NP-MRD: Showing NP-Card for 3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one (NP0315817)

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Record Information

Version

2.0

Created at

2022-09-11 14:38:23 UTC

Updated at

2022-09-11 14:38:23 UTC

NP-MRD ID

NP0315817

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one

Description

CHEMBL523623 belongs to the class of organic compounds known as 7-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C7 atom of the isoflavone backbone. 3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one is found in Psorothamnus arborescens. Based on a literature review very few articles have been published on CHEMBL523623.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112216382D          

 30 32  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
    1.4289    0.8250    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
    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
    4.2868   -0.0000    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
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    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
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -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
    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  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  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 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  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 14 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  2  0  0  0  0
 12 26  1  0  0  0  0
 11 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  2  0  0  0  0
  3 30  1  0  0  0  0
M  END

     RDKit          3D

 56 58  0  0  0  0  0  0  0  0999 V2000
    8.3923    0.6697   -0.1095 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5401   -0.3394    0.3796 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1577   -0.2116    0.2807 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5394    0.8814   -0.2871 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1613    0.9554   -0.3589 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5255    2.0482   -0.9269 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3167    3.0966   -1.4365 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3599   -0.0557    0.1321 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9874    0.0232    0.0580 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3855    0.9980   -0.4498 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2590   -1.0248    0.5697 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2016   -1.0159    0.5275 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9836    0.0462    0.8417 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3843   -0.0178    0.7799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1769    1.1974    1.1236 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6727    1.8736   -0.1061 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9228    2.1460   -0.3946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1012    1.8391    0.4426 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2298    2.8455   -1.7088 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0196   -1.1635    0.3980 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3973   -1.2349    0.3374 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1983   -1.6527    1.4251 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2238   -2.2698    0.0699 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9075   -3.4155   -0.3140 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0973   -4.5465   -0.6496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8521   -2.1859    0.1367 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9557   -2.0977    1.1296 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2597   -2.1156    1.1712 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9919   -1.1477    0.7000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3613   -1.2475    0.7846 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0417    0.9713   -1.1004 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3412    1.5347    0.6111 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.4512    0.3167   -0.1535 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1751    1.6656   -0.6672 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8521    3.6509   -0.6344 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0268    2.6988   -2.1803 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6353    3.8434   -1.9133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5098    0.9684    1.1487 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5632    1.9377    1.6796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0283    0.9619    1.7823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9212    2.1867   -0.8692 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9356    1.1073    1.2426 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9327    1.4053   -0.1849 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5485    2.7777    0.8618 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4020    3.9032   -1.4875 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1545    2.3924   -2.1174 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4182    2.6679   -2.4396 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2383   -1.3124    1.2152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9057   -1.1814    2.3892 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2506   -2.7594    1.5060 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4213   -4.7618    0.2284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4172   -4.3040   -1.4924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6950   -5.4564   -0.8058 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2771   -3.0628   -0.1252 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4053   -2.9335    1.5385 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8659   -2.0960    1.2260 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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  3  4  2  0
  4  5  1  0
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  6  7  1  0
  5  8  2  0
  8  9  1  0
  9 10  2  0
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 11 27  2  0
 27 28  1  0
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 29 30  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  2  3
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 17 19  1  0
 14 20  2  0
 20 21  1  0
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 20 23  1  0
 23 24  1  0
 24 25  1  0
 23 26  2  0
 30  3  1  0
 26 12  1  0
 29  8  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  4 34  1  0
  7 35  1  0
  7 36  1  0
  7 37  1  0
 27 55  1  0
 30 56  1  0
 13 38  1  0
 15 39  1  0
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 22 48  1  0
 22 49  1  0
 22 50  1  0
 25 51  1  0
 25 52  1  0
 25 53  1  0
 26 54  1  0
M  END


  Mrv1652309112216382D          

 30 32  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
    1.4289    0.8250    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
    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
    4.2868   -0.0000    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
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    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
    4.2868    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -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
    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  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  1  0  0  0  0
  6  7  1  0  0  0  0
  5  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 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  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 14 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 23 26  2  0  0  0  0
 12 26  1  0  0  0  0
 11 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
  8 29  1  0  0  0  0
 29 30  2  0  0  0  0
  3 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0315817

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(OC)=C2C(=O)C(=COC2=C1)C1=CC(CC=C(C)C)=C(OC)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C24H26O6/c1-14(2)7-8-15-9-16(10-21(28-5)24(15)29-6)18-13-30-20-12-17(26-3)11-19(27-4)22(20)23(18)25/h7,9-13H,8H2,1-6H3

> <INCHI_KEY>
PCWHSSLCNUSQJY-UHFFFAOYSA-N

> <FORMULA>
C24H26O6

> <MOLECULAR_WEIGHT>
410.466

> <EXACT_MASS>
410.172938557

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
56

> <JCHEM_AVERAGE_POLARIZABILITY>
44.630695378223216

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxy-4H-chromen-4-one

> <JCHEM_LOGP>
4.435450291333333

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.253327089180432

> <JCHEM_POLAR_SURFACE_AREA>
63.22000000000001

> <JCHEM_REFRACTIVITY>
115.83579999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-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  O   UNK     0       2.667   1.540   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.001   2.310   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.335   1.540   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       9.336   3.850   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  C   UNK     0       8.002   6.160   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.668   6.930   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       9.336   6.930   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      10.669   1.540   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      12.003   2.310   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      13.337   1.540   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      10.669  -0.000   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      12.003  -0.770   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.336  -0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       5.335  -3.080   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   30                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    8                                                  
CONECT    6    5    7                                                       
CONECT    7    6                                                            
CONECT    8    5    9   29                                                  
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   27                                                  
CONECT   12   11   13   26                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   20                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   14   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   24   26                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
CONECT   26   23   12                                                       
CONECT   27   11   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28    8   30                                                  
CONECT   30   29    3                                                       
MASTER        0    0    0    0    0    0    0    0   30    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₄H₂₆O₆

Average Mass

410.4660 Da

Monoisotopic Mass

410.17294 Da

IUPAC Name

3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxy-4H-chromen-4-one

Traditional Name

3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one

CAS Registry Number

Not Available

SMILES

COC1=CC(OC)=C2C(=O)C(=COC2=C1)C1=CC(CC=C(C)C)=C(OC)C(OC)=C1

InChI Identifier

InChI=1S/C24H26O6/c1-14(2)7-8-15-9-16(10-21(28-5)24(15)29-6)18-13-30-20-12-17(26-3)11-19(27-4)22(20)23(18)25/h7,9-13H,8H2,1-6H3

InChI Key

PCWHSSLCNUSQJY-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

Species Name	Source	Reference
Psorothamnus arborescens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7-o-methylisoflavones. These are isoflavones with methoxy groups attached to the C7 atom of the isoflavone backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Isoflavonoids

Sub Class

O-methylated isoflavonoids

Direct Parent

7-O-methylisoflavones

Alternative Parents

Substituents

3p-methoxyisoflavone
4p-o-methylisoflavone
7-o-methylisoflavone
Isoflavone
Chromone
Benzopyran
1-benzopyran
O-dimethoxybenzene
Dimethoxybenzene
Phenoxy compound
Anisole
Phenol ether
Methoxybenzene
Pyranone
Alkyl aryl ether
Pyran
Monocyclic benzene moiety
Benzenoid
Heteroaromatic compound
Vinylogous ester
Oxacycle
Ether
Organoheterocyclic compound
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organic oxygen 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	4.44	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	63.22 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	115.84 m³·mol⁻¹	ChemAxon
Polarizability	44.63 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	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

9670037

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11495231

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one (NP0315817)

MOL for NP0315817 (3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one)

3D MOL for NP0315817 (3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one)

3D SDF for NP0315817 (3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one)

3D-SDF for NP0315817 (3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one)

PDB for NP0315817 (3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one)

3D PDB for NP0315817 (3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one)

SMILES for NP0315817 (3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one)

INCHI for NP0315817 (3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one)

Structure for NP0315817 (3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one)

3D Structure for NP0315817 (3-[3,4-dimethoxy-5-(3-methylbut-2-en-1-yl)phenyl]-5,7-dimethoxychromen-4-one)