NP-MRD: Showing NP-Card for (1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate (NP0216586)

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Record Information

Version

2.0

Created at

2022-09-05 16:37:09 UTC

Updated at

2022-09-05 16:37:10 UTC

NP-MRD ID

NP0216586

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate

Description

Euphoscopin N belongs to the class of organic compounds known as jatrophane and cyclojatrophane diterpenoids. These are diterpenoids with a structure based on the jatrophane or the 9,13-jatrophane skeleton. Jatrophane can be derived from casbane by 6,10-cyclization and opening of the cyclopropane. Cyclojatrophane diterpenoids are based on the 9,13-cyclization of the jatrophane skeleton yields the 9,13-cyclojatrophane skeleton. (1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate is found in Euphorbia helioscopia. (1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate was first documented in 2008 (PMID: 18452010). Based on a literature review very few articles have been published on Euphoscopin N.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052218372D          

 43 45  0  0  1  0            999 V2000
    8.0715    3.4576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309052218372D          

 43 45  0  0  1  0            999 V2000
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    4.2072    0.9744    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8234    1.5229    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4240    1.2338    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5055    0.4129    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8353   -0.0682    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9169   -0.8892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0836    0.2716    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7072    0.8254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0973    1.3810    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2893    1.2140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4371    2.1327    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0287    2.8495    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2037    2.8542    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7871    2.1421    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7953    3.5711    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0297    3.5758    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4381    4.2926    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0215    5.0047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8035    5.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2119    4.2832    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2571    2.0418    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.8733    2.5903    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6565    2.3309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2664    1.7754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2727    2.8794    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.1058    3.6873    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7220    4.2359    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5551    5.0438    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5052    3.9764    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
  5  4  1  6  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
  8 11  1  0  0  0  0
 11 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  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  6  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  1  0  0  0
 23 25  1  0  0  0  0
 25 26  1  6  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 32 33  1  0  0  0  0
 33 34  2  0  0  0  0
 29 34  1  0  0  0  0
 25 35  1  0  0  0  0
 17 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
  5 39  1  0  0  0  0
 39 40  1  6  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 41 43  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0216586

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1C[C@@]2(OC(C)=O)[C@@H](\C=C(C)\[C@H](OC(C)=O)[C@H](OC(C)=O)C(=O)C(C)(C)C\C=C(C)/C2=O)[C@H]1OC(=O)C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C33H40O10/c1-18-14-15-32(7,8)30(38)28(41-22(5)35)27(40-21(4)34)19(2)16-25-26(42-31(39)24-12-10-9-11-13-24)20(3)17-33(25,29(18)37)43-23(6)36/h9-14,16,20,25-28H,15,17H2,1-8H3/b18-14-,19-16+/t20-,25+,26+,27+,28+,33-/m1/s1

> <INCHI_KEY>
YCHJWRVSZGGWFE-MQFNCDSZSA-N

> <FORMULA>
C33H40O10

> <MOLECULAR_WEIGHT>
596.673

> <EXACT_MASS>
596.262147488

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
83

> <JCHEM_AVERAGE_POLARIZABILITY>
61.75813079162185

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,2R,3aR,10S,11S,13aS)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1H,2H,3H,3aH,4H,7H,8H,9H,10H,11H,13aH-cyclopenta[12]annulen-1-yl benzoate

> <JCHEM_LOGP>
5.384097025999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.668146133793702

> <JCHEM_PKA_STRONGEST_BASIC>
-5.46388261787262

> <JCHEM_POLAR_SURFACE_AREA>
139.34000000000003

> <JCHEM_REFRACTIVITY>
155.83670000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2R,3aR,10S,11S,13aS)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1H,2H,3H,7H,10H,11H,13aH-cyclopenta[12]annulen-1-yl benzoate

> <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      15.067   6.454   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.916   5.430   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      14.228   3.922   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      12.455   5.915   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.304   4.891   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.616   3.382   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      13.078   2.898   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.466   2.359   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.005   2.404   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.674   1.404   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.777   0.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.627  -0.173   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.165   0.311   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.015  -0.713   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.853   1.819   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       9.004   2.843   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.391   2.303   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.544   0.771   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       5.293  -0.127   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.445  -1.660   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.889   0.507   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.053   1.541   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.915   2.578   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.407   2.266   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.549   3.981   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.787   5.319   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.247   5.328   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       1.469   3.999   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       1.485   6.666   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -0.055   6.675   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -0.818   8.013   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -0.040   9.342   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.500   9.333   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.262   7.995   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       6.080   3.811   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       7.230   4.835   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       8.692   4.351   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       9.831   3.314   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       9.842   5.375   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0       9.531   6.883   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      10.681   7.907   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      10.370   9.415   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      12.143   7.423   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   39                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   10   11                                             
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    8   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18   22   35                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   35                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   34                                                  
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   29                                                       
CONECT   35   25   17   36                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38   39                                                  
CONECT   38   37                                                            
CONECT   39   37    5   40                                                  
CONECT   40   39   41                                                       
CONECT   41   40   42   43                                                  
CONECT   42   41                                                            
CONECT   43   41                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   90    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₄₀O₁₀

Average Mass

596.6730 Da

Monoisotopic Mass

596.26215 Da

IUPAC Name

(1S,2R,3aR,10S,11S,13aS)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1H,2H,3H,3aH,4H,7H,8H,9H,10H,11H,13aH-cyclopenta[12]annulen-1-yl benzoate

Traditional Name

(1S,2R,3aR,10S,11S,13aS)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1H,2H,3H,7H,10H,11H,13aH-cyclopenta[12]annulen-1-yl benzoate

CAS Registry Number

Not Available

SMILES

C[C@@H]1C[C@@]2(OC(C)=O)[C@@H](\C=C(C)\[C@H](OC(C)=O)[C@H](OC(C)=O)C(=O)C(C)(C)C\C=C(C)/C2=O)[C@H]1OC(=O)C1=CC=CC=C1

InChI Identifier

InChI=1S/C33H40O10/c1-18-14-15-32(7,8)30(38)28(41-22(5)35)27(40-21(4)34)19(2)16-25-26(42-31(39)24-12-10-9-11-13-24)20(3)17-33(25,29(18)37)43-23(6)36/h9-14,16,20,25-28H,15,17H2,1-8H3/b18-14-,19-16+/t20-,25+,26+,27+,28+,33-/m1/s1

InChI Key

YCHJWRVSZGGWFE-MQFNCDSZSA-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
Euphorbia helioscopia	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as jatrophane and cyclojatrophane diterpenoids. These are diterpenoids with a structure based on the jatrophane or the 9,13-jatrophane skeleton. Jatrophane can be derived from casbane by 6,10-cyclization and opening of the cyclopropane. Cyclojatrophane diterpenoids are based on the 9,13-cyclization of the jatrophane skeleton yields the 9,13-cyclojatrophane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Jatrophane and cyclojatrophane diterpenoids

Alternative Parents

Substituents

Jatrophane diterpenoid
Tetracarboxylic acid or derivatives
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Alpha-acyloxy ketone
Monocyclic benzene moiety
Benzenoid
Ketone
Carboxylic acid ester
Cyclic ketone
Carboxylic acid derivative
Carbonyl group
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Organooxygen compound
Aromatic homopolycyclic compound

Molecular Framework

Aromatic homopolycyclic 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	5.38	ChemAxon
pKa (Strongest Acidic)	15.67	ChemAxon
pKa (Strongest Basic)	-5.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	139.34 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	155.84 m³·mol⁻¹	ChemAxon
Polarizability	61.76 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

24865736

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Barile E, Borriello M, Di Pietro A, Doreau A, Fattorusso C, Fattorusso E, Lanzotti V: Discovery of a new series of jatrophane and lathyrane diterpenes as potent and specific P-glycoprotein modulators. Org Biomol Chem. 2008 May 21;6(10):1756-62. doi: 10.1039/b800485d. Epub 2008 Mar 28. [PubMed:18452010 ]
LOTUS database [Link]

Showing NP-Card for (1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate (NP0216586)

MOL for NP0216586 ((1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate)

3D MOL for NP0216586 ((1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate)

3D SDF for NP0216586 ((1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate)

3D-SDF for NP0216586 ((1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate)

PDB for NP0216586 ((1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate)

3D PDB for NP0216586 ((1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate)

SMILES for NP0216586 ((1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate)

INCHI for NP0216586 ((1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate)

Structure for NP0216586 ((1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate)

3D Structure for NP0216586 ((1s,2r,3ar,10s,11s,13as)-3a,10,11-tris(acetyloxy)-2,5,8,8,12-pentamethyl-4,9-dioxo-1h,2h,3h,7h,10h,11h,13ah-cyclopenta[12]annulen-1-yl benzoate)