NP-MRD: Showing NP-Card for n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid (NP0213259)

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Record Information

Version

2.0

Created at

2022-09-05 12:11:54 UTC

Updated at

2022-09-05 12:11:54 UTC

NP-MRD ID

NP0213259

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid

Description

N-[(2S,3S,8E)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl). n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid is found in Anemonia sulcata. Based on a literature review very few articles have been published on N-[(2S,3S,8E)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309052214112D          

 38 37  0  0  1  0            999 V2000
    4.7586    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4730    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1875    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9020    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6164    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3309    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4743    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1888    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9033    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6177    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0467    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7612    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4756    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   18.3335    3.9849    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.3335    4.8099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.0480    3.5724    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.0480    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7624    2.3349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   28.3361    3.9849    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
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
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  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
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 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
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 23 24  1  0  0  0  0
 22 25  1  1  0  0  0
 25 26  2  0  0  0  0
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 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
M  END

     RDKit          3D

103102  0  0  0  0  0  0  0  0999 V2000
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M  END


  Mrv1652309052214112D          

 38 37  0  0  1  0            999 V2000
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    7.6164    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3309    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0454    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7599    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.4743    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1888    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9033    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6177    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3322    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0467    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.7612    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4756    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1901    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9046    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.6190    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.3335    3.9849    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.3335    4.8099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.0480    3.5724    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   19.0480    2.7474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7624    2.3349    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.7624    3.9849    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   20.4769    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.4769    2.7474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.1914    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.9059    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6203    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.3348    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.0493    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.7637    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.4782    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.1927    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.9072    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.6216    3.5724    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3361    3.9849    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
  5  6  1  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  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
 18 19  2  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  6  0  0  0
 20 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 22 25  1  1  0  0  0
 25 26  2  0  0  0  0
 26 27  1  4  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0213259

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCC\C=C\CC\C=C\[C@H](O)[C@H](CO)N=C(O)CCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C34H65NO3/c1-3-5-7-9-11-13-14-15-16-17-18-19-20-22-23-25-27-29-33(37)32(31-36)35-34(38)30-28-26-24-21-12-10-8-6-4-2/h20,22,27,29,32-33,36-37H,3-19,21,23-26,28,30-31H2,1-2H3,(H,35,38)/b22-20+,29-27+/t32-,33-/m0/s1

> <INCHI_KEY>
UJRYWTLTIVBMHF-YULZEHSXSA-N

> <FORMULA>
C34H65NO3

> <MOLECULAR_WEIGHT>
535.898

> <EXACT_MASS>
535.496444957

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
103

> <JCHEM_AVERAGE_POLARIZABILITY>
71.71861401863231

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
N-[(2S,3S,4E,8E)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid

> <JCHEM_LOGP>
11.323037614

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
14.105336448543028

> <JCHEM_PKA_STRONGEST_ACIDIC>
6.17608151111364

> <JCHEM_PKA_STRONGEST_BASIC>
3.048240349420818

> <JCHEM_POLAR_SURFACE_AREA>
73.05

> <JCHEM_REFRACTIVITY>
167.41400000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
29

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
N-[(2S,3S,4E,8E)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-SEP-22         0                                  
HETATM    1  C   UNK     0       8.883   6.668   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.216   7.438   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.550   6.668   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      12.884   7.438   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.217   6.668   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      15.551   7.438   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      16.885   6.668   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      18.218   7.438   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      19.552   6.668   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.886   7.438   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      22.219   6.668   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      23.553   7.438   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      24.887   6.668   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      26.220   7.438   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      27.554   6.668   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      28.888   7.438   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      30.222   6.668   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      31.555   7.438   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      32.889   6.668   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      34.223   7.438   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      34.223   8.978   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      35.556   6.668   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      35.556   5.128   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      36.890   4.358   0.000  0.00  0.00           O+0
HETATM   25  N   UNK     0      36.890   7.438   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      38.224   6.668   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      38.224   5.128   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      39.557   7.438   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      40.891   6.668   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      42.225   7.438   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      43.558   6.668   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      44.892   7.438   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      46.226   6.668   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      47.559   7.438   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      48.893   6.668   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      50.227   7.438   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      51.560   6.668   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      52.894   7.438   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    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                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23   25                                                  
CONECT   23   22   24                                                       
CONECT   24   23                                                            
CONECT   25   22   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   74    0
END

View in JSmol

Synonyms

Value	Source
N-[(2S,3S,8E)-1,3-Dihydroxydocosa-4,8-dien-2-yl]dodecanimidate	Generator

Chemical Formula

C₃₄H₆₅NO₃

Average Mass

535.8980 Da

Monoisotopic Mass

535.49644 Da

IUPAC Name

N-[(2S,3S,4E,8E)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid

Traditional Name

N-[(2S,3S,4E,8E)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCC\C=C\CC\C=C\[C@H](O)[C@H](CO)N=C(O)CCCCCCCCCCC

InChI Identifier

InChI=1S/C34H65NO3/c1-3-5-7-9-11-13-14-15-16-17-18-19-20-22-23-25-27-29-33(37)32(31-36)35-34(38)30-28-26-24-21-12-10-8-6-4-2/h20,22,27,29,32-33,36-37H,3-19,21,23-26,28,30-31H2,1-2H3,(H,35,38)/b22-20+,29-27+/t32-,33-/m0/s1

InChI Key

UJRYWTLTIVBMHF-YULZEHSXSA-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
Anemonia sulcata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as secondary alcohols. Secondary alcohols are compounds containing a secondary alcohol functional group, with the general structure HOC(R)(R') (R,R'=alkyl, aryl).

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Secondary alcohols

Alternative Parents

Substituents

Secondary alcohol
Organic 1,3-dipolar compound
Propargyl-type 1,3-dipolar organic compound
Carboximidic acid derivative
Carboximidic acid
Organic nitrogen compound
Organopnictogen compound
Hydrocarbon derivative
Primary alcohol
Organonitrogen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic 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	11.32	ChemAxon
pKa (Strongest Acidic)	6.18	ChemAxon
pKa (Strongest Basic)	3.05	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	73.05 Å²	ChemAxon
Rotatable Bond Count	29	ChemAxon
Refractivity	167.41 m³·mol⁻¹	ChemAxon
Polarizability	71.72 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

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

162874993

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid (NP0213259)

MOL for NP0213259 (n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid)

3D MOL for NP0213259 (n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid)

3D SDF for NP0213259 (n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid)

3D-SDF for NP0213259 (n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid)

PDB for NP0213259 (n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid)

3D PDB for NP0213259 (n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid)

SMILES for NP0213259 (n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid)

INCHI for NP0213259 (n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid)

Structure for NP0213259 (n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid)

3D Structure for NP0213259 (n-[(2s,3s,4e,8e)-1,3-dihydroxydocosa-4,8-dien-2-yl]dodecanimidic acid)