NP-MRD: Showing NP-Card for 2-benzyl-3,4,5,6-tetramethoxybenzoic acid (NP0193306)

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Record Information

Version

2.0

Created at

2022-09-04 10:42:45 UTC

Updated at

2022-09-04 10:42:45 UTC

NP-MRD ID

NP0193306

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-benzyl-3,4,5,6-tetramethoxybenzoic acid

Description

2-Benzyl-3,4,5,6-tetramethoxybenzoic acid belongs to the class of organic compounds known as diphenylmethanes. Diphenylmethanes are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups. 2-benzyl-3,4,5,6-tetramethoxybenzoic acid is found in Blainvillea acmella. Based on a literature review very few articles have been published on 2-benzyl-3,4,5,6-tetramethoxybenzoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 44 45  0  0  0  0  0  0  0  0999 V2000
    0.1983    3.0100   -1.4822 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4855    2.1905   -0.3451 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2361    1.0028   -0.1363 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2418   -0.1850   -0.6858 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4701   -0.2462   -1.4978 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7239   -0.0842   -0.7183 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3068   -1.0805    0.0025 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4798   -0.8860    0.7008 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1312    0.3342    0.7079 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5366    1.3401   -0.0243 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3571    1.1468   -0.7273 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4991   -1.3492   -0.4629 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0827   -2.6268   -1.0163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303   -2.8878   -2.1851 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7213   -3.5362   -0.3985 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6640   -1.3582    0.2703 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3367   -2.5452    0.4461 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3330   -3.0486   -0.3999 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1078   -0.1707    0.7992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2963   -0.1819    1.5470 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2966   -0.3975    2.9407 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4008    1.0186    0.6019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8754    2.1855    1.1456 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7635    3.0889    0.5575 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0664    3.0782   -2.1668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0393    4.0503   -1.1334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7045    2.5915   -1.9963 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4924   -1.2570   -1.9964 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4740    0.5483   -2.2848 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8879   -2.0502    0.0586 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9616   -1.6762    1.2854 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0502    0.4717    1.2599 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0385    2.2998   -0.0253 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0028    2.0092   -1.2669 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5071   -3.9506   -0.8683 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3347   -4.1538   -0.2934 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3297   -2.6953   -0.0481 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2015   -2.7245   -1.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3279   -0.1605    3.2978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5650    0.2352    3.4712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1122   -1.4593    3.2085 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7544    2.6135    0.3339 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9559    3.8930    1.3164 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3856    3.6033   -0.3344 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
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
  4 12  1  0
 12 13  1  0
 13 15  1  0
 13 14  2  0
 12 16  2  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 19 22  2  0
 22 23  1  0
 23 24  1  0
 22  3  1  0
 11  6  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  5 28  1  0
  5 29  1  0
  7 30  1  0
  8 31  1  0
  9 32  1  0
 10 33  1  0
 11 34  1  0
 15 35  1  0
 18 36  1  0
 18 37  1  0
 18 38  1  0
 21 39  1  0
 21 40  1  0
 21 41  1  0
 24 42  1  0
 24 43  1  0
 24 44  1  0
M  END


  Mrv1652309042212422D          

 24 25  0  0  0  0            999 V2000
   -1.4289    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 O   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
    0.0000   -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
    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
    0.7145   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -2.4750    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
   -0.7145   -3.7125    0.0000 O   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
   -1.4289   -2.4750    0.0000 C   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
   -2.1434   -3.7125    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
   -2.1434   -1.2375    0.0000 O   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
  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
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
  4 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 13 15  1  0  0  0  0
 12 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 16 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 19 22  2  0  0  0  0
  3 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0193306

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(CC2=CC=CC=C2)C(C(O)=O)=C(OC)C(OC)=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C18H20O6/c1-21-14-12(10-11-8-6-5-7-9-11)13(18(19)20)15(22-2)17(24-4)16(14)23-3/h5-9H,10H2,1-4H3,(H,19,20)

> <INCHI_KEY>
KNQGZKGKUZSDON-UHFFFAOYSA-N

> <FORMULA>
C18H20O6

> <MOLECULAR_WEIGHT>
332.352

> <EXACT_MASS>
332.125988364

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
44

> <JCHEM_AVERAGE_POLARIZABILITY>
33.995531539388224

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-benzyl-3,4,5,6-tetramethoxybenzoic acid

> <JCHEM_LOGP>
3.091937688333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.3318911251232866

> <JCHEM_PKA_STRONGEST_BASIC>
-4.353393352268801

> <JCHEM_POLAR_SURFACE_AREA>
74.22000000000001

> <JCHEM_REFRACTIVITY>
88.9042

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
2-benzyl-3,4,5,6-tetramethoxybenzoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.334  -0.770   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       2.667  -4.620   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0      -1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      -4.001  -5.390   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      -4.001  -6.930   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -4.001  -2.310   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5   12                                                  
CONECT    5    4    6                                                       
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10    6                                                       
CONECT   12    4   13   16                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16   12   17   19                                                  
CONECT   17   16   18                                                       
CONECT   18   17                                                            
CONECT   19   16   20   22                                                  
CONECT   20   19   21                                                       
CONECT   21   20                                                            
CONECT   22   19    3   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   50    0
END

View in JSmol

Synonyms

Value	Source
2-Benzyl-3,4,5,6-tetramethoxybenzoate	Generator

Chemical Formula

C₁₈H₂₀O₆

Average Mass

332.3520 Da

Monoisotopic Mass

332.12599 Da

IUPAC Name

2-benzyl-3,4,5,6-tetramethoxybenzoic acid

Traditional Name

2-benzyl-3,4,5,6-tetramethoxybenzoic acid

CAS Registry Number

Not Available

SMILES

COC1=C(CC2=CC=CC=C2)C(C(O)=O)=C(OC)C(OC)=C1OC

InChI Identifier

InChI=1S/C18H20O6/c1-21-14-12(10-11-8-6-5-7-9-11)13(18(19)20)15(22-2)17(24-4)16(14)23-3/h5-9H,10H2,1-4H3,(H,19,20)

InChI Key

KNQGZKGKUZSDON-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
Blainvillea acmella	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as diphenylmethanes. Diphenylmethanes are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Diphenylmethanes

Direct Parent

Diphenylmethanes

Alternative Parents

Substituents

Diphenylmethane
Gallic acid or derivatives
P-methoxybenzoic acid or derivatives
O-methoxybenzoic acid or derivatives
M-methoxybenzoic acid or derivatives
Benzoic acid
Benzoic acid or derivatives
Phenoxy compound
Methoxybenzene
Phenol ether
Benzoyl
Anisole
Alkyl aryl ether
Monocarboxylic acid or derivatives
Ether
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
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	3.09	ChemAxon
pKa (Strongest Acidic)	3.33	ChemAxon
pKa (Strongest Basic)	-4.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	74.22 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	88.9 m³·mol⁻¹	ChemAxon
Polarizability	34 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

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

163195729

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-benzyl-3,4,5,6-tetramethoxybenzoic acid (NP0193306)

MOL for NP0193306 (2-benzyl-3,4,5,6-tetramethoxybenzoic acid)

3D MOL for NP0193306 (2-benzyl-3,4,5,6-tetramethoxybenzoic acid)

3D SDF for NP0193306 (2-benzyl-3,4,5,6-tetramethoxybenzoic acid)

3D-SDF for NP0193306 (2-benzyl-3,4,5,6-tetramethoxybenzoic acid)

PDB for NP0193306 (2-benzyl-3,4,5,6-tetramethoxybenzoic acid)

3D PDB for NP0193306 (2-benzyl-3,4,5,6-tetramethoxybenzoic acid)

SMILES for NP0193306 (2-benzyl-3,4,5,6-tetramethoxybenzoic acid)

INCHI for NP0193306 (2-benzyl-3,4,5,6-tetramethoxybenzoic acid)

Structure for NP0193306 (2-benzyl-3,4,5,6-tetramethoxybenzoic acid)

3D Structure for NP0193306 (2-benzyl-3,4,5,6-tetramethoxybenzoic acid)