NP-MRD: Showing NP-Card for 5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one (NP0144170)

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Record Information

Version

2.0

Created at

2022-09-01 23:03:58 UTC

Updated at

2022-09-01 23:03:58 UTC

NP-MRD ID

NP0144170

Secondary Accession Numbers

None

Natural Product Identification

Common Name

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

Description

SCHEMBL1817891 belongs to the class of organic compounds known as 3'-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 3'-position. 5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one is found in Dodonaea polyandra. Based on a literature review very few articles have been published on SCHEMBL1817891.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022201032D          

 28 30  0  0  0  0            999 V2000
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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
    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 O   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
    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 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    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 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
    0.0000   -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
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    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
  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  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  7 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  2  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END

     RDKit          3D

 50 52  0  0  0  0  0  0  0  0999 V2000
    4.0972   -2.9069    0.8053 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6078   -1.7879    0.0953 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2432   -1.5141    0.1231 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3962   -2.3145    0.8250 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0230   -2.0053    0.8289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5080   -0.9417    0.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9155   -0.5672    0.1880 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3250    0.3430   -0.7182 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5467    0.7742   -0.8210 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8730    1.7261   -1.8007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1608    2.1874   -1.9166 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4962    3.1453   -2.9005 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0966    1.6946   -1.0584 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7884    0.7395   -0.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7682    0.2905    0.7535 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4969    0.2719    0.0529 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1721   -0.6555    1.0073 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9588   -1.1492    1.8194 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8173   -1.0716    1.0527 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4829   -2.0022    2.0259 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1330   -1.4100    3.3009 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4002   -0.1550   -0.5370 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7425   -0.4313   -0.5601 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6628    0.4752   -1.3430 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3997    1.3831   -0.4428 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7041    1.4511   -0.4296 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5408    0.6241   -1.3170 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3981    2.3927    0.5088 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1833   -2.9474    0.8595 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7311   -2.8665    1.8695 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7273   -3.8473    0.3571 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7610   -3.1774    1.3752 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5946   -2.7024    1.3757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1109    2.1018   -2.4700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4331    4.1426   -2.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1200    2.0323   -1.1181 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8963   -0.3161    1.4845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4978   -0.5137    3.1500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0709   -1.0932    3.7824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6326   -2.1534    3.9360 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0152    0.7002   -1.0722 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0300    1.0451   -2.0727 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3198   -0.1810   -1.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8087    2.0045    0.2207 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5810    1.0427   -1.4164 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1403    0.5616   -2.3736 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6888   -0.4161   -0.9819 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4406    2.1169    0.6881 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4033    3.4203    0.0368 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8799    2.4599    1.4886 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 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
 25 26  2  3
 26 27  1  0
 26 28  1  0
  6  7  1  0
  7 19  2  0
 19 20  1  0
 20 21  1  0
 19 17  1  0
 17 18  2  0
 17 16  1  0
 16 14  2  0
 14 15  1  0
 14 13  1  0
 13 11  2  0
 11 12  1  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
 23  3  1  0
  8  7  1  0
  9 16  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  4 32  1  0
  5 33  1  0
 22 41  1  0
 24 42  1  0
 24 43  1  0
 25 44  1  0
 27 45  1  0
 27 46  1  0
 27 47  1  0
 28 48  1  0
 28 49  1  0
 28 50  1  0
 21 38  1  0
 21 39  1  0
 21 40  1  0
 15 37  1  0
 13 36  1  0
 12 35  1  0
 10 34  1  0
M  END


  Mrv1652309022201032D          

 28 30  0  0  0  0            999 V2000
   -2.8579    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    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
    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 O   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
    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 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    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 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
    0.0000   -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
   -2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -2.4750    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
  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  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 11 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  2  0  0  0  0
  9 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 17 19  1  0  0  0  0
  7 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  2  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0144170

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1CC=C(C)C)C1=C(OC)C(=O)C2=C(O)C=C(O)C=C2O1

> <INCHI_IDENTIFIER>
InChI=1S/C22H22O6/c1-12(2)5-6-13-9-14(7-8-17(13)26-3)21-22(27-4)20(25)19-16(24)10-15(23)11-18(19)28-21/h5,7-11,23-24H,6H2,1-4H3

> <INCHI_KEY>
HYMQFPWZFNOJGG-UHFFFAOYSA-N

> <FORMULA>
C22H22O6

> <MOLECULAR_WEIGHT>
382.412

> <EXACT_MASS>
382.141638428

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
50

> <JCHEM_AVERAGE_POLARIZABILITY>
40.67694314167259

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
4.03

> <JCHEM_LOGP>
4.447153230333334

> <ALOGPS_LOGS>
-4.66

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
7.97548222637572

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.380966941446971

> <JCHEM_PKA_STRONGEST_BASIC>
-4.558586195789678

> <JCHEM_POLAR_SURFACE_AREA>
85.22000000000001

> <JCHEM_REFRACTIVITY>
108.35759999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.41e-03 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.335   1.540   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -4.001   2.310   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -2.667   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       2.667   0.000   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       8.002  -0.000   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.335  -4.620   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       0.000  -3.080   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -6.668  -2.310   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8   19                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   16                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14    9   17                                                  
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17    7   20                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22    6   23                                                       
CONECT   23   22    3   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₂O₆

Average Mass

382.4120 Da

Monoisotopic Mass

382.14164 Da

IUPAC Name

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

Traditional Name

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

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1CC=C(C)C)C1=C(OC)C(=O)C2=C(O)C=C(O)C=C2O1

InChI Identifier

InChI=1S/C22H22O6/c1-12(2)5-6-13-9-14(7-8-17(13)26-3)21-22(27-4)20(25)19-16(24)10-15(23)11-18(19)28-21/h5,7-11,23-24H,6H2,1-4H3

InChI Key

HYMQFPWZFNOJGG-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
Dodonaea polyandra	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 3'-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 3'-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavones

Direct Parent

3'-prenylated flavones

Alternative Parents

Substituents

3'-prenylated flavone
3-methoxyflavonoid-skeleton
4p-methoxyflavonoid-skeleton
Hydroxyflavonoid
5-hydroxyflavonoid
7-hydroxyflavonoid
3-methoxychromone
Chromone
1-benzopyran
Benzopyran
Anisole
Phenol ether
Phenoxy compound
Methoxybenzene
Phenol
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Pyranone
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Pyran
Vinylogous acid
Heteroaromatic compound
Organoheterocyclic compound
Oxacycle
Ether
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	4.03	ALOGPS
logP	4.45	ChemAxon
logS	-4.7	ALOGPS
pKa (Strongest Acidic)	6.38	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	85.22 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	108.36 m³·mol⁻¹	ChemAxon
Polarizability	40.68 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

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

52935998

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one (NP0144170)

MOL for NP0144170 (5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one)

3D MOL for NP0144170 (5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one)

3D SDF for NP0144170 (5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one)

3D-SDF for NP0144170 (5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one)

PDB for NP0144170 (5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one)

3D PDB for NP0144170 (5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one)

SMILES for NP0144170 (5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one)

INCHI for NP0144170 (5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one)

Structure for NP0144170 (5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one)

3D Structure for NP0144170 (5,7-dihydroxy-3-methoxy-2-[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]chromen-4-one)