NP-MRD: Showing NP-Card for (5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid (NP0208094)

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Record Information

Version

2.0

Created at

2022-09-05 04:57:56 UTC

Updated at

2022-09-05 04:57:56 UTC

NP-MRD ID

NP0208094

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid

Description

(5S,6R,13E,15S)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid belongs to the class of organic compounds known as lipoxins. These are eicosanoids with a trihydroxyicosatetraenoic acid skeleton (a c20-fatty acid, with the chain bearing three hydroxyl groups and four double bonds). Lipoxins have four double bonds, which are all conjugated. In some cases a hydroxyl group is substituted by a C=O group. (5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid is found in Homo sapiens. Based on a literature review very few articles have been published on (5S,6R,13E,15S)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 57 56  0  0  0  0  0  0  0  0999 V2000
    7.8758    2.5366    2.3028 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.1598    1.9903    1.0153 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9808    0.5532    1.2509 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4078   -0.3659    0.2941 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0380   -0.3575   -0.1414 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4458    0.8248   -0.7968 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3175    1.9714   -0.0557 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2699    0.4883   -1.5519 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3253    0.2180   -2.1578 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1754   -0.1108   -2.8980 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0266   -0.5713   -2.3669 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1911   -0.7913   -0.9808 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3228   -1.2543   -0.5035 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4361   -1.5841   -1.3104 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5779   -2.0532   -0.8889 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9369   -2.3304    0.4933 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9542   -2.4583    1.4183 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0359   -1.3188    0.9186 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3433   -0.1314    1.0968 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9371   -1.1589   -0.2687 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0894   -0.2478    0.0405 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5948    1.1250    0.4143 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8252    1.9540    0.6279 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2265    2.6825   -0.2898 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4728    1.8820    1.8309 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.9495    2.3155    2.2322 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4560    2.0515    3.1839 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.7201    3.6145    2.3551 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9107    2.1742    0.1775 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3412    2.6567    0.8564 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4713    0.4393    2.2903 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0334    0.1527    1.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6287   -1.4630    0.6723 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0489   -0.3762   -0.6893 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8911   -1.2628   -0.8402 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3113   -0.6633    0.7027 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2299    1.1048   -1.6432 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0926    1.7229    0.8763 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5738    0.2223   -0.3527 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0837    0.5259   -3.3719 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1526    0.0078   -4.0109 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7965   -0.7892   -3.0550 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5716   -0.5904   -0.2146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3413   -1.3586    0.5951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4028   -1.4533   -2.4162 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3776   -2.2890   -1.6412 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5537   -3.3208    0.4831 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5668   -3.3671    1.4226 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5238   -1.6809    1.8178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6581    0.0808    0.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3082   -2.1224   -0.6848 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3551   -0.6930   -1.1378 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6288   -0.7032    0.9320 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8035   -0.2019   -0.8153 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9620    1.5175   -0.3785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0972    1.1080    1.4240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1698    1.1487    1.9586 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  3
  9 10  1  0
 10 11  2  0
 11 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 25  1  0
 23 24  2  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  2 29  1  0
  2 30  1  0
  3 31  1  0
  3 32  1  0
  4 33  1  0
  4 34  1  0
  5 35  1  0
  5 36  1  0
  6 37  1  6
  7 38  1  0
  8 39  1  0
  9 40  1  0
 10 41  1  0
 11 42  1  0
 12 43  1  0
 13 44  1  0
 14 45  1  0
 15 46  1  0
 16 47  1  6
 17 48  1  0
 18 49  1  1
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 22 56  1  0
 25 57  1  0
M  END


  Mrv1652309052206572D          

 25 24  0  0  1  0            999 V2000
   -8.2421    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5276    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8131    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0987    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3842    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6697    1.4289    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6697    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9552    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2408    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5263    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8118    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0974    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3829    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3316    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0461    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7605    1.8414    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7605    2.6664    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4750    1.4289    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4750    0.6039    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1895    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9039    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6184    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    1.4289    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0474    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3329    0.6039    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  2  0  0  0  0
 10  9  1  4  0  0  0
 10 11  2  0  0  0  0
 12 11  1  4  0  0  0
 12 13  2  0  0  0  0
 14 13  1  4  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  1  0  0  0
 16 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0208094

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC[C@H](O)\C=C\C=CC=CC=C[C@@H](O)[C@@H](O)CCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C20H32O5/c1-2-3-8-12-17(21)13-9-6-4-5-7-10-14-18(22)19(23)15-11-16-20(24)25/h4-7,9-10,13-14,17-19,21-23H,2-3,8,11-12,15-16H2,1H3,(H,24,25)/b6-4?,7-5?,13-9+,14-10?/t17-,18+,19-/m0/s1

> <INCHI_KEY>
IXAQOQZEOGMIQS-FJSMFIKZSA-N

> <FORMULA>
C20H32O5

> <MOLECULAR_WEIGHT>
352.471

> <EXACT_MASS>
352.22497413

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
42.040818827184914

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
4

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(5S,6R,13E,15S)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid

> <JCHEM_LOGP>
3.0506450699999985

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
13.658863253317975

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.475339418208748

> <JCHEM_PKA_STRONGEST_BASIC>
-1.575973533829957

> <JCHEM_POLAR_SURFACE_AREA>
97.99

> <JCHEM_REFRACTIVITY>
104.3465

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(5S,6R,13E,15S)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic 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     -15.385   3.437   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -14.052   2.667   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -12.718   3.437   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -11.384   2.667   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.050   3.437   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -8.717   2.667   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -8.717   1.127   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      -7.383   3.437   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -6.049   2.667   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -4.716   3.437   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -3.382   2.667   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -2.048   3.437   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -0.715   2.667   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.619   3.437   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.953   2.667   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.286   3.437   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       3.286   4.977   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       4.620   2.667   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       4.620   1.127   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       5.954   3.437   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.287   2.667   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       8.621   3.437   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       9.955   2.667   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      11.288   3.437   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0       9.955   1.127   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    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                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   48    0
END

View in JSmol

Synonyms

Value	Source
(5S,6R,13E,15S)-5,6,15-Trihydroxyicosa-7,9,11,13-tetraenoate	Generator

Chemical Formula

C₂₀H₃₂O₅

Average Mass

352.4710 Da

Monoisotopic Mass

352.22497 Da

IUPAC Name

(5S,6R,13E,15S)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid

Traditional Name

(5S,6R,13E,15S)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid

CAS Registry Number

Not Available

SMILES

CCCCC[C@H](O)\C=C\C=CC=CC=C[C@@H](O)[C@@H](O)CCCC(O)=O

InChI Identifier

InChI=1S/C20H32O5/c1-2-3-8-12-17(21)13-9-6-4-5-7-10-14-18(22)19(23)15-11-16-20(24)25/h4-7,9-10,13-14,17-19,21-23H,2-3,8,11-12,15-16H2,1H3,(H,24,25)/b6-4?,7-5?,13-9+,14-10?/t17-,18+,19-/m0/s1

InChI Key

IXAQOQZEOGMIQS-FJSMFIKZSA-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
Homo sapiens	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as lipoxins. These are eicosanoids with a trihydroxyicosatetraenoic acid skeleton (a c20-fatty acid, with the chain bearing three hydroxyl groups and four double bonds). Lipoxins have four double bonds, which are all conjugated. In some cases a hydroxyl group is substituted by a C=O group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Eicosanoids

Direct Parent

Lipoxins

Alternative Parents

Substituents

Lipoxin
Long-chain fatty acid
Hydroxy fatty acid
Fatty acid
Unsaturated fatty acid
Secondary alcohol
Polyol
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Alcohol
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	3.05	ChemAxon
pKa (Strongest Acidic)	4.48	ChemAxon
pKa (Strongest Basic)	-1.6	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	4	ChemAxon
Polar Surface Area	97.99 Å²	ChemAxon
Rotatable Bond Count	14	ChemAxon
Refractivity	104.35 m³·mol⁻¹	ChemAxon
Polarizability	42.04 Å³	ChemAxon
Number of Rings	0	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

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

162876108

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid (NP0208094)

MOL for NP0208094 ((5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid)

3D MOL for NP0208094 ((5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid)

3D SDF for NP0208094 ((5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid)

3D-SDF for NP0208094 ((5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid)

PDB for NP0208094 ((5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid)

3D PDB for NP0208094 ((5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid)

SMILES for NP0208094 ((5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid)

INCHI for NP0208094 ((5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid)

Structure for NP0208094 ((5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid)

3D Structure for NP0208094 ((5s,6r,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoic acid)