NP-MRD: Showing NP-Card for Azaleatin (NP0052915)

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Record Information

Version

2.0

Created at

2022-04-27 23:47:56 UTC

Updated at

2022-04-27 23:47:56 UTC

NP-MRD ID

NP0052915

Secondary Accession Numbers

None

Natural Product Identification

Common Name

Azaleatin

Description

Azaleatin belongs to the class of organic compounds known as flavonols. Flavonols are compounds that contain a flavone (2-phenyl-1-benzopyran-4-one) backbone carrying a hydroxyl group at the 3-position. Thus, azaleatin is considered to be a flavonoid lipid molecule. Azaleatin is found in Beilschmiedia miersii, Carthamus tinctorius , Carya illinoinensis, Carya pecan, Cassiope spp., Eucryphia glutinosa, Kalmiopsis leachiana, Medicago sativa , Parkia biglobosa , Plumbago spp., Rhododendron dauricum, Rhododendron luteum, Rhododendron pneumonanthum, Rhododendron spp., Senna lindheimeriana, Tephrosia watsoniana and Tetracera spp.. Azaleatin is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 35 37  0  0  0  0  0  0  0  0999 V2000
   -5.2353   -1.8230   -0.5218 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8273   -1.7560   -0.5278 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2100   -0.5812   -0.1741 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9387    0.5321    0.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3340    1.7202    0.5441 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0833    2.8312    0.9039 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9578    1.7419    0.5247 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1755    0.6589    0.1730 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1289    0.7131    0.1650 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9007   -0.3137   -0.1690 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3447   -0.0745   -0.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3023   -1.0026   -0.4290 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6525   -0.6848   -0.3558 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1065    0.5586    0.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4539    0.8830    0.0976 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1438    1.4979    0.3329 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5990    2.7549    0.7152 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8118    1.1823    0.2600 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3149   -1.4857   -0.5224 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0256   -2.5802   -0.8764 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0811   -1.5892   -0.5281 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6652   -2.6394   -0.8436 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8338   -0.4926   -0.1727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5172   -2.7958   -1.0048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7139   -0.9670   -1.0040 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5540   -1.8747    0.5519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0319    0.5281    0.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5848    3.6773    1.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4170    2.6580    0.7994 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0416   -1.9838   -0.7292 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4151   -1.4334   -0.6032 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1088    0.1496   -0.1430 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9851    3.5148    0.9633 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1003    1.9580    0.5148 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7257   -3.4822   -1.1512 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 23  2  0
 23 21  1  0
 21 22  2  0
 21 19  1  0
 19 20  1  0
 19 10  2  0
 10  9  1  0
  9  8  1  0
  8  7  2  0
  7  5  1  0
  5  6  1  0
  5  4  2  0
 10 11  1  0
 11 18  2  0
 18 16  1  0
 16 17  1  0
 16 14  2  0
 14 15  1  0
 14 13  1  0
 13 12  2  0
  4  3  1  0
 12 11  1  0
  8 23  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
 20 35  1  0
  7 29  1  0
  6 28  1  0
  4 27  1  0
 18 34  1  0
 17 33  1  0
 15 32  1  0
 13 31  1  0
 12 30  1  0
M  END


  Mrv1652310051715532D          

 23 25  0  0  0  0            999 V2000
   -0.7145   -2.8875    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    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    0.0000    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
   -0.7145   -0.4125    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
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -1.6500    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
    0.7145   -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
    2.1434   -1.2375    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
   -1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  3  2  2  0  0  0  0
  7  2  1  0  0  0  0
  7  4  2  0  0  0  0
  8  5  2  0  0  0  0
  8  6  1  0  0  0  0
  9  3  1  0  0  0  0
 10  4  1  0  0  0  0
 10  9  2  0  0  0  0
 11  5  1  0  0  0  0
 12  6  2  0  0  0  0
 13 11  2  0  0  0  0
 13 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  1  0  0  0  0
 16  7  1  0  0  0  0
 16 15  2  0  0  0  0
 17  8  1  0  0  0  0
 18  9  1  0  0  0  0
 19 10  1  0  0  0  0
 20 14  2  0  0  0  0
 21 15  1  0  0  0  0
 22  1  1  0  0  0  0
 22 11  1  0  0  0  0
 23 12  1  0  0  0  0
 23 16  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0052915

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C(=O)C(O)=C(OC2=CC(O)=C1)C1=CC(O)=C(O)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C16H12O7/c1-22-11-5-8(17)6-12-13(11)14(20)15(21)16(23-12)7-2-3-9(18)10(19)4-7/h2-6,17-19,21H,1H3

> <INCHI_KEY>
RJBAXROZAXAEEM-UHFFFAOYSA-N

> <FORMULA>
C16H12O7

> <MOLECULAR_WEIGHT>
316.265

> <EXACT_MASS>
316.058302726

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
35

> <JCHEM_AVERAGE_POLARIZABILITY>
30.561756194226128

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-4H-chromen-4-one

> <ALOGPS_LOGP>
1.98

> <JCHEM_LOGP>
1.65219352

> <ALOGPS_LOGS>
-3.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
8.434508499632893

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.377463280937571

> <JCHEM_PKA_STRONGEST_BASIC>
-3.9572403137237986

> <JCHEM_POLAR_SURFACE_AREA>
116.45

> <JCHEM_REFRACTIVITY>
81.34450000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.33e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
azaleatin

> <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      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -0.770   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       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -2.667   0.000   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0       9.336   2.310   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       0.000  -4.620   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
CONECT    1   22                                                            
CONECT    2    3    7                                                       
CONECT    3    2    9                                                       
CONECT    4    7   10                                                       
CONECT    5    8   11                                                       
CONECT    6    8   12                                                       
CONECT    7    2    4   16                                                  
CONECT    8    5    6   17                                                  
CONECT    9    3   10   18                                                  
CONECT   10    4    9   19                                                  
CONECT   11    5   13   22                                                  
CONECT   12    6   13   23                                                  
CONECT   13   11   12   14                                                  
CONECT   14   13   15   20                                                  
CONECT   15   14   16   21                                                  
CONECT   16    7   15   23                                                  
CONECT   17    8                                                            
CONECT   18    9                                                            
CONECT   19   10                                                            
CONECT   20   14                                                            
CONECT   21   15                                                            
CONECT   22    1   11                                                       
CONECT   23   12   16                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Value	Source
2-(3,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-4H-1-benzopyran-4-one	ChEBI
5-O-Methylquercetin	ChEBI
Quercetin 5-methyl ether	ChEBI

Chemical Formula

C₁₆H₁₂O₇

Average Mass

316.2650 Da

Monoisotopic Mass

316.05830 Da

IUPAC Name

2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-4H-chromen-4-one

Traditional Name

azaleatin

CAS Registry Number

Not Available

SMILES

COC1=C2C(=O)C(O)=C(OC2=CC(O)=C1)C1=CC(O)=C(O)C=C1

InChI Identifier

InChI=1S/C16H12O7/c1-22-11-5-8(17)6-12-13(11)14(20)15(21)16(23-12)7-2-3-9(18)10(19)4-7/h2-6,17-19,21H,1H3

InChI Key

RJBAXROZAXAEEM-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
Beilschmiedia miersii	Plant	KNApSAcK
Carthamus tinctorius	Plant	KNApSAcK
Carya illinoinensis	LOTUS Database	35616633
Carya pecan	Plant	KNApSAcK
Cassiope spp.	Plant	KNApSAcK
Eucryphia glutinosa	Plant	KNApSAcK
Kalmiopsis leachiana	Plant	KNApSAcK
Medicago sativa	Plant	KNApSAcK
Parkia biglobosa	Plant	KNApSAcK
Plumbago spp.	Plant	KNApSAcK
Rhododendron dauricum	LOTUS Database	35616633
Rhododendron luteum	LOTUS Database	35616633
Rhododendron pneumonanthum	LOTUS Database	35616633
Rhododendron spp.	Plant	KNApSAcK
Senna lindheimeriana	Plant	KNApSAcK
Tephrosia watsoniana	Plant	KNApSAcK
Tetracera spp.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as flavonols. Flavonols are compounds that contain a flavone (2-phenyl-1-benzopyran-4-one) backbone carrying a hydroxyl group at the 3-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavones

Direct Parent

Flavonols

Alternative Parents

Substituents

3-hydroxyflavone
5-methoxyflavonoid-skeleton
7-hydroxyflavonoid
3'-hydroxyflavonoid
3-hydroxyflavonoid
4'-hydroxyflavonoid
Hydroxyflavonoid
Chromone
Benzopyran
1-benzopyran
Anisole
Catechol
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Pyranone
Benzenoid
Pyran
Monocyclic benzene moiety
Vinylogous ester
Heteroaromatic compound
Ether
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

monomethoxyflavone (CHEBI:2945 )
tetrahydroxyflavone (CHEBI:2945 )
7-hydroxyflavonol (CHEBI:2945 )
flavonols (C10022 )
Flavones and Flavonols (C10022 )
Flavones and Flavonols (LMPK12112546 )

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	1.98	ALOGPS
logP	1.65	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	6.38	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	116.45 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	81.34 m³·mol⁻¹	ChemAxon
Polarizability	30.56 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

HMDB0152176

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

C00004633

Chemspider ID

Not Available

KEGG Compound ID

C10022

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Azaleatin

METLIN ID

Not Available

PubChem Compound

5281604

PDB ID

Not Available

ChEBI ID

2945

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for Azaleatin (NP0052915)

MOL for NP0052915 (Azaleatin)

3D MOL for NP0052915 (Azaleatin)

3D SDF for NP0052915 (Azaleatin)

3D-SDF for NP0052915 (Azaleatin)

PDB for NP0052915 (Azaleatin)

3D PDB for NP0052915 (Azaleatin)

SMILES for NP0052915 (Azaleatin)

INCHI for NP0052915 (Azaleatin)

Structure for NP0052915 (Azaleatin)

3D Structure for NP0052915 (Azaleatin)