NP-MRD: Showing NP-Card for 2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate (NP0223991)

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Record Information

Version

2.0

Created at

2022-09-06 02:14:19 UTC

Updated at

2022-09-06 02:14:19 UTC

NP-MRD ID

NP0223991

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate

Description

2-(3,4-Dimethoxyphenyl)-5,7-dimethoxy-4-oxo-4H-chromen-3-yl octadecanoate belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. 2-(3,4-Dimethoxyphenyl)-5,7-dimethoxy-4-oxo-4H-chromen-3-yl octadecanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL SDF PDB SMILES InChI


  Mrv1533004191520402D          

 45 47  0  0  0  0            999 V2000
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -0.4125    0.0000 C   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  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  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 33  2  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  0  0  0  0
 21 34  1  0  0  0  0
 34 35  2  0  0  0  0
 22 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 39 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 42 45  2  0  0  0  0
 36 45  1  0  0  0  0
M  END


  Mrv1533004191520402D          

 45 47  0  0  0  0            999 V2000
   12.8605   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.5749   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2894   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0039   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.7184   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.4328   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.1473   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.8618   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.5762   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.2907   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.0052   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7197   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.4341   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.1486   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.8631   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.5775   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.2920   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.0065   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   30.0078   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.7210   -3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499   -0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.4354    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.1499    1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.5788    0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.2933    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.8644   -0.4125    0.0000 C   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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  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  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 26 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 30 33  2  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  0  0  0  0
 21 34  1  0  0  0  0
 34 35  2  0  0  0  0
 22 36  1  0  0  0  0
 36 37  2  0  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 39 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 42 45  2  0  0  0  0
 36 45  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0223991

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCC(=O)OC1=C(OC2=CC(OC)=CC(OC)=C2C1=O)C1=CC=C(OC)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C37H52O8/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-33(38)45-37-35(39)34-31(43-5)25-28(40-2)26-32(34)44-36(37)27-22-23-29(41-3)30(24-27)42-4/h22-26H,6-21H2,1-5H3

> <INCHI_KEY>
HQICIHYFOSPGLW-UHFFFAOYSA-N

> <FORMULA>
C37H52O8

> <MOLECULAR_WEIGHT>
624.815

> <EXACT_MASS>
624.366218634

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
97

> <JCHEM_AVERAGE_POLARIZABILITY>
73.52406814696992

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxo-4H-chromen-3-yl octadecanoate

> <ALOGPS_LOGP>
8.57

> <JCHEM_LOGP>
9.369767806000002

> <ALOGPS_LOGS>
-8.08

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.260665713751275

> <JCHEM_POLAR_SURFACE_AREA>
89.52000000000001

> <JCHEM_REFRACTIVITY>
177.58479999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
23

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.18e-06 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate

> <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      24.006  -3.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      25.340  -3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      26.674  -3.080   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      28.007  -3.850   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      29.341  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      30.675  -3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      32.008  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      33.342  -3.850   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      34.676  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      36.009  -3.850   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      37.343  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      38.677  -3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      40.010  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      41.344  -3.850   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      42.678  -3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      44.011  -3.850   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      45.345  -3.080   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      46.679  -3.850   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      46.679  -5.390   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      48.012  -3.080   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      49.346  -3.850   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      50.680  -3.080   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      52.013  -3.850   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      52.013  -5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      53.347  -6.160   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      53.347  -7.700   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      54.681  -8.470   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      56.015  -7.700   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      52.013  -8.470   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      50.680  -7.700   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      49.346  -8.470   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      48.012  -7.700   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      50.680  -6.160   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      49.346  -5.390   0.000  0.00  0.00           C+0
HETATM   35  O   UNK     0      48.012  -6.160   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0      50.680  -1.540   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      49.346  -0.770   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      49.346   0.770   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      50.680   1.540   0.000  0.00  0.00           C+0
HETATM   40  O   UNK     0      50.680   3.080   0.000  0.00  0.00           O+0
HETATM   41  C   UNK     0      52.013   3.850   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      52.013   0.770   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      53.347   1.540   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      54.681   0.770   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      52.013  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   34                                                  
CONECT   22   21   23   36                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   33                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   29                                                  
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   26   30                                                       
CONECT   30   29   31   33                                                  
CONECT   31   30   32                                                       
CONECT   32   31                                                            
CONECT   33   30   24   34                                                  
CONECT   34   33   21   35                                                  
CONECT   35   34                                                            
CONECT   36   22   37   45                                                  
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   42                                                  
CONECT   40   39   41                                                       
CONECT   41   40                                                            
CONECT   42   39   43   45                                                  
CONECT   43   42   44                                                       
CONECT   44   43                                                            
CONECT   45   42   36                                                       
MASTER        0    0    0    0    0    0    0    0   45    0   94    0
END

View in JSmol

Synonyms

Value	Source
2-(3,4-Dimethoxyphenyl)-5,7-dimethoxy-4-oxo-4H-chromen-3-yl octadecanoic acid	Generator

Chemical Formula

C₃₇H₅₂O₈

Average Mass

624.8150 Da

Monoisotopic Mass

624.36622 Da

IUPAC Name

2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxo-4H-chromen-3-yl octadecanoate

Traditional Name

2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCC(=O)OC1=C(OC2=CC(OC)=CC(OC)=C2C1=O)C1=CC=C(OC)C(OC)=C1

InChI Identifier

InChI=1S/C37H52O8/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-33(38)45-37-35(39)34-31(43-5)25-28(40-2)26-32(34)44-36(37)27-22-23-29(41-3)30(24-27)42-4/h22-26H,6-21H2,1-5H3

InChI Key

HQICIHYFOSPGLW-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

7-O-methylated flavonoids

Alternative Parents

Substituents

3p-methoxyflavonoid-skeleton
4p-methoxyflavonoid-skeleton
5-methoxyflavonoid-skeleton
7-methoxyflavonoid-skeleton
Flavone
Chromone
1-benzopyran
Benzopyran
Dimethoxybenzene
O-dimethoxybenzene
Anisole
Phenoxy compound
Phenol ether
Methoxybenzene
Pyranone
Alkyl aryl ether
Fatty acid ester
Fatty acyl
Monocyclic benzene moiety
Benzenoid
Pyran
Vinylogous ester
Heteroaromatic compound
Carboxylic acid ester
Ether
Carboxylic acid derivative
Organoheterocyclic compound
Oxacycle
Monocarboxylic acid or derivatives
Carbonyl group
Organic oxide
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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	8.57	ALOGPS
logP	9.37	ChemAxon
logS	-8.1	ALOGPS
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	89.52 Å²	ChemAxon
Rotatable Bond Count	23	ChemAxon
Refractivity	177.58 m³·mol⁻¹	ChemAxon
Polarizability	73.52 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

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

LOTUS database [Link]

Showing NP-Card for 2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate (NP0223991)

MOL for NP0223991 (2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate)

3D MOL for NP0223991 (2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate)

3D SDF for NP0223991 (2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate)

3D-SDF for NP0223991 (2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate)

PDB for NP0223991 (2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate)

3D PDB for NP0223991 (2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate)

SMILES for NP0223991 (2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate)

INCHI for NP0223991 (2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate)

Structure for NP0223991 (2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate)

3D Structure for NP0223991 (2-(3,4-dimethoxyphenyl)-5,7-dimethoxy-4-oxochromen-3-yl octadecanoate)