NP-MRD: Showing NP-Card for 2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone (NP0060772)

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Record Information

Version

2.0

Created at

2022-04-28 05:45:57 UTC

Updated at

2022-04-28 05:45:57 UTC

NP-MRD ID

NP0060772

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone

Description

1-(2,3-Dihydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one belongs to the class of organic compounds known as 2'-hydroxy-dihydrochalcones. These are organic compounds containing dihydrochalcone skeleton that carries a hydroxyl group at the 2'-position. Thus, 1-(2,3-dihydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one is considered to be a flavonoid lipid molecule. 2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone is found in Uvaria dulcis . 1-(2,3-Dihydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 40 41  0  0  0  0  0  0  0  0999 V2000
   -6.1299    0.5457   -0.5030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9276    1.1998   -0.7557 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6722    0.6661   -0.4922 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4984   -0.5874    0.0555 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2157   -1.0768    0.3004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0466   -2.3363    0.8506 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1858   -3.1021    1.1533 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0965   -0.3300    0.0055 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2064   -0.9064    0.2880 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3207   -2.0533    0.7885 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4571   -0.1657   -0.0021 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6844   -0.9665    0.3818 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8672   -0.1230    0.0448 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4569   -0.1993   -1.2014 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5438    0.5906   -1.4789 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0906    1.4758   -0.5601 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5040    1.5490    0.6736 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4172    0.7682    0.9707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2554    0.9236   -0.5418 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1414    1.6607   -0.8326 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5457    1.4045   -0.7833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7225    2.6561   -1.3302 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9375    1.3255   -0.4977 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0979    0.1453    0.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3734   -0.2637   -1.2201 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3687   -1.1842    0.2918 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8781   -3.1974    0.2921 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7464   -2.5584    1.9413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9351   -4.1386    1.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5304    0.7948    0.5483 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5349    0.0604   -1.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7027   -1.2125    1.4563 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6969   -1.8827   -0.2244 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0372   -0.8959   -1.9439 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9818    0.5083   -2.4602 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9511    2.0665   -0.8551 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9017    2.2229    1.4070 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9249    0.7981    1.9378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0745    2.5679   -1.2240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9607    3.2503   -1.5682 H   0  0  0  0  0  0  0  0  0  0  0  0
  7  6  1  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
  3  2  1  0
  2  1  1  0
  3 21  2  0
 21 22  1  0
 21 19  1  0
 19 20  1  0
 19  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
  8  5  1  0
 18 13  1  0
  7 27  1  0
  7 28  1  0
  7 29  1  0
  4 26  1  0
  1 23  1  0
  1 24  1  0
  1 25  1  0
 22 40  1  0
 20 39  1  0
 11 30  1  0
 11 31  1  0
 12 32  1  0
 12 33  1  0
 14 34  1  0
 15 35  1  0
 16 36  1  0
 17 37  1  0
 18 38  1  0
M  END

  Mrv1652308221907242D          

 22 23  0  0  0  0            999 V2000
    1.4289   -1.6500    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
    2.8579   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    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
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   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
    0.7145   -0.4125    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
    1.4289    0.0000    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
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   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
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  2  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  2  0  0  0  0
  9  8  1  0  0  0  0
 11  6  2  0  0  0  0
 11  7  1  0  0  0  0
 11  8  1  0  0  0  0
 12  9  1  0  0  0  0
 13 10  2  0  0  0  0
 14 10  1  0  0  0  0
 15 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16 14  2  0  0  0  0
 17 15  2  0  0  0  0
 17 16  1  0  0  0  0
 18 12  2  0  0  0  0
 19 16  1  0  0  0  0
 20 17  1  0  0  0  0
 21  1  1  0  0  0  0
 21 13  1  0  0  0  0
 22  2  1  0  0  0  0
 22 14  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0060772

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C(O)C(O)=C1C(=O)CCC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H18O5/c1-21-13-10-14(22-2)16(19)17(20)15(13)12(18)9-8-11-6-4-3-5-7-11/h3-7,10,19-20H,8-9H2,1-2H3

> <INCHI_KEY>
RZFPYTZZSXAWPH-UHFFFAOYSA-N

> <FORMULA>
C17H18O5

> <MOLECULAR_WEIGHT>
302.326

> <EXACT_MASS>
302.11542368

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
31.75362628054831

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(2,3-dihydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one

> <ALOGPS_LOGP>
2.84

> <JCHEM_LOGP>
3.537328644666666

> <ALOGPS_LOGS>
-3.82

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.90360914919664

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.287828176134985

> <JCHEM_PKA_STRONGEST_BASIC>
-4.600692138628309

> <JCHEM_POLAR_SURFACE_AREA>
75.99000000000001

> <JCHEM_REFRACTIVITY>
82.6719

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.59e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(2,3-dihydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 22-AUG-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-AUG-19         0                                  
HETATM    1  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.335   0.000   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
CONECT    1   21                                                            
CONECT    2   22                                                            
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3    7                                                       
CONECT    6    4   11                                                       
CONECT    7    5   11                                                       
CONECT    8    9   11                                                       
CONECT    9    8   12                                                       
CONECT   10   13   14                                                       
CONECT   11    6    7    8                                                  
CONECT   12    9   15   18                                                  
CONECT   13   10   15   21                                                  
CONECT   14   10   16   22                                                  
CONECT   15   12   13   17                                                  
CONECT   16   14   17   19                                                  
CONECT   17   15   16   20                                                  
CONECT   18   12                                                            
CONECT   19   16                                                            
CONECT   20   17                                                            
CONECT   21    1   13                                                       
CONECT   22    2   14                                                       
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₈O₅

Average Mass

302.3260 Da

Monoisotopic Mass

302.11542 Da

IUPAC Name

1-(2,3-dihydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one

Traditional Name

1-(2,3-dihydroxy-4,6-dimethoxyphenyl)-3-phenylpropan-1-one

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C(O)C(O)=C1C(=O)CCC1=CC=CC=C1

InChI Identifier

InChI=1S/C17H18O5/c1-21-13-10-14(22-2)16(19)17(20)15(13)12(18)9-8-11-6-4-3-5-7-11/h3-7,10,19-20H,8-9H2,1-2H3

InChI Key

RZFPYTZZSXAWPH-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
Uvaria dulcis	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2'-hydroxy-dihydrochalcones. These are organic compounds containing dihydrochalcone skeleton that carries a hydroxyl group at the 2'-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Linear 1,3-diarylpropanoids

Sub Class

Chalcones and dihydrochalcones

Direct Parent

2'-Hydroxy-dihydrochalcones

Alternative Parents

Substituents

2'-hydroxy-dihydrochalcone
Cinnamylphenol
Alkyl-phenylketone
Butyrophenone
Dimethoxybenzene
Methoxyphenol
M-dimethoxybenzene
4-alkoxyphenol
Phenylketone
Methoxybenzene
Anisole
Benzoyl
Aryl alkyl ketone
Aryl ketone
Phenol ether
Catechol
Phenoxy compound
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Ketone
Ether
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Chalcones and dihydrochalcones (LMPK12120557 )

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	2.84	ALOGPS
logP	3.54	ChemAxon
logS	-3.8	ALOGPS
pKa (Strongest Acidic)	9.29	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	75.99 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	82.67 m³·mol⁻¹	ChemAxon
Polarizability	31.75 Å³	ChemAxon
Number of Rings	2	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

HMDB0132912

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB089968

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone (NP0060772)

MOL for NP0060772 (2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone)

3D MOL for NP0060772 (2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone)

3D SDF for NP0060772 (2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone)

3D-SDF for NP0060772 (2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone)

PDB for NP0060772 (2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone)

3D PDB for NP0060772 (2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone)

SMILES for NP0060772 (2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone)

INCHI for NP0060772 (2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone)

Structure for NP0060772 (2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone)

3D Structure for NP0060772 (2',3'-Dihydroxy-4',6'-dimethoxydihydrochalcone)