      16.523   1.830   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      18.014   2.215   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      19.093   1.117   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      18.681  -0.367   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      19.761  -1.466   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      17.190  -0.753   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      16.779  -2.237   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      16.111   0.346   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      13.952   2.543   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.541   1.059   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.050   0.674   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.971   1.772   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.406   0.339   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.382   3.256   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.098   4.106   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.893   3.148   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.620   4.663   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.432   1.705   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.640   0.384   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.114   0.179   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       6.636  -1.285   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.002   1.245   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.716   0.399   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.828  -0.667   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.924  -0.922   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       3.252   0.876   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.713   2.319   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       1.179   2.459   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       3.504   3.640   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.031   3.845   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       6.142   2.779   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       6.052   4.316   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       7.429   3.625   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      12.873   3.641   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      13.285   5.125   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   11                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8    3                                                       
CONECT   11    2   12   36                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16   20                                             
CONECT   15   14                                                            
CONECT   16   14   17   36                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20   35                                             
CONECT   19   18                                                            
CONECT   20   18   14   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   33                                                  
CONECT   25   24   26   27   28                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   25   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   24   34   35                                             
CONECT   34   33   35                                                       
CONECT   35   34   18   33                                                  
CONECT   36   16   11   37                                                  
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₃₈O₇

Average Mass

510.6270 Da

Monoisotopic Mass

510.26175 Da

IUPAC Name

1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-3,6-dihydro-2H-pyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one

Traditional Name

1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one

CAS Registry Number

Not Available

SMILES

CC(C1CC=C(C)C(=O)O1)C1=CCC2(C)C(CC3(O)C4OC44C=CC(=O)OC(C)(C)C4C(O)CC23)C1=C

InChI Identifier

InChI=1S/C30H38O7/c1-15-7-8-21(35-25(15)33)17(3)18-9-11-28(6)19(16(18)2)14-29(34)22(28)13-20(31)24-27(4,5)36-23(32)10-12-30(24)26(29)37-30/h7,9-10,12,17,19-22,24,26,31,34H,2,8,11,13-14H2,1,3-6H3

InChI Key

COACAZUXJVRXJK-UHFFFAOYSA-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
Kadsura ananosma	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as terpene lactones. These are prenol lipids containing a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Terpene lactones

Direct Parent

Terpene lactones

Alternative Parents

Substituents

Terpene lactone
Sesquiterpenoid
Bisabolane sesquiterpenoid
Dihydropyranone
Dicarboxylic acid or derivatives
Pyran
Cyclic alcohol
Alpha,beta-unsaturated carboxylic ester
Tertiary alcohol
Enoate ester
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Ether
Oxirane
Dialkyl ether
Organoheterocyclic compound
Carboxylic acid derivative
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
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	4.96	ALOGPS
logP	3.25	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	13.46	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	105.59 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	137.93 m³·mol⁻¹	ChemAxon
Polarizability	55.6 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

72987035

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one (NP0222438)

MOL for NP0222438 (1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one)

3D MOL for NP0222438 (1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one)

3D SDF for NP0222438 (1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one)

3D-SDF for NP0222438 (1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one)

PDB for NP0222438 (1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one)

3D PDB for NP0222438 (1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one)

SMILES for NP0222438 (1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one)

INCHI for NP0222438 (1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one)

Structure for NP0222438 (1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one)

3D Structure for NP0222438 (1,11-dihydroxy-9,9,14-trimethyl-17-[1-(5-methyl-6-oxo-2,3-dihydropyran-2-yl)ethyl]-18-methylidene-3,8-dioxapentacyclo[11.7.0.0²,⁴.0⁴,¹⁰.0¹⁴,¹⁹]icosa-5,16-dien-7-one)