NP-MRD: Showing NP-Card for (1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate (NP0328906)

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Record Information

Version

2.0

Created at

2022-09-12 12:47:11 UTC

Updated at

2022-09-12 12:47:11 UTC

NP-MRD ID

NP0328906

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate

Description

Rabdokaurin C belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D. (1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate is found in Isodon longitubus. Based on a literature review very few articles have been published on Rabdokaurin C.

Structure

MOL SDF PDB SMILES InChI


  Mrv1652309122214472D          

 32 36  0  0  1  0            999 V2000
   -0.9961   -0.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2167    0.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0437    0.8570    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5375    1.4840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3754    1.3964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7588    0.6239    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6825    0.4487    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0318    0.0437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2309   -0.6714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5720   -1.0232    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0353   -1.6497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4824   -1.2333    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8068   -1.9918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3120   -2.6520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6364   -3.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4929   -2.5536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9502   -0.4456    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7290   -0.7910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3252   -1.5104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4073   -1.2606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2705   -0.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1071    0.6752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3352    1.0012    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2108    1.8167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8549    2.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7304    3.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6234    2.0322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2313   -0.1724    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4341   -0.5342    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3214   -1.3515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6708    0.4530    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1878    1.0958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 17 12  1  1  0  0  0
  7 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 10 28  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  6  0  0  0
  2 29  1  0  0  0  0
 29 30  1  6  0  0  0
 28 31  1  0  0  0  0
  3 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END


  Mrv1652309122214472D          

 32 36  0  0  1  0            999 V2000
   -0.9961   -0.2564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2167    0.0141    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0437    0.8570    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5375    1.4840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3754    1.3964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7588    0.6239    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6825    0.4487    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0318    0.0437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2309   -0.6714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5720   -1.0232    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0353   -1.6497    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4824   -1.2333    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8068   -1.9918    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3120   -2.6520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6364   -3.4106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4929   -2.5536    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9502   -0.4456    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7290   -0.7910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3252   -1.5104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4073   -1.2606    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2705   -0.1474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1071    0.6752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3352    1.0012    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.2108    1.8167    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8549    2.3323    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7304    3.1478    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6234    2.0322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2313   -0.1724    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4341   -0.5342    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3214   -1.3515    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6708    0.4530    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1878    1.0958    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  6  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 17 12  1  1  0  0  0
  7 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  7 23  1  0  0  0  0
 23 24  1  1  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  2  0  0  0  0
 10 28  1  0  0  0  0
  6 28  1  0  0  0  0
 28 29  1  6  0  0  0
  2 29  1  0  0  0  0
 29 30  1  6  0  0  0
 28 31  1  0  0  0  0
  3 31  1  0  0  0  0
 31 32  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0328906

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@H]1CCC(C)(C)[C@H]2[C@H](OC(C)=O)[C@@]3(O)OC[C@@]12[C@@H]1CC[C@@H]2[C@@H](O)[C@]31[C@H](O)C2=C

> <INCHI_IDENTIFIER>
InChI=1S/C24H34O8/c1-11-14-6-7-15-22-10-30-24(29,23(15,18(11)27)19(14)28)20(32-13(3)26)17(22)21(4,5)9-8-16(22)31-12(2)25/h14-20,27-29H,1,6-10H2,2-5H3/t14-,15-,16-,17+,18+,19+,20-,22+,23-,24+/m0/s1

> <INCHI_KEY>
APQLBUMPCVAYSP-JSIWZPPOSA-N

> <FORMULA>
C24H34O8

> <MOLECULAR_WEIGHT>
450.528

> <EXACT_MASS>
450.225368055

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
46.630006437533424

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,5S,7R,8R,9S,10S,11R,15S,18R)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecan-10-yl acetate

> <JCHEM_LOGP>
0.5033044049999987

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.80058041935867

> <JCHEM_PKA_STRONGEST_ACIDIC>
10.581803559897404

> <JCHEM_PKA_STRONGEST_BASIC>
-3.1727966649979953

> <JCHEM_POLAR_SURFACE_AREA>
122.52000000000001

> <JCHEM_REFRACTIVITY>
110.7968

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,5S,7R,8R,9S,10S,11R,15S,18R)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1^{5,8}.0^{1,11}.0^{2,8}]octadecan-10-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  C   UNK     0      -1.859  -0.479   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.405   0.026   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.082   1.600   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.003   2.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.567   2.607   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.283   1.165   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.007   0.837   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.793   0.081   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       4.164  -1.253   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       2.934  -1.910   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.933  -3.080   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       4.634  -2.302   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       5.239  -3.718   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.316  -4.950   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.921  -6.366   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       2.787  -4.767   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       5.507  -0.832   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.961  -1.477   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.207  -2.819   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       8.227  -2.353   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.972  -0.275   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.667   1.260   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.226   1.869   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       5.993   3.391   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       7.196   4.354   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.963   5.876   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       8.630   3.794   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       2.298  -0.322   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.810  -0.997   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       0.600  -2.523   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       1.252   0.846   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       2.217   2.046   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   29                                                  
CONECT    3    2    4   31                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   28                                                  
CONECT    7    6    8   17   23                                             
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   28                                             
CONECT   11   10                                                            
CONECT   12   10   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14                                                            
CONECT   17   12    7   18                                                  
CONECT   18   17   19   20   21                                             
CONECT   19   18                                                            
CONECT   20   18                                                            
CONECT   21   18   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22    7   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25                                                            
CONECT   28   10    6   29   31                                             
CONECT   29   28    2   30                                                  
CONECT   30   29                                                            
CONECT   31   28    3   32                                                  
CONECT   32   31                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   72    0
END

View in JSmol

Synonyms

Not Available

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]1CCC(C)(C)[C@H]2[C@H](OC(C)=O)[C@@]3(O)OC[C@@]12[C@@H]1CC[C@@H]2[C@@H](O)[C@]31[C@H](O)C2=C

InChI Identifier

InChI=1S/C24H34O8/c1-11-14-6-7-15-22-10-30-24(29,23(15,18(11)27)19(14)28)20(32-13(3)26)17(22)21(4,5)9-8-16(22)31-12(2)25/h14-20,27-29H,1,6-10H2,2-5H3/t14-,15-,16-,17+,18+,19+,20-,22+,23-,24+/m0/s1

InChI Key

APQLBUMPCVAYSP-JSIWZPPOSA-N

Experimental Spectra

Not Available

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Isodon longitubus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as kaurane diterpenoids. These are diterpene alkaloids with a structure that is based on the kaurane skeleton. Kaurane is a tetracyclic compound that arises by cyclisation of a pimarane precursor followed by rearrangement. It possesses a [3,2,1]-bicyclic ring system with C15-C16 bridge connected to C13, forming the five-membered ring D.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Kaurane diterpenoids

Alternative Parents

Substituents

Kaurane diterpenoid
Dicarboxylic acid or derivatives
Oxane
Cyclic alcohol
Carboxylic acid ester
Hemiacetal
Secondary alcohol
Polyol
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Alcohol
Carbonyl group
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

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

100998514

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate (NP0328906)

MOL for NP0328906 ((1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate)

3D MOL for NP0328906 ((1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate)

3D SDF for NP0328906 ((1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate)

3D-SDF for NP0328906 ((1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate)

PDB for NP0328906 ((1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate)

3D PDB for NP0328906 ((1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate)

SMILES for NP0328906 ((1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate)

INCHI for NP0328906 ((1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate)

Structure for NP0328906 ((1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate)

3D Structure for NP0328906 ((1s,2s,5s,7r,8r,9s,10s,11r,15s,18r)-15-(acetyloxy)-7,9,18-trihydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.1⁵,⁸.0¹,¹¹.0²,⁸]octadecan-10-yl acetate)