NP-MRD: Showing NP-Card for 3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate (NP0226806)

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Record Information

Version

2.0

Created at

2022-09-06 05:57:45 UTC

Updated at

2022-09-06 05:57:45 UTC

NP-MRD ID

NP0226806

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate

Description

3,14-Bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]Hexadec-4-en-6-yl acetate belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups. 3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate is found in Taxus canadensis. 3,14-Bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]Hexadec-4-en-6-yl acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004251510142D          

 35 37  0  0  0  0            999 V2000
   -1.4586   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5539   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9664   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9664   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9824   -1.2123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9824   -0.4377    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  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
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 13 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
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  2  0  0  0  0
  5 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 33  1  0  0  0  0
  7 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
M  END


  Mrv1533004251510142D          

 35 37  0  0  0  0            999 V2000
   -1.4586   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6336   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2211   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    1.3184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3164   -0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7289   -2.2539    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5539   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9664   -1.5395    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9664   -2.9684    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4914   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -2.9684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -3.6829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789   -3.6829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -4.3974    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.5395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6039   -2.2539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2539   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9824   -1.2123    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9824   -0.4377    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
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  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
 11 17  1  0  0  0  0
 17 18  1  0  0  0  0
 15 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 13 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
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 25 30  1  0  0  0  0
 30 31  2  0  0  0  0
  5 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 33  1  0  0  0  0
  7 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0226806

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)OC1CC2C(O)CC3CC(C)(C(CC3O)OC(C)=O)C(=O)C(OC(C)=O)C(=C1C)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C26H38O9/c1-12-20(33-13(2)27)9-17-19(31)8-16-11-26(7,21(10-18(16)30)34-14(3)28)24(32)23(35-15(4)29)22(12)25(17,5)6/h16-21,23,30-31H,8-11H2,1-7H3

> <INCHI_KEY>
BGSQOZCYBNXKPC-UHFFFAOYSA-N

> <FORMULA>
C26H38O9

> <MOLECULAR_WEIGHT>
494.581

> <EXACT_MASS>
494.251582804

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
73

> <JCHEM_AVERAGE_POLARIZABILITY>
51.5076143039107

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate

> <ALOGPS_LOGP>
1.42

> <JCHEM_LOGP>
1.0693323616666661

> <ALOGPS_LOGS>
-3.24

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.581747510553207

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.609752071622339

> <JCHEM_PKA_STRONGEST_BASIC>
-2.840369270752344

> <JCHEM_POLAR_SURFACE_AREA>
136.43

> <JCHEM_REFRACTIVITY>
124.09109999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.86e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 25-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-APR-15         0                                  
HETATM    1  C   UNK     0      -2.723  -0.206   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.183  -0.206   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      -0.413   1.127   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -0.413  -1.540   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.127  -1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.897  -0.206   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.437  -0.206   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.207   1.127   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       3.437   2.461   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.747   1.127   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.517  -0.206   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.747  -1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.517  -2.874   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.287  -4.207   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.057  -2.874   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.827  -1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.057  -0.206   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.827   1.127   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       8.827  -4.207   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      10.367  -4.207   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      11.137  -2.874   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      11.137  -5.541   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.747  -4.207   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.517  -5.541   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       4.207  -4.207   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       3.437  -5.541   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       4.207  -6.875   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.747  -6.875   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       3.437  -8.208   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.437  -2.874   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.897  -2.874   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.127  -4.207   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.207  -1.540   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.567  -2.263   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       5.567  -0.817   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   31                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   33                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   17                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   15   23                                             
CONECT   14   13                                                            
CONECT   15   13   16   19                                                  
CONECT   16   15   17                                                       
CONECT   17   16   11   18                                                  
CONECT   18   17                                                            
CONECT   19   15   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   13   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26   30                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   25   31   33                                                  
CONECT   31   30    5   32                                                  
CONECT   32   31                                                            
CONECT   33   30    7   34   35                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
MASTER        0    0    0    0    0    0    0    0   35    0   74    0
END

View in JSmol

Synonyms

Value	Source
3,14-Bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1,]hexadec-4-en-6-yl acetic acid	Generator
3,14-Bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetic acid	Generator

Chemical Formula

C₂₆H₃₈O₉

Average Mass

494.5810 Da

Monoisotopic Mass

494.25158 Da

IUPAC Name

3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate

Traditional Name

3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate

CAS Registry Number

Not Available

SMILES

CC(=O)OC1CC2C(O)CC3CC(C)(C(CC3O)OC(C)=O)C(=O)C(OC(C)=O)C(=C1C)C2(C)C

InChI Identifier

InChI=1S/C26H38O9/c1-12-20(33-13(2)27)9-17-19(31)8-16-11-26(7,21(10-18(16)30)34-14(3)28)24(32)23(35-15(4)29)22(12)25(17,5)6/h16-21,23,30-31H,8-11H2,1-7H3

InChI Key

BGSQOZCYBNXKPC-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Taxus canadensis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as tricarboxylic acids and derivatives. These are carboxylic acids containing exactly three carboxyl groups.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Tricarboxylic acids and derivatives

Direct Parent

Tricarboxylic acids and derivatives

Alternative Parents

Substituents

Tricarboxylic acid or derivatives
Alpha-acyloxy ketone
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic 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	1.42	ALOGPS
logP	1.07	ChemAxon
logS	-3.2	ALOGPS
pKa (Strongest Acidic)	11.61	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	136.43 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	124.09 m³·mol⁻¹	ChemAxon
Polarizability	51.51 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

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 3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate (NP0226806)

MOL for NP0226806 (3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate)

3D MOL for NP0226806 (3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate)

3D SDF for NP0226806 (3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate)

3D-SDF for NP0226806 (3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate)

PDB for NP0226806 (3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate)

3D PDB for NP0226806 (3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate)

SMILES for NP0226806 (3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate)

INCHI for NP0226806 (3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate)

Structure for NP0226806 (3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate)

3D Structure for NP0226806 (3,14-bis(acetyloxy)-9,12-dihydroxy-1,5,16,16-tetramethyl-2-oxotricyclo[9.3.1.1⁴,⁸]hexadec-4-en-6-yl acetate)