NP-MRD: Showing NP-Card for Violanone (NP0137133)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-05-30 16:42:39 UTC

Updated at

2022-05-30 16:42:39 UTC

NP-MRD ID

NP0137133

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Violanone

Description

Violanone belongs to the class of organic compounds known as 2'-o-methylated isoflavonoids. These are isoflavonoids with methoxy groups attached to the C2' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one. Violanone is found in Dalbergia parviflora. Violanone is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
   -1.0906   -2.7559    1.3252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1707   -1.9997    0.1618 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7674   -0.7564    0.0465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0142    0.3789    0.2607 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4186    0.2789    0.6102 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.0589    1.6088    0.8508 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3807    1.3821    1.3051 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2551    0.6185    0.5658 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6294    0.7308    0.6734 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4062   -0.0882   -0.1195 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7823    0.0304   -0.0055 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8670   -0.9991   -1.0004 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4878   -1.0913   -1.0887 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6711   -0.2971   -0.3198 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2223   -0.4113   -0.4292 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7517   -1.0766   -1.3818 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5938    1.6263    0.1497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9405    1.7634   -0.1782 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6715    0.6345   -0.3868 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1179    0.7239   -0.7402 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4912    2.0421   -0.7991 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0966   -0.6162   -0.2771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8210   -1.7831   -0.4851 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6343   -3.7229    1.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0044   -3.0393    1.4548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3728   -2.2298    2.2403 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5019   -0.3109    1.5603 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1385    2.1344   -0.1125 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5093    2.2495    1.5641 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0459    1.4541    1.3730 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2309    0.6687    0.6119 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4761   -1.6450   -1.6257 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9999   -1.7892   -1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0624    2.5559    0.3039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4196    2.7319   -0.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3801    0.1608   -1.6420 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6678    0.2237    0.1095 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7309    2.4269    0.0971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7859   -1.8126   -0.7235 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4 17  1  0
 17 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 22 23  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8 14  2  0
 14 13  1  0
 13 12  2  0
 12 10  1  0
 10 11  1  0
 10  9  2  0
 14 15  1  0
 15 16  2  0
 22  3  1  0
 15  5  1  0
  9  8  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 17 34  1  0
 18 35  1  0
 20 36  1  0
 20 37  1  0
 21 38  1  0
 23 39  1  0
  5 27  1  1
  6 28  1  0
  6 29  1  0
 13 33  1  0
 12 32  1  0
 11 31  1  0
  9 30  1  0
M  END


  Mrv0541 02271201272D          

 23 25  0  0  0  0            999 V2000
    2.3298   -1.1658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6153   -0.7533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9009   -1.1658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1864   -0.7533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1864    0.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9009    0.4842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6153    0.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5281    0.4842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5281    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2426    1.7217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9570    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9570    0.4842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2426    0.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2426   -0.7533    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6715    0.0717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3860    0.4842    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3860    1.3092    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6715    1.7217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1004    1.7217    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5281   -1.1658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5281   -1.9908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9009   -1.9908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3298   -1.9908    0.0000 O   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  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  2  7  1  0  0  0  0
  5  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  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
  8 13  1  0  0  0  0
 13 14  2  0  0  0  0
 12 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 11 18  1  0  0  0  0
 17 19  1  0  0  0  0
  4 20  1  0  0  0  0
 20 21  1  0  0  0  0
  3 22  1  0  0  0  0
  1 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0137133

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(C=CC(CO)=C1O)C1COC2=C(C=CC(O)=C2)C1=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H16O6/c1-22-17-11(4-2-9(7-18)15(17)20)13-8-23-14-6-10(19)3-5-12(14)16(13)21/h2-6,13,18-20H,7-8H2,1H3

> <INCHI_KEY>
NAOWONDUKAFFFO-UHFFFAOYSA-N

> <FORMULA>
C17H16O6

> <MOLECULAR_WEIGHT>
316.3053

> <EXACT_MASS>
316.094688244

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_AVERAGE_POLARIZABILITY>
31.674344759848626

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-hydroxy-3-[3-hydroxy-4-(hydroxymethyl)-2-methoxyphenyl]-3,4-dihydro-2H-1-benzopyran-4-one

> <ALOGPS_LOGP>
1.91

> <JCHEM_LOGP>
1.456202402666666

> <ALOGPS_LOGS>
-3.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.282091813386947

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.781959652775316

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9552847849088586

> <JCHEM_POLAR_SURFACE_AREA>
96.22000000000001

> <JCHEM_REFRACTIVITY>
82.97470000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.06e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-hydroxy-3-[3-hydroxy-4-(hydroxymethyl)-2-methoxyphenyl]-2,3-dihydro-1-benzopyran-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 27-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   27-FEB-12         0                                  
HETATM    1  C   UNK     0       4.349  -2.176   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.015  -1.406   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.682  -2.176   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.348  -1.406   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.348   0.134   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.682   0.904   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.015   0.134   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.986   0.904   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.986   2.444   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -2.320   3.214   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -3.653   2.444   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -3.653   0.904   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.320   0.134   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      -2.320  -1.406   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      -4.987   0.134   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -6.321   0.904   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -6.321   2.444   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -4.987   3.214   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -7.654   3.214   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -0.986  -2.176   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -0.986  -3.716   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       1.682  -3.716   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       4.349  -3.716   0.000  0.00  0.00           O+0
CONECT    1    2   23                                                       
CONECT    2    1    3    7                                                  
CONECT    3    2    4   22                                                  
CONECT    4    3    5   20                                                  
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2                                                       
CONECT    8    5    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   18                                                  
CONECT   12   11   13   15                                                  
CONECT   13   12    8   14                                                  
CONECT   14   13                                                            
CONECT   15   12   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17   11                                                       
CONECT   19   17                                                            
CONECT   20    4   21                                                       
CONECT   21   20                                                            
CONECT   22    3                                                            
CONECT   23    1                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
7,3'-Dihydroxy-2',4'-dimethoxyisoflavone	HMDB

Chemical Formula

C₁₇H₁₆O₆

Average Mass

316.3053 Da

Monoisotopic Mass

316.09469 Da

IUPAC Name

7-hydroxy-3-[3-hydroxy-4-(hydroxymethyl)-2-methoxyphenyl]-3,4-dihydro-2H-1-benzopyran-4-one

Traditional Name

7-hydroxy-3-[3-hydroxy-4-(hydroxymethyl)-2-methoxyphenyl]-2,3-dihydro-1-benzopyran-4-one

CAS Registry Number

Not Available

SMILES

COC1=C(C=CC(CO)=C1O)C1COC2=C(C=CC(O)=C2)C1=O

InChI Identifier

InChI=1S/C17H16O6/c1-22-17-11(4-2-9(7-18)15(17)20)13-8-23-14-6-10(19)3-5-12(14)16(13)21/h2-6,13,18-20H,7-8H2,1H3

InChI Key

NAOWONDUKAFFFO-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, 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
Dalbergia parviflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2'-o-methylated isoflavonoids. These are isoflavonoids with methoxy groups attached to the C2' atom of the isoflavonoid backbone. Isoflavonoids are natural products derived from 3-phenylchromen-4-one.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

O-methylated isoflavonoids

Direct Parent

2'-O-methylated isoflavonoids

Alternative Parents

Substituents

2p-methoxyisoflavonoid-skeleton
Isoflavanol
Hydroxyisoflavonoid
Isoflavanone
Isoflavan
Chromone
Chromane
Benzopyran
Methoxyphenol
1-benzopyran
Phenoxy compound
Anisole
Benzyl alcohol
Methoxybenzene
Phenol ether
Aryl ketone
Aryl alkyl ketone
1-hydroxy-4-unsubstituted benzenoid
Phenol
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Ketone
Oxacycle
Organoheterocyclic compound
Ether
Organooxygen compound
Organic oxygen compound
Organic oxide
Primary alcohol
Aromatic alcohol
Hydrocarbon derivative
Alcohol
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	1.91	ALOGPS
logP	1.46	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	7.78	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	96.22 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	82.97 m³·mol⁻¹	ChemAxon
Polarizability	31.67 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

HMDB0041790

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB029966

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

131753209

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for Violanone (NP0137133)

MOL for NP0137133 (Violanone)

3D MOL for NP0137133 (Violanone)

3D SDF for NP0137133 (Violanone)

3D-SDF for NP0137133 (Violanone)

PDB for NP0137133 (Violanone)

3D PDB for NP0137133 (Violanone)

SMILES for NP0137133 (Violanone)

INCHI for NP0137133 (Violanone)

Structure for NP0137133 (Violanone)

3D Structure for NP0137133 (Violanone)