NP-MRD: Showing NP-Card for 10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol (NP0210610)

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Record Information

Version

2.0

Created at

2022-09-05 08:30:34 UTC

Updated at

2022-09-05 08:30:34 UTC

NP-MRD ID

NP0210610

Secondary Accession Numbers

None

Natural Product Identification

Common Name

10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol

Description

Bisbynin belongs to the class of organic compounds known as pyrans. Pyrans are compounds containing a pyran ring, which is a six-member heterocyclic, non-aromatic ring with five carbon atoms, one oxygen atom and two ring double bonds. Bisbynin is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, bisbynin has been detected, but not quantified in, cereals and cereal products. 10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol is found in Stachybotrys bisbyi. This could make bisbynin a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
    4.7512   -1.1444   -0.7679 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9744   -0.0343   -0.1483 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2371    0.4154    1.2492 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0409    0.5753   -0.8399 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2404    1.6961   -0.2442 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7893    1.2757   -0.3260 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1280    2.1514   -0.8891 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2359    1.0170   -1.6115 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7609   -0.1140   -1.7288 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.5618    0.0051   -2.8503 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6455   -0.0715   -0.5379 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0848   -0.0063    0.6647 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9566   -0.3080    1.8274 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9098   -1.2447    1.5265 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7188   -0.9594    0.4644 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.0518   -0.3457    0.8937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1233   -0.0967   -0.5948 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.4937   -0.4904   -1.8895 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3619    0.3580    0.7982 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1374   -0.7835    0.7466 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2922   -2.1437   -0.5551 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8037   -0.9354   -1.8562 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7975   -1.0875   -0.3789 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5527    1.4909    1.1813 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3245    0.4071    1.8613 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0390   -0.2194    1.6796 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8546    0.2541   -1.8582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5673    1.9460    0.7631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3887    2.5579   -0.9607 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8452    1.1622   -2.5244 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2555   -1.0855   -1.7438 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4817   -0.7890   -3.4414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3708    0.6166    2.2855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2907   -0.7499    2.6102 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9742   -1.9450   -0.0259 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2093    0.6468    0.4164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0452   -0.1403    2.0002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9116   -0.9797    0.5999 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5271    0.9412   -0.4733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1400   -1.2450   -1.8647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4849    0.8380    1.7861 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9221   -1.4354    1.4530 H   0  0  0  0  0  0  0  0  0  0  0  0
 16 15  1  0
 15 14  1  0
 14 13  1  0
 13 12  1  0
 12 11  2  0
 11  9  1  0
  9 10  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  1  6
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
  6 19  1  0
 19 20  1  0
 11 17  1  0
 17 18  1  0
 17 15  1  0
 19 12  1  0
  6  8  1  0
 16 36  1  0
 16 37  1  0
 16 38  1  0
 15 35  1  6
 13 33  1  0
 13 34  1  0
  9 31  1  6
 10 32  1  0
  8 30  1  6
  5 28  1  0
  5 29  1  0
  4 27  1  0
  1 21  1  0
  1 22  1  0
  1 23  1  0
  3 24  1  0
  3 25  1  0
  3 26  1  0
 19 41  1  1
 20 42  1  0
 17 39  1  1
 18 40  1  0
M  END


  Mrv0541 05061312342D          

 20 22  0  0  0  0            999 V2000
    1.4289   -2.0329    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1914   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164    0.1105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0164   -1.3184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  1  1  0  0  0  0
  7  2  1  0  0  0  0
  7  4  2  0  0  0  0
  8  3  1  0  0  0  0
  9  6  1  0  0  0  0
 10  9  2  0  0  0  0
 11  8  1  0  0  0  0
 11 10  1  0  0  0  0
 12 10  1  0  0  0  0
 13  9  1  0  0  0  0
 14 12  1  0  0  0  0
 15  5  1  0  0  0  0
 15 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16 11  1  0  0  0  0
 17 12  1  0  0  0  0
 18 13  1  0  0  0  0
 19  6  1  0  0  0  0
 19  8  1  0  0  0  0
 20 14  1  0  0  0  0
 20 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0210610

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1OCC2=C(C(O)C3OC3(CC=C(C)C)C2O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C15H22O5/c1-7(2)4-5-15-13(18)9-6-19-8(3)11(16)10(9)12(17)14(15)20-15/h4,8,11-14,16-18H,5-6H2,1-3H3

> <INCHI_KEY>
ICHJNTDKHBXTFN-UHFFFAOYSA-N

> <FORMULA>
C15H22O5

> <MOLECULAR_WEIGHT>
282.3322

> <EXACT_MASS>
282.146723814

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
30.161892992409427

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol

> <ALOGPS_LOGP>
-0.24

> <JCHEM_LOGP>
-0.3856206289999996

> <ALOGPS_LOGS>
-1.51

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.420746365590432

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.894434714540878

> <JCHEM_PKA_STRONGEST_BASIC>
-3.449839903750929

> <JCHEM_POLAR_SURFACE_AREA>
82.45

> <JCHEM_REFRACTIVITY>
73.4059

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.74e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       2.667  -3.795   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.357  -2.461   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.667  -1.127   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.897   0.206   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.897  -2.461   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002   3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001   0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       6.668   5.390   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       4.001   5.390   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       8.002   1.540   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1    7                                                            
CONECT    2    7                                                            
CONECT    3    8                                                            
CONECT    4    5    7                                                       
CONECT    5    4   15                                                       
CONECT    6    9   19                                                       
CONECT    7    1    2    4                                                  
CONECT    8    3   11   19                                                  
CONECT    9    6   10   13                                                  
CONECT   10    9   11   12                                                  
CONECT   11    8   10   16                                                  
CONECT   12   10   14   17                                                  
CONECT   13    9   15   18                                                  
CONECT   14   12   15   20                                                  
CONECT   15    5   13   14   20                                             
CONECT   16   11                                                            
CONECT   17   12                                                            
CONECT   18   13                                                            
CONECT   19    6    8                                                       
CONECT   20   14   15                                                       
MASTER        0    0    0    0    0    0    0    0   20    0   44    0
END

View in JSmol

Synonyms

Value	Source
1a,3,5,6,7,7a-Hexahydro-5-methyl-1a-(3-methyl-2-butenyl)-2H-oxireno[g][2]benzopyran-2,6,7-triol, 9ci	HMDB

Chemical Formula

C₁₅H₂₂O₅

Average Mass

282.3322 Da

Monoisotopic Mass

282.14672 Da

IUPAC Name

10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol

Traditional Name

10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol

CAS Registry Number

Not Available

SMILES

CC1OCC2=C(C(O)C3OC3(CC=C(C)C)C2O)C1O

InChI Identifier

InChI=1S/C15H22O5/c1-7(2)4-5-15-13(18)9-6-19-8(3)11(16)10(9)12(17)14(15)20-15/h4,8,11-14,16-18H,5-6H2,1-3H3

InChI Key

ICHJNTDKHBXTFN-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
Stachybotrys bisbyi	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyrans. Pyrans are compounds containing a pyran ring, which is a six-member heterocyclic, non-aromatic ring with five carbon atoms, one oxygen atom and two ring double bonds.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pyrans

Sub Class

Not Available

Direct Parent

Pyrans

Alternative Parents

Substituents

Pyran
Secondary alcohol
Oxacycle
Polyol
Ether
Oxirane
Dialkyl ether
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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
logP	-0.24	ALOGPS
logP	-0.39	ChemAxon
logS	-1.5	ALOGPS
pKa (Strongest Acidic)	12.89	ChemAxon
pKa (Strongest Basic)	-3.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	82.45 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	73.41 m³·mol⁻¹	ChemAxon
Polarizability	30.16 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0041324

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB021244

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

85503029

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol (NP0210610)

MOL for NP0210610 (10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol)

3D MOL for NP0210610 (10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol)

3D SDF for NP0210610 (10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol)

3D-SDF for NP0210610 (10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol)

PDB for NP0210610 (10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol)

3D PDB for NP0210610 (10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol)

SMILES for NP0210610 (10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol)

INCHI for NP0210610 (10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol)

Structure for NP0210610 (10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol)

3D Structure for NP0210610 (10-methyl-5-(3-methylbut-2-en-1-yl)-4,9-dioxatricyclo[5.4.0.0³,⁵]undec-1(7)-ene-2,6,11-triol)