NP-MRD: Showing NP-Card for (1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate (NP0285197)

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Record Information

Version

2.0

Created at

2022-09-09 13:15:24 UTC

Updated at

2022-09-09 13:15:24 UTC

NP-MRD ID

NP0285197

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Description

(1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate is found in Albifimbria verrucaria. Based on a literature review very few articles have been published on (1'R,3'R,6'S,8'R,12'Z,18'Z,20'Z,24'R,25'S)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]Heptacosane]-4',12',18',20'-tetraen-6'-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092215152D          

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 29 40  1  0  0  0  0
  7 40  1  0  0  0  0
 40 41  1  6  0  0  0
M  END

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M  END


  Mrv1652309092215152D          

 41 45  0  0  1  0            999 V2000
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   -1.3373    0.7914    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0150    1.1963    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2280    1.9917    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7283    2.6549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4397    3.0929    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2751    3.1336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5659    3.9057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8789    2.5490    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6205    2.1273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0248    2.9064    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8942    2.7905    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.6712    2.3951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7711    1.5250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5518    1.1862    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6700    0.3634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4356    0.0560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6165    2.1416    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3909    2.4261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2500    1.6132    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2657    1.5053    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.7595    0.8539    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
  2  4  1  0  0  0  0
  5  4  1  1  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  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
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 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
 19 21  1  0  0  0  0
 18 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  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
 31 30  1  1  0  0  0
 31 32  1  0  0  0  0
 33 32  1  6  0  0  0
  7 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
  5 35  1  0  0  0  0
 35 36  1  0  0  0  0
 31 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 37 39  1  0  0  0  0
 37 40  1  0  0  0  0
 29 40  1  0  0  0  0
  7 40  1  0  0  0  0
 40 41  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0285197

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(O)C1OCC\C(C)=C/C(=O)OC[C@]23C[C@H](OC(C)=O)C(C)=C[C@H]2O[C@@H]2C[C@@H](OC(=O)\C=C/C=C\1)[C@@]3(C)C21CO1

> <INCHI_IDENTIFIER>
InChI=1S/C31H40O10/c1-18-10-11-36-22(20(3)32)8-6-7-9-27(34)41-24-14-26-31(17-38-31)29(24,5)30(16-37-28(35)12-18)15-23(39-21(4)33)19(2)13-25(30)40-26/h6-9,12-13,20,22-26,32H,10-11,14-17H2,1-5H3/b8-6-,9-7-,18-12-/t20?,22?,23-,24+,25+,26+,29+,30+,31?/m0/s1

> <INCHI_KEY>
BMAGQNXTRVVGHR-LXWRPICYSA-N

> <FORMULA>
C31H40O10

> <MOLECULAR_WEIGHT>
572.651

> <EXACT_MASS>
572.262147488

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
81

> <JCHEM_AVERAGE_POLARIZABILITY>
59.386567207404006

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1'R,3'R,6'S,8'R,12'E,18'E,20'Z,24'R,25'S)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0^{3,8}.0^{8,25}]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate

> <JCHEM_LOGP>
2.4757707913333316

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.598555428511748

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.451431794827172

> <JCHEM_PKA_STRONGEST_BASIC>
-3.038607496097322

> <JCHEM_POLAR_SURFACE_AREA>
130.12

> <JCHEM_REFRACTIVITY>
149.0882

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1'R,3'R,6'S,8'R,12'E,18'E,20'Z,24'R,25'S)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0^{3,8}.0^{8,25}]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      13.026  -3.932   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      12.842  -2.403   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      14.074  -1.479   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      11.425  -1.798   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.241  -0.269   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.830   0.369   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.408   1.916   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.203   0.773   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       7.680  -0.756   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.624  -2.346   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       8.858  -3.268   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       6.140  -2.843   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.579  -2.944   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.483  -4.481   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.047  -2.650   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.688  -1.898   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.649  -0.743   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.052   0.689   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -1.450   0.347   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.905  -1.124   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -2.496   1.477   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.028   2.233   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.426   3.718   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.359   4.956   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.687   5.773   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       4.247   5.849   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       4.790   7.291   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       5.374   4.758   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       6.758   3.971   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       7.513   5.425   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       9.136   5.209   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      10.586   4.471   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      10.773   2.847   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      12.230   2.214   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      12.451   0.678   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      13.880   0.105   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.617   3.998   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      10.063   4.529   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       9.800   3.011   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       7.963   2.810   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.018   1.594   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   35                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   33   40                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   22                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   18   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30   40                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32   37                                                  
CONECT   32   31   33                                                       
CONECT   33   32    7   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34    5   36                                                  
CONECT   36   35                                                            
CONECT   37   31   38   39   40                                             
CONECT   38   37   39                                                       
CONECT   39   38   37                                                       
CONECT   40   37   29    7   41                                             
CONECT   41   40                                                            
MASTER        0    0    0    0    0    0    0    0   41    0   90    0
END

View in JSmol

Synonyms

Value	Source
(1'r,3'r,6's,8'r,12'z,18'z,20'z,24'r,25's)-17'-(1-Hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0,.0,]heptacosane]-4',12',18',20'-tetraen-6'-yl acetic acid	Generator

Chemical Formula

C₃₁H₄₀O₁₀

Average Mass

572.6510 Da

Monoisotopic Mass

572.26215 Da

IUPAC Name

(1'R,3'R,6'S,8'R,12'E,18'E,20'Z,24'R,25'S)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0^{3,8}.0^{8,25}]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

CC(O)C1OCC\C(C)=C/C(=O)OC[C@]23C[C@H](OC(C)=O)C(C)=C[C@H]2O[C@@H]2C[C@@H](OC(=O)\C=C/C=C\1)[C@@]3(C)C21CO1

InChI Identifier

InChI=1S/C31H40O10/c1-18-10-11-36-22(20(3)32)8-6-7-9-27(34)41-24-14-26-31(17-38-31)29(24,5)30(16-37-28(35)12-18)15-23(39-21(4)33)19(2)13-25(30)40-26/h6-9,12-13,20,22-26,32H,10-11,14-17H2,1-5H3/b8-6-,9-7-,18-12-/t20?,22?,23-,24+,25+,26+,29+,30+,31?/m0/s1

InChI Key

BMAGQNXTRVVGHR-LXWRPICYSA-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
Albifimbria verrucaria	LOTUS Database	35616633

Chemical Taxonomy

Classification

Not classified

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	2.48	ChemAxon
pKa (Strongest Acidic)	14.45	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	130.12 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	149.09 m³·mol⁻¹	ChemAxon
Polarizability	59.39 Å³	ChemAxon
Number of Rings	5	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate (NP0285197)

MOL for NP0285197 ((1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate)

3D MOL for NP0285197 ((1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate)

3D SDF for NP0285197 ((1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate)

3D-SDF for NP0285197 ((1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate)

PDB for NP0285197 ((1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate)

3D PDB for NP0285197 ((1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate)

SMILES for NP0285197 ((1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate)

INCHI for NP0285197 ((1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate)

Structure for NP0285197 ((1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate)

3D Structure for NP0285197 ((1'r,3'r,6's,8'r,12'e,18'e,20'z,24'r,25's)-17'-(1-hydroxyethyl)-5',13',25'-trimethyl-11',22'-dioxo-2',10',16',23'-tetraoxaspiro[oxirane-2,26'-tetracyclo[22.2.1.0³,⁸.0⁸,²⁵]heptacosane]-4',12',18',20'-tetraen-6'-yl acetate)