NP-MRD: Showing NP-Card for (6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid (NP0198056)

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Record Information

Version

2.0

Created at

2022-09-04 16:26:17 UTC

Updated at

2022-09-04 16:26:18 UTC

NP-MRD ID

NP0198056

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid

Description

SCHEMBL22788514, also known as homocapsaicin I, 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. Based on a literature review very few articles have been published on SCHEMBL22788514.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 52 52  0  0  0  0  0  0  0  0999 V2000
   -5.9129   -2.7719    1.4541 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3875   -2.1764    0.2831 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8182   -1.0503   -0.2872 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7244   -0.4719    0.3191 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1266    0.6561   -0.2211 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9530    1.2766    0.4309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5342    2.4174   -0.3248 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4238    2.6175   -0.9104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3151    3.8574   -1.5805 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2633    1.6991   -0.9562 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9118    2.4289   -0.3297 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1664    1.6204   -0.3053 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0513    0.3355    0.4683 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4002   -0.3495    0.3914 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0931   -0.6214    1.4785 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3963   -1.2741    1.5210 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9961   -1.6505    0.2090 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2388   -0.4739   -0.7079 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2205   -2.7373   -0.5016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6236    1.2127   -1.3765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7181    0.6443   -1.9945 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3044   -0.4865   -1.4383 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4120   -1.0847   -2.0388 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7982   -2.8730    1.3369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2950   -3.7879    1.5829 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0494   -2.1531    2.3656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3235   -0.8926    1.2209 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1654    0.5003    0.5641 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2753    1.5899    1.4660 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9593    4.6524   -1.0619 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0036    1.4329   -2.0128 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4127    0.7839   -0.3593 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0870    3.3265   -0.9318 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6554    2.7559    0.6887 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4715    1.4243   -1.3640 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9659    2.2648    0.1143 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7807    0.5551    1.5027 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2713   -0.2973    0.0157 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7975   -0.6237   -0.5669 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6276   -0.3204    2.4223 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1775   -0.6567    2.0575 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3613   -2.2179    2.1427 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0104   -2.0907    0.4416 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8729   -0.6345   -1.7407 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8887    0.4728   -0.2449 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3506   -0.3142   -0.8353 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7989   -3.6789   -0.5527 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0737   -2.4067   -1.5494 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2334   -2.9206   -0.0312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1982    2.0908   -1.8421 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1247    1.0709   -2.9088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7837   -0.6695   -2.9018 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  1  0
  7  8  2  0
  8  9  1  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
  5 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 22  3  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  4 27  1  0
  6 28  1  0
  6 29  1  0
  9 30  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 12 35  1  0
 12 36  1  0
 13 37  1  0
 13 38  1  0
 14 39  1  0
 15 40  1  0
 16 41  1  0
 16 42  1  0
 17 43  1  0
 18 44  1  0
 18 45  1  0
 18 46  1  0
 19 47  1  0
 19 48  1  0
 19 49  1  0
 20 50  1  0
 21 51  1  0
 23 52  1  0
M  END


  Mrv1652309042218262D          

 23 23  0  0  0  0            999 V2000
   -8.5737    4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592    3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8592    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1447    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158    1.6500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579    1.6500    0.0000 C   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
   -1.4289    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
    0.0000    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
    1.4289    1.6500    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
   -7.8592    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5737    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2881    2.8875    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  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  8 10  1  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  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
  5 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
  3 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0198056

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC(CN=C(O)CCCC\C=C\CC(C)C)=CC=C1O

> <INCHI_IDENTIFIER>
InChI=1S/C19H29NO3/c1-15(2)9-7-5-4-6-8-10-19(22)20-14-16-11-12-17(21)18(13-16)23-3/h5,7,11-13,15,21H,4,6,8-10,14H2,1-3H3,(H,20,22)/b7-5+

> <INCHI_KEY>
JZNZUOZRIWOBGG-FNORWQNLSA-N

> <FORMULA>
C19H29NO3

> <MOLECULAR_WEIGHT>
319.445

> <EXACT_MASS>
319.214743798

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
52

> <JCHEM_AVERAGE_POLARIZABILITY>
37.76822838517154

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(6E)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid

> <JCHEM_LOGP>
5.013842336333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.936465082971678

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.885497739499191

> <JCHEM_PKA_STRONGEST_BASIC>
3.714140945511579

> <JCHEM_POLAR_SURFACE_AREA>
62.05

> <JCHEM_REFRACTIVITY>
95.4401

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(6E)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic 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     -16.004   7.700   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0     -14.670   6.930   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0     -14.670   5.390   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -13.337   4.620   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -13.337   3.080   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0     -12.003   2.310   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0     -10.669   3.080   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      -9.336   2.310   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      -9.336   0.770   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      -8.002   3.080   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -5.335   3.080   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.667   3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -14.670   2.310   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0     -16.004   3.080   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0     -16.004   4.620   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0     -17.338   5.390   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   22                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6   20                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20    5   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    3   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Value	Source
Homocapsaicin I	Kegg

Chemical Formula

C₁₉H₂₉NO₃

Average Mass

319.4450 Da

Monoisotopic Mass

319.21474 Da

IUPAC Name

(6E)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid

Traditional Name

(6E)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid

CAS Registry Number

Not Available

SMILES

COC1=CC(CN=C(O)CCCC\C=C\CC(C)C)=CC=C1O

InChI Identifier

InChI=1S/C19H29NO3/c1-15(2)9-7-5-4-6-8-10-19(22)20-14-16-11-12-17(21)18(13-16)23-3/h5,7,11-13,15,21H,4,6,8-10,14H2,1-3H3,(H,20,22)/b7-5+

InChI Key

JZNZUOZRIWOBGG-FNORWQNLSA-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

Not Available

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-2-unsubstituted benzenoid
Monocyclic benzene moiety
Fatty amide
Fatty acyl
N-acyl-amine
Carboxamide group
Secondary carboxylic acid amide
Ether
Carboxylic acid derivative
Organic oxygen compound
Hydrocarbon derivative
Organic nitrogen compound
Carbonyl group
Organic oxide
Organooxygen compound
Organonitrogen 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	5.01	ChemAxon
pKa (Strongest Acidic)	5.89	ChemAxon
pKa (Strongest Basic)	3.71	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	62.05 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	95.44 m³·mol⁻¹	ChemAxon
Polarizability	37.77 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	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

C00057457

Chemspider ID

30790804

KEGG Compound ID

C20215

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71448975

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

rw1854631

References

General References

LOTUS database [Link]

Showing NP-Card for (6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid (NP0198056)

MOL for NP0198056 ((6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid)

3D MOL for NP0198056 ((6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid)

3D SDF for NP0198056 ((6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid)

3D-SDF for NP0198056 ((6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid)

PDB for NP0198056 ((6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid)

3D PDB for NP0198056 ((6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid)

SMILES for NP0198056 ((6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid)

INCHI for NP0198056 ((6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid)

Structure for NP0198056 ((6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid)

3D Structure for NP0198056 ((6e)-n-[(4-hydroxy-3-methoxyphenyl)methyl]-9-methyldec-6-enimidic acid)