NP-MRD: Showing NP-Card for 3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl (NP0061114)

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Record Information

Version

2.0

Created at

2022-04-28 06:01:30 UTC

Updated at

2022-04-28 06:01:30 UTC

NP-MRD ID

NP0061114

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl

Description

Methyl 2,3-dimethoxy-6-[2-(4-methoxyphenyl)ethyl]benzoate 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. 3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl is found in Plagiochila spinulosa. Based on a literature review very few articles have been published on methyl 2,3-dimethoxy-6-[2-(4-methoxyphenyl)ethyl]benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
   -1.3379    1.1554   -3.2972 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5854    0.3822   -2.1156 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8477    0.9984   -0.9097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8659    2.2597   -0.8662 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1138    0.2754    0.3473 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0639   -0.0056    1.1904 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3640    0.3332    0.8966 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0369   -0.6172   -0.0098 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4423   -0.3076   -0.3199 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6699    0.4860   -1.4317 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9603    0.8334   -1.8058 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0417    0.4008   -1.0854 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3123    0.7700   -1.4930 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3980    0.2864   -0.6973 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7978   -0.3870    0.0170 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5165   -0.7323    0.3888 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3853   -0.6670    2.3807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6680   -1.0057    2.6717 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7217   -0.7189    1.8156 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0181   -1.0869    2.1596 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2359   -1.7485    3.3795 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4204   -0.0731    0.6501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4314    0.2444   -0.2545 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8205   -0.6397   -1.2892 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5328    0.5061   -4.1507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0050    2.0418   -3.3300 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2606    1.4509   -3.2968 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8969    0.5613    1.8219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2960    1.3250    0.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0472   -1.6217    0.5177 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5133   -0.8173   -0.9559 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8540    0.8667   -2.0530 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1127    1.4510   -2.6742 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3717    0.6965   -1.0360 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2506    0.6613    0.3558 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3851   -0.8225   -0.6886 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6725   -0.7253    0.5831 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3753   -1.3404    1.2442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5769   -0.8943    3.0525 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8254   -1.5197    3.6200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7334   -1.2307    4.2253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3177   -1.9077    3.5853 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8045   -2.7697    3.2733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8060   -1.1149   -1.1066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0205   -1.3976   -1.4481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9165   -0.0353   -2.2134 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
  3  5  1  0
  5 22  2  0
 22 23  1  0
 23 24  1  0
 22 19  1  0
 19 20  1  0
 20 21  1  0
 19 18  2  0
 18 17  1  0
 17  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  1  0
 12 15  1  0
 15 16  2  0
  6  5  1  0
 16  9  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
 24 44  1  0
 24 45  1  0
 24 46  1  0
 21 41  1  0
 21 42  1  0
 21 43  1  0
 18 40  1  0
 17 39  1  0
  7 28  1  0
  7 29  1  0
  8 30  1  0
  8 31  1  0
 10 32  1  0
 11 33  1  0
 14 34  1  0
 14 35  1  0
 14 36  1  0
 15 37  1  0
 16 38  1  0
M  END


  Mrv1652304282208012D          

 24 25  0  0  0  0            999 V2000
    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 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
   -0.7145   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -2.4750    0.0000 C   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
    0.0000   -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
    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 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -0.0000    0.0000 O   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
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    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    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  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  2  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  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  2  0  0  0  0
  9 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 15 17  1  0  0  0  0
 17 18  1  0  0  0  0
 13 19  1  0  0  0  0
 19 20  1  0  0  0  0
 12 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
M  END
> <DATABASE_ID>
NP0061114

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1=C(OC)C(OC)=CC=C1CCC1=CC=C(OC)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H22O5/c1-21-15-10-6-13(7-11-15)5-8-14-9-12-16(22-2)18(23-3)17(14)19(20)24-4/h6-7,9-12H,5,8H2,1-4H3

> <INCHI_KEY>
VRXWBESJDSINQV-UHFFFAOYSA-N

> <FORMULA>
C19H22O5

> <MOLECULAR_WEIGHT>
330.38

> <EXACT_MASS>
330.146723808

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
36.092090218784946

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2,3-dimethoxy-6-[2-(4-methoxyphenyl)ethyl]benzoate

> <ALOGPS_LOGP>
3.76

> <JCHEM_LOGP>
4.040071674999999

> <ALOGPS_LOGS>
-4.85

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.407926813510963

> <JCHEM_POLAR_SURFACE_AREA>
53.99000000000001

> <JCHEM_REFRACTIVITY>
91.81109999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.67e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2,3-dimethoxy-6-[2-(4-methoxyphenyl)ethyl]benzoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0       4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       5.335  -0.000   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       1.334   3.850   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       2.667   4.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       0.000  -9.240   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       1.334 -10.010   0.000  0.00  0.00           C+0
CONECT    1    2    6                                                       
CONECT    2    1    3   23                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   14                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   21                                                  
CONECT   13   12   14   19                                                  
CONECT   14   13    9   15                                                  
CONECT   15   14   16   17                                                  
CONECT   16   15                                                            
CONECT   17   15   18                                                       
CONECT   18   17                                                            
CONECT   19   13   20                                                       
CONECT   20   19                                                            
CONECT   21   12   22                                                       
CONECT   22   21                                                            
CONECT   23    2   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2,3-dimethoxy-6-[2-(4-methoxyphenyl)ethyl]benzoic acid	Generator

Chemical Formula

C₁₉H₂₂O₅

Average Mass

330.3800 Da

Monoisotopic Mass

330.14672 Da

IUPAC Name

methyl 2,3-dimethoxy-6-[2-(4-methoxyphenyl)ethyl]benzoate

Traditional Name

methyl 2,3-dimethoxy-6-[2-(4-methoxyphenyl)ethyl]benzoate

CAS Registry Number

Not Available

SMILES

COC(=O)C1=C(OC)C(OC)=CC=C1CCC1=CC=C(OC)C=C1

InChI Identifier

InChI=1S/C19H22O5/c1-21-15-10-6-13(7-11-15)5-8-14-9-12-16(22-2)18(23-3)17(14)19(20)24-4/h6-7,9-12H,5,8H2,1-4H3

InChI Key

VRXWBESJDSINQV-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
Plagiochila spinulosa	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
M-methoxybenzoic acid or derivatives
O-methoxybenzoic acid or derivatives
Benzoate ester
Dimethoxybenzene
O-dimethoxybenzene
Benzoic acid or derivatives
Anisole
Methoxybenzene
Phenol ether
Phenoxy compound
Benzoyl
Alkyl aryl ether
Benzenoid
Monocyclic benzene moiety
Methyl ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Carboxylic acid derivative
Organic oxygen compound
Organooxygen compound
Hydrocarbon derivative
Organic oxide
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	3.76	ALOGPS
logP	4.04	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	53.99 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	91.81 m³·mol⁻¹	ChemAxon
Polarizability	36.09 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

C00015294

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

163106344

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl (NP0061114)

MOL for NP0061114 (3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl)

3D MOL for NP0061114 (3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl)

3D SDF for NP0061114 (3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl)

3D-SDF for NP0061114 (3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl)

PDB for NP0061114 (3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl)

3D PDB for NP0061114 (3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl)

SMILES for NP0061114 (3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl)

INCHI for NP0061114 (3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl)

Structure for NP0061114 (3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl)

3D Structure for NP0061114 (3,4,4'-Trimethoxy-2-methoxycarbonylbibenzyl)