NP-MRD: Showing NP-Card for 4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate (NP0182953)

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Record Information

Version

2.0

Created at

2022-09-03 21:46:54 UTC

Updated at

2022-09-03 21:46:54 UTC

NP-MRD ID

NP0182953

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate

Description

4,4',7'',7'',12'',16''-Hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-Pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecane]-6''-yl acetate belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety. 4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate is found in Abies pinsapo. 4,4',7'',7'',12'',16''-Hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-Pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]Octadecane]-6''-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004181501232D          

 37 43  0  0  0  0            999 V2000
    8.0281    2.2525    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2701    1.9269    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.2664    1.0469    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5919    0.2889    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9716   -0.2550    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0470   -1.0765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2626    0.1669    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0804   -0.6377    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2589   -0.7131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9333    0.0450    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3732   -0.5608    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1521    0.3102    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5318   -0.2336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7506    0.0317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0754    3.2550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4448    0.9715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9408    1.8050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5611    2.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4858    3.1704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
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  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
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  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 11 13  1  0  0  0  0
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 23 24  1  0  0  0  0
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 13 25  1  0  0  0  0
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 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
  8 28  1  0  0  0  0
 11 28  1  0  0  0  0
 28 29  1  0  0  0  0
 20 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
  8 34  1  0  0  0  0
  4 34  1  0  0  0  0
  4 35  1  0  0  0  0
 35 36  1  0  0  0  0
  2 36  1  0  0  0  0
 36 37  2  0  0  0  0
M  END

     RDKit          3D

 85 91  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1533004181501232D          

 37 43  0  0  0  0            999 V2000
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    1.5898    0.8408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.6478    1.9153    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2681    2.4592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0493    2.1939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2101    1.3847    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8305    1.9286    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9913    1.1194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6116    1.6633    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3928    1.3980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5537    0.5888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0474    1.2498    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1334    2.1806    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2943    2.9898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0754    3.2550    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3261    3.5336    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4448    0.9715    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9408    1.8050    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5611    2.3489    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4858    3.1704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  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
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 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
 17 19  1  0  0  0  0
 17 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 16 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 13 25  1  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
 27 28  1  0  0  0  0
  8 28  1  0  0  0  0
 11 28  1  0  0  0  0
 28 29  1  0  0  0  0
 20 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 31 33  1  0  0  0  0
  8 34  1  0  0  0  0
  4 34  1  0  0  0  0
  4 35  1  0  0  0  0
 35 36  1  0  0  0  0
  2 36  1  0  0  0  0
 36 37  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0182953

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC2(CC(C)C3(CCC4(C)C5CCC6C7(CC57CCC34C)CCC(OC(C)=O)C6(C)C)O2)OC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C32H48O5/c1-19-16-31(36-25(19)34)17-20(2)32(37-31)15-12-27(6)23-9-8-22-26(4,5)24(35-21(3)33)10-11-29(22)18-30(23,29)14-13-28(27,32)7/h19-20,22-24H,8-18H2,1-7H3

> <INCHI_KEY>
ACMCWGMBFMGKAF-UHFFFAOYSA-N

> <FORMULA>
C32H48O5

> <MOLECULAR_WEIGHT>
512.731

> <EXACT_MASS>
512.350174646

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
85

> <JCHEM_AVERAGE_POLARIZABILITY>
60.00280292364579

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecane]-6''-yl acetate

> <ALOGPS_LOGP>
5.39

> <JCHEM_LOGP>
6.041115849333332

> <ALOGPS_LOGS>
-7.03

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
7

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.387182793110221

> <JCHEM_POLAR_SURFACE_AREA>
61.830000000000005

> <JCHEM_REFRACTIVITY>
139.83239999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
4.76e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecane]-6''-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0      14.986   4.205   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.571   3.597   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.231   2.095   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.697   1.954   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      12.305   0.539   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      11.147  -0.476   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.288  -2.010   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.824   0.312   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.483  -1.190   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.950  -1.331   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       7.342   0.084   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.297  -1.047   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.884   0.579   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.726  -0.436   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.268   0.059   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.968   1.570   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.509   2.065   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.275   0.543   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.030   2.031   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       1.209   3.575   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.367   4.590   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.825   4.095   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.126   2.585   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       5.284   3.600   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.584   2.090   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.742   3.105   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       8.200   2.610   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.500   1.099   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       9.422   2.333   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      -0.249   4.070   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      -0.549   5.581   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      -2.007   6.076   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       0.609   6.596   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      10.164   1.814   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      11.089   3.369   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      12.247   4.385   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      12.107   5.918   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   36                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   34   35                                             
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   28   34                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13   28                                             
CONECT   12   11                                                            
CONECT   13   11   14   25                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   23                                                  
CONECT   17   16   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17   21   30                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   16   24   25                                             
CONECT   24   23   25                                                       
CONECT   25   24   13   23   26                                             
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27    8   11   29                                             
CONECT   29   28                                                            
CONECT   30   20   31                                                       
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31                                                            
CONECT   34    8    4                                                       
CONECT   35    4   36                                                       
CONECT   36   35    2   37                                                  
CONECT   37   36                                                            
MASTER        0    0    0    0    0    0    0    0   37    0   86    0
END

View in JSmol

Synonyms

Value	Source
4,4',7'',7'',12'',16''-Hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0,.0,.0,]octadecane]-6''-yl acetic acid	Generator
4,4',7'',7'',12'',16''-Hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecane]-6''-yl acetic acid	Generator

Chemical Formula

C₃₂H₄₈O₅

Average Mass

512.7310 Da

Monoisotopic Mass

512.35017 Da

IUPAC Name

4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecane]-6''-yl acetate

Traditional Name

4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecane]-6''-yl acetate

CAS Registry Number

Not Available

SMILES

CC1CC2(CC(C)C3(CCC4(C)C5CCC6C7(CC57CCC34C)CCC(OC(C)=O)C6(C)C)O2)OC1=O

InChI Identifier

InChI=1S/C32H48O5/c1-19-16-31(36-25(19)34)17-20(2)32(37-31)15-12-27(6)23-9-8-22-26(4,5)24(35-21(3)33)10-11-29(22)18-30(23,29)14-13-28(27,32)7/h19-20,22-24H,8-18H2,1-7H3

InChI Key

ACMCWGMBFMGKAF-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
Abies pinsapo	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cycloartanols and derivatives. These are steroids containing a cycloartanol moiety.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cycloartanols and derivatives

Direct Parent

Cycloartanols and derivatives

Alternative Parents

Substituents

Cycloartanol-skeleton
9b,19-cyclo-lanostane-skeleton
Cycloartane-skeleton
Triterpenoid
Withanolide-skeleton
Steroid lactone
Steroid ester
Ketal
Dicarboxylic acid or derivatives
Gamma butyrolactone
Tetrahydrofuran
Lactone
Carboxylic acid ester
Acetal
Oxacycle
Organoheterocyclic compound
Carboxylic acid derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Carbonyl group
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	5.39	ALOGPS
logP	6.04	ChemAxon
logS	-7	ALOGPS
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	61.83 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	139.83 m³·mol⁻¹	ChemAxon
Polarizability	60 Å³	ChemAxon
Number of Rings	7	ChemAxon
Bioavailability	No	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

73797072

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate (NP0182953)

MOL for NP0182953 (4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate)

3D MOL for NP0182953 (4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate)

3D SDF for NP0182953 (4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate)

3D-SDF for NP0182953 (4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate)

PDB for NP0182953 (4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate)

3D PDB for NP0182953 (4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate)

SMILES for NP0182953 (4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate)

INCHI for NP0182953 (4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate)

Structure for NP0182953 (4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate)

3D Structure for NP0182953 (4,4',7'',7'',12'',16''-hexamethyl-5-oxodispiro[bis(oxolane)-2,2':5',15''-pentacyclo[9.7.0.0¹,³.0³,⁸.0¹²,¹⁶]octadecan]-6''-yl acetate)