NP-MRD: Showing NP-Card for (+)-Paulownin (NP0075642)

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Record Information

Version

2.0

Created at

2022-04-28 20:54:08 UTC

Updated at

2022-04-28 20:54:09 UTC

NP-MRD ID

NP0075642

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(+)-Paulownin

Description

Paulownin 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. (+)-Paulownin is found in Cleistanthus collinus, Dolichandrone stipulata , Firmiana platanifolia, Gmelina arborea , Markhamia platycalyx, Markhamia stipulata , Paulownia tomentosa and Stereospermum acuminatissimum. Based on a literature review very few articles have been published on Paulownin.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304282222542D          

 27 32  0  0  1  0            999 V2000
    4.0668    2.3479    0.0000 C   0  0  1  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
    5.3725    2.6255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9600    3.3400    0.0000 C   0  0  1  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
    3.7405    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  2  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
    7.1896    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
    7.9742    4.3180    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    5.6529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7669    3.5115    0.0000 O   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
    1.9233    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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  1  6  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
  4 18  1  6  0  0  0
  1 19  1  6  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  2  0  0  0  0
 19 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
M  END

     RDKit          3D

 45 50  0  0  0  0  0  0  0  0999 V2000
   -0.8744    0.0349    1.4240 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6598   -0.9641    0.4945 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0331   -2.1867    1.1261 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2964   -1.7830    1.2588 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5798   -1.3806   -0.0663 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8999   -0.7519   -0.1759 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9612   -1.3786    0.4740 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2358   -0.8435    0.4151 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4825    0.3148   -0.2839 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4465    0.9528   -0.9356 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1908    0.3915   -0.8553 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9964    2.0817   -1.5466 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2620    2.3675   -0.9480 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6366    1.0573   -0.5055 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4336   -0.5760   -0.5123 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1391   -1.1085   -1.7955 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5042   -1.0970   -1.6731 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8415   -1.2717   -0.3547 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9074   -0.2614   -0.0322 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7084    1.0297   -0.4813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6187    2.0253   -0.2408 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7633    1.6976    0.4767 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9674    0.4102    0.9276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0333   -0.5786    0.6722 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1936    0.3901    1.6093 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8929    1.5855    1.2950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8548    2.4763    0.8742 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0122    0.4310    1.6877 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4998   -2.4853    2.0641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0375   -2.9846    0.3503 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6099   -2.3294   -0.6511 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8062   -2.3007    1.0400 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0382   -1.3460    0.9253 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3926    0.8972   -1.3666 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0786    2.9740   -0.0406 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9787    2.7957   -1.6486 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5227    0.5019   -0.4622 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934   -0.5152   -2.6699 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1864   -2.1690   -1.8938 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2403   -2.2959   -0.2180 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8109    1.3100   -1.0500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4851    3.0478   -0.5832 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1693   -1.5922    1.0136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5921    1.4149    0.4522 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3894    2.0122    2.1848 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  1
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 27  1  0
 27 26  1  0
 26 25  1  0
 25 23  1  0
 23 24  2  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 14  1  0
 14 13  1  0
 13 12  1  0
 12 10  1  0
 10 11  2  0
 15  2  1  0
 24 19  1  0
 11  6  1  0
 18  2  1  0
 23 22  1  0
 10  9  1  0
  1 28  1  0
  3 29  1  0
  3 30  1  0
  5 31  1  6
 15 37  1  6
 16 38  1  0
 16 39  1  0
 18 40  1  6
 20 41  1  0
 21 42  1  0
 26 44  1  0
 26 45  1  0
 24 43  1  0
  7 32  1  0
  8 33  1  0
 13 35  1  0
 13 36  1  0
 11 34  1  0
M  END


  Mrv1652304282222542D          

 27 32  0  0  1  0            999 V2000
    4.0668    2.3479    0.0000 C   0  0  1  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
    5.3725    2.6255    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9600    3.3400    0.0000 C   0  0  1  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
    3.7405    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  2  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
    7.1896    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
    7.9742    4.3180    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    5.6529    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7669    3.5115    0.0000 O   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
    1.9233    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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  5  6  1  1  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  4  8  1  0  0  0  0
  8  9  1  6  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
  4 18  1  6  0  0  0
  1 19  1  6  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  2  0  0  0  0
 19 24  1  0  0  0  0
 23 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 22 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0075642

> <DATABASE_NAME>
NP-MRD

> <SMILES>
O[C@]12CO[C@@H]([C@H]1CO[C@@H]2C1=CC=C2OCOC2=C1)C1=CC=C2OCOC2=C1

> <INCHI_IDENTIFIER>
InChI=1S/C20H18O7/c21-20-8-23-18(11-1-3-14-16(5-11)26-9-24-14)13(20)7-22-19(20)12-2-4-15-17(6-12)27-10-25-15/h1-6,13,18-19,21H,7-10H2/t13-,18-,19-,20-/m1/s1

> <INCHI_KEY>
CAQZFLPWHBKTTR-WNISUXOKSA-N

> <FORMULA>
C20H18O7

> <MOLECULAR_WEIGHT>
370.357

> <EXACT_MASS>
370.10525292

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
37.24672140299241

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3aS,4R,6aR)-1,4-bis(2H-1,3-benzodioxol-5-yl)-hexahydrofuro[3,4-c]furan-3a-ol

> <ALOGPS_LOGP>
2.10

> <JCHEM_LOGP>
1.8966909663333333

> <ALOGPS_LOGS>
-2.80

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
6

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.605418107831149

> <JCHEM_PKA_STRONGEST_BASIC>
-3.789871757954018

> <JCHEM_POLAR_SURFACE_AREA>
75.61000000000001

> <JCHEM_REFRACTIVITY>
90.62690000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.93e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3aS,4R,6aR)-1,4-bis(2H-1,3-benzodioxol-5-yl)-tetrahydro-1H-furo[3,4-c]furan-3a-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       7.591   4.383   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.998   3.756   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      10.029   4.901   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.259   6.235   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      10.753   8.536   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.753  10.076   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      12.087  10.846   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.421  10.076   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.421   8.536   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.087   7.766   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      14.885   8.060   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      15.790   9.306   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      14.885  10.552   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      10.765   6.555   0.000  0.00  0.00           O+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  C   UNK     0       3.590   3.613   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.924   4.383   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       1.220   2.843   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       2.126   1.597   0.000  0.00  0.00           O+0
CONECT    1    2    5   19                                                  
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5    8   18                                             
CONECT    5    4    1    6                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    4    9                                                  
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    4                                                            
CONECT   19    1   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   27                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   19                                                       
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   22                                                       
MASTER        0    0    0    0    0    0    0    0   27    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₁₈O₇

Average Mass

370.3570 Da

Monoisotopic Mass

370.10525 Da

IUPAC Name

(1S,3aS,4R,6aR)-1,4-bis(2H-1,3-benzodioxol-5-yl)-hexahydrofuro[3,4-c]furan-3a-ol

Traditional Name

(1S,3aS,4R,6aR)-1,4-bis(2H-1,3-benzodioxol-5-yl)-tetrahydro-1H-furo[3,4-c]furan-3a-ol

CAS Registry Number

Not Available

SMILES

O[C@]12CO[C@@H]([C@H]1CO[C@@H]2C1=CC=C2OCOC2=C1)C1=CC=C2OCOC2=C1

InChI Identifier

InChI=1S/C20H18O7/c21-20-8-23-18(11-1-3-14-16(5-11)26-9-24-14)13(20)7-22-19(20)12-2-4-15-17(6-12)27-10-25-15/h1-6,13,18-19,21H,7-10H2/t13-,18-,19-,20-/m1/s1

InChI Key

CAQZFLPWHBKTTR-WNISUXOKSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Cleistanthus collinus	LOTUS Database	35616633
Dolichandrone stipulata	Plant	KNApSAcK
Firmiana simplex	Plant	KNApSAcK
Gmelina arborea	Plant	KNApSAcK
Markhamia platycalyx	LOTUS Database	35616633
Markhamia stipulata	Plant	KNApSAcK
Paulownia tomentosa	Plant	KNApSAcK
Stereospermum acuminatissimum	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
Benzodioxole
Furofuran
Benzenoid
Oxolane
Tertiary alcohol
Acetal
Dialkyl ether
Ether
Oxacycle
Organoheterocyclic compound
Hydrocarbon derivative
Organic oxygen compound
Organooxygen compound
Alcohol
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	2.1	ALOGPS
logP	1.9	ChemAxon
logS	-2.8	ALOGPS
pKa (Strongest Acidic)	12.61	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	75.61 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	90.63 m³·mol⁻¹	ChemAxon
Polarizability	37.25 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

C00037601

Chemspider ID

2341242

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

3084131

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (+)-Paulownin (NP0075642)

MOL for NP0075642 ((+)-Paulownin)

3D MOL for NP0075642 ((+)-Paulownin)

3D SDF for NP0075642 ((+)-Paulownin)

3D-SDF for NP0075642 ((+)-Paulownin)

PDB for NP0075642 ((+)-Paulownin)

3D PDB for NP0075642 ((+)-Paulownin)

SMILES for NP0075642 ((+)-Paulownin)

INCHI for NP0075642 ((+)-Paulownin)

Structure for NP0075642 ((+)-Paulownin)

3D Structure for NP0075642 ((+)-Paulownin)