NP-MRD: Showing NP-Card for (2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate (NP0212820)

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Record Information

Version

2.0

Created at

2022-09-05 11:36:02 UTC

Updated at

2022-09-05 11:36:02 UTC

NP-MRD ID

NP0212820

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate

Description

Frondogenin belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units. (2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate is found in Cucumaria frondosa. Based on a literature review very few articles have been published on Frondogenin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052213362D          

 37 41  0  0  1  0            999 V2000
   -0.7813    3.2468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309052213362D          

 37 41  0  0  1  0            999 V2000
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    4.0213    0.5217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6990    1.2812    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2024    0.6223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3836    0.7230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0613    1.4824    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0468    0.6575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7057    0.1610    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2579    0.4164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7847    1.0923    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1620    0.5511    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1814    1.6550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6076    1.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7932    0.6100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5822    0.3689    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7679   -0.4350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1855    0.9316    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2813    1.7511    0.0000 C   0  0  1  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  6  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 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  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 12 20  1  0  0  0  0
 20 21  1  1  0  0  0
 20 22  1  0  0  0  0
 22  9  1  6  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  7 25  1  0  0  0  0
 25 26  1  1  0  0  0
 26 27  2  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  6  0  0  0
 29 31  1  1  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
 37 29  1  1  0  0  0
  5 37  1  0  0  0  0
 25 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0212820

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC[C@]1(C)OC(=O)[C@]23CC[C@@H]4C(=CC[C@H]5C(C)(C)[C@@H](O)CC[C@]45C)[C@]2(C)C[C@@H](OC(C)=O)[C@H]13

> <INCHI_IDENTIFIER>
InChI=1S/C32H50O5/c1-19(2)10-9-15-31(8)26-23(36-20(3)33)18-30(7)22-11-12-24-28(4,5)25(34)14-16-29(24,6)21(22)13-17-32(26,30)27(35)37-31/h11,19,21,23-26,34H,9-10,12-18H2,1-8H3/t21-,23-,24+,25+,26-,29-,30+,31+,32-/m1/s1

> <INCHI_KEY>
WKDBZTLJGGVOGW-WDPAYILQSA-N

> <FORMULA>
C32H50O5

> <MOLECULAR_WEIGHT>
514.747

> <EXACT_MASS>
514.36582471

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
87

> <JCHEM_AVERAGE_POLARIZABILITY>
61.070746282056724

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S,4R,5R,6S,9S,12S,13R,16S,18R)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0^{2,9}.0^{5,9}.0^{13,18}]icos-1(20)-en-4-yl acetate

> <JCHEM_LOGP>
5.792829936

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.554178983382673

> <JCHEM_PKA_STRONGEST_BASIC>
-0.806801636509873

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
144.5906

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4R,5R,6S,9S,12S,13R,16S,18R)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0^{2,9}.0^{5,9}.0^{13,18}]icos-1(20)-en-4-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.458   6.061   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.229   5.134   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.417   3.605   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       1.189   5.735   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       2.419   4.808   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.892   5.259   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.775   3.997   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.568   5.317   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.303   3.809   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.230   5.039   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.759   4.851   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.360   3.434   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.889   3.246   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.389   3.592   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.808   4.784   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.490   1.828   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      13.019   1.640   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.563   0.598   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.035   0.786   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.433   2.204   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.506   0.974   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       6.905   2.392   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.978   1.162   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.449   1.350   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       3.848   2.767   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.821   1.227   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.051   0.300   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       2.348   0.777   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.465   2.039   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.302   1.029   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.339   3.089   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -1.134   2.639   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -1.481   1.139   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -2.953   0.689   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -3.300  -0.812   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -4.080   1.739   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       2.392   3.269   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   37                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9   25                                             
CONECT    8    7                                                            
CONECT    9    7   10   22                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   20                                                  
CONECT   13   12   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   12   21   22                                             
CONECT   21   20                                                            
CONECT   22   20    9   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    7   26   37                                             
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   31   37                                             
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34                                                            
CONECT   37   29    5   25                                                  
MASTER        0    0    0    0    0    0    0    0   37    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₂H₅₀O₅

Average Mass

514.7470 Da

Monoisotopic Mass

514.36582 Da

IUPAC Name

(2S,4R,5R,6S,9S,12S,13R,16S,18R)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0^{2,9}.0^{5,9}.0^{13,18}]icos-1(20)-en-4-yl acetate

Traditional Name

(2S,4R,5R,6S,9S,12S,13R,16S,18R)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0^{2,9}.0^{5,9}.0^{13,18}]icos-1(20)-en-4-yl acetate

CAS Registry Number

Not Available

SMILES

CC(C)CCC[C@]1(C)OC(=O)[C@]23CC[C@@H]4C(=CC[C@H]5C(C)(C)[C@@H](O)CC[C@]45C)[C@]2(C)C[C@@H](OC(C)=O)[C@H]13

InChI Identifier

InChI=1S/C32H50O5/c1-19(2)10-9-15-31(8)26-23(36-20(3)33)18-30(7)22-11-12-24-28(4,5)25(34)14-16-29(24,6)21(22)13-17-32(26,30)27(35)37-31/h11,19,21,23-26,34H,9-10,12-18H2,1-8H3/t21-,23-,24+,25+,26-,29-,30+,31+,32-/m1/s1

InChI Key

WKDBZTLJGGVOGW-WDPAYILQSA-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
Cucumaria frondosa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as triterpenoids. These are terpene molecules containing six isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Triterpenoids

Direct Parent

Triterpenoids

Alternative Parents

Substituents

Triterpenoid
Steroid lactone
Steroid ester
3-hydroxysteroid
Hydroxysteroid
3-beta-hydroxysteroid
Steroid
Dicarboxylic acid or derivatives
Gamma butyrolactone
Cyclic alcohol
Tetrahydrofuran
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen 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	5.79	ChemAxon
pKa (Strongest Acidic)	19.55	ChemAxon
pKa (Strongest Basic)	-0.81	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	144.59 m³·mol⁻¹	ChemAxon
Polarizability	61.07 Å³	ChemAxon
Number of Rings	5	ChemAxon
Bioavailability	No	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

10355811

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23247458

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate (NP0212820)

MOL for NP0212820 ((2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate)

3D MOL for NP0212820 ((2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate)

3D SDF for NP0212820 ((2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate)

3D-SDF for NP0212820 ((2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate)

PDB for NP0212820 ((2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate)

3D PDB for NP0212820 ((2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate)

SMILES for NP0212820 ((2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate)

INCHI for NP0212820 ((2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate)

Structure for NP0212820 ((2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate)

3D Structure for NP0212820 ((2s,4r,5r,6s,9s,12s,13r,16s,18r)-16-hydroxy-2,6,13,17,17-pentamethyl-6-(4-methylpentyl)-8-oxo-7-oxapentacyclo[10.8.0.0²,⁹.0⁵,⁹.0¹³,¹⁸]icos-1(20)-en-4-yl acetate)