NP-MRD: Showing NP-Card for (R)-4'-Hydroxy-3,4-dimethoxydalbergione (NP0057209)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-04-28 02:42:39 UTC

Updated at

2022-04-28 02:42:39 UTC

NP-MRD ID

NP0057209

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(R)-4'-Hydroxy-3,4-dimethoxydalbergione

Description

(R)-4'-hydroxy-3,4-dimethoxydalbergione belongs to the class of organic compounds known as ubiquinones. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methyl(1,4-benzoquinone) moiety to which an isoprenyl group is attached at ring position 2(or 6). Thus, (R)-4'-hydroxy-3,4-dimethoxydalbergione is considered to be a flavonoid. (R)-4'-Hydroxy-3,4-dimethoxydalbergione is found in Machaerium nictitans. Based on a literature review very few articles have been published on (r)-4'-hydroxy-3,4-dimethoxydalbergione.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
    1.6658    3.3201   -0.6314 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9344    2.2314   -0.7305 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0365    1.1662    0.2826 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1867    0.3465    0.3822 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0857   -0.9617    0.3251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3044   -1.7932    0.4293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1880   -3.0549    0.3720 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6163   -1.1860    0.5945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7240   -2.0192    0.6865 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4111   -2.4093   -0.4685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7167    0.1273    0.6519 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9512    0.7290    0.8085 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4541    1.6669   -0.1550 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5034    0.9433    0.5477 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5893    2.1923    0.6012 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2517    0.3386    0.0910 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1729    0.1781    1.1037 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3041   -0.5857    0.9121 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5661   -1.2171   -0.2833 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7044   -1.9892   -0.4850 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6436   -1.0576   -1.3006 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5092   -0.2980   -1.1246 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6113    4.1255   -1.3666 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3559    3.4556    0.1941 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2573    2.1325   -1.5683 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1472    1.6793    1.2749 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8604   -1.4915    0.2061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8003   -1.4941   -0.9913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7214   -2.9723   -1.1453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2650   -3.0301   -0.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7550    2.5174   -0.2190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4449    2.0177    0.1406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5352    1.1041   -1.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9988    0.6664    2.0721 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0130   -0.6919    1.7352 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6217   -2.9841   -0.2567 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8270   -1.5472   -2.2580 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7713   -0.1554   -1.9004 H   0  0  0  0  0  0  0  0  0  0  0  0
 10  9  1  0
  9  8  1  0
  8 11  2  0
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  2  0
 14  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  4  3  1  0
  3  2  1  0
  2  1  2  3
  3 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 19 21  1  0
 21 22  2  0
  6  8  1  0
 22 16  1  0
 10 28  1  0
 10 29  1  0
 10 30  1  0
 13 31  1  0
 13 32  1  0
 13 33  1  0
  5 27  1  0
  3 26  1  1
  2 25  1  0
  1 23  1  0
  1 24  1  0
 17 34  1  0
 18 35  1  0
 20 36  1  0
 21 37  1  0
 22 38  1  0
M  END

  Mrv1652304282204422D          

 22 23  0  0  1  0            999 V2000
    2.1434   -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
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   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
    1.4289   -2.4750    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
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  2  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
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   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
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  2  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  6  0  0  0
 10 11  2  0  0  0  0
  9 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 12 17  1  0  0  0  0
 15 18  1  0  0  0  0
  2 19  1  0  0  0  0
 19 20  1  0  0  0  0
  1 21  1  0  0  0  0
 21 22  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0057209

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC)C(=O)C(=CC1=O)[C@H](C=C)C1=CC=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C17H16O5/c1-4-12(10-5-7-11(18)8-6-10)13-9-14(19)16(21-2)17(22-3)15(13)20/h4-9,12,18H,1H2,2-3H3/t12-/m1/s1

> <INCHI_KEY>
XQFOJEJSFFKOCN-GFCCVEGCSA-N

> <FORMULA>
C17H16O5

> <MOLECULAR_WEIGHT>
300.31

> <EXACT_MASS>
300.099773615

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
30.59055638383473

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-[(1R)-1-(4-hydroxyphenyl)prop-2-en-1-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione

> <ALOGPS_LOGP>
2.49

> <JCHEM_LOGP>
2.310410807666666

> <ALOGPS_LOGS>
-3.68

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.493028812085013

> <JCHEM_PKA_STRONGEST_BASIC>
-4.7182664885324845

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
84.6937

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
6.21e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[(1R)-1-(4-hydroxyphenyl)prop-2-en-1-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335  -7.700   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      -1.334 -10.010   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.668  -2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
CONECT    1    2    7   21                                                  
CONECT    2    1    3   19                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    1    8                                                  
CONECT    8    7                                                            
CONECT    9    5   10   12                                                  
CONECT   10    9   11                                                       
CONECT   11   10                                                            
CONECT   12    9   13   17                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18   15                                                            
CONECT   19    2   20                                                       
CONECT   20   19                                                            
CONECT   21    1   22                                                       
CONECT   22   21                                                            
MASTER        0    0    0    0    0    0    0    0   22    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₆O₅

Average Mass

300.3100 Da

Monoisotopic Mass

300.09977 Da

IUPAC Name

5-[(1R)-1-(4-hydroxyphenyl)prop-2-en-1-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione

Traditional Name

5-[(1R)-1-(4-hydroxyphenyl)prop-2-en-1-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione

CAS Registry Number

Not Available

SMILES

COC1=C(OC)C(=O)C(=CC1=O)[C@H](C=C)C1=CC=C(O)C=C1

InChI Identifier

InChI=1S/C17H16O5/c1-4-12(10-5-7-11(18)8-6-10)13-9-14(19)16(21-2)17(22-3)15(13)20/h4-9,12,18H,1H2,2-3H3/t12-/m1/s1

InChI Key

XQFOJEJSFFKOCN-GFCCVEGCSA-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
Machaerium nictitans	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ubiquinones. These are coenzyme Q derivatives containing a 5, 6-dimethoxy-3-methyl(1,4-benzoquinone) moiety to which an isoprenyl group is attached at ring position 2(or 6).

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Quinone and hydroquinone lipids

Direct Parent

Ubiquinones

Alternative Parents

Substituents

Ubiquinone skeleton
Dalbergione skeleton
P-benzoquinone
Quinone
1-hydroxy-2-unsubstituted benzenoid
Phenol
Monocyclic benzene moiety
Benzenoid
Vinylogous ester
Ketone
Cyclic ketone
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Carbonyl group
Organic oxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic compounds

External Descriptors

Neoflavonoids (LMPK12100077 )

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	2.49	ALOGPS
logP	2.31	ChemAxon
logS	-3.7	ALOGPS
pKa (Strongest Acidic)	9.49	ChemAxon
pKa (Strongest Basic)	-4.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	84.69 m³·mol⁻¹	ChemAxon
Polarizability	30.59 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

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00010256

Chemspider ID

24843149

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44257560

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (R)-4'-Hydroxy-3,4-dimethoxydalbergione (NP0057209)

MOL for NP0057209 ((R)-4'-Hydroxy-3,4-dimethoxydalbergione)

3D MOL for NP0057209 ((R)-4'-Hydroxy-3,4-dimethoxydalbergione)

3D SDF for NP0057209 ((R)-4'-Hydroxy-3,4-dimethoxydalbergione)

3D-SDF for NP0057209 ((R)-4'-Hydroxy-3,4-dimethoxydalbergione)

PDB for NP0057209 ((R)-4'-Hydroxy-3,4-dimethoxydalbergione)

3D PDB for NP0057209 ((R)-4'-Hydroxy-3,4-dimethoxydalbergione)

SMILES for NP0057209 ((R)-4'-Hydroxy-3,4-dimethoxydalbergione)

INCHI for NP0057209 ((R)-4'-Hydroxy-3,4-dimethoxydalbergione)

Structure for NP0057209 ((R)-4'-Hydroxy-3,4-dimethoxydalbergione)

3D Structure for NP0057209 ((R)-4'-Hydroxy-3,4-dimethoxydalbergione)