NP-MRD: Showing NP-Card for 7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one (NP0190956)

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Record Information

Version

2.0

Created at

2022-09-04 07:44:09 UTC

Updated at

2022-09-04 07:44:10 UTC

NP-MRD ID

NP0190956

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one

Description

Tephroapollin D 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. Based on a literature review very few articles have been published on Tephroapollin D.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042209442D          

 26 28  0  0  0  0            999 V2000
    0.0000   -2.4750    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
    0.7145   -1.2375    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 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
    2.8579    0.8250    0.0000 O   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
    3.5724   -1.2375    0.0000 C   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
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   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
    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
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    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
   -0.1105   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 O   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
  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  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  2  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 48 50  0  0  0  0  0  0  0  0999 V2000
   -2.9344    0.5915    3.9752 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3380    0.3977    2.7101 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9672    0.3375    2.6183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1800    0.4692    3.7808 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1932    0.4144    3.7289 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8236    0.2248    2.5034 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1964    0.1666    2.4266 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9109    0.2828    3.4569 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7499   -0.0262    1.1579 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9607   -0.1519    0.0388 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5413   -0.3527   -1.2807 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8842   -0.4353   -1.5442 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3309   -0.6306   -2.8577 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4622   -0.7460   -3.9205 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1117   -0.6631   -3.6569 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6677   -0.4711   -2.3667 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6616   -0.0843    0.2034 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0701    0.0951    1.3643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3437    0.1517    1.4186 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0548    0.0073    0.1827 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3347    0.0214   -0.0415 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9236   -0.1464   -1.4162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9136   -0.8880   -2.2443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2050   -0.9263   -1.2393 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1354    1.1030   -1.9729 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0132    1.8757   -1.2092 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0373    0.4923    3.9415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5946   -0.1918    4.7101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6472    1.5636    4.4331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7174    0.6156    4.7139 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7983    0.5119    4.5945 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8178   -0.0734    1.0843 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5881   -0.3487   -0.7338 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3825   -0.6928   -3.0462 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7952   -0.8973   -4.9410 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3856   -0.7502   -4.4767 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5984   -0.4069   -2.1682 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4500   -0.1399   -0.7447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0100    0.1543    0.7442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4221   -1.6893   -1.6344 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1635   -0.1875   -2.6488 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4388   -1.3422   -3.1099 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8871   -1.9854   -1.0123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8344   -0.8798   -2.1412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7335   -0.5885   -0.3159 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9689    1.3264   -1.1632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1318    2.8613   -1.6914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5501    2.0312   -0.2096 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  6  2  0
  6  7  1  0
  7  8  2  0
  7  9  1  0
  9 10  2  0
 10 17  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
 22 24  1  0
 22 25  1  0
 25 26  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
 19  3  1  0
 16 11  1  0
 18  6  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
  9 32  1  0
 20 38  1  0
 21 39  1  0
 23 40  1  0
 23 41  1  0
 23 42  1  0
 24 43  1  0
 24 44  1  0
 24 45  1  0
 26 46  1  0
 26 47  1  0
 26 48  1  0
 12 33  1  0
 13 34  1  0
 14 35  1  0
 15 36  1  0
 16 37  1  0
M  END


  Mrv1652309042209442D          

 26 28  0  0  0  0            999 V2000
    0.0000   -2.4750    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
    0.7145   -1.2375    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 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
    2.8579    0.8250    0.0000 O   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
    3.5724   -1.2375    0.0000 C   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
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   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
    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
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    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
   -0.1105   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5395   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 O   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
  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  2  0  0  0  0
  7  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 10 17  1  0  0  0  0
 17 18  1  0  0  0  0
  6 18  1  0  0  0  0
 18 19  2  0  0  0  0
  3 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0190956

> <DATABASE_NAME>
NP-MRD

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

> <INCHI_IDENTIFIER>
InChI=1S/C22H22O4/c1-22(2,25-4)13-12-17-19(24-3)11-10-16-18(23)14-20(26-21(16)17)15-8-6-5-7-9-15/h5-14H,1-4H3/b13-12+

> <INCHI_KEY>
ZEGZKBKPOMECDI-OUKQBFOZSA-N

> <FORMULA>
C22H22O4

> <MOLECULAR_WEIGHT>
350.414

> <EXACT_MASS>
350.151809188

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
38.5526665627753

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
7-methoxy-8-[(1E)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenyl-4H-chromen-4-one

> <JCHEM_LOGP>
3.9925579356666665

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.800416747878593

> <JCHEM_PKA_STRONGEST_BASIC>
-4.066759623317857

> <JCHEM_POLAR_SURFACE_AREA>
44.760000000000005

> <JCHEM_REFRACTIVITY>
104.37710000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
7-methoxy-8-[(1E)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.000  -3.080   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       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   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  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       6.668  -0.770   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       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -0.206  -6.930   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       2.874  -6.930   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       1.334  -8.470   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   19                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   18                                                  
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10                                                       
CONECT   10    9   11   17                                                  
CONECT   11   10   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17   10   18                                                       
CONECT   18   17    6   19                                                  
CONECT   19   18    3   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24   25                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   22   26                                                       
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

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Synonyms

Not Available

Chemical Formula

C₂₂H₂₂O₄

Average Mass

350.4140 Da

Monoisotopic Mass

350.15181 Da

IUPAC Name

7-methoxy-8-[(1E)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenyl-4H-chromen-4-one

Traditional Name

7-methoxy-8-[(1E)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one

CAS Registry Number

Not Available

SMILES

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

InChI Identifier

InChI=1S/C22H22O4/c1-22(2,25-4)13-12-17-19(24-3)11-10-16-18(23)14-20(26-21(16)17)15-8-6-5-7-9-15/h5-14H,1-4H3/b13-12+

InChI Key

ZEGZKBKPOMECDI-OUKQBFOZSA-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

7-methoxyflavonoid-skeleton
Flavone
Chromone
Benzopyran
1-benzopyran
Anisole
Phenol ether
Styrene
Pyranone
Alkyl aryl ether
Pyran
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Ether
Dialkyl ether
Oxacycle
Organoheterocyclic compound
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
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	3.99	ChemAxon
pKa (Strongest Acidic)	15.8	ChemAxon
pKa (Strongest Basic)	-4.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	44.76 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	104.38 m³·mol⁻¹	ChemAxon
Polarizability	38.55 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

28284551

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

24813966

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one (NP0190956)

MOL for NP0190956 (7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one)

3D MOL for NP0190956 (7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one)

3D SDF for NP0190956 (7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one)

3D-SDF for NP0190956 (7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one)

PDB for NP0190956 (7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one)

3D PDB for NP0190956 (7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one)

SMILES for NP0190956 (7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one)

INCHI for NP0190956 (7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one)

Structure for NP0190956 (7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one)

3D Structure for NP0190956 (7-methoxy-8-[(1e)-3-methoxy-3-methylbut-1-en-1-yl]-2-phenylchromen-4-one)