NP-MRD: Showing NP-Card for 11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one (NP0207995)

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Record Information

Version

1.0

Created at

2022-09-05 04:49:47 UTC

Updated at

2022-09-05 04:49:47 UTC

NP-MRD ID

NP0207995

Secondary Accession Numbers

None

Natural Product Identification

Common Name

11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one

Description

3',4'-Dihydroxy-7-methoxy-8-prenyl-5''-(2-hydroxyisopropyl)-[2'',3'':5,6]Furanoflavanone belongs to the class of organic compounds known as 8-prenylated flavanones. These are flavanones that features a C5-isoprenoid substituent at the 8-position. Thus, 3',4'-dihydroxy-7-methoxy-8-prenyl-5''-(2-hydroxyisopropyl)-[2'',3'':5,6]Furanoflavanone is considered to be a flavonoid lipid molecule. 11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one is found in Paramignya scandens. 3',4'-Dihydroxy-7-methoxy-8-prenyl-5''-(2-hydroxyisopropyl)-[2'',3'':5,6]Furanoflavanone is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004181502332D          

 29 32  0  0  0  0            999 V2000
    2.1072    1.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9318    1.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3664    0.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1910    0.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5810    1.3045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1464    2.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5364    2.7327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1018    3.4340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3610    2.7585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6256   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4502   -0.0980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8849   -0.7992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4949   -1.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6703   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2803   -2.2790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2357   -0.8508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4111   -0.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8784   -1.5066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1147   -1.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1752   -0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9765   -0.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7095   -0.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0994   -0.0465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9240   -0.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3586   -0.7219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1832   -0.6962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9687   -1.4490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4033   -2.1502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1441   -1.4747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  4 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  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  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
  3 21  2  0  0  0  0
 17 21  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 22 29  1  0  0  0  0
M  END

     RDKit          3D

 51 54  0  0  0  0  0  0  0  0999 V2000
   -4.3853   -0.0109    2.5771 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0914   -0.0414    1.1928 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0237   -0.7876    0.7079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7503   -0.2388    0.5861 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5919    1.1756    0.9998 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1672    2.0677   -0.0444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4830    2.9801   -0.6964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0363    3.1677   -0.4033 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1123    3.8368   -1.7252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6653   -0.9297    0.1144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8156   -2.2462   -0.2686 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0720   -2.8206   -0.1589 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4765   -4.0332   -0.4501 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7599   -4.1691   -0.1949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2385   -2.9528    0.3027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1559   -2.1040    0.3207 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3413   -2.9520   -0.7620 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1747   -4.0052   -1.4114 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7354   -2.4867   -0.5358 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7810   -1.1714    0.1962 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9804   -0.4207   -0.1737 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0257    0.3011   -1.3446 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1396    1.0234   -1.7267 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2650    1.0222   -0.8930 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3924    1.7261   -1.2343 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2397    0.3082    0.2795 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3255    0.2841    1.1217 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1166   -0.3878    0.6107 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6067   -0.3914   -0.0106 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2897   -0.6401    2.8109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5315    1.0341    2.9284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5590   -0.4271    3.1889 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5117    1.4277    1.0695 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0786    1.3988    1.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2255    1.9447   -0.2732 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1753    3.3056    0.6700 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3702    4.0697   -0.9249 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5312    2.2996   -0.8356 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9495    3.3301   -2.2605 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5564    4.7693   -1.2969 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3234    4.1844   -2.4389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4123   -5.0173   -0.3128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2483   -2.7258    0.6097 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2265   -3.2965    0.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2945   -2.4584   -1.4882 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8189   -1.3886    1.2898 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1699    0.3309   -2.0264 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2058    1.5975   -2.6354 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1912    1.7111   -0.6195 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3448   -0.2226    1.9815 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0588   -0.9706    1.5413 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 16  2  0
 16 15  1  0
 15 14  2  0
 14 13  1  0
 13 12  1  0
 12 11  2  0
 11 17  1  0
 17 18  2  0
 17 19  1  0
 19 20  1  0
 20 29  1  0
 29 10  1  0
 10  4  2  0
  4  5  1  0
  5  6  1  0
  6  7  2  3
  7  8  1  0
  7  9  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 24 26  1  0
 26 27  1  0
 26 28  2  0
  4  3  1  0
 28 21  1  0
 12 16  1  0
 10 11  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 15 43  1  0
 14 42  1  0
 19 44  1  0
 19 45  1  0
 20 46  1  1
  5 33  1  0
  5 34  1  0
  6 35  1  0
  8 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
  9 40  1  0
  9 41  1  0
 22 47  1  0
 23 48  1  0
 25 49  1  0
 27 50  1  0
 28 51  1  0
M  END


  Mrv1533004181502332D          

 29 32  0  0  0  0            999 V2000
    2.1072    1.2272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9318    1.2530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3664    0.5517    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1910    0.5775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5810    1.3045    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1464    2.0057    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5364    2.7327    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1018    3.4340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3610    2.7585    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6256   -0.1238    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4502   -0.0980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.8849   -0.7992    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4949   -1.5262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6703   -1.5520    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2803   -2.2790    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2357   -0.8508    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4111   -0.8765    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8784   -1.5066    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1147   -1.1947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1752   -0.3719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9765   -0.1753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7095   -0.7735    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0994   -0.0465    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9240   -0.0207    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3586   -0.7219    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1832   -0.6962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9687   -1.4490    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4033   -2.1502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1441   -1.4747    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  4 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  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  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
  3 21  2  0  0  0  0
 17 21  1  0  0  0  0
 12 22  1  0  0  0  0
 22 23  2  0  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  2  0  0  0  0
 22 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207995

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C2C=COC2=C2C(=O)CC(OC2=C1CC=C(C)C)C1=CC=C(O)C(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H22O6/c1-12(2)4-6-14-21(27-3)15-8-9-28-22(15)20-18(26)11-19(29-23(14)20)13-5-7-16(24)17(25)10-13/h4-5,7-10,19,24-25H,6,11H2,1-3H3

> <INCHI_KEY>
POMYWCNEUNRBFJ-UHFFFAOYSA-N

> <FORMULA>
C23H22O6

> <MOLECULAR_WEIGHT>
394.423

> <EXACT_MASS>
394.141638428

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
41.839939059035835

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one

> <ALOGPS_LOGP>
3.07

> <JCHEM_LOGP>
4.218692506333333

> <ALOGPS_LOGS>
-3.86

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.636920966045967

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.212361295794622

> <JCHEM_PKA_STRONGEST_BASIC>
-2.835001747614606

> <JCHEM_POLAR_SURFACE_AREA>
89.13000000000001

> <JCHEM_REFRACTIVITY>
108.856

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.41e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0       3.934   2.291   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.473   2.339   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       6.284   1.030   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.823   1.078   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.551   2.435   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.740   3.744   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.468   5.101   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.657   6.410   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      10.007   5.149   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       8.635  -0.231   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      10.174  -0.183   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      10.985  -1.492   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.257  -2.849   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       8.718  -2.897   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       7.990  -4.254   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       7.907  -1.588   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.367  -1.636   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       5.373  -2.812   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.947  -2.230   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.060  -0.694   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.556  -0.327   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.524  -1.444   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.252  -0.087   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.792  -0.039   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      15.603  -1.348   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      17.142  -1.300   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      14.875  -2.705   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      15.686  -4.014   0.000  0.00  0.00           O+0
HETATM   29  C   UNK     0      13.336  -2.753   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   21                                                  
CONECT    4    3    5   10                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7                                                            
CONECT   10    4   11   16                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   22                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   10   17                                                  
CONECT   17   16   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20    3   17                                                  
CONECT   22   12   23   29                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27   22                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₃H₂₂O₆

Average Mass

394.4230 Da

Monoisotopic Mass

394.14164 Da

IUPAC Name

11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one

Traditional Name

11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one

CAS Registry Number

Not Available

SMILES

COC1=C2C=COC2=C2C(=O)CC(OC2=C1CC=C(C)C)C1=CC=C(O)C(O)=C1

InChI Identifier

InChI=1S/C23H22O6/c1-12(2)4-6-14-21(27-3)15-8-9-28-22(15)20-18(26)11-19(29-23(14)20)13-5-7-16(24)17(25)10-13/h4-5,7-10,19,24-25H,6,11H2,1-3H3

InChI Key

POMYWCNEUNRBFJ-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
Paramignya scandens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 8-prenylated flavanones. These are flavanones that features a C5-isoprenoid substituent at the 8-position.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Flavans

Direct Parent

8-prenylated flavanones

Alternative Parents

Substituents

8-prenylated flavanone
Furanoflavonoid or dihydroflavonoid
7-methoxyflavonoid-skeleton
3'-hydroxyflavonoid
4'-hydroxyflavonoid
Flavanone
Hydroxyflavonoid
Chromone
Chromane
Benzopyran
1-benzopyran
Benzofuran
Anisole
Catechol
Aryl alkyl ketone
Aryl ketone
Phenol
Alkyl aryl ether
1-hydroxy-2-unsubstituted benzenoid
1-hydroxy-4-unsubstituted benzenoid
Benzenoid
Monocyclic benzene moiety
Furan
Heteroaromatic compound
Ketone
Organoheterocyclic compound
Oxacycle
Ether
Organooxygen compound
Organic oxygen compound
Aldehyde
Hydrocarbon derivative
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Flavanones (LMPK12140577 )

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	3.07	ALOGPS
logP	4.22	ChemAxon
logS	-3.9	ALOGPS
pKa (Strongest Acidic)	9.21	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	89.13 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	108.86 m³·mol⁻¹	ChemAxon
Polarizability	41.84 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	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

12019200

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one (NP0207995)

MOL for NP0207995 (11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one)

3D MOL for NP0207995 (11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one)

3D SDF for NP0207995 (11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one)

3D-SDF for NP0207995 (11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one)

PDB for NP0207995 (11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one)

3D PDB for NP0207995 (11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one)

SMILES for NP0207995 (11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one)

INCHI for NP0207995 (11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one)

Structure for NP0207995 (11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one)

3D Structure for NP0207995 (11-(3,4-dihydroxyphenyl)-7-methoxy-8-(3-methylbut-2-en-1-yl)-3,10-dioxatricyclo[7.4.0.0²,⁶]trideca-1,4,6,8-tetraen-13-one)