NP-MRD: Showing NP-Card for rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan (NP0139107)

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Record Information

Version

1.0

Created at

2022-06-29 19:39:40 UTC

Updated at

2022-06-29 19:39:40 UTC

NP-MRD ID

NP0139107

Secondary Accession Numbers

None

Natural Product Identification

Common Name

rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan

Description

GALBACIN 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. rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan is found in Aristolochia holostylis, Bicuiba oleifera, Chamaecyparis obtusa, Holostylis reniformis, Knema elegans, Machilus thunbergii, Myristica fragrans, Piper kadsura, Piper schmidtii, Saururus chinensis and Virola surinamensis. GALBACIN is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161507092D          

 25 29  0  0  0  0            999 V2000
    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  0  0  0  0  0  0  0  0  0  0
    4.8204    2.0124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9920    1.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1530    3.1684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9600    3.3400    0.0000 C   0  0  0  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
    4.8106    4.7611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1462    5.5147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9666    5.6010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4516    6.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2362    6.0135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2362    5.1885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4516    4.9335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1160    4.1799    0.0000 C   0  0  0  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
    1.1387    0.8555    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    2.1904    0.0000 O   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  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 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  2  0  0  0  0
  8 16  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  2  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  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 17 25  1  0  0  0  0
M  END

     RDKit          3D

 45 49  0  0  0  0  0  0  0  0999 V2000
   -1.5861   -2.3850   -0.5168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5878   -1.4879   -1.2038 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.9904   -0.0478   -1.2219 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2595    0.1524   -0.4780 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3137    0.0752    0.8952 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4865    0.2603    1.5825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6625    0.5330    0.9066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6244    0.6133   -0.4660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4333    0.4242   -1.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9193    0.8938   -0.8992 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6736    1.3211    0.2338 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9815    0.7619    1.3542 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0095    0.6766   -0.5542 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1699   -0.0280   -0.7924 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2889    0.4319    0.0241 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1860    0.6912    1.3644 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2930    1.1258    2.0768 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5162    1.3100    1.4750 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6165    1.0489    0.1291 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5211    0.6203   -0.5688 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9252    1.3046   -0.2395 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5765    2.0436    0.7941 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7775    1.7262    1.9160 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7365   -1.4460   -0.4686 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7100   -2.4647   -1.0144 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4671   -2.3949    0.5739 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5661   -3.3779   -0.9823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6001   -1.9598   -0.7366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4313   -1.8947   -2.2452 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0627    0.2873   -2.2629 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3657   -0.1418    1.3947 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4645    0.1873    2.6573 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3995    0.4872   -2.2349 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7141    2.4164    0.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6805    0.8470    0.2443 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4023    0.0049   -1.8610 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2266    0.5450    1.8288 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2143    1.3351    3.1536 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6272    0.4233   -1.6206 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6000    1.6670    0.8590 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4960    3.1103    0.5071 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5407   -1.5897    0.6000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0026   -3.1274   -0.1704 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6228   -1.9388   -1.3487 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2302   -3.0405   -1.8275 H   0  0  0  0  0  0  0  0  0  0  0  0
 25 24  1  0
 24  2  1  0
  2  1  1  0
  2  3  1  0
  3 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 23  1  0
 23 22  1  0
 22 21  1  0
 21 19  1  0
 19 20  2  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  2  0
  7 12  1  0
 12 11  1  0
 11 10  1  0
 10  8  1  0
  8  9  2  0
 14 24  1  0
 20 15  1  0
  9  4  1  0
 19 18  1  0
  8  7  1  0
 25 43  1  0
 25 44  1  0
 25 45  1  0
 24 42  1  1
  2 29  1  6
  1 26  1  0
  1 27  1  0
  1 28  1  0
  3 30  1  6
 14 36  1  6
 16 37  1  0
 17 38  1  0
 22 40  1  0
 22 41  1  0
 20 39  1  0
  5 31  1  0
  6 32  1  0
 11 34  1  0
 11 35  1  0
  9 33  1  0
M  END


  Mrv1533004161507092D          

 25 29  0  0  0  0            999 V2000
    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  0  0  0  0  0  0  0  0  0  0
    4.8204    2.0124    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9920    1.2054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0668    2.3479    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1530    3.1684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9600    3.3400    0.0000 C   0  0  0  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
    4.8106    4.7611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1462    5.5147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9666    5.6010    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4516    6.2684    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.2362    6.0135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2362    5.1885    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4516    4.9335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1160    4.1799    0.0000 C   0  0  0  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
    1.1387    0.8555    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    2.1904    0.0000 O   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  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  2  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 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  2  0  0  0  0
  8 16  1  0  0  0  0
  5 17  1  0  0  0  0
 17 18  2  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  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 20 24  1  0  0  0  0
 24 25  2  0  0  0  0
 17 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0139107

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1C(C)C(OC1C1=CC=C2OCOC2=C1)C1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H20O5/c1-11-12(2)20(14-4-6-16-18(8-14)24-10-22-16)25-19(11)13-3-5-15-17(7-13)23-9-21-15/h3-8,11-12,19-20H,9-10H2,1-2H3

> <INCHI_KEY>
QFUXQRHAJWXPGP-UHFFFAOYSA-N

> <FORMULA>
C20H20O5

> <MOLECULAR_WEIGHT>
340.375

> <EXACT_MASS>
340.131073744

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
36.293293322870184

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
3.73

> <JCHEM_LOGP>
4.075239864333334

> <ALOGPS_LOGS>
-4.77

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
5

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.024051586120543

> <JCHEM_POLAR_SURFACE_AREA>
46.150000000000006

> <JCHEM_REFRACTIVITY>
89.5961

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.80e-03 g/l

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

> <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      11.560   4.740   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.029   4.901   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.998   3.756   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.318   2.250   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       7.752   5.914   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       9.259   6.235   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.885   7.641   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       8.980   8.887   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.606  10.294   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.138  10.455   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0      12.043  11.701   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0      13.508  11.225   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      13.508   9.685   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      12.043   9.209   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      11.417   7.802   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    7                                                  
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   17                                                  
CONECT    6    5    7                                                       
CONECT    7    6    2    8                                                  
CONECT    8    7    9   16                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   15                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   11   16                                                  
CONECT   16   15    8                                                       
CONECT   17    5   18   25                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   24                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   20   25                                                  
CONECT   25   24   17                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₂₀O₅

Average Mass

340.3750 Da

Monoisotopic Mass

340.13107 Da

IUPAC Name

5-[5-(2H-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2H-1,3-benzodioxole

Traditional Name

5-[5-(2H-1,3-benzodioxol-5-yl)-3,4-dimethyloxolan-2-yl]-2H-1,3-benzodioxole

CAS Registry Number

Not Available

SMILES

CC1C(C)C(OC1C1=CC=C2OCOC2=C1)C1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C20H20O5/c1-11-12(2)20(14-4-6-16-18(8-14)24-10-22-16)25-19(11)13-3-5-15-17(7-13)23-9-21-15/h3-8,11-12,19-20H,9-10H2,1-2H3

InChI Key

QFUXQRHAJWXPGP-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
Aristolochia holostylis	LOTUS Database	35616633
Bicuiba oleifera	LOTUS Database	35616633
Chamaecyparis obtusa	LOTUS Database	35616633
Holostylis reniformis	LOTUS Database	35616633
Knema elegans	LOTUS Database	35616633
Machilus thunbergii	LOTUS Database	35616633
Myristica fragrans	LOTUS Database	35616633
Piper kadsura	LOTUS Database	35616633
Piper schmidtii	LOTUS Database	35616633
Saururus chinensis	LOTUS Database	35616633
Virola surinamensis	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
Benzodioxole
Benzenoid
Tetrahydrofuran
Oxacycle
Organoheterocyclic compound
Ether
Dialkyl ether
Acetal
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	3.73	ALOGPS
logP	4.08	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	46.15 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	89.6 m³·mol⁻¹	ChemAxon
Polarizability	36.29 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

234441

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan (NP0139107)

MOL for NP0139107 (rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan)

3D MOL for NP0139107 (rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan)

3D SDF for NP0139107 (rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan)

3D-SDF for NP0139107 (rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan)

PDB for NP0139107 (rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan)

3D PDB for NP0139107 (rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan)

SMILES for NP0139107 (rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan)

INCHI for NP0139107 (rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan)

Structure for NP0139107 (rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan)

3D Structure for NP0139107 (rel-(8R,8'R)-dimethyl-(7S,7'R)-bis(3,4-methylenedioxyphenyl)tetrahydro-furan)