NP-MRD: Showing NP-Card for (-)-Dibalanocarpol (NP0082836)

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Record Information

Version

2.0

Created at

2022-04-29 03:55:13 UTC

Updated at

2022-04-29 03:55:13 UTC

NP-MRD ID

NP0082836

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(-)-Dibalanocarpol

Description

Dibalanocarpol belongs to the class of organic compounds known as 2-arylbenzofuran flavonoids. These are phenylpropanoids containing the 2-phenylbenzofuran moiety. (-)-Dibalanocarpol is found in Hopea malibato. Based on a literature review very few articles have been published on Dibalanocarpol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652304292205552D          

 70 81  0  0  1  0            999 V2000
    2.1525    1.4695    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0355    2.2861    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3241    2.7039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5539    2.4081    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3050    1.6216    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7647    0.9365    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5869    0.8688    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.8826    0.0987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6975   -0.0303    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9240   -0.7066    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4741   -1.4417    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5654   -1.3820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3635   -0.5425    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5310   -2.4101    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4013    0.1959    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4219    0.1403    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0986   -0.7386    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0346    3.0492    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.4839    3.7412    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2808    3.5277    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9726    3.9772    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7078    3.6027    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7511    2.7788    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9141    4.4729    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7892    3.0059    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1637    2.2708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4369    2.9194    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0625    3.6545    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2386    3.6978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2968    2.9123    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    3.1259   -0.9226    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.8744   -0.5757    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0699    0.2258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5652    0.8783    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.9341    1.6162    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4795    2.3047    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    4.6720    3.0921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2627   -0.9143    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.0030   -1.7384    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1892   -1.8737    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8091   -1.1415    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0894   -0.2023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5908   -2.3173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3861   -2.0978    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9739   -2.6767    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7664   -3.4752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9712   -3.6947    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3834   -3.1158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3219   -4.1325    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4015    1.5506    0.0000 O   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
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  1  1  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
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  8 13  1  0  0  0  0
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 17 18  2  0  0  0  0
  5 18  1  0  0  0  0
 17 19  1  0  0  0  0
 15 20  1  0  0  0  0
  4 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
  3 23  1  0  0  0  0
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 25 26  2  0  0  0  0
  2 26  1  0  0  0  0
 25 27  1  0  0  0  0
 21 28  1  6  0  0  0
 28 29  2  0  0  0  0
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 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 32 33  2  0  0  0  0
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 31 34  1  0  0  0  0
  1 35  1  1  0  0  0
  1 36  1  6  0  0  0
 36 37  1  1  0  0  0
 37 38  2  0  0  0  0
 39 38  1  1  0  0  0
 39 40  1  0  0  0  0
 40 41  2  0  0  0  0
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 36 42  1  0  0  0  0
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 46 47  1  0  0  0  0
 47 48  2  0  0  0  0
 43 48  1  0  0  0  0
 46 49  1  0  0  0  0
 41 50  1  0  0  0  0
 50 51  2  0  0  0  0
 51 52  1  0  0  0  0
 52 53  2  0  0  0  0
 40 53  1  0  0  0  0
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 50 55  1  0  0  0  0
 39 56  1  0  0  0  0
 56 57  1  0  0  0  0
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 37 61  1  0  0  0  0
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 66 67  1  0  0  0  0
 67 68  2  0  0  0  0
 63 68  1  0  0  0  0
 66 69  1  0  0  0  0
 36 70  1  1  0  0  0
M  END

     RDKit          3D

112123  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652304292205552D          

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 36 70  1  1  0  0  0
M  END
> <DATABASE_ID>
NP0082836

> <DATABASE_NAME>
NP-MRD

> <SMILES>
OC1=CC=C(C=C1)[C@@H]1OC2=CC(O)=CC3=C2[C@H]1C1=C([C@H](C2=CC=C(O)C=C2)[C@@]3(O)[C@]2(O)[C@@H](C3=CC=C(O)C=C3)C3=C(C=C(O)C=C3O)[C@H]3[C@@H](OC4=CC(O)=CC2=C34)C2=CC=C(O)C=C2)C(O)=CC(O)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C56H42O14/c57-29-9-1-25(2-10-29)51-45-37(17-33(61)21-41(45)65)47-49-39(19-35(63)23-43(49)69-53(47)27-5-13-31(59)14-6-27)55(51,67)56(68)40-20-36(64)24-44-50(40)48(54(70-44)28-7-15-32(60)16-8-28)38-18-34(62)22-42(66)46(38)52(56)26-3-11-30(58)12-4-26/h1-24,47-48,51-54,57-68H/t47-,48-,51+,52+,53+,54+,55-,56-/m1/s1

> <INCHI_KEY>
AETOAAQSGCSQKP-PWJWKHQFSA-N

> <FORMULA>
C56H42O14

> <MOLECULAR_WEIGHT>
938.938

> <EXACT_MASS>
938.257456032

> <JCHEM_ACCEPTOR_COUNT>
14

> <JCHEM_ATOM_COUNT>
112

> <JCHEM_AVERAGE_POLARIZABILITY>
93.79195385023624

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
12

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1R,8S,9S,16R)-8,16-bis(4-hydroxyphenyl)-9-[(1R,8S,9S,16R)-4,6,9,12-tetrahydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0^{2,7}.0^{14,17}]heptadeca-2(7),3,5,10(17),11,13-hexaen-9-yl]-15-oxatetracyclo[8.6.1.0^{2,7}.0^{14,17}]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,9,12-tetrol

> <ALOGPS_LOGP>
5.28

> <JCHEM_LOGP>
8.579484569333331

> <ALOGPS_LOGS>
-4.95

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
12

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.061048871966715

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.663640278413283

> <JCHEM_PKA_STRONGEST_BASIC>
-5.47028007786279

> <JCHEM_POLAR_SURFACE_AREA>
261.21999999999997

> <JCHEM_REFRACTIVITY>
255.7042

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.04e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1R,8S,9S,16R)-8,16-bis(4-hydroxyphenyl)-9-[(1R,8S,9S,16R)-4,6,9,12-tetrahydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0^{2,7}.0^{14,17}]heptadeca-2(7),3,5,10(17),11,13-hexaen-9-yl]-15-oxatetracyclo[8.6.1.0^{2,7}.0^{14,17}]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,9,12-tetrol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  C   UNK     0       4.018   2.743   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       3.800   4.267   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.472   5.047   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.034   4.495   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.569   3.027   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.427   1.748   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.962   1.622   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.514   0.184   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       5.035  -0.057   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.458  -1.319   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.618  -2.691   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.922  -2.580   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.545  -1.013   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.725  -4.499   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       0.749   0.366   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -0.787   0.262   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.646   1.541   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.967   2.923   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -3.237   1.039   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -0.184  -1.379   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       0.065   5.692   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.903   6.984   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       2.391   6.585   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       3.682   7.424   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.055   6.725   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.135   5.187   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       5.440   8.349   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      -1.473   5.611   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -2.172   4.239   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.710   4.158   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.549   5.449   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -3.850   6.822   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      -2.312   6.902   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0      -6.154   5.436   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0       5.371   2.745   0.000  0.00  0.00           O+0
HETATM   36  C   UNK     0       5.115   1.662   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       4.137   0.473   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       4.458  -1.034   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       5.835  -1.722   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       7.232  -1.075   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       7.597   0.421   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0       6.655   1.640   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       7.344   3.017   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       6.495   4.302   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       7.184   5.680   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       8.721   5.772   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       9.570   4.487   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       8.881   3.109   0.000  0.00  0.00           C+0
HETATM   49  O   UNK     0       9.716   7.076   0.000  0.00  0.00           O+0
HETATM   50  C   UNK     0       9.075   0.853   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      10.189  -0.211   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0       9.824  -1.707   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0       8.345  -2.139   0.000  0.00  0.00           C+0
HETATM   54  O   UNK     0      11.371  -2.249   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0      10.673   1.267   0.000  0.00  0.00           O+0
HETATM   56  C   UNK     0       5.606  -3.245   0.000  0.00  0.00           C+0
HETATM   57  O   UNK     0       4.087  -3.498   0.000  0.00  0.00           O+0
HETATM   58  C   UNK     0       3.377  -2.131   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0       1.886  -1.744   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0       1.477  -0.259   0.000  0.00  0.00           C+0
HETATM   61  C   UNK     0       2.557   0.838   0.000  0.00  0.00           C+0
HETATM   62  O   UNK     0      -0.167  -0.378   0.000  0.00  0.00           O+0
HETATM   63  C   UNK     0       6.703  -4.326   0.000  0.00  0.00           C+0
HETATM   64  C   UNK     0       8.187  -3.916   0.000  0.00  0.00           C+0
HETATM   65  C   UNK     0       9.285  -4.996   0.000  0.00  0.00           C+0
HETATM   66  C   UNK     0       8.897  -6.487   0.000  0.00  0.00           C+0
HETATM   67  C   UNK     0       7.413  -6.897   0.000  0.00  0.00           C+0
HETATM   68  C   UNK     0       6.316  -5.816   0.000  0.00  0.00           C+0
HETATM   69  O   UNK     0       9.934  -7.714   0.000  0.00  0.00           O+0
HETATM   70  O   UNK     0       6.349   2.895   0.000  0.00  0.00           O+0
CONECT    1    2    7   35   36                                             
CONECT    2    1    3   26                                                  
CONECT    3    2    4   23                                                  
CONECT    4    3    5   21                                                  
CONECT    5    4    6   18                                                  
CONECT    6    5    7   15                                                  
CONECT    7    6    1    8                                                  
CONECT    8    7    9   13                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   14                                                  
CONECT   12   11   13                                                       
CONECT   13   12    8                                                       
CONECT   14   11                                                            
CONECT   15    6   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17    5                                                       
CONECT   19   17                                                            
CONECT   20   15                                                            
CONECT   21    4   22   28                                                  
CONECT   22   21   23                                                       
CONECT   23   22    3   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25    2                                                       
CONECT   27   25                                                            
CONECT   28   21   29   33                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32   34                                                  
CONECT   32   31   33                                                       
CONECT   33   32   28                                                       
CONECT   34   31                                                            
CONECT   35    1                                                            
CONECT   36    1   37   42   70                                             
CONECT   37   36   38   61                                                  
CONECT   38   37   39   58                                                  
CONECT   39   38   40   56                                                  
CONECT   40   39   41   53                                                  
CONECT   41   40   42   50                                                  
CONECT   42   41   36   43                                                  
CONECT   43   42   44   48                                                  
CONECT   44   43   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47   49                                                  
CONECT   47   46   48                                                       
CONECT   48   47   43                                                       
CONECT   49   46                                                            
CONECT   50   41   51   55                                                  
CONECT   51   50   52                                                       
CONECT   52   51   53   54                                                  
CONECT   53   52   40                                                       
CONECT   54   52                                                            
CONECT   55   50                                                            
CONECT   56   39   57   63                                                  
CONECT   57   56   58                                                       
CONECT   58   57   38   59                                                  
CONECT   59   58   60                                                       
CONECT   60   59   61   62                                                  
CONECT   61   60   37                                                       
CONECT   62   60                                                            
CONECT   63   56   64   68                                                  
CONECT   64   63   65                                                       
CONECT   65   64   66                                                       
CONECT   66   65   67   69                                                  
CONECT   67   66   68                                                       
CONECT   68   67   63                                                       
CONECT   69   66                                                            
CONECT   70   36                                                            
MASTER        0    0    0    0    0    0    0    0   70    0  162    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₅₆H₄₂O₁₄

Average Mass

938.9380 Da

Monoisotopic Mass

938.25746 Da

IUPAC Name

(1R,8S,9S,16R)-8,16-bis(4-hydroxyphenyl)-9-[(1R,8S,9S,16R)-4,6,9,12-tetrahydroxy-8,16-bis(4-hydroxyphenyl)-15-oxatetracyclo[8.6.1.0^{2,7}.0^{14,17}]heptadeca-2(7),3,5,10(17),11,13-hexaen-9-yl]-15-oxatetracyclo[8.6.1.0^{2,7}.0^{14,17}]heptadeca-2(7),3,5,10(17),11,13-hexaene-4,6,9,12-tetrol

Traditional Name

CAS Registry Number

Not Available

SMILES

OC1=CC=C(C=C1)[C@@H]1OC2=CC(O)=CC3=C2[C@H]1C1=C([C@H](C2=CC=C(O)C=C2)[C@@]3(O)[C@]2(O)[C@@H](C3=CC=C(O)C=C3)C3=C(C=C(O)C=C3O)[C@H]3[C@@H](OC4=CC(O)=CC2=C34)C2=CC=C(O)C=C2)C(O)=CC(O)=C1

InChI Identifier

InChI=1S/C56H42O14/c57-29-9-1-25(2-10-29)51-45-37(17-33(61)21-41(45)65)47-49-39(19-35(63)23-43(49)69-53(47)27-5-13-31(59)14-6-27)55(51,67)56(68)40-20-36(64)24-44-50(40)48(54(70-44)28-7-15-32(60)16-8-28)38-18-34(62)22-42(66)46(38)52(56)26-3-11-30(58)12-4-26/h1-24,47-48,51-54,57-68H/t47-,48-,51+,52+,53+,54+,55-,56-/m1/s1

InChI Key

AETOAAQSGCSQKP-PWJWKHQFSA-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
Hopea malibato	Plant	KNApSAcK

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
4-prenylated 2-arybenzofuran
Linear 1,7-diphenylheptane skeleton
Dibenzocycloheptene
Coumaran
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Alkyl aryl ether
Phenol
Monocyclic benzene moiety
Benzenoid
Tertiary alcohol
1,2-diol
Organoheterocyclic compound
Ether
Oxacycle
Polyol
Organooxygen compound
Hydrocarbon derivative
Organic oxygen 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	5.28	ALOGPS
logP	8.58	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	8.66	ChemAxon
pKa (Strongest Basic)	-5.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	14	ChemAxon
Hydrogen Donor Count	12	ChemAxon
Polar Surface Area	261.22 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	255.7 m³·mol⁻¹	ChemAxon
Polarizability	93.79 Å³	ChemAxon
Number of Rings	12	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

C00049785

Chemspider ID

419985

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

478625

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for (-)-Dibalanocarpol (NP0082836)

MOL for NP0082836 ((-)-Dibalanocarpol)

3D MOL for NP0082836 ((-)-Dibalanocarpol)

3D SDF for NP0082836 ((-)-Dibalanocarpol)

3D-SDF for NP0082836 ((-)-Dibalanocarpol)

PDB for NP0082836 ((-)-Dibalanocarpol)

3D PDB for NP0082836 ((-)-Dibalanocarpol)

SMILES for NP0082836 ((-)-Dibalanocarpol)

INCHI for NP0082836 ((-)-Dibalanocarpol)

Structure for NP0082836 ((-)-Dibalanocarpol)

3D Structure for NP0082836 ((-)-Dibalanocarpol)