NP-MRD: Showing NP-Card for 12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione (NP0150984)

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Record Information

Version

2.0

Created at

2022-09-02 07:13:40 UTC

Updated at

2022-09-02 07:13:40 UTC

NP-MRD ID

NP0150984

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione

Description

12'-Hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]Nonacosane]-4',19',21'-triene-11',23'-dione belongs to the class of organic compounds known as trichothecenes. These are sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain. 12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione is found in Paramyrothecium roridum. Based on a literature review very few articles have been published on 12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]Nonacosane]-4',19',21'-triene-11',23'-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022209132D          

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M  END

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M  END


  Mrv1652309022209132D          

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    2.5850   -4.6961    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4328   -3.3824    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7543   -2.8526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8668   -2.7491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1683   -3.5668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7393   -4.2801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1380   -1.8815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9407   -2.0722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4480   -1.5862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0068   -2.2746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3755   -1.5366    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2604   -2.2023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2344   -1.3693    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8928   -0.8722    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  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
  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
 14 13  1  4  0  0  0
 14 15  2  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  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  4 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
  2 30  1  0  0  0  0
 28 31  1  0  0  0  0
  8 31  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
  6 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 33 35  1  0  0  0  0
 18 36  1  0  0  0  0
 36 37  1  0  0  0  0
 16 37  1  0  0  0  0
 37 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0150984

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC2CC(C)C(O)C(=O)OCC34CCC(C)=CC3OC3CC(OC(=O)C=CC=CC1O2)C4(C)C31CO1

> <INCHI_IDENTIFIER>
InChI=1S/C29H38O9/c1-16-9-10-28-14-33-26(32)25(31)17(2)12-24-35-18(3)19(36-24)7-5-6-8-23(30)38-20-13-22(37-21(28)11-16)29(15-34-29)27(20,28)4/h5-8,11,17-22,24-25,31H,9-10,12-15H2,1-4H3

> <INCHI_KEY>
IDKGOOSUZDQUOK-UHFFFAOYSA-N

> <FORMULA>
C29H38O9

> <MOLECULAR_WEIGHT>
530.614

> <EXACT_MASS>
530.251582804

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
54.999920295552556

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1^{15,18}.0^{3,8}.0^{8,26}]nonacosane]-4',19',21'-triene-11',23'-dione

> <ALOGPS_LOGP>
2.92

> <JCHEM_LOGP>
2.853623423666665

> <ALOGPS_LOGS>
-4.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.472818905034927

> <JCHEM_PKA_STRONGEST_BASIC>
-3.688390668488774

> <JCHEM_POLAR_SURFACE_AREA>
113.05000000000001

> <JCHEM_REFRACTIVITY>
136.6399

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.80e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1^{15,18}.0^{3,8}.0^{8,26}]nonacosane]-4',19',21'-triene-11',23'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.999  -9.196   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.153  -7.909   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.836  -6.527   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.020  -5.193   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -0.920  -3.825   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -0.272  -2.320   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.910  -1.170   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.392  -1.887   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.648  -0.902   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.986   0.632   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.758   1.560   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.362   1.371   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.892   1.068   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.311   0.425   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.434  -0.661   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      10.142  -2.079   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       9.286  -3.392   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      10.216  -4.654   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.561  -6.089   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.568  -7.298   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.509  -8.517   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.143  -7.954   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       7.231  -9.492   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       5.645  -7.462   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       4.825  -8.766   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       4.541  -6.314   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       3.275  -5.325   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.618  -5.132   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.181  -6.658   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.380  -7.989   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.124  -3.512   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       3.623  -3.868   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       0.836  -2.961   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.013  -4.246   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      -0.701  -2.868   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      11.686  -4.111   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      11.637  -2.556   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      12.867  -1.628   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   28                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   33                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   31                                                  
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   37                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   36                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27    4   29   31                                             
CONECT   29   28   30                                                       
CONECT   30   29    2                                                       
CONECT   31   28    8   32   33                                             
CONECT   32   31                                                            
CONECT   33   31    6   34   35                                             
CONECT   34   33   35                                                       
CONECT   35   34   33                                                       
CONECT   36   18   37                                                       
CONECT   37   36   16   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

C₂₉H₃₈O₉

Average Mass

530.6140 Da

Monoisotopic Mass

530.25158 Da

IUPAC Name

12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1^{15,18}.0^{3,8}.0^{8,26}]nonacosane]-4',19',21'-triene-11',23'-dione

Traditional Name

12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1^{15,18}.0^{3,8}.0^{8,26}]nonacosane]-4',19',21'-triene-11',23'-dione

CAS Registry Number

Not Available

SMILES

CC1OC2CC(C)C(O)C(=O)OCC34CCC(C)=CC3OC3CC(OC(=O)C=CC=CC1O2)C4(C)C31CO1

InChI Identifier

InChI=1S/C29H38O9/c1-16-9-10-28-14-33-26(32)25(31)17(2)12-24-35-18(3)19(36-24)7-5-6-8-23(30)38-20-13-22(37-21(28)11-16)29(15-34-29)27(20,28)4/h5-8,11,17-22,24-25,31H,9-10,12-15H2,1-4H3

InChI Key

IDKGOOSUZDQUOK-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
Myrothecium roridum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as trichothecenes. These are sesquiterpene mycotoxins structurally characterized by the presence of an epoxide ring and a benzopyran derivative with a variant number of hydroxyl, acetyl, or other substituents. The most important structural features causing the biological activities of trichothecenes are the 12,13-epoxy ring, the presence of hydroxyl or acetyl groups at appropriate positions on the trichothecene nucleus and the structure and position of the side-chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Trichothecenes

Alternative Parents

Substituents

Trichothecene skeleton
Macrolide
Oxepane
Dicarboxylic acid or derivatives
Oxane
Meta-dioxolane
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Secondary alcohol
Lactone
Carboxylic acid ester
Oxacycle
Acetal
Organoheterocyclic compound
Carboxylic acid derivative
Ether
Oxirane
Dialkyl ether
Alcohol
Organic oxygen compound
Organic oxide
Carbonyl group
Organooxygen compound
Hydrocarbon derivative
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	2.92	ALOGPS
logP	2.85	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	12.47	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	113.05 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	136.64 m³·mol⁻¹	ChemAxon
Polarizability	55 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

73237632

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione (NP0150984)

MOL for NP0150984 (12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione)

3D MOL for NP0150984 (12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione)

3D SDF for NP0150984 (12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione)

3D-SDF for NP0150984 (12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione)

PDB for NP0150984 (12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione)

3D PDB for NP0150984 (12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione)

SMILES for NP0150984 (12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione)

INCHI for NP0150984 (12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione)

Structure for NP0150984 (12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione)

3D Structure for NP0150984 (12'-hydroxy-5',13',17',26'-tetramethyl-2',10',16',24',29'-pentaoxaspiro[oxirane-2,27'-pentacyclo[23.2.1.1¹⁵,¹⁸.0³,⁸.0⁸,²⁶]nonacosane]-4',19',21'-triene-11',23'-dione)