NP-MRD: Showing NP-Card for 3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone (NP0060722)

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Record Information

Version

2.0

Created at

2022-04-28 05:43:28 UTC

Updated at

2022-04-28 05:43:28 UTC

NP-MRD ID

NP0060722

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone

Description

2-(2,4-Dihydroxy-6-methoxybenzoyl)-9-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-6-(4-methoxyphenyl)-8H-furo[2,3-g]chromen-8-one belongs to the class of organic compounds known as isoquinolines and derivatives. These are aromatic polycyclic compounds containing an isoquinoline moiety, which consists of a benzene ring fused to a pyridine ring and forming benzo[c]pyridine. 3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone is found in Aristolochia ridicula . 2-(2,4-Dihydroxy-6-methoxybenzoyl)-9-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-6-(4-methoxyphenyl)-8H-furo[2,3-g]chromen-8-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161523082D          

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M  END

     RDKit          3D

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  Mrv1533004161523082D          

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    5.6738   -3.2332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1218   -3.8463    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3767   -4.6309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1837   -4.8025    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3148   -3.6748    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7628   -4.2879    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0599   -2.8902    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    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
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  6  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 11 13  1  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
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 21 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 18 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  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
 35 38  1  0  0  0  0
 38 39  1  0  0  0  0
 38 40  2  0  0  0  0
 32 40  1  0  0  0  0
 31 41  1  0  0  0  0
 16 41  1  0  0  0  0
 41 42  2  0  0  0  0
 42 43  1  0  0  0  0
 13 43  2  0  0  0  0
 43 44  1  0  0  0  0
  9 44  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0060722

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1)C1=CC(=O)C2=C(O1)C=C1C(OC(C(=O)C3=C(O)C=C(O)C=C3OC)=C1C1=CC=C(OC)C(O)=C1)=C2O

> <INCHI_IDENTIFIER>
InChI=1S/C33H24O11/c1-40-18-7-4-15(5-8-18)24-14-22(37)29-26(43-24)13-19-27(16-6-9-23(41-2)20(35)10-16)33(44-32(19)30(29)38)31(39)28-21(36)11-17(34)12-25(28)42-3/h4-14,34-36,38H,1-3H3

> <INCHI_KEY>
WAILTZHTPABBBY-UHFFFAOYSA-N

> <FORMULA>
C33H24O11

> <MOLECULAR_WEIGHT>
596.544

> <EXACT_MASS>
596.131861593

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
68

> <JCHEM_AVERAGE_POLARIZABILITY>
61.78087958352775

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(2,4-dihydroxy-6-methoxybenzoyl)-9-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-6-(4-methoxyphenyl)-8H-furo[2,3-g]chromen-8-one

> <ALOGPS_LOGP>
4.81

> <JCHEM_LOGP>
5.765812938666666

> <ALOGPS_LOGS>
-4.05

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.587254334384376

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.978830892575119

> <JCHEM_PKA_STRONGEST_BASIC>
-3.0956064097028744

> <JCHEM_POLAR_SURFACE_AREA>
165.12

> <JCHEM_REFRACTIVITY>
158.71469999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.26e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(2,4-dihydroxy-6-methoxybenzoyl)-9-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-6-(4-methoxyphenyl)furo[2,3-g]chromen-8-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       8.133  -0.294   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.038  -1.540   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.578  -1.540   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      11.348  -2.874   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      11.348  -0.206   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.578   1.127   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       9.038   1.127   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      11.348   2.461   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.888   2.461   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      13.658   3.795   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      13.658   1.127   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.888  -0.206   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0      13.658  -1.540   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      12.888  -2.874   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       8.133  -2.786   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       8.609  -4.251   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      10.115  -4.571   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      10.591  -6.035   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       9.561  -7.180   0.000  0.00  0.00           C+0
HETATM   36  O   UNK     0      10.037  -8.644   0.000  0.00  0.00           O+0
HETATM   37  C   UNK     0      11.543  -8.965   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       8.054  -6.860   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0       7.024  -8.004   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       7.578  -5.395   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       2.667  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    9                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3                                                       
CONECT    9    6   10   44                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14   43                                                  
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17   41                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   31                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22   28                                                  
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27   21   29                                                  
CONECT   29   28   30                                                       
CONECT   30   29                                                            
CONECT   31   18   32   41                                                  
CONECT   32   31   33   40                                                  
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   38                                                  
CONECT   36   35   37                                                       
CONECT   37   36                                                            
CONECT   38   35   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   32                                                       
CONECT   41   31   16   42                                                  
CONECT   42   41   43                                                       
CONECT   43   42   13   44                                                  
CONECT   44   43    9                                                       
MASTER        0    0    0    0    0    0    0    0   44    0   98    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₃₃H₂₄O₁₁

Average Mass

596.5440 Da

Monoisotopic Mass

596.13186 Da

IUPAC Name

2-(2,4-dihydroxy-6-methoxybenzoyl)-9-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-6-(4-methoxyphenyl)-8H-furo[2,3-g]chromen-8-one

Traditional Name

2-(2,4-dihydroxy-6-methoxybenzoyl)-9-hydroxy-3-(3-hydroxy-4-methoxyphenyl)-6-(4-methoxyphenyl)furo[2,3-g]chromen-8-one

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1)C1=CC(=O)C2=C(O1)C=C1C(OC(C(=O)C3=C(O)C=C(O)C=C3OC)=C1C1=CC=C(OC)C(O)=C1)=C2O

InChI Identifier

InChI=1S/C33H24O11/c1-40-18-7-4-15(5-8-18)24-14-22(37)29-26(43-24)13-19-27(16-6-9-23(41-2)20(35)10-16)33(44-32(19)30(29)38)31(39)28-21(36)11-17(34)12-25(28)42-3/h4-14,34-36,38H,1-3H3

InChI Key

WAILTZHTPABBBY-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Aristolochia ridicula	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as isoquinolines and derivatives. These are aromatic polycyclic compounds containing an isoquinoline moiety, which consists of a benzene ring fused to a pyridine ring and forming benzo[c]pyridine.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isoquinolines and derivatives

Sub Class

Not Available

Direct Parent

Isoquinolines and derivatives

Alternative Parents

Substituents

Isoquinoline
Anisole
Phenol ether
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Pyridine
Heteroaromatic compound
Ether
Azacycle
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organic nitrogen compound
Hydrocarbon derivative
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	4.81	ALOGPS
logP	5.77	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	4.98	ChemAxon
pKa (Strongest Basic)	-3.1	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	165.12 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	158.71 m³·mol⁻¹	ChemAxon
Polarizability	61.78 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	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

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

101717265

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone (NP0060722)

MOL for NP0060722 (3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone)

3D MOL for NP0060722 (3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone)

3D SDF for NP0060722 (3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone)

3D-SDF for NP0060722 (3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone)

PDB for NP0060722 (3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone)

3D PDB for NP0060722 (3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone)

SMILES for NP0060722 (3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone)

INCHI for NP0060722 (3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone)

Structure for NP0060722 (3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone)

3D Structure for NP0060722 (3''',5,5'',7''-Tetrahydroxy-3'',4',4'''-trimethoxy-6-O-alpha,7-beta-flavone-chalcone)