NP-MRD: Showing NP-Card for 1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan (NP0246542)

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Record Information

Version

2.0

Created at

2022-09-07 08:03:22 UTC

Updated at

2022-09-07 08:03:23 UTC

NP-MRD ID

NP0246542

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan

Description

Eudesmin belongs to the class of organic compounds known as furanoid lignans. These are lignans with a structure that contains either a tetrahydrofuran ring, a furan ring, or a furofuan ring system, that arises from the joining of the two phenylpropanoid units. 1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan is found in Achillea holosericea, Acorus calamus, Aglaia abbreviata, Aglaia leptantha, Aglaia perviridis, Araucaria angustifolia, Artemisia absinthium, Artemisia gorgonum, Bupleurum salicifolium, Daphne oleoides, Haplophyllum acutifolium, Haplophyllum villosum, Hernandia sonora, Lindera praecox, Liriodendron tulipifera, Magnolia biondii, Magnolia coco, Magnolia denudata, Magnolia kobus, Magnolia praecocissima, Magnolia stellata, Melicope hayesii, Metrodorea flavida, Metrodorea nigra, Orophea enneandra, Pandanus boninensis, Pandanus odorifer, Annona mucosa, Annona sylvatica, Samadera bidwillii, Zanthoxylum culantrillo and Zanthoxylum simulans. Eudesmin is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161513122D          

 28 31  0  0  0  0            999 V2000
   -1.8267    3.3100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0198    3.1385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7648    2.3539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0422    2.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2971    1.3977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2549    0.7846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0619    0.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3168    1.7408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1238    1.9123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3788    2.6969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4849   -0.6674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692   -1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8242   -2.1195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6312   -2.2910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8861   -3.0756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3341   -3.6887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5890   -4.4734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3960   -4.6449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5271   -3.5172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9751   -4.1303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1681   -3.9588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2721   -2.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 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  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 14 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
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  2  0  0  0  0
 19 28  1  0  0  0  0
M  END

     RDKit          3D

 54 57  0  0  0  0  0  0  0  0999 V2000
   -3.4028    6.8015    3.3296 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3684    5.3951    3.4704 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6318    4.5417    2.6590 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8503    5.0565    1.6095 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1160    4.2085    0.8002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1051    2.8358    0.9719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3155    1.9731    0.1127 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4845    2.0516   -1.2343 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0453    0.8788   -1.8070 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6170    0.0635   -0.6997 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.2660   -1.3680   -0.6391 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9747   -2.3152   -1.4469 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6021   -2.6509   -2.7527 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2911   -3.5508   -3.4665 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4367   -4.2355   -2.9856 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0925   -5.0948   -3.6695 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7447   -5.9521   -4.3549 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8009   -3.8867   -1.6695 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9157   -4.5065   -1.1147 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3914   -4.2378    0.1757 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0945   -2.9808   -0.9703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1150   -1.3757   -0.7556 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5652   -0.2342   -0.0623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3771    0.5272    0.4096 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8739    2.3482    2.0002 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6146    3.1952    2.8159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3878    2.6121    3.8565 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4223    1.2291    4.0334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0501    7.0189    2.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3877    7.2094    3.1168 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8146    7.2314    4.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8585    6.1395    1.4731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5285    4.6619   -0.0031 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7865    2.2549    0.2716 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8255    1.2075   -2.5284 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7801    0.4051   -2.3564 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6421    0.3404   -0.4148 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4377   -1.6697    0.4533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2875   -2.1146   -3.1183 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9843   -3.7992   -4.4780 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7210   -7.0493   -4.0063 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8773   -5.7496   -4.4760 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4453   -6.0892   -5.4507 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7092   -3.1649    0.1905 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6544   -4.3745    0.9845 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3067   -4.8777    0.3341 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3807   -2.7090    0.0641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2637   -0.5661    0.7417 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0952    0.3775   -0.8225 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0021    0.2262    1.3953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9042    1.2977    2.1787 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2654    0.8968    4.6853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5085    0.8033    4.4568 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6710    0.7639    3.0308 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  2  0
  6 25  1  0
 25 26  2  0
 26 27  1  0
 27 28  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 24  1  0
 24 23  1  0
 23 22  1  0
 22 11  1  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  2  0
 26  3  1  0
 24  7  1  0
 21 12  1  0
 11 10  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  4 32  1  0
  5 33  1  0
 25 51  1  0
 28 52  1  0
 28 53  1  0
 28 54  1  0
  7 34  1  6
  9 35  1  0
  9 36  1  0
 10 37  1  1
 24 50  1  1
 23 48  1  0
 23 49  1  0
 11 38  1  1
 13 39  1  0
 14 40  1  0
 17 41  1  0
 17 42  1  0
 17 43  1  0
 20 44  1  0
 20 45  1  0
 20 46  1  0
 21 47  1  0
M  END


  Mrv1533004161513122D          

 28 31  0  0  0  0            999 V2000
   -1.8267    3.3100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0198    3.1385    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7648    2.3539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0422    2.1823    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2971    1.3977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2549    0.7846    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0619    0.9561    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3168    1.7408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1238    1.9123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3788    2.6969    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4849   -0.6674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000   -1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -1.0799    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7846   -0.2549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0542   -0.6674    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5692   -1.3349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8242   -2.1195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6312   -2.2910    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8861   -3.0756    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3341   -3.6887    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5890   -4.4734    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3960   -4.6449    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5271   -3.5172    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9751   -4.1303    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1681   -3.9588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2721   -2.7326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  3  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  6 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  1  0  0  0  0
 11 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 14 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
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 25 28  2  0  0  0  0
 19 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0246542

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(C=C1OC)C1OCC2C1COC2C1=CC=C(OC)C(OC)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C22H26O6/c1-23-17-7-5-13(9-19(17)25-3)21-15-11-28-22(16(15)12-27-21)14-6-8-18(24-2)20(10-14)26-4/h5-10,15-16,21-22H,11-12H2,1-4H3

> <INCHI_KEY>
PEUUVVGQIVMSAW-UHFFFAOYSA-N

> <FORMULA>
C22H26O6

> <MOLECULAR_WEIGHT>
386.444

> <EXACT_MASS>
386.172938557

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
54

> <JCHEM_AVERAGE_POLARIZABILITY>
41.97899034227925

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan

> <ALOGPS_LOGP>
2.97

> <JCHEM_LOGP>
2.569547659333333

> <ALOGPS_LOGS>
-4.85

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7383009447365905

> <JCHEM_POLAR_SURFACE_AREA>
55.38000000000001

> <JCHEM_REFRACTIVITY>
104.0648

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.46e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -3.410   6.179   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.904   5.859   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.428   4.394   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.079   4.074   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.555   2.609   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.476   1.465   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.982   1.785   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -2.458   3.249   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -3.964   3.570   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -4.440   5.034   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      -0.905  -1.246   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      -0.000  -2.492   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       1.465  -2.016   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.465  -0.476   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.929   0.000   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.834  -1.246   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.929  -2.492   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       3.405  -3.956   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.911  -4.277   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       5.387  -5.741   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.357  -6.886   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       4.833  -8.350   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       6.339  -8.670   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       2.851  -6.565   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       1.820  -7.710   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       0.314  -7.390   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       2.375  -5.101   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    8                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    3    9                                                  
CONECT    9    8   10                                                       
CONECT   10    9                                                            
CONECT   11    6   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   18                                                  
CONECT   15   14   11   16                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   14   19                                                  
CONECT   19   18   20   28                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26   28                                                  
CONECT   26   25   27                                                       
CONECT   27   26                                                            
CONECT   28   25   19                                                       
MASTER        0    0    0    0    0    0    0    0   28    0   62    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₂₆O₆

Average Mass

386.4440 Da

Monoisotopic Mass

386.17294 Da

IUPAC Name

1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan

Traditional Name

1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan

CAS Registry Number

Not Available

SMILES

COC1=CC=C(C=C1OC)C1OCC2C1COC2C1=CC=C(OC)C(OC)=C1

InChI Identifier

InChI=1S/C22H26O6/c1-23-17-7-5-13(9-19(17)25-3)21-15-11-28-22(16(15)12-27-21)14-6-8-18(24-2)20(10-14)26-4/h5-10,15-16,21-22H,11-12H2,1-4H3

InChI Key

PEUUVVGQIVMSAW-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
Achillea holosericea	LOTUS Database	35616633
Acorus calamus	LOTUS Database	35616633
Aglaia abbreviata	LOTUS Database	35616633
Aglaia leptantha	LOTUS Database	35616633
Aglaia perviridis	LOTUS Database	35616633
Araucaria angustifolia	LOTUS Database	35616633
Artemisia absinthium	LOTUS Database	35616633
Artemisia gorgonum	LOTUS Database	35616633
Bupleurum salicifolium	LOTUS Database	35616633
Daphne oleoides	LOTUS Database	35616633
Haplophyllum acutifolium	LOTUS Database	35616633
Haplophyllum villosum	LOTUS Database	35616633
Hernandia sonora	LOTUS Database	35616633
Lindera praecox	LOTUS Database	35616633
Liriodendron tulipifera	LOTUS Database	35616633
Magnolia biondii	LOTUS Database	35616633
Magnolia coco	LOTUS Database	35616633
Magnolia denudata	LOTUS Database	35616633
Magnolia kobus	LOTUS Database	35616633
Magnolia praecocissima	LOTUS Database	35616633
Magnolia stellata	LOTUS Database	35616633
Melicope hayesii	LOTUS Database	35616633
Metrodorea flavida	LOTUS Database	35616633
Metrodorea nigra	LOTUS Database	35616633
Orophea enneandra	LOTUS Database	35616633
Pandanus boninensis	LOTUS Database	35616633
Pandanus odorifer	LOTUS Database	35616633
Rollinia mucosa	LOTUS Database	35616633
Rollinia sylvatica	LOTUS Database	35616633
Samadera bidwillii	LOTUS Database	35616633
Zanthoxylum culantrillo	LOTUS Database	35616633
Zanthoxylum simulans	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as furanoid lignans. These are lignans with a structure that contains either a tetrahydrofuran ring, a furan ring, or a furofuan ring system, that arises from the joining of the two phenylpropanoid units.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Furanoid lignans

Sub Class

Not Available

Direct Parent

Furanoid lignans

Alternative Parents

Substituents

Furanoid lignan
Furofuran lignan skeleton
O-dimethoxybenzene
Dimethoxybenzene
Phenoxy compound
Anisole
Methoxybenzene
Furofuran
Phenol ether
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Tetrahydrofuran
Organoheterocyclic compound
Ether
Dialkyl ether
Oxacycle
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

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

Predicted Properties

Property	Value	Source
logP	2.97	ALOGPS
logP	2.57	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	55.38 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	104.06 m³·mol⁻¹	ChemAxon
Polarizability	41.98 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

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

234823

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan (NP0246542)

MOL for NP0246542 (1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan)

3D MOL for NP0246542 (1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan)

3D SDF for NP0246542 (1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan)

3D-SDF for NP0246542 (1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan)

PDB for NP0246542 (1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan)

3D PDB for NP0246542 (1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan)

SMILES for NP0246542 (1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan)

INCHI for NP0246542 (1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan)

Structure for NP0246542 (1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan)

3D Structure for NP0246542 (1,4-bis(3,4-dimethoxyphenyl)-hexahydrofuro[3,4-c]furan)