NP-MRD: Showing NP-Card for 26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione (NP0319421)

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Record Information

Version

2.0

Created at

2022-09-11 20:26:16 UTC

Updated at

2022-09-11 20:26:16 UTC

NP-MRD ID

NP0319421

Secondary Accession Numbers

None

Natural Product Identification

Common Name

26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione

Description

26,27-Dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]Hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members. 26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione is found in Verticimonosporium diffractum. Based on a literature review very few articles have been published on 26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]Hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112222262D          

 39 45  0  0  0  0            999 V2000
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M  END

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M  END


  Mrv1652309112222262D          

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    8.0608    3.9889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0030    1.5506    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1789    1.5887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7176    1.3963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7215    2.2213    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4340    1.8055    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7861    1.6783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3493    2.3782    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5487    2.1790    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9169    2.7096    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4907    1.3560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7908    0.9192    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  2  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
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 12 10  1  4  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 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
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  4  0  0  0
 22 23  2  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
  4 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  2 28  1  0  0  0  0
 26 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
  6 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 33  1  0  0  0  0
 20 34  1  0  0  0  0
 16 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 16 38  1  0  0  0  0
 38 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0319421

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CCC23COC(=O)C=C4CCOC5(CCC=CC(=O)OC6CC(OC2=C1)C1(CO1)C36C)C(O)C(O)OC45

> <INCHI_IDENTIFIER>
InChI=1S/C29H36O10/c1-16-6-9-27-14-34-22(31)12-17-7-10-35-28(23(32)25(33)39-24(17)28)8-4-3-5-21(30)38-18-13-20(37-19(27)11-16)29(15-36-29)26(18,27)2/h3,5,11-12,16,18,20,23-25,32-33H,4,6-10,13-15H2,1-2H3

> <INCHI_KEY>
LERCQWPSQAJZLO-UHFFFAOYSA-N

> <FORMULA>
C29H36O10

> <MOLECULAR_WEIGHT>
544.597

> <EXACT_MASS>
544.230847359

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
55.97436251200637

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1^{8,11}.0^{1,24}.0^{9,18}.0^{13,18}]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione

> <JCHEM_LOGP>
1.6706954106666658

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.11129305720041

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.283046457752961

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7951148123894174

> <JCHEM_POLAR_SURFACE_AREA>
133.28

> <JCHEM_REFRACTIVITY>
136.685

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1^{8,11}.0^{1,24}.0^{9,18}.0^{13,18}]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione

> <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      17.228   8.972   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.583   7.573   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      17.487   6.320   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      16.822   4.915   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      17.943   3.973   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      17.536   2.197   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.646   0.839   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      15.047   1.237   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      13.866   0.215   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      13.955  -1.329   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      15.171  -2.273   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      12.430  -1.628   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.880  -1.406   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.464  -0.733   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.451   0.459   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.944   1.954   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       6.413   1.847   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       5.900   3.749   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.926   4.916   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.688   4.648   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.560   5.796   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.966   6.473   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      11.039   8.011   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      12.313   5.660   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      13.534   4.617   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      15.208   4.586   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      14.452   6.010   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      15.047   7.446   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      14.939   2.894   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      13.401   2.966   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      16.273   2.606   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      16.280   4.146   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      17.610   3.370   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       8.934   3.133   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       8.119   4.439   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       6.624   4.067   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       5.445   5.058   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       6.516   2.531   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       5.210   1.716   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   28                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   26                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   31                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   29                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   34   38                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   34                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    4   27   29                                             
CONECT   27   26   28                                                       
CONECT   28   27    2                                                       
CONECT   29   26    8   30   31                                             
CONECT   30   29                                                            
CONECT   31   29    6   32   33                                             
CONECT   32   31   33                                                       
CONECT   33   32   31                                                       
CONECT   34   20   16   35                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   16   39                                                  
CONECT   39   38                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₉H₃₆O₁₀

Average Mass

544.5970 Da

Monoisotopic Mass

544.23085 Da

IUPAC Name

26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1^{8,11}.0^{1,24}.0^{9,18}.0^{13,18}]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione

Traditional Name

26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1^{8,11}.0^{1,24}.0^{9,18}.0^{13,18}]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione

CAS Registry Number

Not Available

SMILES

CC1CCC23COC(=O)C=C4CCOC5(CCC=CC(=O)OC6CC(OC2=C1)C1(CO1)C36C)C(O)C(O)OC45

InChI Identifier

InChI=1S/C29H36O10/c1-16-6-9-27-14-34-22(31)12-17-7-10-35-28(23(32)25(33)39-24(17)28)8-4-3-5-21(30)38-18-13-20(37-19(27)11-16)29(15-36-29)26(18,27)2/h3,5,11-12,16,18,20,23-25,32-33H,4,6-10,13-15H2,1-2H3

InChI Key

LERCQWPSQAJZLO-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
Verticimonosporium diffractum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as macrolides and analogues. These are organic compounds containing a lactone ring of at least twelve members.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Macrolides and analogues

Sub Class

Not Available

Direct Parent

Macrolides and analogues

Alternative Parents

Substituents

Macrolide
Furopyran
Oxepane
Dicarboxylic acid or derivatives
Monosaccharide
Oxane
Pyran
Furan
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Tetrahydrofuran
Secondary alcohol
Carboxylic acid ester
Hemiacetal
Lactone
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Carbonyl group
Organic oxide
Alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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	1.67	ChemAxon
pKa (Strongest Acidic)	11.28	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	133.28 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	136.68 m³·mol⁻¹	ChemAxon
Polarizability	55.97 Å³	ChemAxon
Number of Rings	7	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

163027325

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione (NP0319421)

MOL for NP0319421 (26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione)

3D MOL for NP0319421 (26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione)

3D SDF for NP0319421 (26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione)

3D-SDF for NP0319421 (26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione)

PDB for NP0319421 (26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione)

3D PDB for NP0319421 (26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione)

SMILES for NP0319421 (26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione)

INCHI for NP0319421 (26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione)

Structure for NP0319421 (26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione)

3D Structure for NP0319421 (26,27-dihydroxy-9,15-dimethyl-7,12,20,25,28-pentaoxaspiro[hexacyclo[21.4.3.1⁸,¹¹.0¹,²⁴.0⁹,¹⁸.0¹³,¹⁸]hentriacontane-10,2'-oxirane]-4,13,22-triene-6,21-dione)