NP-MRD: Showing NP-Card for (1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione (NP0259286)

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Record Information

Version

2.0

Created at

2022-09-08 01:06:09 UTC

Updated at

2022-09-08 01:06:10 UTC

NP-MRD ID

NP0259286

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione

Description

RORIDIN H 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. (1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione is found in Baccharis coridifolia. (1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione was first documented in 2006 (PMID: 17080680). Based on a literature review a small amount of articles have been published on RORIDIN H (PMID: 19938595) (PMID: 24450184) (PMID: 22806769) (PMID: 18663931).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082203062D          

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M  END

     RDKit          3D

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M  END


  Mrv1652309082203062D          

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    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  1  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  2  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  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  8  7  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  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  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  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
  4 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
  2 29  1  0  0  0  0
 27 30  1  0  0  0  0
  8 30  1  0  0  0  0
 30 31  1  1  0  0  0
 30 32  1  0  0  0  0
  6 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 32 34  1  1  0  0  0
 18 35  1  0  0  0  0
 35 36  1  0  0  0  0
 16 36  1  0  0  0  0
 36 37  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0259286

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OC2C\C(C)=C/C(=O)OCC34CCC(C)=C[C@H]3O[C@@H]3C[C@@H](OC(=O)\C=C/C=C\C1O2)[C@@]4(C)[C@]31CO1

> <INCHI_IDENTIFIER>
InChI=1S/C29H36O8/c1-17-9-10-28-15-32-25(31)12-18(2)13-26-34-19(3)20(35-26)7-5-6-8-24(30)37-21-14-23(36-22(28)11-17)29(16-33-29)27(21,28)4/h5-8,11-12,19-23,26H,9-10,13-16H2,1-4H3/b7-5-,8-6-,18-12-/t19?,20?,21-,22-,23-,26?,27-,28?,29+/m1/s1

> <INCHI_KEY>
IWFOIUWPNYEUAI-JYKOLLLESA-N

> <FORMULA>
C29H36O8

> <MOLECULAR_WEIGHT>
512.599

> <EXACT_MASS>
512.241018119

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
53.167806696810246

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'R,2S,3'R,12'Z,19'Z,21'Z,25'R,26'S)-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',12',19',21'-tetraene-11',23'-dione

> <JCHEM_LOGP>
3.8342346126666644

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.858518594157726

> <JCHEM_PKA_STRONGEST_BASIC>
-3.689069770017411

> <JCHEM_POLAR_SURFACE_AREA>
92.82000000000001

> <JCHEM_REFRACTIVITY>
136.0514

> <JCHEM_ROTATABLE_BOND_COUNT>
0

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,2S,3'R,12'Z,19'Z,21'Z,25'R,26'S)-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',12',19',21'-tetraene-11',23'-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-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  C   UNK     0       5.645  -7.462   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       4.825  -8.766   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       4.541  -6.314   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.275  -5.325   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.618  -5.132   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.181  -6.658   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.380  -7.989   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.124  -3.512   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.623  -3.868   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       0.836  -2.961   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -0.013  -4.246   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -0.701  -2.868   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      11.686  -4.111   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      11.637  -2.556   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      12.867  -1.628   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   27                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   32                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   30                                                  
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   36                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   35                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26    4   28   30                                             
CONECT   28   27   29                                                       
CONECT   29   28    2                                                       
CONECT   30   27    8   31   32                                             
CONECT   31   30                                                            
CONECT   32   30    6   33   34                                             
CONECT   33   32   34                                                       
CONECT   34   33   32                                                       
CONECT   35   18   36                                                       
CONECT   36   35   16   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

C₂₉H₃₆O₈

Average Mass

512.5990 Da

Monoisotopic Mass

512.24102 Da

IUPAC Name

(1'R,2S,3'R,12'Z,19'Z,21'Z,25'R,26'S)-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',12',19',21'-tetraene-11',23'-dione

Traditional Name

CAS Registry Number

Not Available

SMILES

CC1OC2C\C(C)=C/C(=O)OCC34CCC(C)=C[C@H]3O[C@@H]3C[C@@H](OC(=O)\C=C/C=C\C1O2)[C@@]4(C)[C@]31CO1

InChI Identifier

InChI=1S/C29H36O8/c1-17-9-10-28-15-32-25(31)12-18(2)13-26-34-19(3)20(35-26)7-5-6-8-24(30)37-21-14-23(36-22(28)11-17)29(16-33-29)27(21,28)4/h5-8,11-12,19-23,26H,9-10,13-16H2,1-4H3/b7-5-,8-6-,18-12-/t19?,20?,21-,22-,23-,26?,27-,28?,29+/m1/s1

InChI Key

IWFOIUWPNYEUAI-JYKOLLLESA-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
Baccharis coridifolia	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
Lactone
Carboxylic acid ester
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Acetal
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
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	3.83	ChemAxon
pKa (Strongest Acidic)	15.86	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	92.82 Å²	ChemAxon
Rotatable Bond Count	0	ChemAxon
Refractivity	136.05 m³·mol⁻¹	ChemAxon
Polarizability	53.17 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

C00012600

Chemspider ID

4513812

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

22524715

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Xu J, Takasaki A, Kobayashi H, Oda T, Yamada J, Mangindaan RE, Ukai K, Nagai H, Namikoshi M: Four new macrocyclic trichothecenes from two strains of marine-derived fungi of the genus Myrothecium. J Antibiot (Tokyo). 2006 Aug;59(8):451-5. doi: 10.1038/ja.2006.63. [PubMed:17080680 ]
Zaichenko AM, Nagornaia SS, Andrienko EV, Tsyganenko ES: [Study of specificity of fungistatic effect of trichothecene mycotoxins]. Mikrobiol Z. 2009 Mar-Apr;71(2):57-62. [PubMed:19938595 ]
Zaichenko AM, Tsyganenko ES, Andrienko EV, Savchuk IaI: [Characteristics of toxigenic properties of Myrothecium cinctum (Corda) sacc., 1886 and Myrothecium commune pidopl., 1969]. Mikrobiol Z. 2013 Nov-Dec;75(6):41-5. [PubMed:24450184 ]
Zhang SY, Li ZL, Guan LP, Wu X, Pan HQ, Bai J, Hua HM: Structure determination of two new trichothecenes from a halotolerant fungus Myrothecium sp. GS-17 by NMR spectroscopy. Magn Reson Chem. 2012 Sep;50(9):632-6. doi: 10.1002/mrc.3845. Epub 2012 Jul 16. [PubMed:22806769 ]
Zaichenko OM: [Biosynthesis of macrocyclic trichothecenes: some aspects of physiology]. Mikrobiol Z. 2008 Mar-Apr;70(2-3):116-21. [PubMed:18663931 ]
LOTUS database [Link]

Showing NP-Card for (1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione (NP0259286)

MOL for NP0259286 ((1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione)

3D MOL for NP0259286 ((1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione)

3D SDF for NP0259286 ((1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione)

3D-SDF for NP0259286 ((1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione)

PDB for NP0259286 ((1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione)

3D PDB for NP0259286 ((1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione)

SMILES for NP0259286 ((1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione)

INCHI for NP0259286 ((1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione)

Structure for NP0259286 ((1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione)

3D Structure for NP0259286 ((1'r,2s,3'r,12'z,19'z,21'z,25'r,26's)-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',12',19',21'-tetraene-11',23'-dione)