NP-MRD: Showing NP-Card for 3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid (NP0283838)

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Record Information

Version

2.0

Created at

2022-09-09 11:16:21 UTC

Updated at

2022-09-09 11:16:22 UTC

NP-MRD ID

NP0283838

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid

Description

3-(2H-1,3-benzodioxol-5-yl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid belongs to the class of organic compounds known as cinnamic acid amides. These are amides of cinnamic acids. Cinnamic acid is an aromatic compound containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. 3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid is found in Zanthoxylum armatum. 3-(2H-1,3-benzodioxol-5-yl)-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

 43 45  0  0  0  0  0  0  0  0999 V2000
    7.5523   -2.1327    1.3046 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0084   -1.9757    0.0076 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9368   -1.1091   -0.1602 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3501   -0.9010   -1.3932 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2709   -0.0202   -1.5280 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7677    0.6581   -0.4447 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6407    1.5761   -0.5934 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3625    0.7924   -0.3894 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2468    1.6705   -0.5303 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1151    1.1832   -0.3839 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1749   -0.0252   -0.1352 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2284    2.0654   -0.5258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4988    2.0348   -0.4758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5185    1.0630   -0.2423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8629    1.4828   -0.2819 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9321    0.6659   -0.0784 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7012   -0.6639    0.1854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4113   -1.1338    0.2371 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3401   -0.2534    0.0205 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4666   -2.4871    0.5155 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8030   -2.9396    0.5291 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5379   -1.7515    0.4363 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.3469    0.4541    0.7785 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4029   -0.4098    0.9021 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4817   -2.7119    1.3101 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8246   -1.1157    1.7095 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7916   -2.5209    2.0336 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7618   -1.4432   -2.2254 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8565    0.0962   -2.5302 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6259    2.0610   -1.6112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6922    2.4176    0.1259 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3987    0.3792    0.6532 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3420   -0.0698   -1.0857 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3564    2.6712   -0.7384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8215    3.1461   -0.7604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9519    3.0902   -0.6757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0966    2.5227   -0.4864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9515    1.0308   -0.1179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3918   -0.7139    0.0820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0441   -3.4698    1.4824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0066   -3.6106   -0.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9735    0.9721    1.6455 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8643   -0.5743    1.8679 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 22  1  0
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  2  0
  6 23  1  0
 23 24  2  0
 24  3  1  0
 19 14  1  0
 18 17  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  4 28  1  0
  5 29  1  0
  7 30  1  0
  7 31  1  0
  8 32  1  0
  8 33  1  0
  9 34  1  0
 12 35  1  0
 13 36  1  0
 15 37  1  0
 16 38  1  0
 21 40  1  0
 21 41  1  0
 19 39  1  0
 23 42  1  0
 24 43  1  0
M  END


  Mrv1533004241514342D          

 24 26  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
    7.7578   -5.5020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4222   -6.2557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6018   -6.1695    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
    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
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 17 21  1  0  0  0  0
 21 22  2  0  0  0  0
 14 22  1  0  0  0  0
  6 23  1  0  0  0  0
 23 24  2  0  0  0  0
  3 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0283838

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(CCNC(=O)C=CC2=CC=C3OCOC3=C2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H19NO4/c1-22-16-6-2-14(3-7-16)10-11-20-19(21)9-5-15-4-8-17-18(12-15)24-13-23-17/h2-9,12H,10-11,13H2,1H3,(H,20,21)

> <INCHI_KEY>
ZDVBEJSAKORDPK-UHFFFAOYSA-N

> <FORMULA>
C19H19NO4

> <MOLECULAR_WEIGHT>
325.364

> <EXACT_MASS>
325.131408096

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
35.55601755963748

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
3-(2H-1,3-benzodioxol-5-yl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enamide

> <ALOGPS_LOGP>
2.71

> <JCHEM_LOGP>
3.031516236333333

> <ALOGPS_LOGS>
-4.76

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.250018291265853

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3880320996859682

> <JCHEM_POLAR_SURFACE_AREA>
56.790000000000006

> <JCHEM_REFRACTIVITY>
91.37650000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
5.64e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(2H-1,3-benzodioxol-5-yl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enamide

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-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      14.481 -10.270   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      13.855 -11.677   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0      12.323 -11.516   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      12.003 -10.010   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.669  -9.240   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM   24  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   24                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   23                                                  
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   22                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   21                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   17   22                                                  
CONECT   22   21   14                                                       
CONECT   23    6   24                                                       
CONECT   24   23    3                                                       
MASTER        0    0    0    0    0    0    0    0   24    0   52    0
END

View in JSmol

Synonyms

Value	Source
3-(2H-1,3-Benzodioxol-5-yl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enimidate	Generator

Chemical Formula

C₁₉H₁₉NO₄

Average Mass

325.3640 Da

Monoisotopic Mass

325.13141 Da

IUPAC Name

3-(2H-1,3-benzodioxol-5-yl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enamide

Traditional Name

3-(2H-1,3-benzodioxol-5-yl)-N-[2-(4-methoxyphenyl)ethyl]prop-2-enamide

CAS Registry Number

Not Available

SMILES

COC1=CC=C(CCNC(=O)C=CC2=CC=C3OCOC3=C2)C=C1

InChI Identifier

InChI=1S/C19H19NO4/c1-22-16-6-2-14(3-7-16)10-11-20-19(21)9-5-15-4-8-17-18(12-15)24-13-23-17/h2-9,12H,10-11,13H2,1H3,(H,20,21)

InChI Key

ZDVBEJSAKORDPK-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
Zanthoxylum armatum	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cinnamic acid amides. These are amides of cinnamic acids. Cinnamic acid is an aromatic compound containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid.

Kingdom

Organic compounds

Super Class

Phenylpropanoids and polyketides

Class

Cinnamic acids and derivatives

Sub Class

Cinnamic acid amides

Direct Parent

Cinnamic acid amides

Alternative Parents

Substituents

Cinnamic acid amide
Benzodioxole
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Styrene
Alkyl aryl ether
Monocyclic benzene moiety
Benzenoid
Carboxamide group
Secondary carboxylic acid amide
Acetal
Carboxylic acid derivative
Oxacycle
Ether
Organoheterocyclic compound
Organic nitrogen compound
Hydrocarbon derivative
Carbonyl group
Organic oxide
Organic oxygen compound
Organonitrogen compound
Organooxygen compound
Organopnictogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic 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	2.71	ALOGPS
logP	3.03	ChemAxon
logS	-4.8	ALOGPS
pKa (Strongest Acidic)	15.25	ChemAxon
pKa (Strongest Basic)	-0.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	56.79 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	91.38 m³·mol⁻¹	ChemAxon
Polarizability	35.56 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

882950

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid (NP0283838)

MOL for NP0283838 (3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

3D MOL for NP0283838 (3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

3D SDF for NP0283838 (3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

3D-SDF for NP0283838 (3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

PDB for NP0283838 (3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

3D PDB for NP0283838 (3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

SMILES for NP0283838 (3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

INCHI for NP0283838 (3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

Structure for NP0283838 (3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)

3D Structure for NP0283838 (3-(2h-1,3-benzodioxol-5-yl)-n-[2-(4-methoxyphenyl)ethyl]prop-2-enimidic acid)