NP-MRD: Showing NP-Card for 5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone (NP0053069)

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Record Information

Version

2.0

Created at

2022-04-27 23:52:48 UTC

Updated at

2022-04-27 23:52:48 UTC

NP-MRD ID

NP0053069

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone

Description

5,7-Dihydroxy-3,6-dimethoxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one belongs to the class of organic compounds known as 6-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone. Thus, 5,7-dihydroxy-3,6-dimethoxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one is considered to be a flavonoid lipid molecule. 5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone is found in Alluaudia ascendens and Gutierrezia spp.. 5,7-Dihydroxy-3,6-dimethoxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652310051719352D          

 26 28  0  0  0  0            999 V2000
   -2.1434   -1.2375    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
    2.8579    0.8250    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
    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
    3.5724    1.2375    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
   -0.7145   -0.4125    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
    4.2868    0.8250    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
    1.4289   -1.6500    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
   -0.7145   -1.2375    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
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    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
    5.0013    1.2375    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   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    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
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  3  2  0  0  0  0
  6  4  1  0  0  0  0
  7  3  1  0  0  0  0
  8  4  2  0  0  0  0
  9  5  2  0  0  0  0
 10  5  1  0  0  0  0
 11 10  2  0  0  0  0
 12  7  2  0  0  0  0
 12  8  1  0  0  0  0
 13 11  1  0  0  0  0
 14 11  1  0  0  0  0
 15  6  1  0  0  0  0
 16  9  1  0  0  0  0
 16 13  2  0  0  0  0
 17 14  1  0  0  0  0
 17 15  2  0  0  0  0
 18  7  1  0  0  0  0
 19  8  1  0  0  0  0
 20  9  1  0  0  0  0
 21 12  1  0  0  0  0
 22 13  1  0  0  0  0
 23 14  2  0  0  0  0
 24  1  1  0  0  0  0
 24 16  1  0  0  0  0
 25  2  1  0  0  0  0
 25 17  1  0  0  0  0
 26 10  1  0  0  0  0
 26 15  1  0  0  0  0
M  END

     RDKit          3D

 40 42  0  0  0  0  0  0  0  0999 V2000
    6.2039    0.0783    0.8048 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4471    0.0619   -0.3988 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0624    0.2944   -0.3112 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5340    1.5479   -0.3961 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4270    2.6043   -0.5752 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1820    1.7569   -0.3087 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3197    0.6755   -0.1295 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0400    0.8739   -0.0466 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8096   -0.1377    0.1240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2228    0.2489    0.1999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2470   -0.5618    0.6006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5748   -0.0972    0.5889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5787   -0.9757    1.0095 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9134    1.1625    0.1872 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2333    1.5749    0.1928 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8942    1.9906   -0.2176 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2333    3.2693   -0.6251 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5998    1.5422   -0.2084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4072   -1.4078    0.2178 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2309   -2.5001    0.3832 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6403   -3.1313   -0.8532 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9768   -1.6663    0.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3705   -2.8607    0.2231 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8255   -0.5997   -0.0406 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1921   -0.7932   -0.1307 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7545   -2.0148   -0.0518 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2514   -0.9021    1.2941 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7699    0.7933    1.5461 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2184    0.4994    0.5653 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1148    3.5597   -0.6472 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7597    2.7279   -0.3735 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0591   -1.5533    0.9568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3654   -1.9132    1.3129 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5545    2.4726   -0.0844 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5180    3.9104   -0.9300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7998    2.1929   -0.5281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1568   -4.0720   -0.6760 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7194   -3.3510   -1.4630 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1956   -2.3712   -1.4067 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5039   -2.9286    0.0613 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 25  2  0
 25 26  1  0
 25 24  1  0
 24  7  2  0
  7  8  1  0
  8  9  1  0
  9 19  2  0
 19 20  1  0
 20 21  1  0
 19 22  1  0
 22 23  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 12 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
 16 18  2  0
  7  6  1  0
  6  4  2  0
  4  5  1  0
  4  3  1  0
 22 24  1  0
 18 10  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
 26 40  1  0
 21 37  1  0
 21 38  1  0
 21 39  1  0
 11 32  1  0
 13 33  1  0
 15 34  1  0
 17 35  1  0
 18 36  1  0
  6 31  1  0
  5 30  1  0
M  END


  Mrv1652310051719352D          

 26 28  0  0  0  0            999 V2000
   -2.1434   -1.2375    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
    2.8579    0.8250    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
    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
    3.5724    1.2375    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
   -0.7145   -0.4125    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
    4.2868    0.8250    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
    1.4289   -1.6500    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
   -0.7145   -1.2375    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
    3.5724    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -0.4125    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
    5.0013    1.2375    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   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.6500    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
    1.4289   -0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  6  3  2  0  0  0  0
  6  4  1  0  0  0  0
  7  3  1  0  0  0  0
  8  4  2  0  0  0  0
  9  5  2  0  0  0  0
 10  5  1  0  0  0  0
 11 10  2  0  0  0  0
 12  7  2  0  0  0  0
 12  8  1  0  0  0  0
 13 11  1  0  0  0  0
 14 11  1  0  0  0  0
 15  6  1  0  0  0  0
 16  9  1  0  0  0  0
 16 13  2  0  0  0  0
 17 14  1  0  0  0  0
 17 15  2  0  0  0  0
 18  7  1  0  0  0  0
 19  8  1  0  0  0  0
 20  9  1  0  0  0  0
 21 12  1  0  0  0  0
 22 13  1  0  0  0  0
 23 14  2  0  0  0  0
 24  1  1  0  0  0  0
 24 16  1  0  0  0  0
 25  2  1  0  0  0  0
 25 17  1  0  0  0  0
 26 10  1  0  0  0  0
 26 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0053069

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C2=C(OC(=C(OC)C2=O)C2=CC(O)=C(O)C(O)=C2)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C17H14O9/c1-24-16-9(20)5-10-11(13(16)22)14(23)17(25-2)15(26-10)6-3-7(18)12(21)8(19)4-6/h3-5,18-22H,1-2H3

> <INCHI_KEY>
ZUBFWGOFMRYWNS-UHFFFAOYSA-N

> <FORMULA>
C17H14O9

> <MOLECULAR_WEIGHT>
362.29

> <EXACT_MASS>
362.063782031

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
40

> <JCHEM_AVERAGE_POLARIZABILITY>
34.48902322609782

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
5

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5,7-dihydroxy-3,6-dimethoxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one

> <ALOGPS_LOGP>
2.38

> <JCHEM_LOGP>
1.8078902659999994

> <ALOGPS_LOGS>
-3.35

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.986657174876062

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.885142777794385

> <JCHEM_PKA_STRONGEST_BASIC>
-4.609528973535809

> <JCHEM_POLAR_SURFACE_AREA>
145.91

> <JCHEM_REFRACTIVITY>
90.0575

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.62e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5,7-dihydroxy-3,6-dimethoxy-2-(3,4,5-trihydroxyphenyl)chromen-4-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      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.668  -0.770   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       5.335  -0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.000  -3.080   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  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       6.668   3.850   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       9.336  -0.770   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -2.667  -0.000   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       9.336   2.310   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  -4.620   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      -2.667  -3.080   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       2.667  -0.000   0.000  0.00  0.00           O+0
CONECT    1   24                                                            
CONECT    2   25                                                            
CONECT    3    6    7                                                       
CONECT    4    6    8                                                       
CONECT    5    9   10                                                       
CONECT    6    3    4   15                                                  
CONECT    7    3   12   18                                                  
CONECT    8    4   12   19                                                  
CONECT    9    5   16   20                                                  
CONECT   10    5   11   26                                                  
CONECT   11   10   13   14                                                  
CONECT   12    7    8   21                                                  
CONECT   13   11   16   22                                                  
CONECT   14   11   17   23                                                  
CONECT   15    6   17   26                                                  
CONECT   16    9   13   24                                                  
CONECT   17   14   15   25                                                  
CONECT   18    7                                                            
CONECT   19    8                                                            
CONECT   20    9                                                            
CONECT   21   12                                                            
CONECT   22   13                                                            
CONECT   23   14                                                            
CONECT   24    1   16                                                       
CONECT   25    2   17                                                       
CONECT   26   10   15                                                       
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₇H₁₄O₉

Average Mass

362.2900 Da

Monoisotopic Mass

362.06378 Da

IUPAC Name

5,7-dihydroxy-3,6-dimethoxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one

Traditional Name

5,7-dihydroxy-3,6-dimethoxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

CAS Registry Number

Not Available

SMILES

COC1=C(O)C2=C(OC(=C(OC)C2=O)C2=CC(O)=C(O)C(O)=C2)C=C1O

InChI Identifier

InChI=1S/C17H14O9/c1-24-16-9(20)5-10-11(13(16)22)14(23)17(25-2)15(26-10)6-3-7(18)12(21)8(19)4-6/h3-5,18-22H,1-2H3

InChI Key

ZUBFWGOFMRYWNS-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
Alluaudia ascendens	Plant	KNApSAcK
Gutierrezia spp.	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 6-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C6 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

6-O-methylated flavonoids

Alternative Parents

Substituents

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

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12113039 )

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	2.38	ALOGPS
logP	1.81	ChemAxon
logS	-3.4	ALOGPS
pKa (Strongest Acidic)	6.89	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	9	ChemAxon
Hydrogen Donor Count	5	ChemAxon
Polar Surface Area	145.91 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	90.06 m³·mol⁻¹	ChemAxon
Polarizability	34.49 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

HMDB0153222

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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone (NP0053069)

MOL for NP0053069 (5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone)

3D MOL for NP0053069 (5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone)

3D SDF for NP0053069 (5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone)

3D-SDF for NP0053069 (5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone)

PDB for NP0053069 (5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone)

3D PDB for NP0053069 (5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone)

SMILES for NP0053069 (5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone)

INCHI for NP0053069 (5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone)

Structure for NP0053069 (5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone)

3D Structure for NP0053069 (5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone)