NP-MRD: Showing NP-Card for 7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate (NP0245252)

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Record Information

Version

1.0

Created at

2022-09-07 06:16:02 UTC

Updated at

2022-09-07 06:16:02 UTC

NP-MRD ID

NP0245252

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate

Description

Triptogelin B-1 belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene). 7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate is found in Celastrus orbiculatus and Tripterygium wilfordii. Based on a literature review very few articles have been published on Triptogelin B-1.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072208162D          

 39 43  0  0  1  0            999 V2000
    0.5136    2.0613    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0881    1.4352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3227    2.2472    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2928    0.5305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0239   -0.2540    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.3646    0.0846    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7712    0.8510    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1102    1.5748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7256    1.7189    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3856    1.2603    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9361   -0.0583    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  1  0  0  0  0
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  8 10  1  0  0  0  0
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  5 35  1  0  0  0  0
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 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
  6 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
M  END

     RDKit          3D

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M  END


  Mrv1652309072208162D          

 39 43  0  0  1  0            999 V2000
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    2.1725   -1.3095    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1802   -2.1746    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6291   -0.6520    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.9217   -1.2071    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1713   -0.7591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1853   -1.5644    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6909   -0.8061    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
  5  4  1  1  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  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
  7 17  1  0  0  0  0
 17 18  1  1  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 21 26  1  0  0  0  0
 17 27  1  0  0  0  0
 27 28  1  1  0  0  0
 27 29  1  0  0  0  0
 29 30  1  1  0  0  0
 29 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  1  0  0  0
 33 35  1  0  0  0  0
  5 35  1  0  0  0  0
 27 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
  6 37  1  0  0  0  0
 37 38  1  0  0  0  0
 37 39  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0245252

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C[C@@H]1CC[C@H](O)[C@@]2(C)[C@@H]([C@@H]([C@@H]3[C@@H](OC(C)=O)[C@]12OC3(C)C)C(=O)OC1=CC=CC=C1)C(=O)OC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C31H36O8/c1-18-16-17-22(33)30(5)25(28(35)38-21-14-10-7-11-15-21)23(27(34)37-20-12-8-6-9-13-20)24-26(36-19(2)32)31(18,30)39-29(24,3)4/h6-15,18,22-26,33H,16-17H2,1-5H3/t18-,22+,23-,24-,25+,26-,30+,31-/m1/s1

> <INCHI_KEY>
SDYCRMLRIREUOM-FQKKMNGFSA-N

> <FORMULA>
C31H36O8

> <MOLECULAR_WEIGHT>
536.621

> <EXACT_MASS>
536.241018119

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
75

> <JCHEM_AVERAGE_POLARIZABILITY>
56.392837299216055

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7,8-diphenyl (1S,2R,5S,6R,7R,8R,9R,12R)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecane-7,8-dicarboxylate

> <JCHEM_LOGP>
4.189892765666666

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
17.261298441555837

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.585938976155251

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9789333327499126

> <JCHEM_POLAR_SURFACE_AREA>
108.36000000000003

> <JCHEM_REFRACTIVITY>
140.02790000000005

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
7,8-diphenyl (1S,2R,5S,6R,7R,8R,9R,12R)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecane-7,8-dicarboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0       0.959   3.848   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       2.031   2.679   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       2.469   4.195   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0       2.413   0.990   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.911  -0.474   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.681   0.158   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.439   1.588   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.206   2.940   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       0.372   4.811   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -1.354   3.209   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -2.586   2.353   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.390   0.825   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.614  -0.109   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -5.035   0.484   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -5.232   2.012   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -4.008   2.946   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       3.034   1.662   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.835   3.360   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.326   4.271   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       3.560   5.249   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       5.107   5.767   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.156   7.306   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.514   8.033   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       7.822   7.221   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.773   5.682   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       6.415   4.955   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       3.812   0.238   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.121   1.435   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.363   0.374   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.025   0.581   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       6.248  -0.893   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.606  -2.302   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       4.055  -2.444   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       4.070  -4.059   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       3.041  -1.217   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       1.721  -2.253   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       0.320  -1.417   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      -0.346  -2.920   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      -1.290  -1.505   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   35                                                  
CONECT    6    5    7   37                                                  
CONECT    7    6    8   17                                                  
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17    7   18   27                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   26                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   21                                                       
CONECT   27   17   28   29   35                                             
CONECT   28   27                                                            
CONECT   29   27   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35                                                  
CONECT   34   33                                                            
CONECT   35   33    5   27   36                                             
CONECT   36   35   37                                                       
CONECT   37   36    6   38   39                                             
CONECT   38   37                                                            
CONECT   39   37                                                            
MASTER        0    0    0    0    0    0    0    0   39    0   86    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₁H₃₆O₈

Average Mass

536.6210 Da

Monoisotopic Mass

536.24102 Da

IUPAC Name

7,8-diphenyl (1S,2R,5S,6R,7R,8R,9R,12R)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecane-7,8-dicarboxylate

Traditional Name

7,8-diphenyl (1S,2R,5S,6R,7R,8R,9R,12R)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0^{1,6}]dodecane-7,8-dicarboxylate

CAS Registry Number

Not Available

SMILES

C[C@@H]1CC[C@H](O)[C@@]2(C)[C@@H]([C@@H]([C@@H]3[C@@H](OC(C)=O)[C@]12OC3(C)C)C(=O)OC1=CC=CC=C1)C(=O)OC1=CC=CC=C1

InChI Identifier

InChI=1S/C31H36O8/c1-18-16-17-22(33)30(5)25(28(35)38-21-14-10-7-11-15-21)23(27(34)37-20-12-8-6-9-13-20)24-26(36-19(2)32)31(18,30)39-29(24,3)4/h6-15,18,22-26,33H,16-17H2,1-5H3/t18-,22+,23-,24-,25+,26-,30+,31-/m1/s1

InChI Key

SDYCRMLRIREUOM-FQKKMNGFSA-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
Celastrus orbiculatus	LOTUS Database	35616633
Tripterygium wilfordii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as agarofurans. These are organic compounds containing an agarofuran moiety( a three-ring system, with core fragment oxatricyclo[7.2.1.0^{1,6}]Dodec-2-ene).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Agarofurans

Alternative Parents

Substituents

Agarofuran
Phenol ester
Tricarboxylic acid or derivatives
Phenoxy compound
Oxepane
Benzenoid
Monocyclic benzene moiety
Tetrahydrofuran
Cyclic alcohol
Secondary alcohol
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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
logP	4.19	ChemAxon
pKa (Strongest Acidic)	14.59	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	108.36 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	140.03 m³·mol⁻¹	ChemAxon
Polarizability	56.39 Å³	ChemAxon
Number of Rings	5	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

101589351

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate (NP0245252)

MOL for NP0245252 (7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate)

3D MOL for NP0245252 (7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate)

3D SDF for NP0245252 (7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate)

3D-SDF for NP0245252 (7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate)

PDB for NP0245252 (7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate)

3D PDB for NP0245252 (7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate)

SMILES for NP0245252 (7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate)

INCHI for NP0245252 (7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate)

Structure for NP0245252 (7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate)

3D Structure for NP0245252 (7,8-diphenyl (1s,2r,5s,6r,7r,8r,9r,12r)-12-(acetyloxy)-5-hydroxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.0¹,⁶]dodecane-7,8-dicarboxylate)