NP-MRD: Showing NP-Card for 2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one (NP0086488)

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Record Information

Version

2.0

Created at

2022-04-29 06:46:36 UTC

Updated at

2022-04-29 06:46:36 UTC

NP-MRD ID

NP0086488

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one

Description

SCHEMBL18417920 belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety. 2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one is found in Cucumis melo var. reticulatus . Based on a literature review very few articles have been published on SCHEMBL18417920.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 37 39  0  0  0  0  0  0  0  0999 V2000
    3.6770    2.5732   -0.2466 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9752    1.5263   -0.2987 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6104    1.5540   -0.5522 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8660    0.3933   -0.6038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6084    0.4154   -0.8771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2895    0.5261    0.4633 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7476    0.5619    0.3891 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4035    1.7671    0.2730 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7786    1.7986    0.2032 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5177    0.6075    0.2498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8979    0.6918    0.1760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8799   -0.6040    0.3654 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5865   -1.7954    0.4136 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4827   -0.6030    0.4341 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4943   -0.7411   -0.4045 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7622   -0.8473   -0.1631 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3210   -2.1151    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6767   -2.1503    0.2856 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2844   -3.3790    0.4881 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4605   -1.0320    0.3476 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8892    0.2089    0.1509 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6272    1.3841    0.2003 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5444    0.2804   -0.1021 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1458    2.5220   -0.7091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8897    1.2011   -1.5817 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8312   -0.5570   -1.3636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0100   -0.4139    1.0255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8608    1.3497    1.0698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8043    2.6585    0.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2891    2.7429    0.1123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5212   -0.0902    0.1998 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5876   -1.8701    0.3696 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0159   -1.5809    0.5251 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6921   -2.9888   -0.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8215   -4.2569    0.4675 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5266   -1.0964    0.5488 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6278    1.3584    0.3866 H   0  0  0  0  0  0  0  0  0  0  0  0
 19 18  1  0
 18 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 12 14  2  0
  4 15  1  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 16 23  1  0
 14  7  1  0
 19 35  1  0
 20 36  1  0
 22 37  1  0
  3 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  8 29  1  0
  9 30  1  0
 11 31  1  0
 13 32  1  0
 14 33  1  0
 17 34  1  0
M  END


  Mrv1652304292208462D          

 23 25  0  0  0  0            999 V2000
   -0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.6500    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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 O   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
    2.8579   -0.0000    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
    3.5724    1.2375    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
    4.2868    2.4750    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
    5.7158    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.8250    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   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
   -1.4289   -0.0000    0.0000 O   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  2  1  0  0  0  0
  2  3  2  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
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  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
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
  9 16  1  0  0  0  0
  6 17  2  0  0  0  0
 17 18  1  0  0  0  0
  3 18  1  0  0  0  0
 18 19  2  0  0  0  0
  4 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
  2 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086488

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC(O)=C2C(=O)C=C(CCC3=CC=C(O)C(O)=C3)OC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O6/c18-10-6-14(21)17-15(22)8-11(23-16(17)7-10)3-1-9-2-4-12(19)13(20)5-9/h2,4-8,18-21H,1,3H2

> <INCHI_KEY>
FIOQHGFHIGXAOW-UHFFFAOYSA-N

> <FORMULA>
C17H14O6

> <MOLECULAR_WEIGHT>
314.293

> <EXACT_MASS>
314.079038171

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
37

> <JCHEM_AVERAGE_POLARIZABILITY>
31.627373253903208

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-[2-(3,4-dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-chromen-4-one

> <ALOGPS_LOGP>
2.92

> <JCHEM_LOGP>
3.408187015333333

> <ALOGPS_LOGS>
-3.75

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.175519269063335

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.592771868965674

> <JCHEM_PKA_STRONGEST_BASIC>
-5.351196097962434

> <JCHEM_POLAR_SURFACE_AREA>
107.22000000000001

> <JCHEM_REFRACTIVITY>
84.2508

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.60e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[2-(3,4-dihydroxyphenyl)ethyl]-5,7-dihydroxychromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0      -0.000  -4.620   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      10.669   4.620   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      10.669   1.540   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4   18                                                  
CONECT    4    3    5   20                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   17                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    9                                                       
CONECT   17    6   18                                                       
CONECT   18   17    3   19                                                  
CONECT   19   18                                                            
CONECT   20    4   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21    2                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄O₆

Average Mass

314.2930 Da

Monoisotopic Mass

314.07904 Da

IUPAC Name

2-[2-(3,4-dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-chromen-4-one

Traditional Name

2-[2-(3,4-dihydroxyphenyl)ethyl]-5,7-dihydroxychromen-4-one

CAS Registry Number

Not Available

SMILES

OC1=CC(O)=C2C(=O)C=C(CCC3=CC=C(O)C(O)=C3)OC2=C1

InChI Identifier

InChI=1S/C17H14O6/c18-10-6-14(21)17-15(22)8-11(23-16(17)7-10)3-1-9-2-4-12(19)13(20)5-9/h2,4-8,18-21H,1,3H2

InChI Key

FIOQHGFHIGXAOW-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
Cucumis melo var. reticulatus	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as chromones. Chromones are compounds containing a benzopyran-4-one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Benzopyrans

Sub Class

1-benzopyrans

Direct Parent

Chromones

Alternative Parents

Substituents

Chromone
Catechol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Pyranone
Phenol
Monocyclic benzene moiety
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous acid
Oxacycle
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
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	2.92	ALOGPS
logP	3.41	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	6.59	ChemAxon
pKa (Strongest Basic)	-5.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	107.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	84.25 m³·mol⁻¹	ChemAxon
Polarizability	31.63 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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00056780

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

91162275

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one (NP0086488)

MOL for NP0086488 (2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one)

3D MOL for NP0086488 (2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one)

3D SDF for NP0086488 (2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one)

3D-SDF for NP0086488 (2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one)

PDB for NP0086488 (2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one)

3D PDB for NP0086488 (2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one)

SMILES for NP0086488 (2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one)

INCHI for NP0086488 (2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one)

Structure for NP0086488 (2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one)

3D Structure for NP0086488 (2-[2-(3,4-Dihydroxyphenyl)ethyl]-5,7-dihydroxy-4H-1-benzopyran-4-one)