NP-MRD: Showing NP-Card for 4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid (NP0259212)

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Record Information

Version

2.0

Created at

2022-09-08 01:00:14 UTC

Updated at

2022-09-08 01:00:14 UTC

NP-MRD ID

NP0259212

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid

Description

Secoisoodorinol 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. 4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid is found in Aglaia tenuicaulis. Based on a literature review very few articles have been published on Secoisoodorinol.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 49 49  0  0  0  0  0  0  0  0999 V2000
   -5.9102    1.7011    0.4586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5285    0.2642    0.2124 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3065   -0.2962   -0.9605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7826   -0.2019   -0.6139 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0588   -0.9286    0.5259 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0730    0.1893   -0.0042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4421   -1.0159   -0.2546 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3699    1.2585    0.0388 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9250    1.2308   -0.1700 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3223    0.5875    1.0416 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1589    0.5290    0.8949 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6494   -0.2537   -0.2920 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0964   -0.2020   -0.2689 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.7582   -1.2764   -0.0622 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0923   -2.4666    0.1357 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2280   -1.2757   -0.0295 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9349   -0.1892   -0.2079 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3789   -0.0751   -0.1961 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0173    1.1401   -0.3990 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3968    1.2080   -0.3804 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1703    0.0838   -0.1624 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5401   -1.1179    0.0383 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1632   -1.1730    0.0174 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8841    2.2923   -0.4714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9158    1.7787    0.9282 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1195    2.1352    1.1299 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8177   -0.3425    1.1135 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0845    0.2587   -1.8772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0526   -1.3528   -1.1013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0453    0.8754   -0.5136 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4083   -0.5821   -1.4626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.1137   -0.3708    1.3425 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5882   -1.8476    0.2970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6713    0.6371   -1.0819 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5301    2.2436   -0.2729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7191   -0.4327    1.2290 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5409    1.2218    1.9294 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5864    0.0242    1.7987 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5996    1.5461    0.8673 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2954    0.1645   -1.2653 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3011   -1.3004   -0.2702 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2710   -3.3170   -0.4020 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7547   -2.1987    0.1472 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3434    0.7222   -0.3840 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4170    2.0285   -0.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9353    2.1332   -0.5337 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.2650    0.1419   -0.1484 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1259   -2.0307    0.2144 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7310   -2.1481    0.1820 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  2  6  1  0
  6  7  1  0
  6  8  2  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 14 16  1  0
 16 17  2  0
 17 18  1  0
 18 19  2  0
 19 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  2  0
 23 18  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  1
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
  5 32  1  0
  7 33  1  0
  9 34  1  0
  9 35  1  0
 10 36  1  0
 10 37  1  0
 11 38  1  0
 11 39  1  0
 12 40  1  0
 12 41  1  0
 15 42  1  0
 16 43  1  0
 17 44  1  0
 19 45  1  0
 20 46  1  0
 21 47  1  0
 22 48  1  0
 23 49  1  0
M  END


  Mrv1652309082203002D          

 23 23  0  0  0  0            999 V2000
   -2.8579   -5.7750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724   -4.5375    0.0000 C   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   -4.5375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -4.5375    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -5.7750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -4.5375    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
    4.2868   -3.3000    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   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158   -3.3000    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
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  2  6  1  0  0  0  0
  6  7  1  0  0  0  0
  6  8  2  0  0  0  0
  8  9  1  4  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 13 12  1  4  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 21 22  1  0  0  0  0
 22 23  2  0  0  0  0
 18 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0259212

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(CCO)C(O)=NCCCCN=C(O)\C=C\C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C18H26N2O3/c1-15(11-14-21)18(23)20-13-6-5-12-19-17(22)10-9-16-7-3-2-4-8-16/h2-4,7-10,15,21H,5-6,11-14H2,1H3,(H,19,22)(H,20,23)/b10-9+

> <INCHI_KEY>
AZFOWFPALBQOTD-MDZDMXLPSA-N

> <FORMULA>
C18H26N2O3

> <MOLECULAR_WEIGHT>
318.417

> <EXACT_MASS>
318.194342705

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
37.13575739100497

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-hydroxy-N-(4-{[(2E)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid

> <JCHEM_LOGP>
1.6144602646107722

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
6.3675230725458665

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.027775602025945

> <JCHEM_PKA_STRONGEST_BASIC>
7.012544433701452

> <JCHEM_POLAR_SURFACE_AREA>
85.41000000000001

> <JCHEM_REFRACTIVITY>
93.45690000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-hydroxy-N-(4-{[(2E)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0      -5.335 -10.780   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -5.335  -9.240   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -6.668  -8.470   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -8.002  -9.240   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -9.336  -8.470   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -4.001  -8.470   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -4.001  -6.930   0.000  0.00  0.00           O+0
HETATM    8  N   UNK     0      -2.667  -9.240   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      -1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334  -8.470   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0       4.001  -8.470   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0       5.335  -9.240   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       5.335 -10.780   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.668  -8.470   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -6.930   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002  -6.160   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.002  -4.620   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       9.336  -3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      10.669  -4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      10.669  -6.160   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.336  -6.930   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    6                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4                                                            
CONECT    6    2    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   18                                                       
MASTER        0    0    0    0    0    0    0    0   23    0   46    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₆N₂O₃

Average Mass

318.4170 Da

Monoisotopic Mass

318.19434 Da

IUPAC Name

4-hydroxy-N-(4-{[(2E)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid

Traditional Name

4-hydroxy-N-(4-{[(2E)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid

CAS Registry Number

Not Available

SMILES

CC(CCO)C(O)=NCCCCN=C(O)\C=C\C1=CC=CC=C1

InChI Identifier

InChI=1S/C18H26N2O3/c1-15(11-14-21)18(23)20-13-6-5-12-19-17(22)10-9-16-7-3-2-4-8-16/h2-4,7-10,15,21H,5-6,11-14H2,1H3,(H,19,22)(H,20,23)/b10-9+

InChI Key

AZFOWFPALBQOTD-MDZDMXLPSA-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
Aglaia tenuicaulis	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
Styrene
Monocyclic benzene moiety
Fatty amide
Fatty acyl
Benzenoid
N-acyl-amine
Carboxamide group
Secondary carboxylic acid amide
Carboxylic acid derivative
Organonitrogen compound
Primary alcohol
Hydrocarbon derivative
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Organooxygen 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	1.61	ChemAxon
pKa (Strongest Acidic)	5.03	ChemAxon
pKa (Strongest Basic)	7.01	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	85.41 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	93.46 m³·mol⁻¹	ChemAxon
Polarizability	37.14 Å³	ChemAxon
Number of Rings	1	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

C00034226

Chemspider ID

59650575

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

101844317

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid (NP0259212)

MOL for NP0259212 (4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid)

3D MOL for NP0259212 (4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid)

3D SDF for NP0259212 (4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid)

3D-SDF for NP0259212 (4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid)

PDB for NP0259212 (4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid)

3D PDB for NP0259212 (4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid)

SMILES for NP0259212 (4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid)

INCHI for NP0259212 (4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid)

Structure for NP0259212 (4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid)

3D Structure for NP0259212 (4-hydroxy-n-(4-{[(2e)-1-hydroxy-3-phenylprop-2-en-1-ylidene]amino}butyl)-2-methylbutanimidic acid)