NP-MRD: Showing NP-Card for 4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol (NP0206804)

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Record Information

Version

2.0

Created at

2022-09-05 03:11:21 UTC

Updated at

2022-09-05 03:11:21 UTC

NP-MRD ID

NP0206804

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol

Description

Chicanin belongs to the class of organic compounds known as 7,7'-epoxylignans. These are lignans with a structure based on a 2,5-diaryl-3, 4-dimethyltetrahydrofuran skeleton. 4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol is found in Leucas aspera and Piper kadsura. Based on a literature review very few articles have been published on Chicanin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052205112D          

 25 28  0  0  1  0            999 V2000
    8.5050    0.8594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6845    0.9457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3490    1.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5285    1.7856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1929    2.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3725    2.6255    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8204    2.0124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1530    3.1684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5399    3.7205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9600    3.3400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2955    4.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6779    3.2067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4983    3.1204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8339    2.3668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6544    2.2805    0.0000 O   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
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  6  0  0  0
  5 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END

     RDKit          3D

 47 50  0  0  0  0  0  0  0  0999 V2000
   -5.1521    0.6410   -1.8975 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1880    1.0901   -0.5348 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0820    0.9554    0.2914 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9048    0.3864   -0.1595 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8585    0.2872    0.7108 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5809   -0.2973    0.3390 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0772    0.0443   -0.8891 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0745   -0.7318   -1.0090 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2223    0.1577   -0.6726 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2463    1.4757   -1.1389 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2821    2.3269   -0.8614 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3476    1.9090   -0.1050 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3636    0.6242    0.3716 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3032   -0.2392    0.0845 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5432    0.4891    1.0897 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4360    1.5577    0.7539 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5075    2.5537    0.3181 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9434   -1.9159   -0.0939 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.2923   -3.2196   -0.7146 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5676   -1.8121    0.2235 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2731   -2.2070   -1.0231 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9949    0.7519    2.0087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1433    1.3166    2.4781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2126    1.4167    1.5855 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3792    1.9882    2.0560 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3895    1.2013   -2.4589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8418   -0.4283   -1.8719 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1432    0.7868   -2.3503 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8468    0.0375   -1.1940 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2326   -0.0678    1.0949 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1633   -1.1382   -2.0389 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3920    1.7780   -1.7334 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2157    3.3301   -1.2643 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3617   -1.2299    0.4727 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0401    1.2996   -0.1562 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0444    1.8816    1.5965 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4761   -1.7577    0.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6501   -4.0327   -0.3003 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3393   -3.4959   -0.4713 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1696   -3.1746   -1.8200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8349   -2.3323    1.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3723   -2.2852   -0.9124 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8671   -3.1586   -1.4705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0740   -1.4421   -1.8018 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1575    0.6784    2.7230 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2329    1.6762    3.5005 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4727    2.3250    3.0027 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 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 17  1  0
 17 16  1  0
 16 15  1  0
 15 13  1  0
 13 14  2  0
 24  3  1  0
 20  6  1  0
 14  9  1  0
 13 12  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
 22 45  1  0
 23 46  1  0
 25 47  1  0
  6 30  1  1
  8 31  1  6
 18 37  1  1
 19 38  1  0
 19 39  1  0
 19 40  1  0
 20 41  1  1
 21 42  1  0
 21 43  1  0
 21 44  1  0
 10 32  1  0
 11 33  1  0
 16 35  1  0
 16 36  1  0
 14 34  1  0
M  END


  Mrv1652309052205112D          

 25 28  0  0  1  0            999 V2000
    8.5050    0.8594    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6845    0.9457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3490    1.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5285    1.7856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1929    2.5392    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3725    2.6255    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.8204    2.0124    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3523    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233    1.9354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    2.1904    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538    1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387    0.8555    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1530    3.1684    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5399    3.7205    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9600    3.3400    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2955    4.0936    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6779    3.2067    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4983    3.1204    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8339    2.3668    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6544    2.2805    0.0000 O   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
  6  5  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  1  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
  9 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 12 17  1  0  0  0  0
  8 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
  6 20  1  0  0  0  0
 20 21  1  6  0  0  0
  5 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
  3 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0206804

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(=CC=C1O)[C@@H]1O[C@H]([C@H](C)[C@@H]1C)C1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H22O5/c1-11-12(2)20(14-5-7-16-18(9-14)24-10-23-16)25-19(11)13-4-6-15(21)17(8-13)22-3/h4-9,11-12,19-21H,10H2,1-3H3/t11-,12+,19+,20+/m0/s1

> <INCHI_KEY>
JPDORDSJPIKURD-OCBHBYCGSA-N

> <FORMULA>
C20H22O5

> <MOLECULAR_WEIGHT>
342.391

> <EXACT_MASS>
342.146723808

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
47

> <JCHEM_AVERAGE_POLARIZABILITY>
36.750346527295385

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-[(2R,3S,4R,5R)-5-(2H-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol

> <JCHEM_LOGP>
3.990769809333334

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.910800516313147

> <JCHEM_PKA_STRONGEST_BASIC>
-4.049220177016412

> <JCHEM_POLAR_SURFACE_AREA>
57.150000000000006

> <JCHEM_REFRACTIVITY>
92.27330000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-[(2R,3S,4R,5R)-5-(2H-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0      15.876   1.604   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      14.344   1.765   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      13.718   3.172   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.187   3.333   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.560   4.740   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.029   4.901   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.998   3.756   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       7.752   5.914   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.608   6.945   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.259   6.235   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       9.885   7.641   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      12.465   5.986   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      13.997   5.825   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      14.623   4.418   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      16.155   4.257   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   24                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   22                                                  
CONECT    6    5    7   20                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   18                                                  
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   17                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13    9                                                       
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   12                                                       
CONECT   18    8   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18    6   21                                                  
CONECT   21   20                                                            
CONECT   22    5   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23    3   25                                                  
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   56    0
END

View in JSmol

Synonyms

Value	Source
Chicanine	MeSH

Chemical Formula

C₂₀H₂₂O₅

Average Mass

342.3910 Da

Monoisotopic Mass

342.14672 Da

IUPAC Name

4-[(2R,3S,4R,5R)-5-(2H-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol

Traditional Name

4-[(2R,3S,4R,5R)-5-(2H-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol

CAS Registry Number

Not Available

SMILES

COC1=CC(=CC=C1O)[C@@H]1O[C@H]([C@H](C)[C@@H]1C)C1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C20H22O5/c1-11-12(2)20(14-5-7-16-18(9-14)24-10-23-16)25-19(11)13-4-6-15(21)17(8-13)22-3/h4-9,11-12,19-21H,10H2,1-3H3/t11-,12+,19+,20+/m0/s1

InChI Key

JPDORDSJPIKURD-OCBHBYCGSA-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
Leucas aspera	LOTUS Database	35616633
Piper kadsura	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 7,7'-epoxylignans. These are lignans with a structure based on a 2,5-diaryl-3, 4-dimethyltetrahydrofuran skeleton.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Furanoid lignans

Sub Class

Tetrahydrofuran lignans

Direct Parent

7,7'-epoxylignans

Alternative Parents

Substituents

7,7p-epoxylignan
Dibenzylbutane lignan skeleton
Methoxyphenol
Benzodioxole
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Oxolane
Ether
Acetal
Dialkyl ether
Organoheterocyclic compound
Oxacycle
Hydrocarbon derivative
Organic oxygen compound
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	3.99	ChemAxon
pKa (Strongest Acidic)	9.91	ChemAxon
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	57.15 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	92.27 m³·mol⁻¹	ChemAxon
Polarizability	36.75 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

C00031445

Chemspider ID

9253541

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

11078392

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol (NP0206804)

MOL for NP0206804 (4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol)

3D MOL for NP0206804 (4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol)

3D SDF for NP0206804 (4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol)

3D-SDF for NP0206804 (4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol)

PDB for NP0206804 (4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol)

3D PDB for NP0206804 (4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol)

SMILES for NP0206804 (4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol)

INCHI for NP0206804 (4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol)

Structure for NP0206804 (4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol)

3D Structure for NP0206804 (4-[(2r,3s,4r,5r)-5-(2h-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol)