NP-MRD: Showing NP-Card for 5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone (NP0053291)

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Record Information

Version

2.0

Created at

2022-04-27 23:59:53 UTC

Updated at

2022-04-27 23:59:53 UTC

NP-MRD ID

NP0053291

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone

Description

5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone belongs to the class of organic compounds known as 8-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone. Thus, 5-hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone is considered to be a flavonoid. 5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone is found in Melicope triphylla. Based on a literature review very few articles have been published on 5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282201592D          

 31 34  0  0  0  0            999 V2000
    4.2135    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    4.6654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    3.3305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6424    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  2  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 18 24  1  0  0  0  0
  3 25  1  0  0  0  0
  1 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
M  END

     RDKit          3D

 53 56  0  0  0  0  0  0  0  0999 V2000
    3.4294    0.1115   -4.0933 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0235    1.0695   -3.0903 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0399    0.6183   -2.2176 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3581    0.0336   -1.0339 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7054   -0.1827   -0.5321 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8539    0.3559   -1.0225 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0965    0.0944   -0.4152 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2156   -0.7099    0.6952 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0716   -1.2529    1.1942 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8481   -0.9975    0.5982 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4283   -2.0259    2.3115 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.7356   -1.6360    2.6764 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3062   -1.1160    1.4667 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3164   -0.3623   -0.3002 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0700   -0.2073   -0.6720 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9275   -0.6580    0.1740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5677   -1.2497    1.3696 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3918   -0.5296    2.5734 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2904   -0.5368   -0.1362 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2366   -0.9995    0.7478 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5977   -0.8750    0.5602 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0105    0.5492    0.5897 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9036    0.9664    1.5214 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3176    2.3770    1.5567 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4584   -0.0232    2.5075 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6012    0.0528   -1.3280 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6327    0.5345   -2.2352 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0254    1.1013   -3.3828 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3120    0.3862   -1.8715 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7248    0.8119   -2.6673 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5015    1.3577   -3.7641 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7402    0.1893   -4.9566 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4843    0.3203   -4.4085 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3256   -0.9126   -3.6823 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8261    1.0048   -1.8637 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9980    0.5312   -0.8205 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9607   -1.4398    1.0127 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3743   -2.4964    2.9593 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7520   -0.8800    3.4873 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2800    0.3255    2.3850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3587   -0.1896    3.0015 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0477   -1.2360    3.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2092   -1.4925    1.2523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8093   -1.2223   -0.4962 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6606    1.3152   -0.0681 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3930    2.8065    0.5408 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3233    2.4465    2.0156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5549    2.9598    2.1351 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6013   -0.4262    3.0743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0081   -0.8117    1.9455 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1528    0.5068    3.1737 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6144    0.1579   -1.6557 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5549    1.4851   -4.1199 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 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  2  3
 23 24  1  0
 23 25  1  0
 19 26  2  0
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 27 28  1  0
 27 29  2  0
 29 30  1  0
 30 31  2  0
  4  5  1  0
  5 10  2  0
 10  9  1  0
  9  8  2  0
  8 13  1  0
 13 12  1  0
 12 11  1  0
  8  7  1  0
  7  6  2  0
 30  3  1  0
  6  5  1  0
 29 15  1  0
 11  9  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
 18 40  1  0
 18 41  1  0
 18 42  1  0
 21 43  1  0
 21 44  1  0
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 25 51  1  0
 26 52  1  0
 28 53  1  0
 10 37  1  0
 12 38  1  0
 12 39  1  0
  7 36  1  0
  6 35  1  0
M  END


  Mrv1652304282201592D          

 31 34  0  0  0  0            999 V2000
    4.2135    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    0.6979    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279    3.5854    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990    4.4104    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    3.1729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6411    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556    4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701    4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    4.6654    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6284    3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1435    3.3305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6424    2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -0.1271    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -0.5396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4990   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.7771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -2.6021    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -1.3646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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
  1  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  5  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  2  0  0  0  0
 11 14  1  0  0  0  0
 14 15  1  0  0  0  0
 10 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 16 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 18 24  1  0  0  0  0
  3 25  1  0  0  0  0
  1 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 29 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0053291

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(OC2=C(OC)C(OCC=C(C)C)=CC(O)=C2C1=O)C1=CC2=C(OCO2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H22O8/c1-12(2)7-8-28-17-10-14(24)18-19(25)23(27-4)20(31-22(18)21(17)26-3)13-5-6-15-16(9-13)30-11-29-15/h5-7,9-10,24H,8,11H2,1-4H3

> <INCHI_KEY>
IBKHFDNXHBVBAD-UHFFFAOYSA-N

> <FORMULA>
C23H22O8

> <MOLECULAR_WEIGHT>
426.421

> <EXACT_MASS>
426.131467668

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
44.39410884706516

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-(2H-1,3-benzodioxol-5-yl)-5-hydroxy-3,8-dimethoxy-7-[(3-methylbut-2-en-1-yl)oxy]-4H-chromen-4-one

> <ALOGPS_LOGP>
2.93

> <JCHEM_LOGP>
3.8489598443333337

> <ALOGPS_LOGS>
-4.34

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.65524033222564

> <JCHEM_PKA_STRONGEST_BASIC>
-4.28007421787777

> <JCHEM_POLAR_SURFACE_AREA>
92.68000000000002

> <JCHEM_REFRACTIVITY>
113.4822

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.93e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-(2H-1,3-benzodioxol-5-yl)-5-hydroxy-3,8-dimethoxy-7-[(3-methylbut-2-en-1-yl)oxy]chromen-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       7.865   1.303   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       9.199   2.073   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.199   3.613   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.865   4.383   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       6.531   3.613   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.531   2.073   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.198   1.303   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.198  -0.237   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.198   4.383   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       5.198   5.923   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.531   6.693   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       7.865   5.923   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       9.199   6.693   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       6.531   8.233   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       7.865   9.003   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.864   6.693   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       2.530   5.923   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.197   6.693   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.197   8.233   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       2.530   9.003   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       3.864   8.233   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      -0.268   8.709   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      -1.173   7.463   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.268   6.217   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      10.533   4.383   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       7.865  -0.237   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.531  -1.007   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       6.531  -2.547   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       5.198  -3.317   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       5.198  -4.857   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.864  -2.547   0.000  0.00  0.00           C+0
CONECT    1    2    6   26                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5   12                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    1    7                                                  
CONECT    7    6    8                                                       
CONECT    8    7                                                            
CONECT    9    5   10                                                       
CONECT   10    9   11   16                                                  
CONECT   11   10   12   14                                                  
CONECT   12   11    4   13                                                  
CONECT   13   12                                                            
CONECT   14   11   15                                                       
CONECT   15   14                                                            
CONECT   16   10   17   21                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   24                                                  
CONECT   19   18   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20   16                                                       
CONECT   22   19   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   18                                                       
CONECT   25    3                                                            
CONECT   26    1   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30   31                                                  
CONECT   30   29                                                            
CONECT   31   29                                                            
MASTER        0    0    0    0    0    0    0    0   31    0   68    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₂O₈

Average Mass

426.4210 Da

Monoisotopic Mass

426.13147 Da

IUPAC Name

2-(2H-1,3-benzodioxol-5-yl)-5-hydroxy-3,8-dimethoxy-7-[(3-methylbut-2-en-1-yl)oxy]-4H-chromen-4-one

Traditional Name

2-(2H-1,3-benzodioxol-5-yl)-5-hydroxy-3,8-dimethoxy-7-[(3-methylbut-2-en-1-yl)oxy]chromen-4-one

CAS Registry Number

Not Available

SMILES

COC1=C(OC2=C(OC)C(OCC=C(C)C)=CC(O)=C2C1=O)C1=CC2=C(OCO2)C=C1

InChI Identifier

InChI=1S/C23H22O8/c1-12(2)7-8-28-17-10-14(24)18-19(25)23(27-4)20(31-22(18)21(17)26-3)13-5-6-15-16(9-13)30-11-29-15/h5-7,9-10,24H,8,11H2,1-4H3

InChI Key

IBKHFDNXHBVBAD-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Melicope triphylla	Plant	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C8 atom of the flavonoid backbone.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

O-methylated flavonoids

Direct Parent

8-O-methylated flavonoids

Alternative Parents

Substituents

3-methoxyflavonoid-skeleton
8-methoxyflavonoid-skeleton
5-hydroxyflavonoid
Hydroxyflavonoid
Flavone
3-methoxychromone
Chromone
Benzopyran
1-benzopyran
Benzodioxole
Anisole
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Pyranone
Benzenoid
Pyran
Heteroaromatic compound
Vinylogous acid
Oxacycle
Organoheterocyclic compound
Acetal
Ether
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavones and Flavonols (LMPK12113227 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	2.93	ALOGPS
logP	3.85	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	7.66	ChemAxon
pKa (Strongest Basic)	-4.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	92.68 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	113.48 m³·mol⁻¹	ChemAxon
Polarizability	44.39 Å³	ChemAxon
Number of Rings	4	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

C00005057

Chemspider ID

24845756

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

44260025

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone (NP0053291)

MOL for NP0053291 (5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone)

3D MOL for NP0053291 (5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone)

3D SDF for NP0053291 (5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone)

3D-SDF for NP0053291 (5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone)

PDB for NP0053291 (5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone)

3D PDB for NP0053291 (5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone)

SMILES for NP0053291 (5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone)

INCHI for NP0053291 (5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone)

Structure for NP0053291 (5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone)

3D Structure for NP0053291 (5-Hydroxy-3,8-dimethoxy-3',4'-methylenedioxy-7-prenyloxyflavone)