NP-MRD: Showing NP-Card for 3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one (NP0239694)

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Record Information

Version

2.0

Created at

2022-09-06 23:20:42 UTC

Updated at

2022-09-06 23:20:43 UTC

NP-MRD ID

NP0239694

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one

Description

Aspulvinone O belongs to the class of organic compounds known as resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3. 3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one was first documented in 2019 (PMID: 31470862). Based on a literature review very few articles have been published on Aspulvinone O (PMID: 30602325).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072201202D          

 33 35  0  0  0  0            999 V2000
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -1.7224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1830   -3.1745    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1526   -3.9282    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3323   -4.5956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0032   -5.3493    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8237   -5.4355    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1593   -6.1892    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9798   -6.2754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6744   -6.8566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1528   -4.5094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6377   -5.1768    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4884   -3.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0034   -3.0882    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3390   -2.3346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7376   -1.4675    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    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
   -2.1434    1.2375    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
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  5  6  1  0  0  0  0
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 17 23  2  0  0  0  0
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  8 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
  6 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END

     RDKit          3D

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   -6.7317    0.4859   -1.4313 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6291    1.6184   -0.8001 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4510    2.7878   -1.3733 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8127    1.8747    0.3845 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7868   -1.1061    1.1969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1580   -1.0191    1.3331 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9683   -1.2977    2.2813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5852   -1.3789    2.0943 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.8094    1.4628    0.3803 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END


  Mrv1652309072201202D          

 33 35  0  0  0  0            999 V2000
   -2.1434    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
> <DATABASE_ID>
NP0239694

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=CC(C=C2OC(=O)C(=C2O)C2=CC(CC=C(C)C)=C(O)C=C2O)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C27H28O6/c1-15(2)5-8-18-11-17(7-10-21(18)28)12-24-26(31)25(27(32)33-24)20-13-19(9-6-16(3)4)22(29)14-23(20)30/h5-7,10-14,28-31H,8-9H2,1-4H3

> <INCHI_KEY>
IAHWCROWFXOMDG-UHFFFAOYSA-N

> <FORMULA>
C27H28O6

> <MOLECULAR_WEIGHT>
448.515

> <EXACT_MASS>
448.188588622

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
50.27064269623404

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}-2,5-dihydrofuran-2-one

> <JCHEM_LOGP>
5.903639308000001

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.71221821094261

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.6058473507823505

> <JCHEM_PKA_STRONGEST_BASIC>
-5.762422934993261

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
132.55129999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one

> <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      -4.001   6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.580  -3.215   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       2.104  -4.680   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       3.009  -5.926   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       0.564  -4.680   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.342  -5.926   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.285  -7.333   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.620  -8.578   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.006  -9.985   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.538 -10.146   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.164 -11.553   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.696 -11.714   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.259 -12.799   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.152  -8.417   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -3.057  -9.663   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.778  -7.011   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.873  -5.765   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -2.499  -4.358   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       0.088  -3.215   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.377  -2.739   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      -4.001   2.310   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   32                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   30                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   28                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   28                                                  
CONECT   15   14   16   26                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   23                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   17   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   15   27                                                  
CONECT   27   26                                                            
CONECT   28   14   10   29                                                  
CONECT   29   28                                                            
CONECT   30    8   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31    6   33                                                  
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   70    0
END

View in JSmol

Synonyms

Value	Source
3-(2,4-Dihydroxy-5-(3-methyl-2-buten-1-yl) phenyl)-4-hydroxy-5-((4-hydroxy-3-(3-methyl-2-buten-1-yl) phenyl) methylene)-2(5H)-furanone	MeSH

Chemical Formula

C₂₇H₂₈O₆

Average Mass

448.5150 Da

Monoisotopic Mass

448.18859 Da

IUPAC Name

3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}-2,5-dihydrofuran-2-one

Traditional Name

3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=CC(C=C2OC(=O)C(=C2O)C2=CC(CC=C(C)C)=C(O)C=C2O)=CC=C1O

InChI Identifier

InChI=1S/C27H28O6/c1-15(2)5-8-18-11-17(7-10-21(18)28)12-24-26(31)25(27(32)33-24)20-13-19(9-6-16(3)4)22(29)14-23(20)30/h5-7,10-14,28-31H,8-9H2,1-4H3

InChI Key

IAHWCROWFXOMDG-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as resorcinols. Resorcinols are compounds containing a resorcinol moiety, which is a benzene ring bearing two hydroxyl groups at positions 1 and 3.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Resorcinol
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
2-furanone
Dihydrofuran
Enol ester
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Carboxylic acid ester
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Enol
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxygen compound
Organic oxide
Carbonyl group
Organooxygen compound
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	5.9	ChemAxon
pKa (Strongest Acidic)	6.61	ChemAxon
pKa (Strongest Basic)	-5.8	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	132.55 m³·mol⁻¹	ChemAxon
Polarizability	50.27 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	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

78435902

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

76178391

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Sun W, Luan S, Qi C, Tong Q, Yan S, Li H, Zhang Y: Aspulvinone O, a natural inhibitor of GOT1 suppresses pancreatic ductal adenocarcinoma cells growth by interfering glutamine metabolism. Cell Commun Signal. 2019 Aug 30;17(1):111. doi: 10.1186/s12964-019-0425-4. [PubMed:31470862 ]
Hamed A, Abdel-Razek AS, Omran DA, El-Metwally MM, El-Hosari DG, Frese M, Soliman HSM, Sewald N, Shaaban M: Terretonin O: a new meroterpenoid from Aspergillus terreus. Nat Prod Res. 2020 Apr;34(7):965-974. doi: 10.1080/14786419.2018.1544977. Epub 2019 Jan 3. [PubMed:30602325 ]
LOTUS database [Link]

Showing NP-Card for 3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one (NP0239694)

MOL for NP0239694 (3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one)

3D MOL for NP0239694 (3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one)

3D SDF for NP0239694 (3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one)

3D-SDF for NP0239694 (3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one)

PDB for NP0239694 (3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one)

3D PDB for NP0239694 (3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one)

SMILES for NP0239694 (3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one)

INCHI for NP0239694 (3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one)

Structure for NP0239694 (3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one)

3D Structure for NP0239694 (3-[2,4-dihydroxy-5-(3-methylbut-2-en-1-yl)phenyl]-4-hydroxy-5-{[4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl]methylidene}furan-2-one)