NP-MRD: Showing NP-Card for (1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate (NP0214220)

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Record Information

Version

2.0

Created at

2022-09-05 13:27:28 UTC

Updated at

2022-09-05 13:27:29 UTC

NP-MRD ID

NP0214220

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Description

(1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate is found in Albifimbria verrucaria. Based on a literature review very few articles have been published on (1R)-1-[(1'R,2S,3'R,8'R,12'Z,17'R,18'Z,20'Z,24'R,25'S)-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-17'-yl]ethyl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052215272D          

 40 44  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1652309052215272D          

 40 44  0  0  1  0            999 V2000
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    5.3092   -0.3593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0824    0.4637    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4458   -0.1477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1474   -0.9815    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1428   -1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8023   -2.3369    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3350   -2.0801    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4932   -2.1369    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4419   -2.9603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6715   -1.9772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9503   -1.5750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3928   -0.9524    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3157    0.9330    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8139    0.2781    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6666    1.5740    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4205    1.9091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3338    1.0887    0.0000 O   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
  4  5  1  0  0  0  0
  5  6  1  1  0  0  0
  7  5  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  6  0  0  0
 17 16  1  1  0  0  0
 17 18  1  0  0  0  0
 19 18  1  6  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 25 24  1  6  0  0  0
 19 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
 28 29  2  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
  7 35  1  0  0  0  0
 25 36  1  0  0  0  0
 15 36  1  0  0  0  0
 36 37  1  6  0  0  0
 36 38  1  0  0  0  0
 17 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 38 40  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0214220

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H](OC(C)=O)[C@@H]1OCC\C(C)=C/C(=O)OC[C@]23CCC(C)=C[C@H]2O[C@@H]2C[C@@H](OC(=O)\C=C/C=C\1)[C@@]3(C)[C@]21CO1

> <INCHI_IDENTIFIER>
InChI=1S/C31H40O9/c1-19-10-12-30-17-36-28(34)15-20(2)11-13-35-23(21(3)38-22(4)32)8-6-7-9-27(33)40-24-16-26(39-25(30)14-19)31(18-37-31)29(24,30)5/h6-9,14-15,21,23-26H,10-13,16-18H2,1-5H3/b8-6-,9-7-,20-15-/t21-,23-,24-,25-,26-,29-,30-,31+/m1/s1

> <INCHI_KEY>
UMMRHXXIVGSHOW-HOBFAORDSA-N

> <FORMULA>
C31H40O9

> <MOLECULAR_WEIGHT>
556.652

> <EXACT_MASS>
556.267232868

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
57.79496537174774

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R)-1-[(1'R,2S,3'R,8'R,12'E,17'R,18'E,20'Z,24'R,25'S)-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-17'-yl]ethyl acetate

> <JCHEM_LOGP>
3.7065818583333323

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.595948891870844

> <JCHEM_PKA_STRONGEST_BASIC>
-3.734723058047598

> <JCHEM_POLAR_SURFACE_AREA>
109.89000000000001

> <JCHEM_REFRACTIVITY>
147.5727

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R)-1-[(1'R,2S,3'R,8'R,12'E,17'R,18'E,20'Z,24'R,25'S)-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-17'-yl]ethyl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      -4.950   1.242   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.906   0.110   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -4.365  -1.360   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -2.404   0.448   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -1.360  -0.685   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.819  -2.155   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.143  -0.347   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.065   1.182   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.521   2.673   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.444   3.897   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.773   4.721   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.339   4.817   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       4.885   6.257   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       5.447   3.708   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       6.821   2.911   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       7.565   4.357   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.204   4.152   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.653   3.438   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      10.861   1.808   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      12.332   1.146   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.533  -0.383   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      13.954  -0.975   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.309  -1.317   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       9.911  -0.671   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       9.487   0.866   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.299  -0.276   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.742  -1.832   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       7.733  -3.437   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.964  -4.362   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       6.225  -3.883   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.654  -3.989   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.558  -5.526   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       3.120  -3.691   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.774  -2.940   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       0.733  -1.778   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       8.056   1.742   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.119   0.519   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.711   2.938   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      10.118   3.564   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       9.956   2.032   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8   35                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16   36                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   38                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   25                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   19   26   36                                             
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34    7                                                       
CONECT   36   25   15   37   38                                             
CONECT   37   36                                                            
CONECT   38   36   17   39   40                                             
CONECT   39   38   40                                                       
CONECT   40   39   38                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   88    0
END

View in JSmol

Synonyms

Value	Source
(1R)-1-[(1'r,2S,3'r,8'r,12'z,17'r,18'z,20'z,24'r,25's)-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-17'-yl]ethyl acetic acid	Generator

Chemical Formula

C₃₁H₄₀O₉

Average Mass

556.6520 Da

Monoisotopic Mass

556.26723 Da

IUPAC Name

(1R)-1-[(1'R,2S,3'R,8'R,12'E,17'R,18'E,20'Z,24'R,25'S)-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-17'-yl]ethyl acetate

Traditional Name

CAS Registry Number

Not Available

SMILES

C[C@@H](OC(C)=O)[C@@H]1OCC\C(C)=C/C(=O)OC[C@]23CCC(C)=C[C@H]2O[C@@H]2C[C@@H](OC(=O)\C=C/C=C\1)[C@@]3(C)[C@]21CO1

InChI Identifier

InChI=1S/C31H40O9/c1-19-10-12-30-17-36-28(34)15-20(2)11-13-35-23(21(3)38-22(4)32)8-6-7-9-27(33)40-24-16-26(39-25(30)14-19)31(18-37-31)29(24,30)5/h6-9,14-15,21,23-26H,10-13,16-18H2,1-5H3/b8-6-,9-7-,20-15-/t21-,23-,24-,25-,26-,29-,30-,31+/m1/s1

InChI Key

UMMRHXXIVGSHOW-HOBFAORDSA-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	3.71	ChemAxon
pKa (Strongest Acidic)	17.6	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	109.89 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	147.57 m³·mol⁻¹	ChemAxon
Polarizability	57.79 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

58139614

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162988371

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate (NP0214220)

MOL for NP0214220 ((1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate)

3D MOL for NP0214220 ((1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate)

3D SDF for NP0214220 ((1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate)

3D-SDF for NP0214220 ((1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate)

PDB for NP0214220 ((1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate)

3D PDB for NP0214220 ((1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate)

SMILES for NP0214220 ((1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate)

INCHI for NP0214220 ((1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate)

Structure for NP0214220 ((1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate)

3D Structure for NP0214220 ((1r)-1-[(1'r,2s,3'r,8'r,12'e,17'r,18'e,20'z,24'r,25's)-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-17'-yl]ethyl acetate)