NP-MRD: Showing NP-Card for 7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione (NP0300382)

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Record Information

Version

2.0

Created at

2022-09-10 12:45:19 UTC

Updated at

2022-09-10 12:45:19 UTC

NP-MRD ID

NP0300382

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione

Description

7',17',20'-Trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]Henicosane]-2'(11'),18'-diene-3',5,12'-trione belongs to the class of organic compounds known as withanolides and derivatives. These are c28 steroids structurally characterized by an ergostane skeleton usually functionalized at carbons 1, 22 and 26 to form a lactone ring. 7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione is found in Ganoderma australe. 7',17',20'-Trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]Henicosane]-2'(11'),18'-diene-3',5,12'-trione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004171523582D          

 38 43  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004171523582D          

 38 43  0  0  0  0            999 V2000
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    7.1915   -1.8175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9111   -2.2209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6203   -1.7994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3400   -2.2028    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6099   -0.9745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4241   -1.1074    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8822   -0.1957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8902   -0.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8798    0.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1601    0.6573    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1497    1.4822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7016   -1.6733    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9925   -2.0948    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9166   -2.9163    0.0000 O   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  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  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
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
  4 20  1  0  0  0  0
 19 21  1  0  0  0  0
  9 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
 29 32  1  0  0  0  0
 23 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 15 34  1  0  0  0  0
 34 35  2  0  0  0  0
  4 36  1  0  0  0  0
 36 37  1  0  0  0  0
  2 37  1  0  0  0  0
 37 38  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0300382

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2(CC(C)(O)C3=CC(O)C4(C)C5=C(C(=O)C(O2)C34C)C2(C)CCC(O)C(C)(C)C2CC5=O)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H40O8/c1-14-12-30(38-24(14)35)13-27(5,36)17-11-19(33)29(7)20-15(31)10-16-25(2,3)18(32)8-9-26(16,4)21(20)22(34)23(37-30)28(17,29)6/h11,14,16,18-19,23,32-33,36H,8-10,12-13H2,1-7H3

> <INCHI_KEY>
SZXITMVEKFHHKF-UHFFFAOYSA-N

> <FORMULA>
C30H40O8

> <MOLECULAR_WEIGHT>
528.642

> <EXACT_MASS>
528.272318248

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
78

> <JCHEM_AVERAGE_POLARIZABILITY>
56.103959993863725

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione

> <ALOGPS_LOGP>
2.57

> <JCHEM_LOGP>
2.439135691000001

> <ALOGPS_LOGS>
-3.70

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.53788355411833

> <JCHEM_PKA_STRONGEST_ACIDIC>
13.919052724053898

> <JCHEM_PKA_STRONGEST_BASIC>
-0.7784771682497266

> <JCHEM_POLAR_SURFACE_AREA>
130.36

> <JCHEM_REFRACTIVITY>
137.71490000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.05e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-APR-15         0                                  
HETATM    1  C   UNK     0       2.926  -3.234   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.429  -2.894   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.037  -1.480   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.570  -1.621   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.968  -0.204   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.701   1.151   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.218   1.564   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       6.774   2.689   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       8.217   1.422   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.826   2.837   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.359   2.695   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      11.375   3.853   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      10.698   1.193   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      11.933   2.114   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.042   0.440   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.061  -1.100   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      10.737  -1.887   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.778  -3.426   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       9.302  -1.132   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       8.054  -2.034   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       9.375   0.406   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.957  -0.196   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.405  -1.853   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.081  -2.640   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      13.424  -3.393   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.767  -4.146   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      16.091  -3.359   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      17.435  -4.112   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      16.072  -1.819   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      17.592  -2.067   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      16.580  -0.365   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      14.728  -1.066   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      14.709   0.474   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      13.366   1.227   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      13.346   2.767   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0       6.910  -3.123   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       5.586  -3.910   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       5.444  -5.444   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   37                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   20   36                                             
CONECT    5    4    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6   10   21                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   21                                             
CONECT   14   13                                                            
CONECT   15   13   16   34                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19    4                                                       
CONECT   21   19    9   13   22                                             
CONECT   22   21                                                            
CONECT   23   16   24   25   32                                             
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31   32                                             
CONECT   30   29                                                            
CONECT   31   29                                                            
CONECT   32   29   23   33                                                  
CONECT   33   32   34                                                       
CONECT   34   33   15   35                                                  
CONECT   35   34                                                            
CONECT   36    4   37                                                       
CONECT   37   36    2   38                                                  
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₀H₄₀O₈

Average Mass

528.6420 Da

Monoisotopic Mass

528.27232 Da

IUPAC Name

7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione

Traditional Name

7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione

CAS Registry Number

Not Available

SMILES

CC1CC2(CC(C)(O)C3=CC(O)C4(C)C5=C(C(=O)C(O2)C34C)C2(C)CCC(O)C(C)(C)C2CC5=O)OC1=O

InChI Identifier

InChI=1S/C30H40O8/c1-14-12-30(38-24(14)35)13-27(5,36)17-11-19(33)29(7)20-15(31)10-16-25(2,3)18(32)8-9-26(16,4)21(20)22(34)23(37-30)28(17,29)6/h11,14,16,18-19,23,32-33,36H,8-10,12-13H2,1-7H3

InChI Key

SZXITMVEKFHHKF-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
Ganoderma australe	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as withanolides and derivatives. These are c28 steroids structurally characterized by an ergostane skeleton usually functionalized at carbons 1, 22 and 26 to form a lactone ring.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Steroid lactones

Direct Parent

Withanolides and derivatives

Alternative Parents

Substituents

Withanolide-skeleton
20-hydroxysteroid
3-hydroxysteroid
15-hydroxysteroid
Hydroxysteroid
11-oxosteroid
Oxosteroid
7-oxosteroid
Ketal
Cyclohexenone
Oxepane
Gamma butyrolactone
Tetrahydrofuran
Tertiary alcohol
Cyclic alcohol
Secondary alcohol
Lactone
Ketone
Carboxylic acid ester
Polyol
Oxacycle
Organoheterocyclic compound
Monocarboxylic acid or derivatives
Acetal
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Carbonyl group
Organooxygen compound
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	2.57	ALOGPS
logP	2.44	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	13.92	ChemAxon
pKa (Strongest Basic)	-0.78	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	130.36 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	137.71 m³·mol⁻¹	ChemAxon
Polarizability	56.1 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

85154996

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione (NP0300382)

MOL for NP0300382 (7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione)

3D MOL for NP0300382 (7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione)

3D SDF for NP0300382 (7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione)

3D-SDF for NP0300382 (7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione)

PDB for NP0300382 (7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione)

3D PDB for NP0300382 (7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione)

SMILES for NP0300382 (7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione)

INCHI for NP0300382 (7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione)

Structure for NP0300382 (7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione)

3D Structure for NP0300382 (7',17',20'-trihydroxy-1',4,6',6',10',17',21'-heptamethyl-14'-oxaspiro[oxolane-2,15'-pentacyclo[11.7.1.0²,¹¹.0⁵,¹⁰.0¹⁸,²¹]henicosane]-2'(11'),18'-diene-3',5,12'-trione)