NP-MRD: Showing NP-Card for Europinidin (NP0054451)

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Record Information

Version

2.0

Created at

2022-04-28 00:48:13 UTC

Updated at

2022-04-28 00:48:13 UTC

NP-MRD ID

NP0054451

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Europinidin

Description

Europinidin belongs to the class of organic compounds known as 5-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone. Thus, europinidin is considered to be a flavonoid lipid molecule. Europinidin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. It is a water-soluble, bluish red plant dye. It is a rare O-methylated flavonoid, a derivative of delphinidin. Europinidin (Eu) is an O-methylated anthocyanidin. Europinidin is found in Ceratostigma plumbaginoides and Plumbago europaea . It can be found in some species of Plumbago and Ceratostigma.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 39 41  0  0  0  0  0  0  0  0999 V2000
    4.4000    0.0275   -2.1379 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8948   -0.1198   -0.8235 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9935   -0.1936    0.2292 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6420   -0.1249    0.0015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7166   -0.1975    1.0509 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2833   -0.1160    0.7236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0677    0.0220   -0.5450 O   0  0  0  0  0  3  0  0  0  0  0  0
   -1.2815    0.1076   -0.9900 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5574    0.2522   -2.3512 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8567    0.3415   -2.8030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1515    0.4856   -4.1527 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8941    0.2862   -1.8904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6386    0.1420   -0.5267 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6375    0.0819    0.4217 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0075    0.1549    0.1575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3308    0.0548   -0.0978 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0658   -0.0873    1.2411 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7305   -0.1719    1.6341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4817   -0.3132    2.9711 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2425   -0.3391    2.2966 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6264   -0.4111    2.5459 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0925   -0.5557    3.8433 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5077   -0.3381    1.5078 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8758   -0.4010    1.6715 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8344    0.9862   -2.2561 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2355    0.0415   -2.8677 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7591   -0.8470   -2.4395 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2555   -0.0122   -1.0002 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7563    0.2967   -3.0736 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2396    1.3866   -4.6040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9220    0.3553   -2.2332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5614    0.5563    1.0348 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2401    0.7759   -0.7318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3723   -0.8838   -0.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8762   -0.1281    1.9299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2166   -0.3555    3.6494 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5958   -0.4013    3.1455 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4202   -0.6082    4.6025 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5102   -0.3473    0.9125 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  5  1  0
  5 20  2  0
 20 21  1  0
 21 22  1  0
 21 23  2  0
 23 24  1  0
  5  6  1  0
  6 18  2  0
 18 19  1  0
 18 17  1  0
 17 16  2  0
 16 13  1  0
 13 14  1  0
 14 15  1  0
 13 12  2  0
 12 10  1  0
 10 11  1  0
 10  9  2  0
  9  8  1  0
  8  7  2  0
 23  3  1  0
  7  6  1  0
  8 16  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
 20 37  1  0
 22 38  1  0
 24 39  1  0
 19 36  1  0
 17 35  1  0
 15 32  1  0
 15 33  1  0
 15 34  1  0
 12 31  1  0
 11 30  1  0
  9 29  1  0
M  CHG  1   7   1
M  END

  Mrv1533004191513182D          

 24 26  0  0  0  0            999 V2000
   -1.4289    2.4750    0.0000 C   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
   -0.7145    1.2375    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
    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 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    0.8250    0.0000 C   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   -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  3  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
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -0.0000    0.0000 O   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
    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 O   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   -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
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  2  0  0  0  0
  3  9  1  0  0  0  0
  9 10  1  0  0  0  0
  5 11  1  0  0  0  0
 11 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
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  1  0  0  0  0
 13 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 11 23  2  0  0  0  0
 23 24  1  0  0  0  0
M  CHG  1  12   1
M  END
> <DATABASE_ID>
NP0054451

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC(O)=C1O)C1=C(O)C=C2C(OC)=CC(O)=CC2=[O+]1

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O7/c1-22-13-5-9(18)6-14-10(13)7-12(20)17(24-14)8-3-11(19)16(21)15(4-8)23-2/h3-7H,1-2H3,(H3-,18,19,20,21)/p+1

> <INCHI_KEY>
XJXMPIWHBIOJSH-UHFFFAOYSA-O

> <FORMULA>
C17H15O7

> <MOLECULAR_WEIGHT>
331.299

> <EXACT_MASS>
331.081229243

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
39

> <JCHEM_AVERAGE_POLARIZABILITY>
33.04054142134069

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
1

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxy-5-methoxyphenyl)-3,7-dihydroxy-5-methoxy-1λ⁴-chromen-1-ylium

> <ALOGPS_LOGP>
2.48

> <JCHEM_LOGP>
2.8293

> <ALOGPS_LOGS>
-4.16

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
7.0496875568218185

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.068305793769855

> <JCHEM_PKA_STRONGEST_BASIC>
-4.6042499453596175

> <JCHEM_POLAR_SURFACE_AREA>
112.52000000000001

> <JCHEM_REFRACTIVITY>
95.0586

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.53e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
europinidin

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.334   3.850   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -4.001  -0.770   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+1
HETATM   13  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    9                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   11                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7    3   10                                                  
CONECT   10    9                                                            
CONECT   11    5   12   23                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   21                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   13   22                                                  
CONECT   22   21   23                                                       
CONECT   23   22   11   24                                                  
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₅O₇

Average Mass

331.2990 Da

Monoisotopic Mass

331.08123 Da

IUPAC Name

2-(3,4-dihydroxy-5-methoxyphenyl)-3,7-dihydroxy-5-methoxy-1λ⁴-chromen-1-ylium

Traditional Name

europinidin

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC(O)=C1O)C1=C(O)C=C2C(OC)=CC(O)=CC2=[O+]1

InChI Identifier

InChI=1S/C17H14O7/c1-22-13-5-9(18)6-14-10(13)7-12(20)17(24-14)8-3-11(19)16(21)15(4-8)23-2/h3-7H,1-2H3,(H3-,18,19,20,21)/p+1

InChI Key

XJXMPIWHBIOJSH-UHFFFAOYSA-O

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
Ceratostigma plumbaginoides	Plant	KNApSAcK
Plumbago europaea	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 5-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C5 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

5-O-methylated flavonoids

Alternative Parents

Substituents

3p-methoxyflavonoid-skeleton
5-methoxyflavonoid-skeleton
3'-hydroxyflavonoid
3-hydroxyflavonoid
4'-hydroxyflavonoid
7-hydroxyflavonoid
Hydroxyflavonoid
Anthocyanidin
Benzopyran
Methoxyphenol
1-benzopyran
Phenoxy compound
Anisole
Methoxybenzene
Catechol
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Organoheterocyclic compound
Ether
Oxacycle
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic cation
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Anthocyanidins (LMPK12010416 )

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	2.48	ALOGPS
logP	2.83	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	6.07	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	112.52 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	95.06 m³·mol⁻¹	ChemAxon
Polarizability	33.04 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

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Europinidin

METLIN ID

Not Available

PubChem Compound

14496547

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Europinidin (NP0054451)

MOL for NP0054451 (Europinidin)

3D MOL for NP0054451 (Europinidin)

3D SDF for NP0054451 (Europinidin)

3D-SDF for NP0054451 (Europinidin)

PDB for NP0054451 (Europinidin)

3D PDB for NP0054451 (Europinidin)

SMILES for NP0054451 (Europinidin)

INCHI for NP0054451 (Europinidin)

Structure for NP0054451 (Europinidin)

3D Structure for NP0054451 (Europinidin)