NP-MRD: Showing NP-Card for 13-hode (NP0174539)

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Record Information

Version

2.0

Created at

2022-09-03 11:48:35 UTC

Updated at

2022-09-03 11:48:35 UTC

NP-MRD ID

NP0174539

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-hode

Description

13-HODE, also known as coriolic acid or coriolate, belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions. Thus, 13-HODE is considered to be an octadecanoid lipid molecule. A HODE that consists of 9Z,11E-octadecadienoic acid carrying a 13-hydroxy substituent. 13-hode is found in Astragalus mongholicus. 13-HODE is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 53 52  0  0  0  0  0  0  0  0999 V2000
    7.9823    1.0397    0.6231 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4923   -0.3751    0.8942 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1667   -0.5104    0.1628 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1673    0.4824    0.6463 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8383    0.3976   -0.0062 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7987    0.5961   -1.4794 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5587   -0.3360   -2.2053 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4329    0.6552   -2.0304 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3301    0.5252   -1.2712 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0160    0.5929   -1.8781 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0695    0.4760   -1.1832 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1016    0.2683    0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7997   -1.0289    0.5631 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1947   -1.0319    0.0134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0080    0.0732    0.6024 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4009    0.0662    0.0430 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1022   -1.2113    0.3598 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5267   -1.1756   -0.1928 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2626   -0.0600    0.4085 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7112   -0.1788    1.5841 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4795    1.1247   -0.2815 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5116    1.4564   -0.2898 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.0801    1.0766    0.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7017    1.6366    1.5291 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1947   -1.0917    0.3771 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3786   -0.6007    1.9550 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7707   -1.5346    0.1910 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4379   -0.3017   -0.9123 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9998    0.3414    1.7460 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5811    1.4996    0.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2853   -0.5164    0.3244 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2261    1.2467    0.4338 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2799    1.5951   -1.6802 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6160    0.0619   -3.1318 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2747    0.8077   -3.0823 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5440    0.3726   -0.2281 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0312    0.7504   -2.9676 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0299    0.5420   -1.7321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6389    1.0882    0.8141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0895    0.2093    0.7313 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7906   -1.2492    1.6643 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2522   -1.8646    0.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6972   -2.0176    0.2369 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2170   -0.9635   -1.0909 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0157   -0.0996    1.7160 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5407    1.0797    0.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9811    0.9681    0.3523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3772    0.1342   -1.0858 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5703   -2.0488   -0.1470 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0850   -1.3760    1.4513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4438   -1.1363   -1.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9717   -2.1520    0.0725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2771    1.6967   -0.1035 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
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 21  1  0
 19 20  2  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  5 31  1  0
  5 32  1  0
  6 33  1  1
  7 34  1  0
  8 35  1  0
  9 36  1  0
 10 37  1  0
 11 38  1  0
 12 39  1  0
 12 40  1  0
 13 41  1  0
 13 42  1  0
 14 43  1  0
 14 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 18 51  1  0
 18 52  1  0
 21 53  1  0
M  END

      
  Mrv1652309151721502D          

 21 20  0  0  1  0            999 V2000
    5.2477  -10.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9621  -11.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6766  -10.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3910  -11.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1056  -10.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8200  -11.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5345  -10.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3595  -10.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0740  -11.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7884  -10.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5029  -11.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.2174  -10.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5332  -11.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9318  -11.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6463  -10.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3608  -11.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0752  -10.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0753  -10.1154    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7897  -11.3530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.3909  -12.1779    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8187  -10.9403    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  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  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
  1 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 19  1  0  0  0  0
 17 18  2  0  0  0  0
  4 20  1  0  0  0  0
 13 21  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0174539

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCC(O)\C=C\C=C/CCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C18H32O3/c1-2-3-11-14-17(19)15-12-9-7-5-4-6-8-10-13-16-18(20)21/h7,9,12,15,17,19H,2-6,8,10-11,13-14,16H2,1H3,(H,20,21)/b9-7-,15-12+

> <INCHI_KEY>
HNICUWMFWZBIFP-BSZOFBHHSA-N

> <FORMULA>
C18H32O3

> <MOLECULAR_WEIGHT>
296.451

> <EXACT_MASS>
296.23514489

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
36.53117396068553

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(9Z,11E)-13-hydroxyoctadeca-9,11-dienoic acid

> <ALOGPS_LOGP>
5.88

> <JCHEM_LOGP>
5.191065727333333

> <ALOGPS_LOGS>
-5.00

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
17.795677909269454

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.9881674023842

> <JCHEM_PKA_STRONGEST_BASIC>
-1.5759706009659333

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
90.03429999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.98e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(9Z,11E)-13-hydroxyoctadeca-9,11-dienoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-SEP-17   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-SEP-17         0                                  
HETATM    1  C   UNK     0       9.796 -20.422   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      11.129 -21.192   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      12.463 -20.422   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      13.797 -21.192   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      15.130 -20.422   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      16.464 -21.192   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      17.798 -20.422   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      19.338 -20.422   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      20.671 -21.192   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      22.005 -20.422   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      23.339 -21.192   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      24.672 -20.422   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.462 -21.192   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      26.006 -21.192   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      27.340 -20.422   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      28.673 -21.192   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      30.007 -20.422   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      30.007 -18.882   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      31.341 -21.192   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      13.796 -22.732   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       7.128 -20.422   0.000  0.00  0.00           C+0
CONECT    1    2   13                                                       
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5   20                                                  
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   14                                                       
CONECT   13    1   21                                                       
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   19   18                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20    4                                                            
CONECT   21   13                                                            
MASTER        0    0    0    0    0    0    0    0   21    0   40    0
END

View in JSmol

Synonyms

Value	Source
13-Hydroxy-9Z,11E-octadecadienoic acid	ChEBI
13-Hydroxy-cis-9,trans-11-octadecadienoic acid	ChEBI
Coriolic acid	ChEBI
13-Hydroxy-9Z,11E-octadecadienoate	Generator
13-Hydroxy-cis-9,trans-11-octadecadienoate	Generator
Coriolate	Generator
(9Z,11E)-13-hydroxy-9,11-octadecadienoic acid	SMPDB, HMDB
13-hydroxy-(9Z,11E)-octadeca-9,11-dienoic acid	SMPDB, HMDB
13-hydroxy-9(Z),11(E)-octadecadienoic acid	SMPDB, HMDB
13-hydroxy-9,11-cis,trans-octadecadienoic acid	SMPDB, HMDB
13-hydroxy-9-cis-11-trans-octadecadienoic acid	SMPDB, HMDB
13-hydroxy-cis-9-trans-11-octadecadienoic acid	SMPDB, HMDB
13-hydroxyoctadeca-9,11-dienoic acid	SMPDB, HMDB
13-(Z,E)-HODE	SMPDB, HMDB
13-HODE	SMPDB, MeSH, HMDB
13-hydroxylinoleic acid	SMPDB, HMDB
(9Z,11E)-13-HODE	SMPDB
13-HODD	MeSH, HMDB
13-LOX	MeSH, HMDB
13-Hydroxy-9,11-octadecadienoic acid	MeSH, HMDB
13-Hydroxy-9,11-octadecadienoic acid, (e,e)-isomer	MeSH, HMDB
13-Hydroxy-9,11-octadecadienoic acid, (Z,e)-isomer	MeSH, HMDB
13-Hydroxyoctadecadienoic acid	MeSH, HMDB
13-Hydroxy-9,11-octadecadienoic acid, (e,Z)-isomer	MeSH, HMDB
13-Hydroxy-9,11-octadecadienoic acid, (R)-(e,Z)-isomer	MeSH, HMDB
13-Hydroxy-9,11-octadecadienoic acid, (S)-(e,Z)-isomer	MeSH, HMDB

Chemical Formula

C₁₈H₃₂O₃

Average Mass

296.4510 Da

Monoisotopic Mass

296.23514 Da

IUPAC Name

(9Z,11E)-13-hydroxyoctadeca-9,11-dienoic acid

Traditional Name

(9Z,11E)-13-hydroxyoctadeca-9,11-dienoic acid

CAS Registry Number

Not Available

SMILES

CCCCCC(O)\C=C\C=C/CCCCCCCC(O)=O

InChI Identifier

InChI=1S/C18H32O3/c1-2-3-11-14-17(19)15-12-9-7-5-4-6-8-10-13-16-18(20)21/h7,9,12,15,17,19H,2-6,8,10-11,13-14,16H2,1H3,(H,20,21)/b9-7-,15-12+

InChI Key

HNICUWMFWZBIFP-BSZOFBHHSA-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
Astragalus mongholicus	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lineolic acids and derivatives. These are derivatives of lineolic acid. Lineolic acid is a polyunsaturated omega-6 18 carbon long fatty acid, with two CC double bonds at the 9- and 12-positions.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Lineolic acids and derivatives

Direct Parent

Lineolic acids and derivatives

Alternative Parents

Substituents

Octadecanoid
Long-chain fatty acid
Hydroxy fatty acid
Fatty acid
Unsaturated fatty acid
Secondary alcohol
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxide
Organic oxygen compound
Alcohol
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

HODE (CHEBI:72639 )
Other Octadecanoids (LMFA02000154 )

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	5.88	ALOGPS
logP	5.19	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	4.99	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	90.03 m³·mol⁻¹	ChemAxon
Polarizability	36.53 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

HMDB0112194

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

13-Hydroxyoctadecadienoic acid

METLIN ID

Not Available

PubChem Compound

5282947

PDB ID

Not Available

ChEBI ID

72639

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13-hode (NP0174539)

MOL for NP0174539 (13-hode)

3D MOL for NP0174539 (13-hode)

3D SDF for NP0174539 (13-hode)

3D-SDF for NP0174539 (13-hode)

PDB for NP0174539 (13-hode)

3D PDB for NP0174539 (13-hode)

SMILES for NP0174539 (13-hode)

INCHI for NP0174539 (13-hode)

Structure for NP0174539 (13-hode)

3D Structure for NP0174539 (13-hode)