NP-MRD: Showing NP-Card for 4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid (NP0316956)

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Record Information

Version

2.0

Created at

2022-09-11 16:30:06 UTC

Updated at

2022-09-11 16:30:06 UTC

NP-MRD ID

NP0316956

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid

Description

4-(4-Hydroxy-3-methoxyphenyl)-N-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. 4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid is found in Pisonia aculeata. Based on a literature review very few articles have been published on 4-(4-hydroxy-3-methoxyphenyl)-N-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309112218302D          

 26 27  0  0  0  0            999 V2000
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   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
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  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  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  2  0  0  0  0
 15 23  1  0  0  0  0
  6 24  1  0  0  0  0
 24 25  2  0  0  0  0
  3 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 49 50  0  0  0  0  0  0  0  0999 V2000
   -5.5124    2.6127    1.3841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3589    2.5260    0.5793 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8950    1.3411    0.0384 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6179    0.1988    0.3170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2161   -1.0240   -0.1885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0957   -1.1636   -0.9807 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6705   -2.4789   -1.5193 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7272   -3.2044   -0.5917 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5247   -2.4766   -0.3349 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.4262   -2.3376   -1.1909 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3152   -2.9125   -2.4461 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6184   -1.5790   -0.8462 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5905   -1.4437   -1.7382 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8280   -0.6884   -1.4583 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8287   -0.1225   -0.0843 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3623   -0.9115    0.9256 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3681   -0.3965    2.2037 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8617    0.8637    2.4830 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8865    1.3470    3.7885 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3331    1.6468    1.4862 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8203    2.9093    1.7363 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2734    3.7423    0.7617 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3234    1.1391    0.2044 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3827   -0.0110   -1.2506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7889    1.2250   -0.7395 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0544    2.3862   -1.0224 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3510    2.0711    0.8667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7808    3.6352    1.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3060    2.0438    2.3191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4999    0.2195    0.9240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7952   -1.9084    0.0405 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0902   -2.2615   -2.4496 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5365   -3.1160   -1.7667 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4528   -4.1544   -1.0959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1970   -3.4807    0.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7611   -3.8074   -2.6027 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7240   -1.1179    0.1403 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4994   -1.8938   -2.7160 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7156   -1.3576   -1.6126 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9202    0.1018   -2.2277 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7602   -1.8855    0.7455 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7653   -0.9554    3.0241 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2633    0.8097    4.5497 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1157    4.2139    0.2031 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6313    4.5342    1.1464 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6606    3.1368    0.0510 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9239    1.6946   -0.6384 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4985   -0.0559   -1.8634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2240    2.3457   -1.5973 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  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 16 17  1  0
 17 18  2  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 20 23  2  0
  6 24  1  0
 24 25  2  0
 25 26  1  0
 25  3  1  0
 23 15  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
  4 30  1  0
  5 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
 11 36  1  0
 12 37  1  0
 13 38  1  0
 14 39  1  0
 14 40  1  0
 16 41  1  0
 17 42  1  0
 19 43  1  0
 22 44  1  0
 22 45  1  0
 22 46  1  0
 23 47  1  0
 24 48  1  0
 26 49  1  0
M  END


  Mrv1652309112218302D          

 26 27  0  0  0  0            999 V2000
    3.5724   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.1250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -6.6000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -7.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -8.6625    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -8.6625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -12.7875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000  -12.3750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -12.7875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0000  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145  -11.1375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 O   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
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  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  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 20 23  2  0  0  0  0
 15 23  1  0  0  0  0
  6 24  1  0  0  0  0
 24 25  2  0  0  0  0
  3 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0316956

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(CCN=C(O)C=CCC2=CC=C(O)C(OC)=C2)C=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C20H23NO5/c1-25-18-9-7-15(12-17(18)23)10-11-21-20(24)5-3-4-14-6-8-16(22)19(13-14)26-2/h3,5-9,12-13,22-23H,4,10-11H2,1-2H3,(H,21,24)

> <INCHI_KEY>
ZGCSDBMDEGSSAY-UHFFFAOYSA-N

> <FORMULA>
C20H23NO5

> <MOLECULAR_WEIGHT>
357.406

> <EXACT_MASS>
357.157622845

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
38.37333648915683

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-(4-hydroxy-3-methoxyphenyl)-N-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid

> <JCHEM_LOGP>
3.2460029533236003

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.621224941605309

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.454542466503571

> <JCHEM_PKA_STRONGEST_BASIC>
6.436597057482237

> <JCHEM_POLAR_SURFACE_AREA>
91.51

> <JCHEM_REFRACTIVITY>
101.1573

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-(4-hydroxy-3-methoxyphenyl)-N-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 11-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   11-SEP-22         0                                  
HETATM    1  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       8.002  -7.700   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.336 -10.010   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       9.336 -11.550   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.002 -12.320   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       8.002 -13.860   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.668 -14.630   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0       6.668 -16.170   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0       5.335 -16.940   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       4.001 -16.170   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       5.335 -18.480   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.001 -19.250   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.001 -20.790   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.667 -21.560   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       2.667 -23.100   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334 -23.870   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -0.000 -23.100   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -1.334 -23.870   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -0.000 -21.560   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -1.334 -20.790   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -1.334 -19.250   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.334 -20.790   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668 -11.550   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.668 -10.010   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       5.335  -9.240   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   24                                                  
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                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   23                                                  
CONECT   21   20   22                                                       
CONECT   22   21                                                            
CONECT   23   20   15                                                       
CONECT   24    6   25                                                       
CONECT   25   24    3   26                                                  
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   54    0
END

View in JSmol

Synonyms

Value	Source
4-(4-Hydroxy-3-methoxyphenyl)-N-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidate	Generator

Chemical Formula

C₂₀H₂₃NO₅

Average Mass

357.4060 Da

Monoisotopic Mass

357.15762 Da

IUPAC Name

Not Available

Traditional Name

Not Available

CAS Registry Number

Not Available

SMILES

COC1=CC=C(CCN=C(O)C=CCC2=CC=C(O)C(OC)=C2)C=C1O

InChI Identifier

InChI=1S/C20H23NO5/c1-25-18-9-7-15(12-17(18)23)10-11-21-20(24)5-3-4-14-6-8-16(22)19(13-14)26-2/h3,5-9,12-13,22-23H,4,10-11H2,1-2H3,(H,21,24)

InChI Key

ZGCSDBMDEGSSAY-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
Pisonia aculeata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Methoxyphenol
Phenoxy compound
Anisole
Methoxybenzene
Phenol ether
Alkyl aryl ether
1-hydroxy-4-unsubstituted benzenoid
1-hydroxy-2-unsubstituted benzenoid
Monocyclic benzene moiety
Carboximidic acid
Carboximidic acid derivative
Ether
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Organic oxygen compound
Hydrocarbon derivative
Organonitrogen compound
Organooxygen compound
Organopnictogen 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

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

163093777

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid (NP0316956)

MOL for NP0316956 (4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid)

3D MOL for NP0316956 (4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid)

3D SDF for NP0316956 (4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid)

3D-SDF for NP0316956 (4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid)

PDB for NP0316956 (4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid)

3D PDB for NP0316956 (4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid)

SMILES for NP0316956 (4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid)

INCHI for NP0316956 (4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid)

Structure for NP0316956 (4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid)

3D Structure for NP0316956 (4-(4-hydroxy-3-methoxyphenyl)-n-[2-(3-hydroxy-4-methoxyphenyl)ethyl]but-2-enimidic acid)