NP-MRD: Showing NP-Card for (1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate (NP0291322)

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Record Information

Version

2.0

Created at

2022-09-09 22:22:08 UTC

Updated at

2022-09-09 22:22:08 UTC

NP-MRD ID

NP0291322

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate

Description

CHEMBL338319 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. (1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate is found in Taxus cuspidata. Based on a literature review very few articles have been published on CHEMBL338319.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309102200222D          

 58 63  0  0  1  0            999 V2000
    4.8045    2.3012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9601    1.4910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7396    1.2207    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.3634    1.7606    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    5.4283    2.8411    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8316    3.1106    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6760    3.9208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2998    4.4607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1442    5.2709    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
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  9 10  2  0  0  0  0
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  9 14  1  0  0  0  0
  3 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
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 19  2  1  6  0  0  0
 19 20  1  0  0  0  0
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 25 26  1  1  0  0  0
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M  END

     RDKit          3D

108113  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309102200222D          

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M  END
> <DATABASE_ID>
NP0291322

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=O)O[C@@H]1[C@@H]2CC(=O)C(C)=C([C@@H](OC(=O)\C=C\C3=CC=CC=C3)[C@H](OC(=O)\C=C\C3=CC=CC=C3)[C@]3(C)CC[C@H](OC(=O)\C=C\C4=CC=CC=C4)C(=C)[C@@H]13)C2(C)C

> <INCHI_IDENTIFIER>
InChI=1S/C49H50O9/c1-31-38(51)30-37-45(55-33(3)50)44-32(2)39(56-40(52)25-22-34-16-10-7-11-17-34)28-29-49(44,6)47(58-42(54)27-24-36-20-14-9-15-21-36)46(43(31)48(37,4)5)57-41(53)26-23-35-18-12-8-13-19-35/h7-27,37,39,44-47H,2,28-30H2,1,3-6H3/b25-22+,26-23+,27-24+/t37-,39-,44-,45+,46+,47-,49+/m0/s1

> <INCHI_KEY>
PCZGAGIIBAOCAI-UUGOILRDSA-N

> <FORMULA>
C49H50O9

> <MOLECULAR_WEIGHT>
782.93

> <EXACT_MASS>
782.34548319

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
108

> <JCHEM_AVERAGE_POLARIZABILITY>
85.77026514700981

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,3R,5S,8R,9R,10R)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2E)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0^{3,8}]pentadec-11-en-5-yl (2E)-3-phenylprop-2-enoate

> <JCHEM_LOGP>
10.039233161999999

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
18.484527995475574

> <JCHEM_PKA_STRONGEST_BASIC>
-5.887498461001402

> <JCHEM_POLAR_SURFACE_AREA>
122.27000000000001

> <JCHEM_REFRACTIVITY>
222.45969999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,3R,5S,8R,9R,10R)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2E)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0^{3,8}]pentadec-11-en-5-yl (2E)-3-phenylprop-2-enoate

> <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       8.968   4.296   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.259   2.783   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      10.714   2.279   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      11.878   3.286   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      11.588   4.799   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      10.133   5.303   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      12.752   5.807   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.462   7.319   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      13.626   8.327   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      13.336   9.839   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.500  10.847   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      15.955  10.342   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      16.246   8.830   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      15.081   7.822   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.004   0.766   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.840  -0.241   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.385   0.263   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.843  -1.207   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.094   1.775   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.740   2.662   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       7.080   4.164   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       5.949   5.210   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.478   4.753   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       6.289   6.712   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       5.125   2.443   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       3.533   2.727   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       2.422   1.606   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.920   1.945   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       2.945   0.118   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       1.896  -1.009   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       4.505  -0.309   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.870  -1.199   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       5.523  -2.699   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       6.648  -3.750   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       8.122  -3.301   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       6.301  -5.251   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       7.427  -6.302   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       7.079  -7.802   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       8.205  -8.853   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.857 -10.353   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.384 -10.803   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.259  -9.752   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       5.606  -8.251   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.456  -1.003   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0       8.235  -2.332   0.000  0.00  0.00           O+0
HETATM   46  C   UNK     0       9.775  -2.321   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0      10.536  -0.982   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0      10.554  -3.650   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      12.094  -3.639   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      12.873  -4.968   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      14.413  -4.957   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      15.192  -6.286   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      14.431  -7.624   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      12.891  -7.635   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      12.112  -6.306   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0       4.937   1.040   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0       6.200   0.159   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0       6.456   1.294   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   19                                                  
CONECT    3    2    4   15                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    9                                                       
CONECT   15    3   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19   44                                             
CONECT   18   17                                                            
CONECT   19   17    2   20                                                  
CONECT   20   19   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   20   26   56                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32   56                                                  
CONECT   32   31   33   44                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39   43                                                  
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   38                                                       
CONECT   44   32   17   45                                                  
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51   55                                                  
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   50                                                       
CONECT   56   31   25   57   58                                             
CONECT   57   56                                                            
CONECT   58   56                                                            
MASTER        0    0    0    0    0    0    0    0   58    0  126    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₉H₅₀O₉

Average Mass

782.9300 Da

Monoisotopic Mass

782.34548 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(=O)O[C@@H]1[C@@H]2CC(=O)C(C)=C([C@@H](OC(=O)\C=C\C3=CC=CC=C3)[C@H](OC(=O)\C=C\C3=CC=CC=C3)[C@]3(C)CC[C@H](OC(=O)\C=C\C4=CC=CC=C4)C(=C)[C@@H]13)C2(C)C

InChI Identifier

InChI=1S/C49H50O9/c1-31-38(51)30-37-45(55-33(3)50)44-32(2)39(56-40(52)25-22-34-16-10-7-11-17-34)28-29-49(44,6)47(58-42(54)27-24-36-20-14-9-15-21-36)46(43(31)48(37,4)5)57-41(53)26-23-35-18-12-8-13-19-35/h7-27,37,39,44-47H,2,28-30H2,1,3-6H3/b25-22+,26-23+,27-24+/t37-,39-,44-,45+,46+,47-,49+/m0/s1

InChI Key

PCZGAGIIBAOCAI-UUGOILRDSA-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
Taxus cuspidata	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
Tetracarboxylic acid or derivatives
Cinnamic acid or derivatives
Cinnamic acid ester
Styrene
Cyclohexenone
Fatty acid ester
Fatty acyl
Benzenoid
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Cyclic ketone
Carboxylic acid ester
Ketone
Carboxylic acid derivative
Organic oxide
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxygen 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

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

23207906

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44351436

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate (NP0291322)

MOL for NP0291322 ((1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate)

3D MOL for NP0291322 ((1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate)

3D SDF for NP0291322 ((1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate)

3D-SDF for NP0291322 ((1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate)

PDB for NP0291322 ((1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate)

3D PDB for NP0291322 ((1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate)

SMILES for NP0291322 ((1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate)

INCHI for NP0291322 ((1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate)

Structure for NP0291322 ((1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate)

3D Structure for NP0291322 ((1r,2r,3r,5s,8r,9r,10r)-2-(acetyloxy)-8,12,15,15-tetramethyl-4-methylidene-13-oxo-9,10-bis({[(2e)-3-phenylprop-2-enoyl]oxy})tricyclo[9.3.1.0³,⁸]pentadec-11-en-5-yl (2e)-3-phenylprop-2-enoate)