NP-MRD: Showing NP-Card for 12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one (NP0321936)

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Record Information

Version

2.0

Created at

2022-09-12 00:24:56 UTC

Updated at

2022-09-12 00:24:56 UTC

NP-MRD ID

NP0321936

Secondary Accession Numbers

None

Natural Product Identification

Common Name

12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one

Description

12-(2H-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]Trideca-1,3,6,8-tetraen-10-one belongs to the class of organic compounds known as furanoflavonoids and dihydrofuranoflavonoids. These are flavonoids possessing a furan (or dihydrofuran) ring fused to the benzopyran moiety of the flavonoid skeleton. 12-(2H-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]Trideca-1,3,6,8-tetraen-10-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004191523122D          

 29 33  0  0  0  0            999 V2000
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.7604    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
    2.7845   -3.9979    0.0000 O   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
    3.4990   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 O   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
    4.2135   -1.5229    0.0000 O   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   -2.7604    0.0000 C   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
    6.3569   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5410   -4.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2055   -4.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3850   -4.8049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -3.9979    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
    0.6411   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0734   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8580   -5.0779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3429   -4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8580   -3.7430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0734   -3.9979    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
  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  1  0  0  0  0
  7  8  1  0  0  0  0
  3  8  1  0  0  0  0
  8  9  2  0  0  0  0
  7 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  2  0  0  0  0
 16 17  1  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
  6 20  2  0  0  0  0
 16 20  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  2  0  0  0  0
 21 29  1  0  0  0  0
M  END

     RDKit          3D

 47 51  0  0  0  0  0  0  0  0999 V2000
   -3.9772   -1.6005    1.6576 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8332   -1.1003    0.3490 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0560   -0.0037    0.0332 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7458   -0.2101   -0.2858 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9632    0.8814   -0.6026 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4727    2.1668   -0.6037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9842    3.4291   -0.8618 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0067    4.3366   -0.6904 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0566    3.6398   -0.3453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8069    2.3620   -0.2774 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5961    1.2601    0.0422 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9276    1.4742    0.3659 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9511    1.4723   -0.6005 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3456    0.6857   -0.9223 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0725   -0.4994   -0.9177 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3630   -0.2474   -0.2164 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4338    0.4517    0.9723 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6250    0.6865    1.6238 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8150    0.2274    1.1103 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7670   -0.4728   -0.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5788   -0.7078   -0.7265 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0844   -0.8060   -0.3507 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9249    0.0905    0.3767 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1541    0.3119    1.5420 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3528   -1.6938   -0.3931 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.5986   -2.8500   -1.1341 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1972   -3.8378   -0.3570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1136   -1.5170   -0.3143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8297   -2.5315   -0.2708 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8223   -2.6913    1.6180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3237   -1.0861    2.3948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0245   -1.4009    1.9647 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0336    3.6389   -1.1481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9256    5.4222   -0.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5994    0.9557   -1.5269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8630    0.9622   -0.2521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2294    2.4993   -0.8931 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3320   -0.7241   -1.9950 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4733    0.8123    1.3701 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6125    1.2401    2.5502 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5311   -1.2613   -1.6658 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8420   -0.4539    0.7153 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1516    0.9968   -0.1829 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7138   -1.8831    0.6496 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3540   -4.7158   -1.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5414   -4.1763    0.4599 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2107   -3.5323   -0.0041 H   0  0  0  0  0  0  0  0  0  0  0  0
 27 26  1  0
 26 25  1  0
 25 15  1  0
 15 14  1  0
 14  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 11  3  1  0
  3  2  1  0
  2  1  1  0
  3  4  2  0
  4 28  1  0
 28 29  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 24  1  0
 24 23  1  0
 23 22  1  0
 22 20  1  0
 20 21  2  0
 28 25  1  0
 21 16  1  0
  4  5  1  0
 20 19  1  0
 10  6  1  0
 27 45  1  0
 27 46  1  0
 27 47  1  0
 25 44  1  1
 15 38  1  6
  7 33  1  0
  8 34  1  0
 13 35  1  0
 13 36  1  0
 13 37  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
 17 39  1  0
 18 40  1  0
 23 42  1  0
 23 43  1  0
 21 41  1  0
M  END


  Mrv1533004191523122D          

 29 33  0  0  0  0            999 V2000
    1.3556   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -2.3479    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0701   -2.7604    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
    2.7845   -3.9979    0.0000 O   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
    3.4990   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7845   -1.5229    0.0000 O   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
    4.2135   -1.5229    0.0000 O   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   -2.7604    0.0000 C   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
    6.3569   -2.7604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9279   -3.5854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5410   -4.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2055   -4.8912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3850   -4.8049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2135   -3.9979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3556   -3.9979    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
    0.6411   -5.2354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0734   -4.8229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8580   -5.0779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3429   -4.4104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8580   -3.7430    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0734   -3.9979    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
  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  1  0  0  0  0
  7  8  1  0  0  0  0
  3  8  1  0  0  0  0
  8  9  2  0  0  0  0
  7 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 13 16  2  0  0  0  0
 16 17  1  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
  6 20  2  0  0  0  0
 16 20  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 24 28  1  0  0  0  0
 28 29  2  0  0  0  0
 21 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0321936

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1C(OC2=C3C=COC3=C(OC)C(OC)=C2C1=O)C1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H18O8/c1-23-19-14-15(22)20(24-2)16(10-4-5-12-13(8-10)28-9-27-12)29-17(14)11-6-7-26-18(11)21(19)25-3/h4-8,16,20H,9H2,1-3H3

> <INCHI_KEY>
FLULTMWANDINQB-UHFFFAOYSA-N

> <FORMULA>
C21H18O8

> <MOLECULAR_WEIGHT>
398.367

> <EXACT_MASS>
398.10016754

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
40.18069538736188

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
12-(2H-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one

> <ALOGPS_LOGP>
2.80

> <JCHEM_LOGP>
2.490786395333333

> <ALOGPS_LOGS>
-3.52

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.420392069362293

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8123724269095045

> <JCHEM_POLAR_SURFACE_AREA>
85.59000000000002

> <JCHEM_REFRACTIVITY>
98.97090000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.19e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-(2H-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-APR-15         0                                  
HETATM    1  C   UNK     0       2.530  -2.843   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       2.530  -4.383   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       3.864  -5.153   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.864  -6.693   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       5.198  -7.463   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0       6.531  -6.693   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.531  -5.153   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       5.198  -4.383   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.198  -2.843   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       7.865  -4.383   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       7.865  -2.843   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       9.199  -2.073   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.199  -5.153   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      10.533  -4.383   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      11.866  -5.153   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.199  -6.693   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      10.343  -7.723   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       9.717  -9.130   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.185  -8.969   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       7.865  -7.463   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.530  -7.463   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.530  -9.003   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.197  -9.773   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.137  -9.003   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -1.602  -9.479   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -2.507  -8.233   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      -1.602  -6.987   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -0.137  -7.463   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.197  -6.693   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5   21                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   20                                                  
CONECT    7    6    8   10                                                  
CONECT    8    7    3    9                                                  
CONECT    9    8                                                            
CONECT   10    7   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   16                                                  
CONECT   14   13   15                                                       
CONECT   15   14                                                            
CONECT   16   13   17   20                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19    6   16                                                  
CONECT   21    4   22   29                                                  
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   28                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   24   29                                                  
CONECT   29   28   21                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   66    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₁₈O₈

Average Mass

398.3670 Da

Monoisotopic Mass

398.10017 Da

IUPAC Name

12-(2H-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one

Traditional Name

12-(2H-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one

CAS Registry Number

Not Available

SMILES

COC1C(OC2=C3C=COC3=C(OC)C(OC)=C2C1=O)C1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C21H18O8/c1-23-19-14-15(22)20(24-2)16(10-4-5-12-13(8-10)28-9-27-12)29-17(14)11-6-7-26-18(11)21(19)25-3/h4-8,16,20H,9H2,1-3H3

InChI Key

FLULTMWANDINQB-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furanoflavonoids and dihydrofuranoflavonoids. These are flavonoids possessing a furan (or dihydrofuran) ring fused to the benzopyran moiety of the flavonoid skeleton.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Flavonoids

Sub Class

Furanoflavonoids and dihydrofuranoflavonoids

Direct Parent

Furanoflavonoids and dihydrofuranoflavonoids

Alternative Parents

Substituents

Furanoflavonoid or dihydroflavonoid
3-methoxyflavonoid-skeleton
5-methoxyflavonoid-skeleton
6-methoxyflavonoid-skeleton
Flavanone
Flavanonol
Flavan
Chromone
Chromane
Benzopyran
1-benzopyran
Benzodioxole
Benzofuran
Aryl ketone
Aryl alkyl ketone
Anisole
Alkyl aryl ether
Benzenoid
Furan
Heteroaromatic compound
Ketone
Oxacycle
Ether
Acetal
Organoheterocyclic compound
Dialkyl ether
Organic oxide
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
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	2.8	ALOGPS
logP	2.49	ChemAxon
logS	-3.5	ALOGPS
pKa (Strongest Acidic)	14.42	ChemAxon
pKa (Strongest Basic)	-2.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	85.59 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	98.97 m³·mol⁻¹	ChemAxon
Polarizability	40.18 Å³	ChemAxon
Number of Rings	5	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

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one (NP0321936)

MOL for NP0321936 (12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one)

3D MOL for NP0321936 (12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one)

3D SDF for NP0321936 (12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one)

3D-SDF for NP0321936 (12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one)

PDB for NP0321936 (12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one)

3D PDB for NP0321936 (12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one)

SMILES for NP0321936 (12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one)

INCHI for NP0321936 (12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one)

Structure for NP0321936 (12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one)

3D Structure for NP0321936 (12-(2h-1,3-benzodioxol-5-yl)-7,8,11-trimethoxy-5,13-dioxatricyclo[7.4.0.0²,⁶]trideca-1,3,6,8-tetraen-10-one)