NP-MRD: Showing NP-Card for N-trans-Isoferuloyl-3-O-methyldopamine (NP0086452)

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Record Information

Version

2.0

Created at

2022-04-29 06:45:07 UTC

Updated at

2022-04-29 06:45:07 UTC

NP-MRD ID

NP0086452

Secondary Accession Numbers

None

Natural Product Identification

Common Name

N-trans-Isoferuloyl-3-O-methyldopamine

Description

N-trans-4-O-methylcaffeoyl 3'-O-methyldopamine 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. N-trans-Isoferuloyl-3-O-methyldopamine is found in Chenopodium album . Based on a literature review very few articles have been published on N-trans-4-O-methylcaffeoyl 3'-O-methyldopamine.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 46 47  0  0  0  0  0  0  0  0999 V2000
    8.4393    2.2612   -0.4006 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9198    1.0946    0.1976 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5410    0.8501    0.0259 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7713    1.7286   -0.6963 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4339    1.4711   -0.8503 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8663    0.3226   -0.2744 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4388    0.0640   -0.4488 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8081   -0.9586    0.0345 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3927   -1.2482   -0.1180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0538   -2.2980    0.4254 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4410   -0.3910   -0.8420 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8488   -0.6740   -0.9886 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5098   -0.6854    0.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9644   -0.9585    0.2864 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3693   -2.2747    0.3586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7248   -2.5497    0.3147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6491   -1.5311    0.2015 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0021   -1.7946    0.1570 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2304   -0.2041    0.1292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1278    0.8363    0.0157 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6498    2.1577   -0.0535 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8786    0.0605    0.1736 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6533   -0.5256    0.4331 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9881   -0.2705    0.5880 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7895   -1.1591    1.3238 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9463    3.1373    0.0861 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5434    2.2563   -0.2225 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.2215    2.3287   -1.4848 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2137    2.6266   -1.1468 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7997    2.1276   -1.4038 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8480    0.7825   -1.0303 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3767   -1.6986    0.6241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0474    0.4634   -1.2833 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3327   -0.0108   -1.7385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8851   -1.6937   -1.4783 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0649   -1.4564    0.9804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3876    0.2736    0.9010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6866   -3.1087    0.4478 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0944   -3.5590    0.3673 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6472   -1.0313    0.0743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8516    2.2621   -0.8062 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2298    2.4101    0.9607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4476    2.8757   -0.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4840    1.0660    0.1224 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2666   -1.4060    0.8858 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3507   -1.9693    1.7211 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3 24  2  0
 24 25  1  0
 24 23  1  0
 23  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
  9 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 22  2  0
 22 19  1  0
 19 20  1  0
 20 21  1  0
 19 17  2  0
 17 18  1  0
 17 16  1  0
 16 15  2  0
  6  5  1  0
  5  4  2  0
  4  3  1  0
 15 14  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
 25 46  1  0
 23 45  1  0
  7 31  1  0
  8 32  1  0
 11 33  1  0
 12 34  1  0
 12 35  1  0
 13 36  1  0
 13 37  1  0
 22 44  1  0
 21 41  1  0
 21 42  1  0
 21 43  1  0
 18 40  1  0
 16 39  1  0
 15 38  1  0
  5 30  1  0
  4 29  1  0
M  END


  Mrv1652304292208452D          

 25 26  0  0  0  0            999 V2000
   -2.8579   -1.6500    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.2375    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
   -2.8579    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
   -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 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
    0.0000   -1.6500    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
    1.4289   -2.4750    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0013   -2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302   -2.8875    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 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
    3.5724   -3.7125    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   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  3  6  1  0  0  0  0
  6  7  2  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  1  0  0  0  0
 12 13  1  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  1  0  0  0  0
 18 19  1  0  0  0  0
 17 20  2  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 22 23  2  0  0  0  0
 15 23  1  0  0  0  0
 11 24  2  0  0  0  0
  8 25  2  0  0  0  0
  2 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0086452

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=C(O)C=C(\C=C\C(=O)NCCC2=CC(OC)=C(O)C=C2)C=C1

> <INCHI_IDENTIFIER>
InChI=1S/C19H21NO5/c1-24-17-7-4-13(11-16(17)22)5-8-19(23)20-10-9-14-3-6-15(21)18(12-14)25-2/h3-8,11-12,21-22H,9-10H2,1-2H3,(H,20,23)/b8-5+

> <INCHI_KEY>
QGYGWYUQPCKNKZ-VMPITWQZSA-N

> <FORMULA>
C19H21NO5

> <MOLECULAR_WEIGHT>
343.379

> <EXACT_MASS>
343.14197278

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
46

> <JCHEM_AVERAGE_POLARIZABILITY>
37.468665163562555

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

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

> <ALOGPS_LOGP>
2.37

> <JCHEM_LOGP>
2.6434808596666666

> <ALOGPS_LOGS>
-4.20

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
10.191138718242993

> <JCHEM_PKA_STRONGEST_ACIDIC>
9.581091097724073

> <JCHEM_PKA_STRONGEST_BASIC>
-0.3880084047443634

> <JCHEM_POLAR_SURFACE_AREA>
88.02000000000001

> <JCHEM_REFRACTIVITY>
96.0346

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
2.14e-02 g/l

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

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 29-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   29-APR-22         0                                  
HETATM    1  O   UNK     0      -5.335  -3.080   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -4.001  -2.310   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -5.335   0.000   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -6.668  -0.770   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334  -0.770   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       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -5.390   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0       2.667  -4.620   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0       4.001  -5.390   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       5.335  -4.620   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.668  -5.390   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       9.336  -5.390   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      10.669  -4.620   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0      12.003  -5.390   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      10.669  -7.700   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       8.002  -7.700   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0       1.334  -6.930   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.667  -3.080   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   25                                                  
CONECT    3    2    4    6                                                  
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    3    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   25                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12   24                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   23                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18   20                                                  
CONECT   18   17   19                                                       
CONECT   19   18                                                            
CONECT   20   17   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   15                                                       
CONECT   24   11                                                            
CONECT   25    8    2                                                       
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₉H₂₁NO₅

Average Mass

343.3790 Da

Monoisotopic Mass

343.14197 Da

IUPAC Name

(2E)-N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-(3-hydroxy-4-methoxyphenyl)prop-2-enamide

Traditional Name

(2E)-N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-(3-hydroxy-4-methoxyphenyl)prop-2-enamide

CAS Registry Number

Not Available

SMILES

COC1=C(O)C=C(\C=C\C(=O)NCCC2=CC(OC)=C(O)C=C2)C=C1

InChI Identifier

InChI=1S/C19H21NO5/c1-24-17-7-4-13(11-16(17)22)5-8-19(23)20-10-9-14-3-6-15(21)18(12-14)25-2/h3-8,11-12,21-22H,9-10H2,1-2H3,(H,20,23)/b8-5+

InChI Key

QGYGWYUQPCKNKZ-VMPITWQZSA-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
Chenopodium album	Plant	KNApSAcK

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
Styrene
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
logP	2.37	ALOGPS
logP	2.64	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	9.58	ChemAxon
pKa (Strongest Basic)	-0.39	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	88.02 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	96.03 m³·mol⁻¹	ChemAxon
Polarizability	37.47 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

C00056727

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

14412558

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for N-trans-Isoferuloyl-3-O-methyldopamine (NP0086452)

MOL for NP0086452 (N-trans-Isoferuloyl-3-O-methyldopamine)

3D MOL for NP0086452 (N-trans-Isoferuloyl-3-O-methyldopamine)

3D SDF for NP0086452 (N-trans-Isoferuloyl-3-O-methyldopamine)

3D-SDF for NP0086452 (N-trans-Isoferuloyl-3-O-methyldopamine)

PDB for NP0086452 (N-trans-Isoferuloyl-3-O-methyldopamine)

3D PDB for NP0086452 (N-trans-Isoferuloyl-3-O-methyldopamine)

SMILES for NP0086452 (N-trans-Isoferuloyl-3-O-methyldopamine)

INCHI for NP0086452 (N-trans-Isoferuloyl-3-O-methyldopamine)

Structure for NP0086452 (N-trans-Isoferuloyl-3-O-methyldopamine)

3D Structure for NP0086452 (N-trans-Isoferuloyl-3-O-methyldopamine)