NP-MRD: Showing NP-Card for (1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione (NP0208909)

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Record Information

Version

2.0

Created at

2022-09-05 06:07:07 UTC

Updated at

2022-09-05 06:07:07 UTC

NP-MRD ID

NP0208909

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione

Description

(1S,4R,8S,9S,10R)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]Dodec-2(6)-ene-7,12-dione belongs to the class of organic compounds known as monoterpenoids. Monoterpenoids are compounds containing a chain of two isoprene units. (1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione is found in Hypericum perforatum. Based on a literature review very few articles have been published on (1S,4R,8S,9S,10R)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]Dodec-2(6)-ene-7,12-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052208072D          

 40 42  0  0  1  0            999 V2000
    7.0096   -0.8872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

     RDKit          3D

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M  END


  Mrv1652309052208072D          

 40 42  0  0  1  0            999 V2000
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    5.4259    1.0148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6129    0.8746    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.9587    0.1256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6879    1.6962    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.4757    1.9413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6573    2.7460    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4450    2.9911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0512    2.4315    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6266    3.7959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1600    2.3302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3384    2.4052    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0933    3.1930    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6530    3.7991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4578    3.6175    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0174    4.2236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7029    2.8297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9160    1.4560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6973    1.1913    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9789    0.3467    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.2240   -0.4410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0287   -0.6227    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6643   -1.0472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9094   -1.8349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8595   -0.8656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1573    0.4217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7736   -0.3086    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6294    1.0557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7044    1.8773    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9462    2.2025    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4026    1.5820    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.5810    1.6570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2405    1.7320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5060    0.8354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6561    2.4786    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8248    0.8732    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
  2  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  7  6  1  6  0  0  0
  7  8  1  1  0  0  0
  7  9  1  0  0  0  0
  9 10  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
  9 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 16 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
  7 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
 32 33  2  0  0  0  0
 16 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 36 38  1  0  0  0  0
 36 39  1  0  0  0  0
 35 40  1  0  0  0  0
 32 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0208909

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)C(=O)[C@]12C(=O)C3=C(O[C@H](C3)C(C)(C)O)[C@](CC=C(C)C)(C[C@@H](CC=C(C)C)[C@]1(C)CCC=C(C)C)C2=O

> <INCHI_IDENTIFIER>
InChI=1S/C35H52O5/c1-21(2)13-12-17-33(11)25(15-14-22(3)4)20-34(18-16-23(5)6)30-26(19-27(40-30)32(9,10)39)29(37)35(33,31(34)38)28(36)24(7)8/h13-14,16,24-25,27,39H,12,15,17-20H2,1-11H3/t25-,27-,33+,34+,35-/m1/s1

> <INCHI_KEY>
MGDKDTTZQJLKED-MNVUCGFOSA-N

> <FORMULA>
C35H52O5

> <MOLECULAR_WEIGHT>
552.796

> <EXACT_MASS>
552.381474774

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
92

> <JCHEM_AVERAGE_POLARIZABILITY>
64.560783790496

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,4R,8S,9S,10R)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0^{2,6}]dodec-2(6)-ene-7,12-dione

> <JCHEM_LOGP>
8.157324218333335

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
19.100431933104794

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.297368714694244

> <JCHEM_PKA_STRONGEST_BASIC>
-3.106127934611351

> <JCHEM_POLAR_SURFACE_AREA>
80.67

> <JCHEM_REFRACTIVITY>
165.52

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,4R,8S,9S,10R)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0^{2,6}]dodec-2(6)-ene-7,12-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      13.085  -1.656   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.567  -1.918   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.035  -3.363   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.582  -0.734   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.114   0.711   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.128   1.894   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.611   1.633   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.256   0.234   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.751   3.166   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.221   3.624   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.560   5.126   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.031   5.583   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.162   4.539   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.370   7.086   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.765   4.350   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.232   4.490   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.774   5.960   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.819   7.092   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.321   6.753   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.366   7.884   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.779   5.282   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.310   2.718   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       8.768   2.224   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       7.427   0.647   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       7.885  -0.823   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       9.387  -1.162   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.840  -1.955   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       7.298  -3.425   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.338  -1.616   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.894   0.787   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       5.177  -0.576   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0       4.908   1.971   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       5.048   3.504   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       3.633   4.111   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       2.618   2.953   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.085   3.093   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      -0.449   3.233   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.945   1.559   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       1.225   4.627   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       3.406   1.630   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                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9   24                                             
CONECT    8    7                                                            
CONECT    9    7   10   15                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15    9   16                                                       
CONECT   16   15   17   22   33                                             
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   16   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22    7   25   30                                             
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   24   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   33   40                                                  
CONECT   33   32   16   34                                                  
CONECT   34   33   35                                                       
CONECT   35   34   36   40                                                  
CONECT   36   35   37   38   39                                             
CONECT   37   36                                                            
CONECT   38   36                                                            
CONECT   39   36                                                            
CONECT   40   35   32                                                       
MASTER        0    0    0    0    0    0    0    0   40    0   84    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₅H₅₂O₅

Average Mass

552.7960 Da

Monoisotopic Mass

552.38147 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

CC(C)C(=O)[C@]12C(=O)C3=C(O[C@H](C3)C(C)(C)O)[C@](CC=C(C)C)(C[C@@H](CC=C(C)C)[C@]1(C)CCC=C(C)C)C2=O

InChI Identifier

InChI=1S/C35H52O5/c1-21(2)13-12-17-33(11)25(15-14-22(3)4)20-34(18-16-23(5)6)30-26(19-27(40-30)32(9,10)39)29(37)35(33,31(34)38)28(36)24(7)8/h13-14,16,24-25,27,39H,12,15,17-20H2,1-11H3/t25-,27-,33+,34+,35-/m1/s1

InChI Key

MGDKDTTZQJLKED-MNVUCGFOSA-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
Hypericum perforatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monoterpenoids. Monoterpenoids are compounds containing a chain of two isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Monoterpenoids

Direct Parent

Monoterpenoids

Alternative Parents

Substituents

Monoterpenoid
Cyclohexenone
Vinylogous ester
Tertiary alcohol
Dihydrofuran
Ketone
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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

163078272

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione (NP0208909)

MOL for NP0208909 ((1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione)

3D MOL for NP0208909 ((1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione)

3D SDF for NP0208909 ((1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione)

3D-SDF for NP0208909 ((1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione)

PDB for NP0208909 ((1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione)

3D PDB for NP0208909 ((1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione)

SMILES for NP0208909 ((1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione)

INCHI for NP0208909 ((1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione)

Structure for NP0208909 ((1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione)

3D Structure for NP0208909 ((1s,4r,8s,9s,10r)-4-(2-hydroxypropan-2-yl)-9-methyl-1,10-bis(3-methylbut-2-en-1-yl)-9-(4-methylpent-3-en-1-yl)-8-(2-methylpropanoyl)-3-oxatricyclo[6.3.1.0²,⁶]dodec-2(6)-ene-7,12-dione)