NP-MRD: Showing NP-Card for 2',4'-Dihydroxydihydrochalcone (NP0055286)

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Record Information

Version

2.0

Created at

2022-04-28 01:23:43 UTC

Updated at

2022-04-28 01:23:43 UTC

NP-MRD ID

NP0055286

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2',4'-Dihydroxydihydrochalcone

Description

1-(2,4-Dihydroxyphenyl)-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-(2,4-dihydroxyphenyl)-3-phenylpropan-1-one is considered to be a flavonoid lipid molecule. 2',4'-Dihydroxydihydrochalcone is found in Ceratiola ericoides, Muntingia calabura and Oxytropis falcata. 1-(2,4-Dihydroxyphenyl)-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

 32 33  0  0  0  0  0  0  0  0999 V2000
    0.7799   -2.3301    0.5434 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9017   -1.1398    0.1373 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3066   -0.3341   -0.0102 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5235   -1.1617    0.3609 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7784   -0.3740    0.2234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5148   -0.3194   -0.9395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6758    0.4128   -1.0585 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1212    1.1237    0.0372 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4226    1.0993    1.2134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2492    0.3471    1.3012 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2458   -0.6645   -0.1526 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3407   -1.4954    0.0183 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6341   -1.0786   -0.2454 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8798    0.2059   -0.6968 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1608    0.6082   -0.9544 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8086    1.0523   -0.8751 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5078    0.6126   -0.6031 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4227    1.4565   -0.7796 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822    0.6205    0.5582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4615   -0.0288   -1.0749 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5578   -2.0918   -0.2422 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3727   -1.4880    1.4138 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1780   -0.8647   -1.7889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2666    0.4674   -1.9628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0320    1.7145   -0.0125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7293    1.6374    2.0967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6973    0.3298    2.2354 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1857   -2.5185    0.3739 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4396   -1.7830   -0.0887 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4238    1.5089   -1.2797 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9255    2.0743   -1.2267 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5126    2.4010   -1.1029 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 16  2  0
 16 17  1  0
 17 18  1  0
 17 11  2  0
 11 12  1  0
 12 13  2  0
 11  2  1  0
  2  1  2  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 13 14  1  0
 10  5  1  0
 15 30  1  0
 16 31  1  0
 18 32  1  0
 12 28  1  0
 13 29  1  0
  3 19  1  0
  3 20  1  0
  4 21  1  0
  4 22  1  0
  6 23  1  0
  7 24  1  0
  8 25  1  0
  9 26  1  0
 10 27  1  0
M  END


  Mrv1652310051715242D          

 18 19  0  0  0  0            999 V2000
    5.0013   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   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
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592    3.7125    0.0000 C   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
    7.8592    4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5737    4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  2  0  0  0  0
  3  1  1  0  0  0  0
  4  2  1  0  0  0  0
  5  3  2  0  0  0  0
  8  7  2  0  0  0  0
  9  6  1  0  0  0  0
 11  4  2  0  0  0  0
 11  5  1  0  0  0  0
 11  6  1  0  0  0  0
 12  7  1  0  0  0  0
 12 10  2  0  0  0  0
 13  8  1  0  0  0  0
 14  9  1  0  0  0  0
 14 13  1  0  0  0  0
 15 10  1  0  0  0  0
 15 13  2  0  0  0  0
 16 12  1  0  0  0  0
 17 14  2  0  0  0  0
 18 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0055286

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC(O)=C(C=C1)C(=O)CCC1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C15H14O3/c16-12-7-8-13(15(18)10-12)14(17)9-6-11-4-2-1-3-5-11/h1-5,7-8,10,16,18H,6,9H2

> <INCHI_KEY>
ZUKLXLKVCGZHAA-UHFFFAOYSA-N

> <FORMULA>
C15H14O3

> <MOLECULAR_WEIGHT>
242.274

> <EXACT_MASS>
242.094294311

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
32

> <JCHEM_AVERAGE_POLARIZABILITY>
26.023225571619193

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-(2,4-dihydroxyphenyl)-3-phenylpropan-1-one

> <ALOGPS_LOGP>
3.12

> <JCHEM_LOGP>
3.852671176

> <ALOGPS_LOGS>
-3.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.83927647746614

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.8656325493732275

> <JCHEM_PKA_STRONGEST_BASIC>
-4.908504640641795

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
69.7455

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.10e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-(2,4-dihydroxyphenyl)-3-phenylpropan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-OCT-17   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-OCT-17         0                                  
HETATM    1  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      13.337   9.240   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      12.003   8.470   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      14.670   6.930   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      14.670   8.470   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.003   6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.669   6.160   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      13.337   6.160   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      16.004   9.240   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       9.336   6.930   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      13.337   4.620   0.000  0.00  0.00           O+0
CONECT    1    2    3                                                       
CONECT    2    1    4                                                       
CONECT    3    1    5                                                       
CONECT    4    2   11                                                       
CONECT    5    3   11                                                       
CONECT    6    9   11                                                       
CONECT    7    8   12                                                       
CONECT    8    7   13                                                       
CONECT    9    6   14                                                       
CONECT   10   12   15                                                       
CONECT   11    4    5    6                                                  
CONECT   12    7   10   16                                                  
CONECT   13    8   14   15                                                  
CONECT   14    9   13   17                                                  
CONECT   15   10   13   18                                                  
CONECT   16   12                                                            
CONECT   17   14                                                            
CONECT   18   15                                                            
MASTER        0    0    0    0    0    0    0    0   18    0   38    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₅H₁₄O₃

Average Mass

242.2740 Da

Monoisotopic Mass

242.09429 Da

IUPAC Name

1-(2,4-dihydroxyphenyl)-3-phenylpropan-1-one

Traditional Name

1-(2,4-dihydroxyphenyl)-3-phenylpropan-1-one

CAS Registry Number

Not Available

SMILES

OC1=CC(O)=C(C=C1)C(=O)CCC1=CC=CC=C1

InChI Identifier

InChI=1S/C15H14O3/c16-12-7-8-13(15(18)10-12)14(17)9-6-11-4-2-1-3-5-11/h1-5,7-8,10,16,18H,6,9H2

InChI Key

ZUKLXLKVCGZHAA-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
Ceratiola ericoides	Plant	KNApSAcK
Muntingia calabura	LOTUS Database	35616633
Oxytropis falcata	LOTUS Database	35616633

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
Phenylketone
Benzoyl
Resorcinol
Aryl alkyl ketone
Aryl ketone
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Vinylogous acid
Ketone
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Chalcones and dihydrochalcones (LMPK12120442 )

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	3.12	ALOGPS
logP	3.85	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	7.87	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	69.75 m³·mol⁻¹	ChemAxon
Polarizability	26.02 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

HMDB0151857

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

586491

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 2',4'-Dihydroxydihydrochalcone (NP0055286)

MOL for NP0055286 (2',4'-Dihydroxydihydrochalcone)

3D MOL for NP0055286 (2',4'-Dihydroxydihydrochalcone)

3D SDF for NP0055286 (2',4'-Dihydroxydihydrochalcone)

3D-SDF for NP0055286 (2',4'-Dihydroxydihydrochalcone)

PDB for NP0055286 (2',4'-Dihydroxydihydrochalcone)

3D PDB for NP0055286 (2',4'-Dihydroxydihydrochalcone)

SMILES for NP0055286 (2',4'-Dihydroxydihydrochalcone)

INCHI for NP0055286 (2',4'-Dihydroxydihydrochalcone)

Structure for NP0055286 (2',4'-Dihydroxydihydrochalcone)

3D Structure for NP0055286 (2',4'-Dihydroxydihydrochalcone)