NP-MRD: Showing NP-Card for (1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol (NP0320651)

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Record Information

Version

2.0

Created at

2022-09-11 22:25:23 UTC

Updated at

2022-09-11 22:25:23 UTC

NP-MRD ID

NP0320651

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol

Description

(2S)-2alpha,2'alpha-Bis(4-hydroxyphenyl)-3'beta-(3,5-dihydroxyphenyl)-4,5'-[(S)-2-(2,4-dihydroxyphenyl)ethane-1,2-diyl]-4',6-dihydroxy-2,2',3,3'-tetrahydro-3beta,6'-bibenzofuran belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. (1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol is found in Gnetum gnemon. Based on a literature review very few articles have been published on (2S)-2alpha,2'alpha-Bis(4-hydroxyphenyl)-3'beta-(3,5-dihydroxyphenyl)-4,5'-[(S)-2-(2,4-dihydroxyphenyl)ethane-1,2-diyl]-4',6-dihydroxy-2,2',3,3'-tetrahydro-3beta,6'-bibenzofuran.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309122200252D          

 52 60  0  0  1  0            999 V2000
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M  END

     RDKit          3D

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 13 58  1  0
 15 59  1  1
 17 60  1  0
 19 61  1  0
 20 62  1  0
 22 63  1  0
 23 64  1  0
M  END


  Mrv1652309122200252D          

 52 60  0  0  1  0            999 V2000
    8.4362   -1.4735    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6230   -1.3348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0962   -1.9697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2830   -1.8310    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9965   -1.0574    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1832   -0.9187    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5930   -1.4951    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8624   -1.1119    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0887   -1.3984    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4538   -0.8716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5925   -0.0584    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3661    0.2281    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5048    1.0414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.0011   -0.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8174   -0.1792    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2006    0.5514    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7595    1.2486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1427    1.9791    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7016    2.6763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9671    2.0126    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4082    1.3154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2325    1.3488    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.0249    0.5848    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0431    0.5571    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3593    1.3191    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1773    1.4263    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4935    2.1883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9917    2.8431    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3079    3.6051    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1737    2.7360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8575    1.9740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0395    1.8668    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2194    0.5114    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7416   -0.1612    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1165   -0.0254    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6527   -0.6524    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4638   -0.5015    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3778   -1.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4333   -1.5811    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9695   -0.9541    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7315   -1.2702    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.6662   -2.0927    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2932   -2.6289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0711   -2.3539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6981   -2.8901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5472   -3.7012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1742   -4.2374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7694   -3.9761    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1424   -3.4399    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8639   -2.2848    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5232   -0.4224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3365   -0.5611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  6  5  1  1  0  0  0
  6  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
 12 14  2  0  0  0  0
  8 14  1  0  0  0  0
 14 15  1  0  0  0  0
  6 15  1  0  0  0  0
 15 16  1  6  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 18 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  2  0  0  0  0
 16 23  1  0  0  0  0
 11 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  2  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 25 31  1  0  0  0  0
 31 32  1  0  0  0  0
 24 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  2  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 36 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 34 40  1  0  0  0  0
 41 40  1  6  0  0  0
 10 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  1  0  0  0
 43 44  2  0  0  0  0
 44 45  1  0  0  0  0
 45 46  2  0  0  0  0
 46 47  1  0  0  0  0
 46 48  1  0  0  0  0
 48 49  2  0  0  0  0
 43 49  1  0  0  0  0
 42 50  1  0  0  0  0
 39 50  1  0  0  0  0
  5 51  1  0  0  0  0
 51 52  2  0  0  0  0
  2 52  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0320651

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)[C@H]1OC2=CC3=C([C@@H](CC4=CC(O)=CC5=C4[C@H]3[C@H](O5)C3=CC=C(O)C=C3)C3=CC=C(O)C=C3O)C(O)=C2[C@@H]1C1=CC(O)=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C42H32O10/c43-23-5-1-19(2-6-23)41-36(21-11-26(46)15-27(47)12-21)39-34(52-41)18-31-37(40(39)50)30(29-10-9-25(45)16-32(29)49)14-22-13-28(48)17-33-35(22)38(31)42(51-33)20-3-7-24(44)8-4-20/h1-13,15-18,30,36,38,41-50H,14H2/t30-,36-,38-,41+,42+/m0/s1

> <INCHI_KEY>
XIHCOJVIUYCWST-OOUVTCTBSA-N

> <FORMULA>
C42H32O10

> <MOLECULAR_WEIGHT>
696.708

> <EXACT_MASS>
696.19954723

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
73.32294431317344

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S,6S,7S,11S,19S)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0^{2,10}.0^{4,8}.0^{17,20}]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol

> <JCHEM_LOGP>
7.859131641666667

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
9

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.072480308544357

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.678443416771422

> <JCHEM_PKA_STRONGEST_BASIC>
-5.292217948306697

> <JCHEM_POLAR_SURFACE_AREA>
180.29999999999998

> <JCHEM_REFRACTIVITY>
192.07339999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S,6S,7S,11S,19S)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0^{2,10}.0^{4,8}.0^{17,20}]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 12-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   12-SEP-22         0                                  
HETATM    1  O   UNK     0      15.748  -2.751   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      14.230  -2.492   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.246  -3.677   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      11.728  -3.418   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      11.193  -1.974   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.675  -1.715   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       8.574  -2.791   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       7.210  -2.075   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.766  -2.610   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.580  -1.627   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.839  -0.109   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.283   0.426   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       6.542   1.944   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       7.469  -0.557   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       8.992  -0.335   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       9.708   1.029   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.884   2.331   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.600   3.694   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.776   4.996   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      11.139   3.757   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      11.962   2.455   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      13.501   2.518   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      11.247   1.092   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.814   1.040   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.404   2.462   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.931   2.662   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       6.521   4.085   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       5.585   5.307   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       6.175   6.730   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       4.058   5.107   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       3.467   3.685   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       1.940   3.485   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       2.276   0.955   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       1.384  -0.301   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -0.218  -0.047   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      -1.218  -1.218   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -2.732  -0.936   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -0.705  -2.670   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.809  -2.951   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.810  -1.781   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.232  -2.371   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       3.110  -3.906   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       4.281  -4.907   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       5.733  -4.394   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       6.903  -5.395   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       6.621  -6.909   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       7.792  -7.910   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       5.169  -7.422   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       3.999  -6.421   0.000  0.00  0.00           C+0
HETATM   50  O   UNK     0       1.613  -4.265   0.000  0.00  0.00           O+0
HETATM   51  C   UNK     0      12.177  -0.789   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      13.695  -1.047   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   52                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   51                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   14                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   41                                                  
CONECT   11   10   12   24                                                  
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    8   15                                                  
CONECT   15   14    6   16                                                  
CONECT   16   15   17   23                                                  
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   16                                                       
CONECT   24   11   25   33                                                  
CONECT   25   24   26   31                                                  
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31                                                       
CONECT   31   30   25   32                                                  
CONECT   32   31                                                            
CONECT   33   24   34                                                       
CONECT   34   33   35   40                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37   38                                                  
CONECT   37   36                                                            
CONECT   38   36   39                                                       
CONECT   39   38   40   50                                                  
CONECT   40   39   34   41                                                  
CONECT   41   40   10   42                                                  
CONECT   42   41   43   50                                                  
CONECT   43   42   44   49                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47   48                                                  
CONECT   47   46                                                            
CONECT   48   46   49                                                       
CONECT   49   48   43                                                       
CONECT   50   42   39                                                       
CONECT   51    5   52                                                       
CONECT   52   51    2                                                       
MASTER        0    0    0    0    0    0    0    0   52    0  120    0
END

View in JSmol

Synonyms

Value	Source
(2S)-2a,2'a-Bis(4-hydroxyphenyl)-3'b-(3,5-dihydroxyphenyl)-4,5'-[(S)-2-(2,4-dihydroxyphenyl)ethane-1,2-diyl]-4',6-dihydroxy-2,2',3,3'-tetrahydro-3b,6'-bibenzofuran	Generator
(2S)-2Α,2'α-bis(4-hydroxyphenyl)-3'β-(3,5-dihydroxyphenyl)-4,5'-[(S)-2-(2,4-dihydroxyphenyl)ethane-1,2-diyl]-4',6-dihydroxy-2,2',3,3'-tetrahydro-3β,6'-bibenzofuran	Generator

Chemical Formula

C₄₂H₃₂O₁₀

Average Mass

696.7080 Da

Monoisotopic Mass

696.19955 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)[C@H]1OC2=CC3=C([C@@H](CC4=CC(O)=CC5=C4[C@H]3[C@H](O5)C3=CC=C(O)C=C3)C3=CC=C(O)C=C3O)C(O)=C2[C@@H]1C1=CC(O)=CC(O)=C1

InChI Identifier

InChI=1S/C42H32O10/c43-23-5-1-19(2-6-23)41-36(21-11-26(46)15-27(47)12-21)39-34(52-41)18-31-37(40(39)50)30(29-10-9-25(45)16-32(29)49)14-22-13-28(48)17-33-35(22)38(31)42(51-33)20-3-7-24(44)8-4-20/h1-13,15-18,30,36,38,41-50H,14H2/t30-,36-,38-,41+,42+/m0/s1

InChI Key

XIHCOJVIUYCWST-OOUVTCTBSA-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
Gnetum gnemon	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

2-arylbenzofuran flavonoids

Sub Class

Not Available

Direct Parent

2-arylbenzofuran flavonoids

Alternative Parents

Substituents

2-arylbenzofuran flavonoid
Linear 1,7-diphenylheptane skeleton
Neolignan skeleton
1-phenylcoumaran
Dibenzocycloheptene
Stilbene
Coumaran
Benzofuran
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Oxacycle
Organoheterocyclic compound
Ether
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

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

9116734

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

10941505

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol (NP0320651)

MOL for NP0320651 ((1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol)

3D MOL for NP0320651 ((1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol)

3D SDF for NP0320651 ((1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol)

3D-SDF for NP0320651 ((1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol)

PDB for NP0320651 ((1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol)

3D PDB for NP0320651 ((1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol)

SMILES for NP0320651 ((1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol)

INCHI for NP0320651 ((1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol)

Structure for NP0320651 ((1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol)

3D Structure for NP0320651 ((1s,6s,7s,11s,19s)-11-(2,4-dihydroxyphenyl)-7-(3,5-dihydroxyphenyl)-6,19-bis(4-hydroxyphenyl)-5,18-dioxapentacyclo[11.6.1.0²,¹⁰.0⁴,⁸.0¹⁷,²⁰]icosa-2(10),3,8,13,15,17(20)-hexaene-9,15-diol)