NP-MRD: Showing NP-Card for (1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione (NP0244129)

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Record Information

Version

2.0

Created at

2022-09-07 04:50:24 UTC

Updated at

2022-09-07 04:50:24 UTC

NP-MRD ID

NP0244129

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione

Description

(1R,2R,4R,6Z,8S,9R)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]Undecane-5,7-dione belongs to the class of organic compounds known as oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms. Based on a literature review very few articles have been published on (1R,2R,4R,6Z,8S,9R)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]Undecane-5,7-dione.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072206502D          

 38 41  0  0  1  0            999 V2000
   -3.0450    0.3635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4890    0.9730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.1272    1.4058    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3214    1.2291    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2590    1.9161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1125    1.7393    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0982    2.5642    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8055    2.9890    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7912    3.8139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4985    4.2386    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0697    4.2140    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9565    1.9448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 36 37  1  0  0  0  0
  8 37  1  0  0  0  0
 27 37  1  0  0  0  0
 37 38  1  1  0  0  0
M  END

     RDKit          3D

 80 83  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309072206502D          

 38 41  0  0  1  0            999 V2000
   -3.0450    0.3635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    2.9219   -0.0223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4913    0.2575    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8377   -0.4913    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3624   -1.1656    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7087   -1.9144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2334   -2.5887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5303   -1.9888    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6987   -0.2083    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0735    0.3324    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7474   -0.1434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4136    0.6382    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1306    0.9451    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9294    1.1516    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
  8 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  2  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
 19 24  1  0  0  0  0
 16 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  1  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 27 33  1  0  0  0  0
 33 34  1  0  0  0  0
  6 34  1  0  0  0  0
 34 35  1  1  0  0  0
 34 36  1  0  0  0  0
 36 37  1  0  0  0  0
  8 37  1  0  0  0  0
 27 37  1  0  0  0  0
 37 38  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0244129

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(=C)CC[C@@H]1C[C@]2(CC=C(C)C)C(=O)\C(=C(\O)C3=CC=CC=C3)C(=O)[C@]3(CC=C(C)C)C[C@@]1(C)O[C@]23O

> <INCHI_IDENTIFIER>
InChI=1S/C33H42O5/c1-21(2)13-14-25-19-31(17-15-22(3)4)28(35)26(27(34)24-11-9-8-10-12-24)29(36)32(18-16-23(5)6)20-30(25,7)38-33(31,32)37/h8-12,15-16,25,34,37H,1,13-14,17-20H2,2-7H3/b27-26-/t25-,30-,31-,32+,33-/m1/s1

> <INCHI_KEY>
YSWMOTQKYHHEFG-WEXSKNODSA-N

> <FORMULA>
C33H42O5

> <MOLECULAR_WEIGHT>
518.694

> <EXACT_MASS>
518.303224452

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
80

> <JCHEM_AVERAGE_POLARIZABILITY>
58.94860215294955

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,2R,4R,6Z,8S,9R)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0^{4,9}]undecane-5,7-dione

> <JCHEM_LOGP>
7.6045406006666685

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
11.124946930885413

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.1312470242303805

> <JCHEM_PKA_STRONGEST_BASIC>
-4.392468029058539

> <JCHEM_POLAR_SURFACE_AREA>
83.83

> <JCHEM_REFRACTIVITY>
153.16040000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1R,2R,4R,6Z,8S,9R)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0^{4,9}]undecane-5,7-dione

> <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      -5.684   0.678   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.646   1.816   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -5.113   3.284   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.142   1.486   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.104   2.624   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.600   2.294   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.483   3.577   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.077   3.247   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.050   4.787   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.370   5.579   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.344   7.119   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.664   7.912   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.997   7.866   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.652   3.630   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.046   5.119   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.799   2.549   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.287   2.947   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.375   1.858   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       6.685   4.435   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.596   5.524   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.995   7.011   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.482   7.410   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       8.571   6.321   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       8.173   4.833   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.342   1.023   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.454  -0.042   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       2.784   0.481   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       3.430  -0.917   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.543  -2.176   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       3.190  -3.574   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       2.302  -4.832   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       4.723  -3.713   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       1.304  -0.389   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      -0.137   0.621   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.395  -0.268   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0       0.772   1.191   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0       2.111   1.764   0.000  0.00  0.00           C+0
HETATM   38  O   UNK     0       3.602   2.150   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   34                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14   37                                             
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11                                                            
CONECT   14    8   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   25                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19                                                       
CONECT   25   16   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   33   37                                             
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
CONECT   33   27   34                                                       
CONECT   34   33    6   35   36                                             
CONECT   35   34                                                            
CONECT   36   34   37                                                       
CONECT   37   36    8   27   38                                             
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₄₂O₅

Average Mass

518.6940 Da

Monoisotopic Mass

518.30322 Da

IUPAC Name

(1R,2R,4R,6Z,8S,9R)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0^{4,9}]undecane-5,7-dione

Traditional Name

(1R,2R,4R,6Z,8S,9R)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0^{4,9}]undecane-5,7-dione

CAS Registry Number

Not Available

SMILES

CC(=C)CC[C@@H]1C[C@]2(CC=C(C)C)C(=O)\C(=C(\O)C3=CC=CC=C3)C(=O)[C@]3(CC=C(C)C)C[C@@]1(C)O[C@]23O

InChI Identifier

InChI=1S/C33H42O5/c1-21(2)13-14-25-19-31(17-15-22(3)4)28(35)26(27(34)24-11-9-8-10-12-24)29(36)32(18-16-23(5)6)20-30(25,7)38-33(31,32)37/h8-12,15-16,25,34,37H,1,13-14,17-20H2,2-7H3/b27-26-/t25-,30-,31-,32+,33-/m1/s1

InChI Key

YSWMOTQKYHHEFG-WEXSKNODSA-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 oxanes. Oxanes are compounds containing an oxane (tetrahydropyran) ring, which is a six-member saturated aliphatic heterocycle with one oxygen atom and five carbon atoms.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Oxanes

Sub Class

Not Available

Direct Parent

Oxanes

Alternative Parents

Substituents

Monocyclic benzene moiety
Benzenoid
Oxane
Cyclic alcohol
Vinylogous acid
Tetrahydrofuran
Hemiacetal
Ketone
Enol
Oxacycle
Hydrocarbon derivative
Organic oxide
Carbonyl group
Organic oxygen compound
Organooxygen compound
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	7.6	ChemAxon
pKa (Strongest Acidic)	6.13	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	83.83 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	153.16 m³·mol⁻¹	ChemAxon
Polarizability	58.95 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	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

163194873

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,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione (NP0244129)

MOL for NP0244129 ((1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione)

3D MOL for NP0244129 ((1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione)

3D SDF for NP0244129 ((1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione)

3D-SDF for NP0244129 ((1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione)

PDB for NP0244129 ((1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione)

3D PDB for NP0244129 ((1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione)

SMILES for NP0244129 ((1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione)

INCHI for NP0244129 ((1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione)

Structure for NP0244129 ((1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione)

3D Structure for NP0244129 ((1r,2r,4r,6z,8s,9r)-9-hydroxy-6-[hydroxy(phenyl)methylidene]-1-methyl-4,8-bis(3-methylbut-2-en-1-yl)-2-(3-methylbut-3-en-1-yl)-10-oxatricyclo[6.2.1.0⁴,⁹]undecane-5,7-dione)