NP-MRD: Showing NP-Card for 3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl (NP0045204)

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Record Information

Version

2.0

Created at

2022-03-10 18:59:45 UTC

Updated at

2022-03-10 22:17:25 UTC

NP-MRD ID

NP0045204

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl

Description

3,4'-Dihydroxy-5,3'-dimethoxy-5'-isoprenyl bibenzyl, 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 the phenyl ring leads to stilbenoids. Stilbenoids were first detected and isolated from the stems of cannabis plants in 1982, from cannabis leaves in 1978 and from cannabis resin in 1986 (https://Doi.Org/10.1007/S11101-008-9094-4). 3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl is a derivative of Bibenzyl. Bibenzyl is a compound consisting to two benzene rings linked together via ethane. Bibenzyls typically form a white solid. Bibenzyl forms the central core of several natural products such as dihydrostilbenoids and isoquinoline alkaloids. 3,4'-Dihydroxy-5,3'-dimethoxy-5'-isoprenyl bibenzyl is one of a small number of bibenzyls including 3,4'-dihydroxy-5-methoxybibenzyl and 3,3'-dihydroxy-5,4'-dimethoxy bibenzyl found in Cannabis sativa (https://Doi.Org/10.1007/S11101-008-9094-4). Bibenzyls and bibenzyl derivatives exhibit anti-inflammatory and antineoplastic activities (PMID: 27310249 ).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 51 52  0  0  0  0  0  0  0  0999 V2000
    6.5007    3.6178    0.7946 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2522    3.0717    0.4202 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0284    1.7187    0.2694 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9984    0.7577    0.4681 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7156   -0.5901    0.3017 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7490   -1.4889    0.5218 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4426   -0.9751   -0.0687 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4498   -0.0387   -0.2752 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1294   -0.4884   -0.6638 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1833   -0.7801    0.4559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1476   -1.2348   -0.0268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4317   -2.5771   -0.2439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6551   -3.0186   -0.6911 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8827   -4.3750   -0.8909 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6610   -2.0786   -0.9394 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8531   -2.5608   -1.3810 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9550   -2.9872   -0.6538 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4206   -0.7510   -0.7378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4313    0.2998   -0.9711 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4317    0.4458    0.0949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5805    1.6018    0.7727 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7036    2.7488    0.4223 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5873    1.7597    1.8497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1636   -0.3373   -0.2822 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7633    1.3034   -0.1009 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2760    3.4907    0.0343 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7872    3.1273    1.7583 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3793    4.7056    0.9764 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0017    1.0925    0.7621 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3171   -1.7117   -0.3070 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2685   -2.0453   -0.1872 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2330   -1.4328   -1.2633 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6922    0.2538   -1.3639 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9961    0.1845    0.9938 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5717   -1.4694    1.2107 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3733   -3.2649   -0.0392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1421   -5.0315   -0.7044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0784   -4.0900   -0.7769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8875   -2.7464    0.4234 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8902   -2.5005   -1.0195 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9476    1.3080   -1.1185 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9598    0.1413   -1.9620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0941   -0.3510    0.3903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6258    2.4920    0.5086 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9557    3.0157   -0.6460 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9517    3.6258    1.0439 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2959    2.5860    1.6331 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1222    2.0217    2.8337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2234    0.8463    1.9546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9766    0.7199   -0.1237 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9468    1.9886   -0.2764 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  4  5  1  0
  5  6  1  0
  5  7  2  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 24  2  0
 24 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  2  3
 21 22  1  0
 21 23  1  0
 18 15  2  0
 15 16  1  0
 16 17  1  0
 15 13  1  0
 13 14  1  0
 13 12  2  0
  8 25  2  0
 25  3  1  0
 12 11  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  6 30  1  0
  7 31  1  0
  9 32  1  0
  9 33  1  0
 10 34  1  0
 10 35  1  0
 24 50  1  0
 19 41  1  0
 19 42  1  0
 20 43  1  0
 22 44  1  0
 22 45  1  0
 22 46  1  0
 23 47  1  0
 23 48  1  0
 23 49  1  0
 17 38  1  0
 17 39  1  0
 17 40  1  0
 14 37  1  0
 12 36  1  0
 25 51  1  0
M  END


  Mrv1652303192001543D          

 25 26  0  0  0  0            999 V2000
    7.3684   -2.0515   -1.3923 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9826   -1.7787   -1.3983 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4669   -0.6859   -0.7389 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3228    0.1470   -0.0669 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8330    1.2535    0.6057 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7320    2.0732    1.2744 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4675    1.4948    0.5821 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5733    0.6916   -0.0753 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1125    0.9226   -0.1164 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3716    0.2443    0.9931 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0730    0.5569    0.8354 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9150   -0.2362    0.0739 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2608    0.0295   -0.0877 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0646   -0.9021   -0.9044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8062   -1.8103   -0.0052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0998   -2.0215   -0.0571 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9398   -1.3473   -1.0522 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7703   -2.9589    0.8967 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7974    1.1111    0.5187 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1298    1.4380    0.3975 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4448    2.3203   -0.6893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0003    1.9361    1.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5663    3.0393    1.9060 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6470    1.6504    1.4414 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0937   -0.4142   -0.7433 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  3  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 13 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
  8 25  2  0  0  0  0
 25  3  1  0  0  0  0
 24 11  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0045204

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(O)=CC(CCC2=CC(CC=C(C)C)=C(OC)C(O)=C2)=C1

> <INCHI_IDENTIFIER>
InChI=1S/C21H26O4/c1-14(2)5-8-17-9-15(12-20(23)21(17)25-4)6-7-16-10-18(22)13-19(11-16)24-3/h5,9-13,22-23H,6-8H2,1-4H3

> <INCHI_KEY>
ZRAWGGRJVKXQIK-UHFFFAOYSA-N

> <FORMULA>
C21H26O4

> <MOLECULAR_WEIGHT>
342.435

> <EXACT_MASS>
342.183109317

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
51

> <JCHEM_AVERAGE_POLARIZABILITY>
38.86730656822449

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxy-3-(3-methylbut-2-en-1-yl)phenol

> <ALOGPS_LOGP>
4.54

> <JCHEM_LOGP>
5.315702332666667

> <ALOGPS_LOGS>
-4.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.114854368021563

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.429018167858535

> <JCHEM_PKA_STRONGEST_BASIC>
-4.5628721751332515

> <JCHEM_POLAR_SURFACE_AREA>
58.92

> <JCHEM_REFRACTIVITY>
101.52720000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.52e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxy-3-(3-methylbut-2-en-1-yl)phenol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 19-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-MAR-20         0                                  
HETATM    1  C   UNK     0       7.368  -2.051  -1.392  0.00  0.00           C+0
HETATM    2  O   UNK     0       5.983  -1.779  -1.398  0.00  0.00           O+0
HETATM    3  C   UNK     0       5.467  -0.686  -0.739  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.323   0.147  -0.067  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.833   1.254   0.606  0.00  0.00           C+0
HETATM    6  O   UNK     0       6.732   2.073   1.274  0.00  0.00           O+0
HETATM    7  C   UNK     0       4.468   1.495   0.582  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.573   0.692  -0.075  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.112   0.923  -0.116  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.372   0.244   0.993  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.073   0.557   0.835  0.00  0.00           C+0
HETATM   12  C   UNK     0      -0.915  -0.236   0.074  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.261   0.030  -0.088  0.00  0.00           C+0
HETATM   14  C   UNK     0      -3.065  -0.902  -0.904  0.00  0.00           C+0
HETATM   15  C   UNK     0      -3.806  -1.810  -0.005  0.00  0.00           C+0
HETATM   16  C   UNK     0      -5.100  -2.022  -0.057  0.00  0.00           C+0
HETATM   17  C   UNK     0      -5.940  -1.347  -1.052  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.770  -2.959   0.897  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.797   1.111   0.519  0.00  0.00           C+0
HETATM   20  O   UNK     0      -4.130   1.438   0.398  0.00  0.00           O+0
HETATM   21  C   UNK     0      -4.445   2.320  -0.689  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.000   1.936   1.291  0.00  0.00           C+0
HETATM   23  O   UNK     0      -2.566   3.039   1.906  0.00  0.00           O+0
HETATM   24  C   UNK     0      -0.647   1.650   1.441  0.00  0.00           C+0
HETATM   25  C   UNK     0       4.094  -0.414  -0.743  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   25                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   24                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   13   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   11                                                       
CONECT   25    8    3                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₆O₄

Average Mass

342.4350 Da

Monoisotopic Mass

342.18311 Da

IUPAC Name

5-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxy-3-(3-methylbut-2-en-1-yl)phenol

Traditional Name

5-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxy-3-(3-methylbut-2-en-1-yl)phenol

CAS Registry Number

Not Available

SMILES

COC1=CC(O)=CC(CCC2=CC(CC=C(C)C)=C(OC)C(O)=C2)=C1

InChI Identifier

InChI=1S/C21H26O4/c1-14(2)5-8-17-9-15(12-20(23)21(17)25-4)6-7-16-10-18(22)13-19(11-16)24-3/h5,9-13,22-23H,6-8H2,1-4H3

InChI Key

ZRAWGGRJVKXQIK-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
Cannabis sativa	NULL	Not Available

Chemical Taxonomy

Classification

Not classified

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	4.54	ALOGPS
logP	5.32	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	9.43	ChemAxon
pKa (Strongest Basic)	-4.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	58.92 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	101.53 m³·mol⁻¹	ChemAxon
Polarizability	38.87 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

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

Showing NP-Card for 3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl (NP0045204)

MOL for NP0045204 (3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl)

3D MOL for NP0045204 (3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl)

3D SDF for NP0045204 (3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl)

3D-SDF for NP0045204 (3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl)

PDB for NP0045204 (3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl)

3D PDB for NP0045204 (3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl)

SMILES for NP0045204 (3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl)

INCHI for NP0045204 (3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl)

Structure for NP0045204 (3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl)

3D Structure for NP0045204 (3,4'-Dihydroxy-5,3'-dimethoxy-5' isoprenyl bibenzyl)