NP-MRD: Showing NP-Card for 5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one (NP0161563)

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Record Information

Version

2.0

Created at

2022-09-02 19:46:20 UTC

Updated at

2022-09-02 19:46:20 UTC

NP-MRD ID

NP0161563

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one

Description

5-(1,2-Dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]Dodeca-1(12),8,10-trien-3-one belongs to the class of organic compounds known as coumarans. Coumarans are compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 2,3-dihydrofuran ring. 5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one is found in Sargassum spinuligerum. Based on a literature review very few articles have been published on 5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]Dodeca-1(12),8,10-trien-3-one.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 33 35  0  0  0  0  0  0  0  0999 V2000
   -0.3901    0.9357   -2.6738 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3389    0.6512   -1.6943 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6042    1.0971   -1.3427 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6810    1.1360    0.0675 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0674    0.7624    0.4816 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9411    1.7079   -0.1009 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4993   -0.5855   -0.0512 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8234   -0.8183    0.3211 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6029    0.2952    0.6271 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.0088   -0.6898    1.4974 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4334    1.0257    1.2503 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6694    0.5474    0.8509 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9529    0.7436    1.3752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0242    0.1324    0.7620 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3047    0.3044    1.2529 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8212   -0.6576   -0.3500 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5544   -0.8502   -0.8661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3338   -1.6469   -1.9908 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4690   -0.2366   -0.2523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0412   -0.3019   -0.6246 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4121   -1.5775   -0.8551 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5428    2.2177    0.3594 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2291    0.8264    1.5746 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9868    1.5109   -1.0899 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5015   -0.5384   -1.1680 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9014   -1.4206    0.3364 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3144    0.0081    0.5457 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6620   -1.5773    1.1874 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0534    1.3755    2.2522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9180    1.0678    0.9362 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6430   -1.1615   -0.8681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1340   -2.0908   -2.4318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3742   -2.1926   -0.7988 H   0  0  0  0  0  0  0  0  0  0  0  0
  8  7  1  0
  7  5  1  0
  5  6  1  0
  5  4  1  0
  4  3  1  0
  3  2  1  0
  2  1  2  0
  2 20  1  0
 20 21  1  6
 20 19  1  0
 19 17  2  0
 17 18  1  0
 17 16  1  0
 16 14  2  0
 14 15  1  0
 14 13  1  0
 13 12  2  0
 12 11  1  0
 11  9  1  0
  9 10  1  1
  9  4  1  0
  9 20  1  0
 12 19  1  0
  8 27  1  0
  7 25  1  0
  7 26  1  0
  5 23  1  1
  6 24  1  0
  4 22  1  1
 21 33  1  0
 18 32  1  0
 16 31  1  0
 15 30  1  0
 13 29  1  0
 10 28  1  0
M  END


  Mrv1652309022221462D          

 21 23  0  0  0  0            999 V2000
    2.4230   -2.6863    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4068   -1.8614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7299   -1.3898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9693   -0.6003    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4713    0.0575    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7920    0.8176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6527   -0.0449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1547    0.6128    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7942   -0.5840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5238    0.1954    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4519   -0.0860    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1288   -0.5577    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9322   -0.3703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4962   -0.9724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2997   -0.7850    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2568   -1.7619    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4534   -1.9493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2139   -2.7388    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8894   -1.3472    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0645   -1.3635    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3349   -2.1429    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
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  2  0  0  0  0
 12 19  1  0  0  0  0
 19 20  1  0  0  0  0
  2 20  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0161563

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OCC(O)C1OC(=O)C2(O)C3=C(O)C=C(O)C=C3OC12O

> <INCHI_IDENTIFIER>
InChI=1S/C12H12O9/c13-3-6(16)9-12(19)11(18,10(17)20-9)8-5(15)1-4(14)2-7(8)21-12/h1-2,6,9,13-16,18-19H,3H2

> <INCHI_KEY>
CNGYVGSYKOQCPS-UHFFFAOYSA-N

> <FORMULA>
C12H12O9

> <MOLECULAR_WEIGHT>
300.219

> <EXACT_MASS>
300.048131966

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
33

> <JCHEM_AVERAGE_POLARIZABILITY>
26.555145643053336

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-trien-3-one

> <ALOGPS_LOGP>
-1.13

> <JCHEM_LOGP>
-1.3807510193333332

> <ALOGPS_LOGS>
-0.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.537790388216344

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.876267771105788

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9772793420193073

> <JCHEM_POLAR_SURFACE_AREA>
156.91

> <JCHEM_REFRACTIVITY>
62.9871

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.02e+02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-trien-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  O   UNK     0       4.523  -5.014   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.493  -3.475   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       3.229  -2.594   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       3.676  -1.121   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.746   0.107   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       3.345   1.526   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       1.218  -0.084   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       0.289   1.144   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       5.216  -1.090   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.711   0.365   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0       6.444  -0.161   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       7.707  -1.041   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.207  -0.691   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.260  -1.815   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      11.759  -1.465   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       9.813  -3.289   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.313  -3.639   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       7.866  -5.112   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       7.260  -2.515   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.720  -2.545   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       6.225  -4.000   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3   20                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    9                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7                                                            
CONECT    9    4   10   11   20                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   19                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   12   20                                                  
CONECT   20   19    2    9   21                                             
CONECT   21   20                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₂H₁₂O₉

Average Mass

300.2190 Da

Monoisotopic Mass

300.04813 Da

IUPAC Name

5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-trien-3-one

Traditional Name

5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0^{2,6}]dodeca-1(12),8,10-trien-3-one

CAS Registry Number

Not Available

SMILES

OCC(O)C1OC(=O)C2(O)C3=C(O)C=C(O)C=C3OC12O

InChI Identifier

InChI=1S/C12H12O9/c13-3-6(16)9-12(19)11(18,10(17)20-9)8-5(15)1-4(14)2-7(8)21-12/h1-2,6,9,13-16,18-19H,3H2

InChI Key

CNGYVGSYKOQCPS-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
Sargassum spinuligerum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarans. Coumarans are compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 2,3-dihydrofuran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Coumarans

Sub Class

Not Available

Direct Parent

Coumarans

Alternative Parents

Substituents

Coumaran
Furofuran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Benzenoid
Gamma butyrolactone
Tetrahydrofuran
Tertiary alcohol
Carboxylic acid ester
Secondary alcohol
Hemiacetal
Lactone
Carboxylic acid derivative
Oxacycle
Polyol
Monocarboxylic acid or derivatives
Alcohol
Organooxygen compound
Primary alcohol
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
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	-1.1	ALOGPS
logP	-1.4	ChemAxon
logS	-0.17	ALOGPS
pKa (Strongest Acidic)	8.88	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	156.91 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	62.99 m³·mol⁻¹	ChemAxon
Polarizability	26.56 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	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

76427590

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one (NP0161563)

MOL for NP0161563 (5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one)

3D MOL for NP0161563 (5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one)

3D SDF for NP0161563 (5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one)

3D-SDF for NP0161563 (5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one)

PDB for NP0161563 (5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one)

3D PDB for NP0161563 (5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one)

SMILES for NP0161563 (5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one)

INCHI for NP0161563 (5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one)

Structure for NP0161563 (5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one)

3D Structure for NP0161563 (5-(1,2-dihydroxyethyl)-2,6,10,12-tetrahydroxy-4,7-dioxatricyclo[6.4.0.0²,⁶]dodeca-1(12),8,10-trien-3-one)