NP-MRD: Showing NP-Card for 3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one (NP0258448)

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Record Information

Version

2.0

Created at

2022-09-07 23:54:24 UTC

Updated at

2022-09-07 23:54:24 UTC

NP-MRD ID

NP0258448

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one

Description

3,6-Bis(2H-1,3-benzodioxol-5-yl)-hexahydrofuro[3,4-c]furan-1-one belongs to the class of organic compounds known as lignan lactones. These are lignans that contain a lactone moiety. They include 1-aryltetralin lactones, dibenzylbutyrolactone lignans, and podophyllotoxins, among others. 3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one is found in Vitex negundo. 3,6-Bis(2H-1,3-benzodioxol-5-yl)-hexahydrofuro[3,4-c]furan-1-one is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201503442D          

 27 32  0  0  0  0            999 V2000
    6.1929    2.5392    0.0000 O   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 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7405    3.8829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2925    4.4960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0462    4.1604    0.0000 C   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
    5.7607    4.5729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7607    5.3979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4751    5.8104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1896    5.3979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9742    5.6529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4592    4.9854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9742    4.3180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1896    4.5729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4751    4.1604    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  2  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
  8  9  1  0  0  0  0
  2  9  1  0  0  0  0
  5  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 18  1  0  0  0  0
  4 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 19 27  1  0  0  0  0
M  END

     RDKit          3D

 43 48  0  0  0  0  0  0  0  0999 V2000
   -0.3386    2.3519   -0.7086 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0279    1.2489   -0.1852 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9217    0.9731    0.7767 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3890   -0.3474    0.5918 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8275   -0.2736    0.2414 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3822   -1.0769   -0.7234 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7455   -0.9614   -1.0198 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5582   -0.0582   -0.3677 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0109    0.7552    0.6053 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6691    0.6292    0.8846 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0025    1.5640    1.1101 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0515    1.5782    0.1692 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9034    0.2900   -0.4278 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5880   -0.9405   -0.5335 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0613   -2.2414   -0.1643 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0463   -1.9446    0.7375 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3944   -0.6064    0.6420 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8497   -0.3940    0.5825 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7107   -1.0770    1.4081 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0927   -0.8663    1.3465 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6101    0.0358    0.4498 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7549    0.7233   -0.3799 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3705    0.5065   -0.3119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5510    1.5450   -1.1591 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8384    1.6727   -0.5881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9047    0.4500    0.1623 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6662   -0.0330   -0.5292 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.2524   -0.9065    1.5466 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8200   -1.8036   -1.2681 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2087   -1.5826   -1.7766 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2303    1.2575    1.6411 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0164    1.6457    0.7067 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9597    2.3864   -0.5761 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0580   -0.9041   -1.5166 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6511   -2.9799    0.2462 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5635   -2.6236   -1.0926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0346   -0.1189    1.5835 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2967   -1.7784    2.1039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7668   -1.4028    1.9948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7578    1.0830   -0.9928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6435    1.7480   -1.3267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7916    2.5465    0.1104 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1742   -0.0699   -1.4863 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
  3  4  1  0
  4 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 27  1  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 26  1  0
 26 25  1  0
 25 24  1  0
 24 22  1  0
 22 23  2  0
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8 13  1  0
 13 12  1  0
 12 11  1  0
 11  9  1  0
  9 10  2  0
 27  2  1  0
 23 18  1  0
 10  5  1  0
 27 14  1  0
 22 21  1  0
  9  8  1  0
  4 28  1  1
 14 34  1  6
 15 35  1  0
 15 36  1  0
 17 37  1  1
 27 43  1  6
 19 38  1  0
 20 39  1  0
 25 41  1  0
 25 42  1  0
 23 40  1  0
  6 29  1  0
  7 30  1  0
 12 32  1  0
 12 33  1  0
 10 31  1  0
M  END


  Mrv1533004201503442D          

 27 32  0  0  0  0            999 V2000
    6.1929    2.5392    0.0000 O   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 O   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 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7405    3.8829    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2925    4.4960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0462    4.1604    0.0000 C   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
    5.7607    4.5729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7607    5.3979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4751    5.8104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1896    5.3979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9742    5.6529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.4592    4.9854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9742    4.3180    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.1896    4.5729    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4751    4.1604    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  2  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
  8  9  1  0  0  0  0
  2  9  1  0  0  0  0
  5  9  1  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 13 17  1  0  0  0  0
 17 18  2  0  0  0  0
 10 18  1  0  0  0  0
  4 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
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 22 26  1  0  0  0  0
 26 27  2  0  0  0  0
 19 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0258448

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O=C1OC(C2COC(C12)C1=CC=C2OCOC2=C1)C1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O7/c21-20-17-12(18(27-20)10-1-3-13-15(5-10)25-8-23-13)7-22-19(17)11-2-4-14-16(6-11)26-9-24-14/h1-6,12,17-19H,7-9H2

> <INCHI_KEY>
UIPQDOWYNRWNGN-UHFFFAOYSA-N

> <FORMULA>
C20H16O7

> <MOLECULAR_WEIGHT>
368.341

> <EXACT_MASS>
368.089602855

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
36.616324014702926

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3,6-bis(2H-1,3-benzodioxol-5-yl)-hexahydrofuro[3,4-c]furan-1-one

> <ALOGPS_LOGP>
2.50

> <JCHEM_LOGP>
2.3582682463333335

> <ALOGPS_LOGS>
-3.34

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-3.993069801193291

> <JCHEM_POLAR_SURFACE_AREA>
72.45000000000002

> <JCHEM_REFRACTIVITY>
89.5481

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.70e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,6-bis(2H-1,3-benzodioxol-5-yl)-tetrahydro-3H-furo[3,4-c]furan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 20-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-APR-15         0                                  
HETATM    1  O   UNK     0      11.560   4.740   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      10.029   4.901   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       8.998   3.756   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.752   5.914   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.982   7.248   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.013   8.393   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       9.420   7.766   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.259   6.235   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.753   8.536   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.753  10.076   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.087  10.846   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.421  10.076   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      14.885  10.552   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      15.790   9.306   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      14.885   8.060   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      13.421   8.536   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      12.087   7.766   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.258   3.613   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       6.258   2.073   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.924   1.303   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.590   2.073   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.126   4.089   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.924   4.383   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    9                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   19                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8    2    5                                                  
CONECT   10    8   11   18                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   13   18                                                  
CONECT   18   17   10                                                       
CONECT   19    4   20   27                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   26                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   22   27                                                  
CONECT   27   26   19                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₆O₇

Average Mass

368.3410 Da

Monoisotopic Mass

368.08960 Da

IUPAC Name

3,6-bis(2H-1,3-benzodioxol-5-yl)-hexahydrofuro[3,4-c]furan-1-one

Traditional Name

3,6-bis(2H-1,3-benzodioxol-5-yl)-tetrahydro-3H-furo[3,4-c]furan-1-one

CAS Registry Number

Not Available

SMILES

O=C1OC(C2COC(C12)C1=CC=C2OCOC2=C1)C1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C20H16O7/c21-20-17-12(18(27-20)10-1-3-13-15(5-10)25-8-23-13)7-22-19(17)11-2-4-14-16(6-11)26-9-24-14/h1-6,12,17-19H,7-9H2

InChI Key

UIPQDOWYNRWNGN-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
Vitex negundo	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lignan lactones. These are lignans that contain a lactone moiety. They include 1-aryltetralin lactones, dibenzylbutyrolactone lignans, and podophyllotoxins, among others.

Kingdom

Organic compounds

Super Class

Lignans, neolignans and related compounds

Class

Lignan lactones

Sub Class

Not Available

Direct Parent

Lignan lactones

Alternative Parents

Substituents

Lignan lactone
Furanoid lignan
Furofuran lignan skeleton
Benzodioxole
Furofuran
Gamma butyrolactone
Benzenoid
Oxolane
Carboxylic acid ester
Lactone
Organoheterocyclic compound
Oxacycle
Ether
Dialkyl ether
Acetal
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Hydrocarbon derivative
Organic oxide
Carbonyl group
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	2.5	ALOGPS
logP	2.36	ChemAxon
logS	-3.3	ALOGPS
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	72.45 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	89.55 m³·mol⁻¹	ChemAxon
Polarizability	36.62 Å³	ChemAxon
Number of Rings	6	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 3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one (NP0258448)

MOL for NP0258448 (3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one)

3D MOL for NP0258448 (3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one)

3D SDF for NP0258448 (3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one)

3D-SDF for NP0258448 (3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one)

PDB for NP0258448 (3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one)

3D PDB for NP0258448 (3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one)

SMILES for NP0258448 (3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one)

INCHI for NP0258448 (3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one)

Structure for NP0258448 (3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one)

3D Structure for NP0258448 (3,6-bis(2h-1,3-benzodioxol-5-yl)-tetrahydro-3h-furo[3,4-c]furan-1-one)