NP-MRD: Showing NP-Card for (1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate (NP0304310)

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Record Information

Version

2.0

Created at

2022-09-10 19:18:46 UTC

Updated at

2022-09-10 19:18:46 UTC

NP-MRD ID

NP0304310

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate

Description

(3S,4S,6S,9R,11S,12S,14S)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]Hexadeca-1,7-dien-6-yl acetate belongs to the class of organic compounds known as taxanes and derivatives. These are diterpenoids with a structure based either on the taxane skeleton, or a derivative thereof. In term of phytochemistry, several derivatives of the taxane skeleton exist: 2(3->20)-Abeotaxane, 3,11-cyclotaxane, 11(15->1),11(10->9)-abeotaxane, 3,8-seco-taxane, and 11(15->1)-abeotaxane, among others. More complex skeletons have been found recently, which include the taxane-derived [3.3.3] Propellane ring system. (1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate is found in Taxus baccata. Based on a literature review very few articles have been published on (3S,4S,6S,9R,11S,12S,14S)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]Hexadeca-1,7-dien-6-yl acetate.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309102221182D          

 32 34  0  0  1  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  1  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  2  0  0  0  0  0  0  0  0  0
    2.2539    0.6039    0.0000 C   0  0  1  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
    2.2539    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    2.0329    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  2  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
    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  2  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
    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
    4.3164   -1.5395    0.0000 C   0  0  1  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
    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  2  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
  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  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
  7 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 16 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 14 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END


  Mrv1652309102221182D          

 32 34  0  0  1  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  1  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  2  0  0  0  0  0  0  0  0  0
    2.2539    0.6039    0.0000 C   0  0  1  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
    2.2539    2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8414    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0789    2.0329    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  2  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
    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  2  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
    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
    4.3164   -1.5395    0.0000 C   0  0  1  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
    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  2  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
  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  1  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  2  0  0  0  0
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  6  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
  7 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 16 28  1  0  0  0  0
 28 29  1  6  0  0  0
 28 30  1  0  0  0  0
 30 31  1  0  0  0  0
 14 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0304310

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1C[C@@H]2[C@@H](OC(C)=O)\C=C3/C[C@@](C)([C@@H](O)C[C@@H]3O)C(=O)[C@H](O)C(=C1C)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C24H34O8/c1-11-17(31-12(2)25)8-15-18(32-13(3)26)7-14-10-24(6,19(28)9-16(14)27)22(30)21(29)20(11)23(15,4)5/h7,15-19,21,27-29H,8-10H2,1-6H3/b14-7+/t15-,16+,17+,18+,19+,21-,24+/m1/s1

> <INCHI_KEY>
CYDOOPFWDIWLOT-ZDKNXHBOSA-N

> <FORMULA>
C24H34O8

> <MOLECULAR_WEIGHT>
450.528

> <EXACT_MASS>
450.225368055

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.15970125402319

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1E,3S,4S,6S,9R,11S,12S,14S)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1^{4,8}]hexadeca-1,7-dien-6-yl acetate

> <JCHEM_LOGP>
0.45648865999999955

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.304425524243467

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.996962009382838

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0089931451960563

> <JCHEM_POLAR_SURFACE_AREA>
130.36

> <JCHEM_REFRACTIVITY>
115.55859999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1E,3S,4S,6S,9R,11S,12S,14S)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1^{4,8}]hexadeca-1,7-dien-6-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 10-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-SEP-22         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       4.207   3.795   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.437   5.128   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       5.747   3.795   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       5.747   1.127   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.517  -0.206   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.747  -1.540   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.517  -2.874   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.287  -4.207   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.747  -4.207   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.517  -5.541   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       4.207  -4.207   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       3.437  -5.541   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       3.437  -2.874   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.897  -2.874   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.127  -4.207   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.207  -1.540   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.567  -2.263   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       5.567  -0.817   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       8.057  -2.874   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       8.827  -4.207   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       8.827  -1.540   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.057  -0.206   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       8.827   1.127   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   23                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   25                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13    8   14                                                       
CONECT   14   13   15   31                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18   28                                             
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22    5   24                                                  
CONECT   24   23                                                            
CONECT   25   22    7   26   27                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   16   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   14   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
(3S,4S,6S,9R,11S,12S,14S)-3-(Acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1,]hexadeca-1,7-dien-6-yl acetic acid	Generator

Chemical Formula

C₂₄H₃₄O₈

Average Mass

450.5280 Da

Monoisotopic Mass

450.22537 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@H]1C[C@@H]2[C@@H](OC(C)=O)\C=C3/C[C@@](C)([C@@H](O)C[C@@H]3O)C(=O)[C@H](O)C(=C1C)C2(C)C

InChI Identifier

InChI=1S/C24H34O8/c1-11-17(31-12(2)25)8-15-18(32-13(3)26)7-14-10-24(6,19(28)9-16(14)27)22(30)21(29)20(11)23(15,4)5/h7,15-19,21,27-29H,8-10H2,1-6H3/b14-7+/t15-,16+,17+,18+,19+,21-,24+/m1/s1

InChI Key

CYDOOPFWDIWLOT-ZDKNXHBOSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Taxus baccata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as taxanes and derivatives. These are diterpenoids with a structure based either on the taxane skeleton, or a derivative thereof. In term of phytochemistry, several derivatives of the taxane skeleton exist: 2(3->20)-Abeotaxane, 3,11-cyclotaxane, 11(15->1),11(10->9)-abeotaxane, 3,8-seco-taxane, and 11(15->1)-abeotaxane, among others. More complex skeletons have been found recently, which include the taxane-derived [3.3.3] Propellane ring system.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Taxanes and derivatives

Alternative Parents

Substituents

Taxane diterpenoid
Dicarboxylic acid or derivatives
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid ester
Polyol
Carboxylic acid derivative
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

External Links

HMDB ID

Not Available

DrugBank ID

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Phenol Explorer Compound ID

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FoodDB ID

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KNApSAcK ID

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Chemspider ID

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KEGG Compound ID

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BioCyc ID

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BiGG ID

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Wikipedia Link

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METLIN ID

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PubChem Compound

163094053

PDB ID

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ChEBI ID

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Good Scents ID

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References

General References

LOTUS database [Link]

Showing NP-Card for (1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate (NP0304310)

MOL for NP0304310 ((1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate)

3D MOL for NP0304310 ((1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate)

3D SDF for NP0304310 ((1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate)

3D-SDF for NP0304310 ((1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate)

PDB for NP0304310 ((1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate)

3D PDB for NP0304310 ((1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate)

SMILES for NP0304310 ((1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate)

INCHI for NP0304310 ((1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate)

Structure for NP0304310 ((1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate)

3D Structure for NP0304310 ((1e,3s,4s,6s,9r,11s,12s,14s)-3-(acetyloxy)-9,12,14-trihydroxy-7,11,16,16-tetramethyl-10-oxotricyclo[9.3.1.1⁴,⁸]hexadeca-1,7-dien-6-yl acetate)