NP-MRD: Showing NP-Card for 11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate (NP0242080)

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Record Information

Version

2.0

Created at

2022-09-07 02:18:10 UTC

Updated at

2022-09-07 02:18:10 UTC

NP-MRD ID

NP0242080

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate

Description

11-(Acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]Hexadeca-1(16),2,4,6,12,14-hexaen-8-yl benzoate belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit. 11-(Acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]Hexadeca-1(16),2,4,6,12,14-hexaen-8-yl benzoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004251510042D          

 42 45  0  0  0  0            999 V2000
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    3.9633    0.6398    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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 41 42  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1533004251510042D          

 42 45  0  0  0  0            999 V2000
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    3.2011   -0.5009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9980   -0.7145    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2115   -1.5114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0084   -1.7249    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5918   -1.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6282   -2.0947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8417   -2.8916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6386   -3.1051    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8313   -1.8812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2479   -2.4646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6178   -1.0843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7928   -1.0843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5792   -1.8812    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9538   -2.6163    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7823   -2.0947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5688   -2.8916    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2281   -3.1051    0.0000 C   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  2  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  2  0  0  0  0
  8 10  1  0  0  0  0
  6 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
 13 15  1  0  0  0  0
 13 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 20 25  1  0  0  0  0
 16 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 28 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 31 34  1  0  0  0  0
 34 35  1  0  0  0  0
 34 36  2  0  0  0  0
 26 36  1  0  0  0  0
 36 37  1  0  0  0  0
  5 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
  3 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0242080

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC2=C(C(O)=C1OC)C1=C(O)C(OC)=C(OC)C=C1C(OC(=O)C1=CC=CC=C1)C(C)(O)C(C)C2OC(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H34O11/c1-15-26(41-16(2)32)18-13-20(37-4)27(39-6)24(33)22(18)23-19(14-21(38-5)28(40-7)25(23)34)29(31(15,3)36)42-30(35)17-11-9-8-10-12-17/h8-15,26,29,33-34,36H,1-7H3

> <INCHI_KEY>
FJCBKSYUDCSWLR-UHFFFAOYSA-N

> <FORMULA>
C31H34O11

> <MOLECULAR_WEIGHT>
582.602

> <EXACT_MASS>
582.210111915

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
76

> <JCHEM_AVERAGE_POLARIZABILITY>
59.064326375597545

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2,4,6,13,15-hexaen-8-yl benzoate

> <ALOGPS_LOGP>
4.20

> <JCHEM_LOGP>
3.921915417666666

> <ALOGPS_LOGS>
-4.57

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.889136011532138

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.046621243088145

> <JCHEM_PKA_STRONGEST_BASIC>
-3.4163539953129227

> <JCHEM_POLAR_SURFACE_AREA>
150.21

> <JCHEM_REFRACTIVITY>
150.868

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.55e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2,4,6,13,15-hexaen-8-yl benzoate

> <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      -2.205  -2.131   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.116  -3.220   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.371  -2.821   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.770  -1.334   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.258  -0.935   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.258   0.605   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       0.835   1.194   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       0.634   2.721   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.789   3.310   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       1.856   3.659   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.346   1.694   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.757   3.117   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.886   1.694   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.488   3.181   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       6.220   2.464   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.975   0.605   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       7.398   1.194   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.599   2.721   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       6.377   3.659   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       9.022   3.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.223   4.837   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.646   5.427   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.868   4.489   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      11.667   2.962   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.244   2.373   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.975  -0.935   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       7.463  -1.334   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.862  -2.821   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       9.349  -3.220   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      10.438  -2.131   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.773  -3.910   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       7.171  -5.398   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       8.659  -5.796   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       5.285  -3.512   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0       4.196  -4.601   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       4.886  -2.024   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       3.346  -2.024   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       2.948  -3.512   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       3.647  -4.884   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       1.460  -3.910   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       1.062  -5.398   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0      -0.426  -5.796   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   40                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   37                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8                                                            
CONECT   11    6   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   15   16                                             
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   13   17   26                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   25                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   20                                                       
CONECT   26   16   27   36                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29   31                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   28   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32                                                            
CONECT   34   31   35   36                                                  
CONECT   35   34                                                            
CONECT   36   34   26   37                                                  
CONECT   37   36    5   38                                                  
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38    3   41                                                  
CONECT   41   40   42                                                       
CONECT   42   41                                                            
MASTER        0    0    0    0    0    0    0    0   42    0   90    0
END

View in JSmol

Synonyms

Value	Source
11-(Acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0,]hexadeca-1(16),2,4,6,12,14-hexaen-8-yl benzoic acid	Generator
11-(Acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(16),2,4,6,12,14-hexaen-8-yl benzoic acid	Generator

Chemical Formula

C₃₁H₃₄O₁₁

Average Mass

582.6020 Da

Monoisotopic Mass

582.21011 Da

IUPAC Name

11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2,4,6,13,15-hexaen-8-yl benzoate

Traditional Name

11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2,4,6,13,15-hexaen-8-yl benzoate

CAS Registry Number

Not Available

SMILES

COC1=CC2=C(C(O)=C1OC)C1=C(O)C(OC)=C(OC)C=C1C(OC(=O)C1=CC=CC=C1)C(C)(O)C(C)C2OC(C)=O

InChI Identifier

InChI=1S/C31H34O11/c1-15-26(41-16(2)32)18-13-20(37-4)27(39-6)24(33)22(18)23-19(14-21(38-5)28(40-7)25(23)34)29(31(15,3)36)42-30(35)17-11-9-8-10-12-17/h8-15,26,29,33-34,36H,1-7H3

InChI Key

FJCBKSYUDCSWLR-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as hydrolyzable tannins. These are tannins with a structure characterized by either of the following models. In model 1, the structure contains galloyl units (in some cases, shikimic acid units) that are linked to diverse polyol carbohydrate-, catechin-, or triterpenoid units. In model 2, contains at least two galloyl units C-C coupled to each other, and do not contain a glycosidically linked catechin unit.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Tannins

Sub Class

Hydrolyzable tannins

Direct Parent

Hydrolyzable tannins

Alternative Parents

Substituents

Hydrolyzable tannin
Dibenzocyclooctane lignan
Benzoate ester
Benzoic acid or derivatives
Anisole
Benzoyl
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Dicarboxylic acid or derivatives
Tertiary alcohol
Carboxylic acid ester
Polyol
Ether
Carboxylic acid derivative
Hydrocarbon derivative
Alcohol
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen 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
logP	4.2	ALOGPS
logP	3.92	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	9.05	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	150.21 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	150.87 m³·mol⁻¹	ChemAxon
Polarizability	59.06 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

73319570

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate (NP0242080)

MOL for NP0242080 (11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate)

3D MOL for NP0242080 (11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate)

3D SDF for NP0242080 (11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate)

3D-SDF for NP0242080 (11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate)

PDB for NP0242080 (11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate)

3D PDB for NP0242080 (11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate)

SMILES for NP0242080 (11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate)

INCHI for NP0242080 (11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate)

Structure for NP0242080 (11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate)

3D Structure for NP0242080 (11-(acetyloxy)-3,9,16-trihydroxy-4,5,14,15-tetramethoxy-9,10-dimethyltricyclo[10.4.0.0²,⁷]hexadeca-1(12),2(7),3,5,13,15-hexaen-8-yl benzoate)