NP-MRD: Showing NP-Card for 5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione (NP0307574)

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Record Information

Version

2.0

Created at

2022-09-11 00:47:18 UTC

Updated at

2022-09-11 00:47:19 UTC

NP-MRD ID

NP0307574

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione

Description

Bambamalone A belongs to the class of organic compounds known as naphthols and derivatives. These are naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position. 5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione is found in Bombax ceiba. Based on a literature review very few articles have been published on Bambamalone A.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 40  0  0  0  0  0  0  0  0999 V2000
    4.7156    0.1742   -0.0757 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6567   -0.6967    0.1067 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3070   -0.4282    0.0931 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8784    0.7932    0.3843 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4711    2.0219    0.7466 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4779    2.9912    0.9528 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6246    4.1850    1.2881 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1854    2.3579    0.7069 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1387    2.7101    0.7568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5342    3.9909    1.1081 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0915    1.7739    0.4533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8383    0.4450    0.0775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8674   -0.5064   -0.3856 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4106   -1.4887    0.5949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0528   -0.7227   -1.8455 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4640    0.1248    0.0438 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4628    1.0723    0.3647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0399   -1.2175   -0.2993 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9120   -2.0506   -0.6337 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4135   -1.5516   -0.2421 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8610   -2.1845   -1.5283 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5325   -2.4999    0.8300 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7385    0.6859   -1.0597 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7820    0.9736    0.6926 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6632   -0.4087    0.0149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8925    4.7328    1.3511 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1232    2.0803    0.5181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8030    0.2743   -0.2673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5953   -2.4995    0.0945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6878   -1.6573    1.4598 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3631   -1.2775    1.0907 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0873   -0.3561   -2.2288 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0955   -1.7653   -2.2053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4006   -0.0486   -2.4522 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0285   -2.7104   -2.0467 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6499   -2.9436   -1.2508 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3030   -1.4698   -2.2485 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6461   -2.9040    1.0004 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  8  9  1  0
  9 10  1  0
  9 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 12 16  2  0
 16 17  1  0
 16 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 20 22  1  1
 20  3  1  0
 17  4  1  0
 17  8  2  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 10 26  1  0
 11 27  1  0
 13 28  1  0
 14 29  1  0
 14 30  1  0
 14 31  1  0
 15 32  1  0
 15 33  1  0
 15 34  1  0
 21 35  1  0
 21 36  1  0
 21 37  1  0
 22 38  1  0
M  END


  Mrv1652309112202472D          

 22 24  0  0  0  0            999 V2000
   -0.4835    0.2931    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2702    0.6287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9377    0.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6913    0.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9463    1.2639    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7713    1.2639    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2562    1.9314    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0262    0.4793    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7799    0.1437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4473    0.6287    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8661   -0.6767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1987   -1.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3141   -1.9785    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0793   -2.2870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6644   -2.4869    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2725   -0.8261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3588   -0.0056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5189   -1.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4326   -1.9821    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -0.6767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3435   -1.3268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0284   -0.6192    0.0000 O   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  2  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 12 16  1  0  0  0  0
 16 17  2  0  0  0  0
  8 17  1  0  0  0  0
  4 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
  3 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0307574

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2OC(=O)C3=C(O)C=C(C(C)C)C(=C23)C(=O)C1(C)O

> <INCHI_IDENTIFIER>
InChI=1S/C16H16O6/c1-6(2)7-5-8(17)10-11-9(7)13(18)16(3,20)14(21-4)12(11)22-15(10)19/h5-6,17,20H,1-4H3

> <INCHI_KEY>
JYUFSZQBCUGFJN-UHFFFAOYSA-N

> <FORMULA>
C16H16O6

> <MOLECULAR_WEIGHT>
304.298

> <EXACT_MASS>
304.094688235

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
30.422611478355837

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,10-dihydroxy-11-methoxy-10-methyl-7-(propan-2-yl)-2-oxatricyclo[6.3.1.0^{4,12}]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione

> <JCHEM_LOGP>
1.7911427756666662

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
11.8793837011918

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.644679334320681

> <JCHEM_PKA_STRONGEST_BASIC>
-4.179813624842454

> <JCHEM_POLAR_SURFACE_AREA>
93.06000000000002

> <JCHEM_REFRACTIVITY>
79.9663

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0^{4,12}]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.902   0.547   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.504   1.174   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       1.750   0.268   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.157   0.895   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       3.633   2.359   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       5.173   2.359   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       6.078   3.605   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.649   0.895   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.056   0.268   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       8.302   1.174   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       7.217  -1.263   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.971  -2.168   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.186  -3.693   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.615  -4.269   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.973  -4.642   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.242  -1.542   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.403  -0.010   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.835  -2.168   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.674  -3.700   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.589  -1.263   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.641  -2.477   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.053  -1.156   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   20                                                  
CONECT    4    3    5   17                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9   17                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   16                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   12   17   18                                                  
CONECT   17   16    8    4                                                  
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    3   21   22                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   48    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₆H₁₆O₆

Average Mass

304.2980 Da

Monoisotopic Mass

304.09469 Da

IUPAC Name

5,10-dihydroxy-11-methoxy-10-methyl-7-(propan-2-yl)-2-oxatricyclo[6.3.1.0^{4,12}]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione

Traditional Name

5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0^{4,12}]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione

CAS Registry Number

Not Available

SMILES

COC1=C2OC(=O)C3=C(O)C=C(C(C)C)C(=C23)C(=O)C1(C)O

InChI Identifier

InChI=1S/C16H16O6/c1-6(2)7-5-8(17)10-11-9(7)13(18)16(3,20)14(21-4)12(11)22-15(10)19/h5-6,17,20H,1-4H3

InChI Key

JYUFSZQBCUGFJN-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

Species Name	Source	Reference
Bombax ceiba	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as naphthols and derivatives. These are naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Naphthalenes

Sub Class

Naphthols and derivatives

Direct Parent

Naphthols and derivatives

Alternative Parents

Substituents

2-naphthol
Isobenzofuranone
Cumene
Isocoumaran
Aryl ketone
Aryl alkyl ketone
1-hydroxy-2-unsubstituted benzenoid
Phenol
Acyloin
Enol ester
Tertiary alcohol
Vinylogous acid
Lactone
Ketone
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
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	1.79	ChemAxon
pKa (Strongest Acidic)	7.64	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	93.06 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	79.97 m³·mol⁻¹	ChemAxon
Polarizability	30.42 Å³	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

23311433

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

23642715

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione (NP0307574)

MOL for NP0307574 (5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione)

3D MOL for NP0307574 (5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione)

3D SDF for NP0307574 (5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione)

3D-SDF for NP0307574 (5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione)

PDB for NP0307574 (5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione)

3D PDB for NP0307574 (5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione)

SMILES for NP0307574 (5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione)

INCHI for NP0307574 (5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione)

Structure for NP0307574 (5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione)

3D Structure for NP0307574 (5,10-dihydroxy-7-isopropyl-11-methoxy-10-methyl-2-oxatricyclo[6.3.1.0⁴,¹²]dodeca-1(11),4,6,8(12)-tetraene-3,9-dione)