NP-MRD: Showing NP-Card for 2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl (NP0061069)

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Record Information

Version

2.0

Created at

2022-04-28 05:59:55 UTC

Updated at

2022-04-28 05:59:55 UTC

NP-MRD ID

NP0061069

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl

Description

Gancaonin R 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. Gancaonin R is an extremely weak basic (essentially neutral) compound (based on its pKa). Outside of the human body, Gancaonin R has been detected, but not quantified in, herbs and spices. 2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl is found in Glycyrrhiza glabra and Glycyrrhiza uralensis . This could make gancaonin R a potential biomarker for the consumption of these foods.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv0541 05061309522D          

 28 29  0  0  0  0            999 V2000
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    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
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  5  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 12  8  2  0  0  0  0
 15  1  1  0  0  0  0
 15  2  1  0  0  0  0
 15  5  2  0  0  0  0
 16  3  1  0  0  0  0
 16  4  1  0  0  0  0
 16  6  2  0  0  0  0
 17  7  1  0  0  0  0
 17  8  1  0  0  0  0
 17 13  2  0  0  0  0
 18 11  1  0  0  0  0
 19  9  1  0  0  0  0
 19 18  2  0  0  0  0
 20 10  1  0  0  0  0
 20 18  1  0  0  0  0
 21 12  1  0  0  0  0
 22 14  2  0  0  0  0
 22 19  1  0  0  0  0
 23 14  1  0  0  0  0
 23 20  2  0  0  0  0
 24 13  1  0  0  0  0
 24 21  2  0  0  0  0
 25 21  1  0  0  0  0
 26 22  1  0  0  0  0
 27 23  1  0  0  0  0
 28 24  1  0  0  0  0
M  END

     RDKit          3D

 58 59  0  0  0  0  0  0  0  0999 V2000
   -4.3652   -2.8772    1.9187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7612   -2.6573    0.5832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4572   -3.1997   -0.5968 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6374   -2.0076    0.4673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8847   -1.6878   -0.7636 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6253   -0.2308   -0.9227 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5206    0.5182   -1.6268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6407    0.0009   -2.3045 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3755    1.9089   -1.7241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3286    2.4969   -1.1045 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2048    3.8914   -1.2148 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4217    1.7416   -0.3932 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7081    2.4708    0.2685 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3821    3.9176    0.3985 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0854    4.9076   -0.1253 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6777    6.3306    0.0611 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2947    4.5580   -0.9044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5546    0.3557   -0.2913 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5166   -0.4182    0.4023 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5870   -0.9012   -0.5489 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6364   -1.6843    0.1447 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7710   -1.1180    0.6882 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7262   -1.8812    1.3295 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5803   -3.2493    1.4510 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5732   -3.9893    2.1094 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4626   -3.8282    0.9183 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3416   -5.2168    1.0568 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5134   -3.0568    0.2794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0639   -3.8852    2.2759 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4831   -2.9333    1.7981 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0790   -2.0961    2.6493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0739   -4.0990   -0.3459 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1626   -2.4771   -1.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7407   -3.5388   -1.3646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1935   -1.6409    1.4144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4548   -2.0481   -1.6262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9076   -2.2129   -0.6538 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8679   -0.9501   -2.3211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1002    2.4852   -2.2914 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8459    4.4538   -1.7212 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8792    2.1168    1.3134 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6051    2.4053   -0.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5027    4.1737    0.9711 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5535    6.9299    0.3243 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2750    6.6786   -0.9076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1250    6.3869    0.8330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0149    4.0420   -1.8582 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9854    3.9062   -0.3365 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7936    5.4988   -1.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0125   -1.2842    0.8984 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9623    0.1736    1.1901 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1551   -1.5007   -1.3337 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1223    0.0096   -0.9343 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8656   -0.0446    0.5807 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6055   -1.4458    1.7530 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5095   -4.9880    2.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5359   -5.6755    0.6776 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6469   -3.5346   -0.1320 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
  5  6  1  0
  6 18  2  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 21 28  2  0
 28 26  1  0
 26 27  1  0
 26 24  2  0
 24 25  1  0
 24 23  1  0
 23 22  2  0
 18 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  3
 15 16  1  0
 15 17  1  0
 12 10  2  0
 10 11  1  0
 10  9  1  0
  9  7  2  0
  7  8  1  0
  7  6  1  0
 22 21  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
  3 33  1  0
  3 34  1  0
  4 35  1  0
  5 36  1  0
  5 37  1  0
 19 50  1  0
 19 51  1  0
 20 52  1  0
 20 53  1  0
 28 58  1  0
 27 57  1  0
 25 56  1  0
 23 55  1  0
 22 54  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 16 44  1  0
 16 45  1  0
 16 46  1  0
 17 47  1  0
 17 48  1  0
 17 49  1  0
 11 40  1  0
  9 39  1  0
  8 38  1  0
M  END


  Mrv0541 05061309522D          

 28 29  0  0  0  0            999 V2000
    6.4302   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -1.6500    0.0000 C   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
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -1.2375    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
    4.2868    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    3.3000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  5  1  0  0  0  0
 10  6  1  0  0  0  0
 11  7  1  0  0  0  0
 12  8  2  0  0  0  0
 15  1  1  0  0  0  0
 15  2  1  0  0  0  0
 15  5  2  0  0  0  0
 16  3  1  0  0  0  0
 16  4  1  0  0  0  0
 16  6  2  0  0  0  0
 17  7  1  0  0  0  0
 17  8  1  0  0  0  0
 17 13  2  0  0  0  0
 18 11  1  0  0  0  0
 19  9  1  0  0  0  0
 19 18  2  0  0  0  0
 20 10  1  0  0  0  0
 20 18  1  0  0  0  0
 21 12  1  0  0  0  0
 22 14  2  0  0  0  0
 22 19  1  0  0  0  0
 23 14  1  0  0  0  0
 23 20  2  0  0  0  0
 24 13  1  0  0  0  0
 24 21  2  0  0  0  0
 25 21  1  0  0  0  0
 26 22  1  0  0  0  0
 27 23  1  0  0  0  0
 28 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0061069

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1=C(CCC2=CC(O)=C(O)C=C2)C(CC=C(C)C)=C(O)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C24H30O4/c1-15(2)5-9-19-18(11-7-17-8-12-21(25)24(28)13-17)20(10-6-16(3)4)23(27)14-22(19)26/h5-6,8,12-14,25-28H,7,9-11H2,1-4H3

> <INCHI_KEY>
QFAPONVNJTUMHF-UHFFFAOYSA-N

> <FORMULA>
C24H30O4

> <MOLECULAR_WEIGHT>
382.4926

> <EXACT_MASS>
382.214409448

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
43.82086627618359

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
5-[2-(3,4-dihydroxyphenyl)ethyl]-4,6-bis(3-methylbut-2-en-1-yl)benzene-1,3-diol

> <ALOGPS_LOGP>
4.70

> <JCHEM_LOGP>
6.75248122

> <ALOGPS_LOGS>
-5.09

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.62156084508902

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.975754918587098

> <JCHEM_PKA_STRONGEST_BASIC>
-5.718758134440564

> <JCHEM_POLAR_SURFACE_AREA>
80.92

> <JCHEM_REFRACTIVITY>
116.80539999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.10e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[2-(3,4-dihydroxyphenyl)ethyl]-4,6-bis(3-methylbut-2-en-1-yl)benzene-1,3-diol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      12.003  -0.770   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      13.337  -3.080   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.669  -3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       9.336   2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.336  -2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       9.336   3.850   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.003  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       8.002   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002  -3.080   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       8.002   6.160   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       9.336  -5.390   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   28  O   UNK     0       5.335   4.620   0.000  0.00  0.00           O+0
CONECT    1   15                                                            
CONECT    2   15                                                            
CONECT    3   16                                                            
CONECT    4   16                                                            
CONECT    5    9   15                                                       
CONECT    6   10   16                                                       
CONECT    7   11   17                                                       
CONECT    8   12   17                                                       
CONECT    9    5   19                                                       
CONECT   10    6   20                                                       
CONECT   11    7   18                                                       
CONECT   12    8   21                                                       
CONECT   13   17   24                                                       
CONECT   14   22   23                                                       
CONECT   15    1    2    5                                                  
CONECT   16    3    4    6                                                  
CONECT   17    7    8   13                                                  
CONECT   18   11   19   20                                                  
CONECT   19    9   18   22                                                  
CONECT   20   10   18   23                                                  
CONECT   21   12   24   25                                                  
CONECT   22   14   19   26                                                  
CONECT   23   14   20   27                                                  
CONECT   24   13   21   28                                                  
CONECT   25   21                                                            
CONECT   26   22                                                            
CONECT   27   23                                                            
CONECT   28   24                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   58    0
END

View in JSmol

Synonyms

Value	Source
2,6-Diisopentenyl-3,3'4',5-tetrahydroxybibenzyl	HMDB
3,3',4',5-Tetrahydroxy-2,6-diprenylbibenzyl	HMDB

Chemical Formula

C₂₄H₃₀O₄

Average Mass

382.4926 Da

Monoisotopic Mass

382.21441 Da

IUPAC Name

5-[2-(3,4-dihydroxyphenyl)ethyl]-4,6-bis(3-methylbut-2-en-1-yl)benzene-1,3-diol

Traditional Name

5-[2-(3,4-dihydroxyphenyl)ethyl]-4,6-bis(3-methylbut-2-en-1-yl)benzene-1,3-diol

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1=C(CCC2=CC(O)=C(O)C=C2)C(CC=C(C)C)=C(O)C=C1O

InChI Identifier

InChI=1S/C24H30O4/c1-15(2)5-9-19-18(11-7-17-8-12-21(25)24(28)13-17)20(10-6-16(3)4)23(27)14-22(19)26/h5-6,8,12-14,25-28H,7,9-11H2,1-4H3

InChI Key

QFAPONVNJTUMHF-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, 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
Glycyrrhiza glabra	Plant	KNApSAcK
Glycyrrhiza uralensis	Plant	KNApSAcK

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
Resorcinol
Catechol
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	4.7	ALOGPS
logP	6.75	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Acidic)	8.98	ChemAxon
pKa (Strongest Basic)	-5.7	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	80.92 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	116.81 m³·mol⁻¹	ChemAxon
Polarizability	43.82 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0037588

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB016692

KNApSAcK ID

C00015247

Chemspider ID

421876

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

480815

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl (NP0061069)

MOL for NP0061069 (2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl)

3D MOL for NP0061069 (2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl)

3D SDF for NP0061069 (2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl)

3D-SDF for NP0061069 (2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl)

PDB for NP0061069 (2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl)

3D PDB for NP0061069 (2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl)

SMILES for NP0061069 (2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl)

INCHI for NP0061069 (2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl)

Structure for NP0061069 (2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl)

3D Structure for NP0061069 (2,6-Diisopentenyl-3,3'4',5-Tetrahydroxybibenzyl)