NP-MRD: Showing NP-Card for (2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one (NP0264553)

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Record Information

Version

2.0

Created at

2022-09-08 08:07:12 UTC

Updated at

2022-09-08 08:07:12 UTC

NP-MRD ID

NP0264553

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one

Description

Disulfuretin belongs to the class of organic compounds known as aurone flavonoids. These are flavonoids containing a 2-Benzylidene-1-benzofuran-3-one based core. Aurone flavonoids provide the bright yellow color of some important ornamental flowers, such as snapdragon (Antirrhinum majus). (2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one is found in Cotinus coggygria. (2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one was first documented in 2000 (PMID: 11141121). Based on a literature review very few articles have been published on Disulfuretin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082210072D          

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M  END

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M  END


  Mrv1652309082210072D          

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 30 32  2  0  0  0  0
 25 32  1  0  0  0  0
  3 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 34 40  1  0  0  0  0
  2 40  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0264553

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C2C(O\C(=C(/C(=C3\OC4=CC(O)=CC=C4C3=O)/C3=CC=C(O)C(O)=C3)\C3=CC=C(O)C(O)=C3)C2=O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C30H18O10/c31-15-3-5-17-23(11-15)39-29(27(17)37)25(13-1-7-19(33)21(35)9-13)26(14-2-8-20(34)22(36)10-14)30-28(38)18-6-4-16(32)12-24(18)40-30/h1-12,31-36H/b29-25-,30-26-

> <INCHI_KEY>
MZVYXDUSVXNKLC-IDDWGTJGSA-N

> <FORMULA>
C30H18O10

> <MOLECULAR_WEIGHT>
538.464

> <EXACT_MASS>
538.08999678

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
58

> <JCHEM_AVERAGE_POLARIZABILITY>
53.853603738930566

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2Z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2Z)-6-hydroxy-3-oxo-2,3-dihydro-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-2,3-dihydro-1-benzofuran-3-one

> <JCHEM_LOGP>
3.82908268

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.48408177956742

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.9175289626894525

> <JCHEM_PKA_STRONGEST_BASIC>
-5.184468863587674

> <JCHEM_POLAR_SURFACE_AREA>
173.98

> <JCHEM_REFRACTIVITY>
143.5378

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2Z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2Z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  O   UNK     0       3.730 -10.283   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0       4.206  -8.819   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.300  -7.573   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.760  -7.573   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.990  -6.239   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.550  -6.239   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.455  -7.485   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -2.919  -7.009   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -4.253  -7.779   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -5.587  -7.009   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -6.920  -7.779   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -5.587  -5.469   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.253  -4.699   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.919  -5.469   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.455  -4.993   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -0.979  -3.529   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.760  -4.905   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.990  -3.572   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.760  -2.238   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.300  -2.238   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.070  -0.904   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.070  -3.572   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       5.610  -3.572   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.300  -4.905   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.990  -8.907   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.760 -10.240   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.990 -11.574   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -0.550 -11.574   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      -1.320 -12.908   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      -1.320 -10.240   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      -2.860 -10.240   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      -0.550  -8.907   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0       4.206  -6.327   0.000  0.00  0.00           O+0
HETATM   34  C   UNK     0       5.670  -6.803   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       7.004  -6.033   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       8.338  -6.803   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0       9.671  -6.033   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0       8.338  -8.343   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       7.004  -9.113   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       5.670  -8.343   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   40                                                  
CONECT    3    2    4   33                                                  
CONECT    4    3    5   25                                                  
CONECT    5    4    6   17                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13    8   15                                                  
CONECT   15   14    6   16                                                  
CONECT   16   15                                                            
CONECT   17    5   18   24                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   17                                                       
CONECT   25    4   26   32                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30   25                                                       
CONECT   33    3   34                                                       
CONECT   34   33   35   40                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   34    2                                                  
MASTER        0    0    0    0    0    0    0    0   40    0   90    0
END

View in JSmol

Synonyms

Value	Source
Disulphuretin	Generator

Chemical Formula

C₃₀H₁₈O₁₀

Average Mass

538.4640 Da

Monoisotopic Mass

538.09000 Da

IUPAC Name

(2Z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2Z)-6-hydroxy-3-oxo-2,3-dihydro-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-2,3-dihydro-1-benzofuran-3-one

Traditional Name

(2Z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2Z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one

CAS Registry Number

Not Available

SMILES

OC1=CC=C2C(O\C(=C(/C(=C3\OC4=CC(O)=CC=C4C3=O)/C3=CC=C(O)C(O)=C3)\C3=CC=C(O)C(O)=C3)C2=O)=C1

InChI Identifier

InChI=1S/C30H18O10/c31-15-3-5-17-23(11-15)39-29(27(17)37)25(13-1-7-19(33)21(35)9-13)26(14-2-8-20(34)22(36)10-14)30-28(38)18-6-4-16(32)12-24(18)40-30/h1-12,31-36H/b29-25-,30-26-

InChI Key

MZVYXDUSVXNKLC-IDDWGTJGSA-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
Cotinus coggygria	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as aurone flavonoids. These are flavonoids containing a 2-Benzylidene-1-benzofuran-3-one based core. Aurone flavonoids provide the bright yellow color of some important ornamental flowers, such as snapdragon (Antirrhinum majus).

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Aurone flavonoids

Sub Class

Not Available

Direct Parent

Aurone flavonoids

Alternative Parents

Substituents

Aurone
Stilbene
Benzofuran
Coumaran
Catechol
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Ketone
Oxacycle
Organoheterocyclic compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen 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	3.83	ChemAxon
pKa (Strongest Acidic)	6.92	ChemAxon
pKa (Strongest Basic)	-5.2	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	173.98 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	143.54 m³·mol⁻¹	ChemAxon
Polarizability	53.85 Å³	ChemAxon
Number of Rings	6	ChemAxon
Bioavailability	No	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

C00014672

Chemspider ID

8182991

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10007411

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Westenburg HE, Lee KJ, Lee SK, Fong HH, van Breemen RB, Pezzuto JM, Kinghorn AD: Activity-guided isolation of antioxidative constituents of Cotinus coggygria. J Nat Prod. 2000 Dec;63(12):1696-8. doi: 10.1021/np000292h. [PubMed:11141121 ]
LOTUS database [Link]

Showing NP-Card for (2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one (NP0264553)

MOL for NP0264553 ((2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one)

3D MOL for NP0264553 ((2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one)

3D SDF for NP0264553 ((2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one)

3D-SDF for NP0264553 ((2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one)

PDB for NP0264553 ((2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one)

3D PDB for NP0264553 ((2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one)

SMILES for NP0264553 ((2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one)

INCHI for NP0264553 ((2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one)

Structure for NP0264553 ((2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one)

3D Structure for NP0264553 ((2z)-2-[1,2-bis(3,4-dihydroxyphenyl)-2-[(2z)-6-hydroxy-3-oxo-1-benzofuran-2-ylidene]ethylidene]-6-hydroxy-1-benzofuran-3-one)