NP-MRD: Showing NP-Card for 5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol (NP0207176)

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Record Information

Version

2.0

Created at

2022-09-05 03:40:51 UTC

Updated at

2022-09-05 03:40:51 UTC

NP-MRD ID

NP0207176

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol

Description

5-[2-(2,4-Dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids. 5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol is found in Milicia excelsa. 5-[2-(2,4-Dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004201504032D          

 48 51  0  0  0  0            999 V2000
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M  END

     RDKit          3D

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M  END


  Mrv1533004201504032D          

 48 51  0  0  0  0            999 V2000
    5.0013   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -13.6125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.0250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -14.8500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -16.5000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158  -17.3250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -16.0875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013  -15.2625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -14.8500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -6.6000    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  4  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
 10  9  1  4  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
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 15 16  1  0  0  0  0
 15 17  1  0  0  0  0
 17 18  2  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
  9 20  1  0  0  0  0
 20 21  2  0  0  0  0
  5 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 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
 26 27  1  0  0  0  0
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 28 29  1  4  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  2  0  0  0  0
 35 34  1  4  0  0  0
 35 36  2  0  0  0  0
 36 37  1  0  0  0  0
 37 38  2  0  0  0  0
 38 39  1  0  0  0  0
 39 40  2  0  0  0  0
 40 41  1  0  0  0  0
 40 42  1  0  0  0  0
 42 43  2  0  0  0  0
 37 43  1  0  0  0  0
 43 44  1  0  0  0  0
 34 45  1  0  0  0  0
 45 46  2  0  0  0  0
 30 46  1  0  0  0  0
 46 47  1  0  0  0  0
 27 48  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0207176

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCCCC(C)=CCC1=C(O)C=C(C=CC2=CC=C(O)C=C2O)C=C1O)=CCC1=C(O)C=C(C=CC2=CC=C(O)C=C2O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C40H42O8/c1-25(7-17-33-37(45)19-27(20-38(33)46)9-11-29-13-15-31(41)23-35(29)43)5-3-4-6-26(2)8-18-34-39(47)21-28(22-40(34)48)10-12-30-14-16-32(42)24-36(30)44/h7-16,19-24,41-48H,3-6,17-18H2,1-2H3

> <INCHI_KEY>
QXZYEWXVQKXLIF-UHFFFAOYSA-N

> <FORMULA>
C40H42O8

> <MOLECULAR_WEIGHT>
650.768

> <EXACT_MASS>
650.287968312

> <JCHEM_ACCEPTOR_COUNT>
8

> <JCHEM_ATOM_COUNT>
90

> <JCHEM_AVERAGE_POLARIZABILITY>
74.13383839143815

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol

> <ALOGPS_LOGP>
5.82

> <JCHEM_LOGP>
10.080196555333332

> <ALOGPS_LOGS>
-5.93

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
8.860794036462243

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.439997280119798

> <JCHEM_PKA_STRONGEST_BASIC>
-5.6447397428456165

> <JCHEM_POLAR_SURFACE_AREA>
161.84

> <JCHEM_REFRACTIVITY>
194.7582

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
7.67e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol

> <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  C   UNK     0       9.336 -16.170   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.002 -16.940   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       8.002 -18.480   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.336 -19.250   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336 -20.790   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.669 -21.560   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      12.003 -20.790   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      10.669 -23.100   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.336 -23.870   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       9.336 -25.410   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      10.669 -26.180   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      10.669 -27.720   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      12.003 -28.490   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      12.003 -30.030   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      10.669 -30.800   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      10.669 -32.340   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       9.336 -30.030   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       9.336 -28.490   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       8.002 -27.720   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       8.002 -23.100   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002 -21.560   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       6.668 -20.790   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       6.668 -16.170   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.335 -13.860   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.335 -12.320   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       4.001 -11.550   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       4.001 -10.010   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0       0.000  -7.700   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   41  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   42  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   44  O   UNK     0       4.001  -0.770   0.000  0.00  0.00           O+0
HETATM   45  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   47  O   UNK     0       5.335  -7.700   0.000  0.00  0.00           O+0
HETATM   48  C   UNK     0       2.667 -12.320   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6   21                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   20                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17   12   19                                                  
CONECT   19   18                                                            
CONECT   20    9   21                                                       
CONECT   21   20    5   22                                                  
CONECT   22   21                                                            
CONECT   23    2   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   48                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31   46                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35   45                                                  
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38   43                                                  
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40   43                                                       
CONECT   43   42   37   44                                                  
CONECT   44   43                                                            
CONECT   45   34   46                                                       
CONECT   46   45   30   47                                                  
CONECT   47   46                                                            
CONECT   48   27                                                            
MASTER        0    0    0    0    0    0    0    0   48    0  102    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₄₀H₄₂O₈

Average Mass

650.7680 Da

Monoisotopic Mass

650.28797 Da

IUPAC Name

5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol

Traditional Name

5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol

CAS Registry Number

Not Available

SMILES

CC(CCCCC(C)=CCC1=C(O)C=C(C=CC2=CC=C(O)C=C2O)C=C1O)=CCC1=C(O)C=C(C=CC2=CC=C(O)C=C2O)C=C1O

InChI Identifier

InChI=1S/C40H42O8/c1-25(7-17-33-37(45)19-27(20-38(33)46)9-11-29-13-15-31(41)23-35(29)43)5-3-4-6-26(2)8-18-34-39(47)21-28(22-40(34)48)10-12-30-14-16-32(42)24-36(30)44/h7-16,19-24,41-48H,3-6,17-18H2,1-2H3

InChI Key

QXZYEWXVQKXLIF-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
Milicia excelsa	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as stilbenes. These are organic compounds containing a 1,2-diphenylethylene moiety. Stilbenes (C6-C2-C6 ) are derived from the common phenylpropene (C6-C3) skeleton building block. The introduction of one or more hydroxyl groups to a phenyl ring lead to stilbenoids.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Stilbenes

Sub Class

Not Available

Direct Parent

Stilbenes

Alternative Parents

Substituents

Stilbene
Styrene
Resorcinol
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Phenol
Benzenoid
Monocyclic benzene moiety
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	5.82	ALOGPS
logP	10.08	ChemAxon
logS	-5.9	ALOGPS
pKa (Strongest Acidic)	8.44	ChemAxon
pKa (Strongest Basic)	-5.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	8	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	161.84 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	194.76 m³·mol⁻¹	ChemAxon
Polarizability	74.13 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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 5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol (NP0207176)

MOL for NP0207176 (5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol)

3D MOL for NP0207176 (5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol)

3D SDF for NP0207176 (5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol)

3D-SDF for NP0207176 (5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol)

PDB for NP0207176 (5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol)

3D PDB for NP0207176 (5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol)

SMILES for NP0207176 (5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol)

INCHI for NP0207176 (5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol)

Structure for NP0207176 (5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol)

3D Structure for NP0207176 (5-[2-(2,4-dihydroxyphenyl)ethenyl]-2-(10-{4-[2-(2,4-dihydroxyphenyl)ethenyl]-2,6-dihydroxyphenyl}-3,8-dimethyldeca-2,8-dien-1-yl)benzene-1,3-diol)