NP-MRD: Showing NP-Card for 3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid (NP0297824)

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Record Information

Version

2.0

Created at

2022-09-10 08:31:45 UTC

Updated at

2022-09-10 08:31:45 UTC

NP-MRD ID

NP0297824

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid

Description

3-(3,4-Dihydroxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid belongs to the class of organic compounds known as catechols. Catechols are compounds containing a 1,2-benzenediol moiety. 3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid is found in Fissistigma oldhamii. 3-(3,4-Dihydroxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 42 43  0  0  0  0  0  0  0  0999 V2000
   -8.3480   -0.0871   -0.9335 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5205   -0.6778    0.0239 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1370   -0.6804   -0.0651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4777   -0.0958   -1.1131 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0815   -0.1340   -1.1419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3418   -0.7384   -0.1544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8739   -0.7327   -0.2635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2406    0.4567    0.3848 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1983    0.3873    0.2338 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.0214    1.4017    0.7651 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4775    2.3789    1.3793 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4570    1.3868    0.6463 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1425    0.4436    0.0410 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5777    0.4259   -0.0795 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3660    1.4093    0.4364 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7617    1.3848    0.3149 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3883    0.3473   -0.3412 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7646    0.2814   -0.4854 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5850   -0.6573   -0.8682 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2322   -1.7006   -1.5293 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2126   -0.6259   -0.7446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0033   -1.3264    0.8996 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3755   -1.2875    0.9255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4689   -0.7667   -1.8007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3452    0.2131   -0.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9354    0.8891   -1.3236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0463    0.3821   -1.8952 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6153    0.3395   -1.9861 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5362   -0.8214   -1.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5009   -1.6379    0.2623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5572    1.4192   -0.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4515    0.4733    1.4791 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6297   -0.4076   -0.2650 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9938    2.2318    1.1002 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5988   -0.3719   -0.3952 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9483    2.2505    0.9614 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3697    2.1782    0.7332 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1612   -0.5051   -0.9768 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6548   -2.4354   -1.9156 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5923   -1.4293   -1.1678 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4064   -1.7969    1.6669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8701   -1.7643    1.7773 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  2  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 19 21  2  0
  6 22  1  0
 22 23  2  0
 23  3  1  0
 21 14  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  5 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
 12 34  1  0
 13 35  1  0
 15 36  1  0
 16 37  1  0
 18 38  1  0
 20 39  1  0
 21 40  1  0
 22 41  1  0
 23 42  1  0
M  END


  Mrv1533005011514092D          

 23 24  0  0  0  0            999 V2000
   -2.1434   -2.8875    0.0000 C   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
    0.0000   -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 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
    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 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.8592   -5.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -6.1875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -4.9500    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
  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  2  0  0  0  0
  6  7  1  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  2  0  0  0  0
 12 10  1  4  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  2  0  0  0  0
 14 21  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  2  0  0  0  0
  3 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0297824

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(CCNC(=O)C=CC2=CC=C(O)C(O)=C2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H19NO4/c1-23-15-6-2-13(3-7-15)10-11-19-18(22)9-5-14-4-8-16(20)17(21)12-14/h2-9,12,20-21H,10-11H2,1H3,(H,19,22)

> <INCHI_KEY>
JRKPLTBLTYEYJJ-UHFFFAOYSA-N

> <FORMULA>
C18H19NO4

> <MOLECULAR_WEIGHT>
313.353

> <EXACT_MASS>
313.131408096

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
34.023272399347576

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(3,4-dihydroxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enamide

> <ALOGPS_LOGP>
2.52

> <JCHEM_LOGP>
2.801152125333333

> <ALOGPS_LOGS>
-4.41

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.625527755734765

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.220676918420638

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3880112165105255

> <JCHEM_POLAR_SURFACE_AREA>
78.79

> <JCHEM_REFRACTIVITY>
89.57140000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.21e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(3,4-dihydroxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 01-MAY-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   01-MAY-15         0                                  
HETATM    1  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -2.667  -4.620   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.667  -7.700   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001  -6.930   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       5.335  -7.700   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       6.668  -5.390   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      10.669  -7.700   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      12.003  -6.930   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      13.337  -7.700   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      13.337  -9.240   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      14.670 -10.010   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.003 -11.550   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   21                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   14                                                       
CONECT   22    6   23                                                       
CONECT   23   22    3                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Value	Source
3-(3,4-Dihydroxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enimidate	Generator

Chemical Formula

C₁₈H₁₉NO₄

Average Mass

313.3530 Da

Monoisotopic Mass

313.13141 Da

IUPAC Name

3-(3,4-dihydroxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enamide

Traditional Name

3-(3,4-dihydroxyphenyl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enamide

CAS Registry Number

Not Available

SMILES

COC1=CC=C(CCNC(=O)C=CC2=CC=C(O)C(O)=C2)C=C1

InChI Identifier

InChI=1S/C18H19NO4/c1-23-15-6-2-13(3-7-15)10-11-19-18(22)9-5-14-4-8-16(20)17(21)12-14/h2-9,12,20-21H,10-11H2,1H3,(H,19,22)

InChI Key

JRKPLTBLTYEYJJ-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
Fissistigma oldhamii	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as catechols. Catechols are compounds containing a 1,2-benzenediol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenoxy compound
Anisole
Methoxybenzene
Catechol
Phenol ether
Styrene
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Carboximidic acid
Carboximidic acid derivative
Organic 1,3-dipolar compound
Ether
Propargyl-type 1,3-dipolar organic compound
Organic oxygen compound
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Organic nitrogen 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	2.52	ALOGPS
logP	2.8	ChemAxon
logS	-4.4	ALOGPS
pKa (Strongest Acidic)	9.22	ChemAxon
pKa (Strongest Basic)	-0.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	78.79 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	89.57 m³·mol⁻¹	ChemAxon
Polarizability	34.02 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

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References

General References

LOTUS database [Link]

Showing NP-Card for 3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid (NP0297824)

MOL for NP0297824 (3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

3D MOL for NP0297824 (3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

3D SDF for NP0297824 (3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

3D-SDF for NP0297824 (3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

PDB for NP0297824 (3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

3D PDB for NP0297824 (3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

SMILES for NP0297824 (3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

INCHI for NP0297824 (3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

Structure for NP0297824 (3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

3D Structure for NP0297824 (3-(3,4-dihydroxyphenyl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)