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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2012-09-11 21:54:39 UTC

Update Date

2022-03-07 02:55:02 UTC

HMDB ID

HMDB0036741

Secondary Accession Numbers

HMDB36741

Metabolite Identification

Common Name

1-Hydroxy-2,12,15-heneicosatrien-4-one

Description

1-Hydroxy-2,12,15-heneicosatrien-4-one belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms. Thus, 1-hydroxy-2,12,15-heneicosatrien-4-one is considered to be a fatty alcohol. Based on a literature review a small amount of articles have been published on 1-Hydroxy-2,12,15-heneicosatrien-4-one.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI

HMDB0036741
     RDKit          3D
1-Hydroxy-2,12,15-heneicosatrien-4-one
 59 58  0  0  0  0  0  0  0  0999 V2000
   -8.3745   -1.9330    1.7066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3276   -1.4129    2.6666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2976   -0.5539    1.9812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3123   -0.0929    3.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2315    0.7910    2.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5106    0.0162    1.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5194    0.4427    0.0912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8225   -0.2852   -0.9766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7662    0.5322   -1.6488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5080    1.7726   -1.3007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5355    2.7039   -1.8256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4202    2.2980   -2.8588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3959    1.2720   -2.3448 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3633    0.8485   -3.4344 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3062   -0.1714   -2.9024 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1058    0.3605   -1.7537 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0732   -0.6915   -1.2266 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8421   -0.1214   -0.0921 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6322    1.0629    0.2799 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8448   -0.9031    0.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5503   -0.4522    1.6155 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5682   -1.3397    2.2818 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2712   -1.5142    3.6121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9277   -2.4718    0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0743   -2.5564    2.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9857   -1.1043    1.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8034   -0.8164    3.4580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8332   -2.2993    3.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7977    0.3366    1.5414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8123   -1.0847    1.1394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7750   -0.9594    3.4543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8513    0.4829    3.7838 H   0  0  0  0  0  0  0  0  0  0  0  0
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    3.4807    0.6501   -0.8815 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4099    0.5405    1.9663 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5515   -0.8624    2.1002 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5662   -2.3415    1.7874 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1210   -1.4842    4.1249 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  2  0
  7  8  1  0
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  9 10  2  0
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  1 24  1  0
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  2 27  1  0
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  3 29  1  0
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  5 34  1  0
  6 35  1  0
  7 36  1  0
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 20 55  1  0
 21 56  1  0
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 22 58  1  0
 23 59  1  0
M  END


  Mrv0541 02241209392D          

 23 22  0  0  0  0            999 V2000
   -7.5036    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7890    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0744    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3598    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6451    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9304    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2158    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5012    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7866    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0719    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3573    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3573    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0719    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7866    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5012    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2158    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9304    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6451    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3598    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0744    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7890    0.6184    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6451   -0.6184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5036    0.2062    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  2  0  0  0  0
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  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
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 12 13  1  0  0  0  0
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 18 22  2  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 23  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0036741

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCC\C=C\C\C=C\CCCCCCCC(=O)\C=C\CO

> <INCHI_IDENTIFIER>
InChI=1S/C21H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-18-21(23)19-17-20-22/h6-7,9-10,17,19,22H,2-5,8,11-16,18,20H2,1H3/b7-6+,10-9+,19-17+

> <INCHI_KEY>
HYSAQRFMZWHDTN-ZLMPDQHQSA-N

> <FORMULA>
C21H36O2

> <MOLECULAR_WEIGHT>
320.5093

> <EXACT_MASS>
320.271530396

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_AVERAGE_POLARIZABILITY>
40.55856146709888

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E,12E,15E)-1-hydroxyhenicosa-2,12,15-trien-4-one

> <ALOGPS_LOGP>
6.66

> <JCHEM_LOGP>
6.613659162

> <ALOGPS_LOGS>
-6.31

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
15.595553874363596

> <JCHEM_PKA_STRONGEST_BASIC>
-2.538304735353363

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
104.16579999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
16

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.55e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2E,12E,15E)-1-hydroxyhenicosa-2,12,15-trien-4-one

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0036741
     RDKit          3D
1-Hydroxy-2,12,15-heneicosatrien-4-one
 59 58  0  0  0  0  0  0  0  0999 V2000
   -8.3745   -1.9330    1.7066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3276   -1.4129    2.6666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2976   -0.5539    1.9812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3123   -0.0929    3.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2315    0.7910    2.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5106    0.0162    1.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5194    0.4427    0.0912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8225   -0.2852   -0.9766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7662    0.5322   -1.6488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5080    1.7726   -1.3007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5355    2.7039   -1.8256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4202    2.2980   -2.8588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3959    1.2720   -2.3448 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3633    0.8485   -3.4344 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3062   -0.1714   -2.9024 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1058    0.3605   -1.7537 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0732   -0.6915   -1.2266 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8421   -0.1214   -0.0921 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6322    1.0629    0.2799 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8448   -0.9031    0.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5503   -0.4522    1.6155 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5682   -1.3397    2.2818 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2712   -1.5142    3.6121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9277   -2.4718    0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0743   -2.5564    2.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9857   -1.1043    1.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8034   -0.8164    3.4580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8332   -2.2993    3.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7977    0.3366    1.5414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8123   -1.0847    1.1394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7750   -0.9594    3.4543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8513    0.4829    3.7838 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.0300    2.0007   -3.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8783    0.4150   -1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.7329    0.4047   -4.2440 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8576    1.7250   -3.8813 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0080   -0.4637   -3.7077 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6973   -1.0599   -2.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6688    1.2516   -2.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4807    0.6501   -0.8815 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5124   -1.5578   -0.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7386   -1.0624   -2.0363 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0205   -1.9189    0.2874 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4099    0.5405    1.9663 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5515   -0.8624    2.1002 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5662   -2.3415    1.7874 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1210   -1.4842    4.1249 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  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  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  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 15 50  1  0
 16 51  1  0
 16 52  1  0
 17 53  1  0
 17 54  1  0
 20 55  1  0
 21 56  1  0
 22 57  1  0
 22 58  1  0
 23 59  1  0
M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0     -14.007   1.154   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -12.673   0.385   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -11.339   1.154   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.005   0.385   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -8.671   1.154   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -7.337   0.385   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -6.003   1.154   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -4.669   0.385   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      -3.335   1.154   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.001   0.385   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.667   1.154   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.667   0.385   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.001   1.154   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.335   0.385   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.669   1.154   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.003   0.385   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       7.337   1.154   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.671   0.385   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      10.005   1.154   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      11.339   0.385   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      12.673   1.154   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       8.671  -1.154   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      14.007   0.385   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                                                       
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   22                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   23                                                       
CONECT   22   18                                                            
CONECT   23   21                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   44    0
END

COMPND    HMDB0036741
HETATM    1  C1  UNL     1      -8.375  -1.933   1.707  1.00  0.00           C  
HETATM    2  C2  UNL     1      -7.328  -1.413   2.667  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.298  -0.554   1.981  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.312  -0.093   3.018  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.231   0.791   2.381  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.511   0.016   1.344  1.00  0.00           C  
HETATM    7  C7  UNL     1      -3.519   0.443   0.091  1.00  0.00           C  
HETATM    8  C8  UNL     1      -2.822  -0.285  -0.977  1.00  0.00           C  
HETATM    9  C9  UNL     1      -1.766   0.532  -1.649  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.508   1.773  -1.301  1.00  0.00           C  
HETATM   11  C11 UNL     1      -0.535   2.704  -1.826  1.00  0.00           C  
HETATM   12  C12 UNL     1       0.420   2.298  -2.859  1.00  0.00           C  
HETATM   13  C13 UNL     1       1.396   1.272  -2.345  1.00  0.00           C  
HETATM   14  C14 UNL     1       2.363   0.848  -3.434  1.00  0.00           C  
HETATM   15  C15 UNL     1       3.306  -0.171  -2.902  1.00  0.00           C  
HETATM   16  C16 UNL     1       4.106   0.360  -1.754  1.00  0.00           C  
HETATM   17  C17 UNL     1       5.073  -0.691  -1.227  1.00  0.00           C  
HETATM   18  C18 UNL     1       5.842  -0.121  -0.092  1.00  0.00           C  
HETATM   19  O1  UNL     1       5.632   1.063   0.280  1.00  0.00           O  
HETATM   20  C19 UNL     1       6.845  -0.903   0.611  1.00  0.00           C  
HETATM   21  C20 UNL     1       7.550  -0.452   1.615  1.00  0.00           C  
HETATM   22  C21 UNL     1       8.568  -1.340   2.282  1.00  0.00           C  
HETATM   23  O2  UNL     1       8.271  -1.514   3.612  1.00  0.00           O  
HETATM   24  H1  UNL     1      -7.928  -2.472   0.870  1.00  0.00           H  
HETATM   25  H2  UNL     1      -9.074  -2.556   2.298  1.00  0.00           H  
HETATM   26  H3  UNL     1      -8.986  -1.104   1.287  1.00  0.00           H  
HETATM   27  H4  UNL     1      -7.803  -0.816   3.458  1.00  0.00           H  
HETATM   28  H5  UNL     1      -6.833  -2.299   3.116  1.00  0.00           H  
HETATM   29  H6  UNL     1      -6.798   0.337   1.541  1.00  0.00           H  
HETATM   30  H7  UNL     1      -5.812  -1.085   1.139  1.00  0.00           H  
HETATM   31  H8  UNL     1      -4.775  -0.959   3.454  1.00  0.00           H  
HETATM   32  H9  UNL     1      -5.851   0.483   3.784  1.00  0.00           H  
HETATM   33  H10 UNL     1      -3.489   1.085   3.146  1.00  0.00           H  
HETATM   34  H11 UNL     1      -4.678   1.694   1.945  1.00  0.00           H  
HETATM   35  H12 UNL     1      -2.979  -0.890   1.593  1.00  0.00           H  
HETATM   36  H13 UNL     1      -4.061   1.354  -0.131  1.00  0.00           H  
HETATM   37  H14 UNL     1      -2.379  -1.226  -0.602  1.00  0.00           H  
HETATM   38  H15 UNL     1      -3.570  -0.532  -1.775  1.00  0.00           H  
HETATM   39  H16 UNL     1      -1.229   0.092  -2.459  1.00  0.00           H  
HETATM   40  H17 UNL     1      -2.143   2.149  -0.474  1.00  0.00           H  
HETATM   41  H18 UNL     1      -1.091   3.651  -2.089  1.00  0.00           H  
HETATM   42  H19 UNL     1       0.089   3.049  -0.932  1.00  0.00           H  
HETATM   43  H20 UNL     1       1.029   3.215  -3.132  1.00  0.00           H  
HETATM   44  H21 UNL     1      -0.030   2.001  -3.831  1.00  0.00           H  
HETATM   45  H22 UNL     1       0.878   0.415  -1.934  1.00  0.00           H  
HETATM   46  H23 UNL     1       1.980   1.814  -1.525  1.00  0.00           H  
HETATM   47  H24 UNL     1       1.733   0.405  -4.244  1.00  0.00           H  
HETATM   48  H25 UNL     1       2.858   1.725  -3.881  1.00  0.00           H  
HETATM   49  H26 UNL     1       4.008  -0.464  -3.708  1.00  0.00           H  
HETATM   50  H27 UNL     1       2.697  -1.060  -2.586  1.00  0.00           H  
HETATM   51  H28 UNL     1       4.669   1.252  -2.078  1.00  0.00           H  
HETATM   52  H29 UNL     1       3.481   0.650  -0.881  1.00  0.00           H  
HETATM   53  H30 UNL     1       4.512  -1.558  -0.826  1.00  0.00           H  
HETATM   54  H31 UNL     1       5.739  -1.062  -2.036  1.00  0.00           H  
HETATM   55  H32 UNL     1       7.020  -1.919   0.287  1.00  0.00           H  
HETATM   56  H33 UNL     1       7.410   0.540   1.966  1.00  0.00           H  
HETATM   57  H34 UNL     1       9.552  -0.862   2.100  1.00  0.00           H  
HETATM   58  H35 UNL     1       8.566  -2.342   1.787  1.00  0.00           H  
HETATM   59  H36 UNL     1       9.121  -1.484   4.125  1.00  0.00           H  
CONECT    1    2   24   25   26
CONECT    2    3   27   28
CONECT    3    4   29   30
CONECT    4    5   31   32
CONECT    5    6   33   34
CONECT    6    7    7   35
CONECT    7    8   36
CONECT    8    9   37   38
CONECT    9   10   10   39
CONECT   10   11   40
CONECT   11   12   41   42
CONECT   12   13   43   44
CONECT   13   14   45   46
CONECT   14   15   47   48
CONECT   15   16   49   50
CONECT   16   17   51   52
CONECT   17   18   53   54
CONECT   18   19   19   20
CONECT   20   21   21   55
CONECT   21   22   56
CONECT   22   23   57   58
CONECT   23   59
END

HMDB0036741
     RDKit          3D
1-Hydroxy-2,12,15-heneicosatrien-4-one
 59 58  0  0  0  0  0  0  0  0999 V2000
   -8.3745   -1.9330    1.7066 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3276   -1.4129    2.6666 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2976   -0.5539    1.9812 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3123   -0.0929    3.0184 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2315    0.7910    2.3814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5106    0.0162    1.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5194    0.4427    0.0912 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8225   -0.2852   -0.9766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7662    0.5322   -1.6488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5080    1.7726   -1.3007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5355    2.7039   -1.8256 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4202    2.2980   -2.8588 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3959    1.2720   -2.3448 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3633    0.8485   -3.4344 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3062   -0.1714   -2.9024 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1058    0.3605   -1.7537 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0732   -0.6915   -1.2266 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8421   -0.1214   -0.0921 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6322    1.0629    0.2799 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8448   -0.9031    0.6113 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5503   -0.4522    1.6155 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5682   -1.3397    2.2818 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2712   -1.5142    3.6121 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9277   -2.4718    0.8700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0743   -2.5564    2.2984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9857   -1.1043    1.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8034   -0.8164    3.4580 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8332   -2.2993    3.1165 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7977    0.3366    1.5414 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8123   -1.0847    1.1394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7750   -0.9594    3.4543 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8513    0.4829    3.7838 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4890    1.0848    3.1464 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6780    1.6935    1.9449 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9790   -0.8899    1.5933 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0607    1.3544   -0.1305 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3786   -1.2261   -0.6024 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5702   -0.5317   -1.7754 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2291    0.0922   -2.4590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1430    2.1487   -0.4745 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0907    3.6511   -2.0892 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0885    3.0495   -0.9323 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0293    3.2146   -3.1321 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0300    2.0007   -3.8312 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8783    0.4150   -1.9335 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9799    1.8139   -1.5245 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7329    0.4047   -4.2440 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8576    1.7250   -3.8813 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0080   -0.4637   -3.7077 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6973   -1.0599   -2.5857 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6688    1.2516   -2.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4807    0.6501   -0.8815 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5124   -1.5578   -0.8258 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7386   -1.0624   -2.0363 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0205   -1.9189    0.2874 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4099    0.5405    1.9663 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5515   -0.8624    2.1002 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5662   -2.3415    1.7874 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.1210   -1.4842    4.1249 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  2  0
  7  8  1  0
  8  9  1  0
  9 10  2  0
 10 11  1  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  2  0
 18 20  1  0
 20 21  2  0
 21 22  1  0
 22 23  1  0
  1 24  1  0
  1 25  1  0
  1 26  1  0
  2 27  1  0
  2 28  1  0
  3 29  1  0
  3 30  1  0
  4 31  1  0
  4 32  1  0
  5 33  1  0
  5 34  1  0
  6 35  1  0
  7 36  1  0
  8 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  0
 11 41  1  0
 11 42  1  0
 12 43  1  0
 12 44  1  0
 13 45  1  0
 13 46  1  0
 14 47  1  0
 14 48  1  0
 15 49  1  0
 15 50  1  0
 16 51  1  0
 16 52  1  0
 17 53  1  0
 17 54  1  0
 20 55  1  0
 21 56  1  0
 22 57  1  0
 22 58  1  0
 23 59  1  0
M  END

View in JSmol View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₂₁H₃₆O₂

Average Molecular Weight

320.5093

Monoisotopic Molecular Weight

320.271530396

IUPAC Name

(2E,12E,15E)-1-hydroxyhenicosa-2,12,15-trien-4-one

Traditional Name

(2E,12E,15E)-1-hydroxyhenicosa-2,12,15-trien-4-one

CAS Registry Number

Not Available

SMILES

CCCCC\C=C\C\C=C\CCCCCCCC(=O)\C=C\CO

InChI Identifier

InChI=1S/C21H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-18-21(23)19-17-20-22/h6-7,9-10,17,19,22H,2-5,8,11-16,18,20H2,1H3/b7-6+,10-9+,19-17+

InChI Key

HYSAQRFMZWHDTN-ZLMPDQHQSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty alcohols. These are fatty alcohols that have an aliphatic tail of 13 to 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty alcohols

Direct Parent

Long-chain fatty alcohols

Alternative Parents

Substituents

Long chain fatty alcohol
Alpha,beta-unsaturated ketone
Enone
Acryloyl-group
Ketone
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Primary alcohol
Organooxygen compound
Carbonyl group
Alcohol
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Excreta

Biofluid or Excreta

Urine (HMDB: HMDB0036741)

Route of exposure

Enteral

Ingestion (HMDB: HMDB0036741)

Source

Endogenous

Endogenous (HMDB: HMDB0036741)

Plant

Plant (HMDB: HMDB0036741)

Animal

Animal (HMDB: HMDB0036741)

Exogenous

Food

Food (HMDB: HMDB0036741)

Fruit

Fruits (FooDB: FOOD00871)

Exogenous (HMDB: HMDB0036741)

Process

Naturally occurring process

Biological process

Chemical reaction

Lipid Peroxidation (HMDB: HMDB0036741)

Biochemical pathway

Metabolic pathway

Fatty Acid Metabolism (HMDB: HMDB0036741)

Lipid metabolism pathway (HMDB: HMDB0036741)

Cellular process

Cell signaling (HMDB: HMDB0036741)

Biochemical process

Lipid transport (HMDB: HMDB0036741)

Role

Biological role

Energy source (HMDB: HMDB0036741)

Industrial application

Manufacturing industry

Material processing agent

Fluid processing agent

Surfactant

Surfactant (HMDB: HMDB0036741)

Physical Properties

State

Not Available

Experimental Molecular 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

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.00016 g/L	ALOGPS
logP	6.66	ALOGPS
logP	6.61	ChemAxon
logS	-6.3	ALOGPS
pKa (Strongest Acidic)	15.6	ChemAxon
pKa (Strongest Basic)	-2.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	16	ChemAxon
Refractivity	104.17 m³·mol⁻¹	ChemAxon
Polarizability	40.56 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

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	190.051	30932474
DeepCCS	[M-H]-	187.693	30932474
DeepCCS	[M-2H]-	220.7	30932474
DeepCCS	[M+Na]+	196.39	30932474
AllCCS	[M+H]+	188.8	32859911
AllCCS	[M+H-H2O]+	186.0	32859911
AllCCS	[M+NH4]+	191.4	32859911
AllCCS	[M+Na]+	192.1	32859911
AllCCS	[M-H]-	188.9	32859911
AllCCS	[M+Na-2H]-	191.0	32859911
AllCCS	[M+HCOO]-	193.4	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
1-Hydroxy-2,12,15-heneicosatrien-4-one	CCCCC\C=C\C\C=C\CCCCCCCC(=O)\C=C\CO	3169.6	Standard polar	33892256
1-Hydroxy-2,12,15-heneicosatrien-4-one	CCCCC\C=C\C\C=C\CCCCCCCC(=O)\C=C\CO	2411.1	Standard non polar	33892256
1-Hydroxy-2,12,15-heneicosatrien-4-one	CCCCC\C=C\C\C=C\CCCCCCCC(=O)\C=C\CO	2573.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
1-Hydroxy-2,12,15-heneicosatrien-4-one,1TMS,isomer #1	CCCCC/C=C/C/C=C/CCCCCCCC(=O)/C=C/CO[Si](C)(C)C	2659.2	Semi standard non polar	33892256
1-Hydroxy-2,12,15-heneicosatrien-4-one,1TMS,isomer #2	CCCCC/C=C/C/C=C/CCCCCCC=C(/C=C/CO)O[Si](C)(C)C	2717.7	Semi standard non polar	33892256
1-Hydroxy-2,12,15-heneicosatrien-4-one,2TMS,isomer #1	CCCCC/C=C/C/C=C/CCCCCCC=C(/C=C/CO[Si](C)(C)C)O[Si](C)(C)C	2787.9	Semi standard non polar	33892256
1-Hydroxy-2,12,15-heneicosatrien-4-one,2TMS,isomer #1	CCCCC/C=C/C/C=C/CCCCCCC=C(/C=C/CO[Si](C)(C)C)O[Si](C)(C)C	2664.8	Standard non polar	33892256
1-Hydroxy-2,12,15-heneicosatrien-4-one,1TBDMS,isomer #1	CCCCC/C=C/C/C=C/CCCCCCCC(=O)/C=C/CO[Si](C)(C)C(C)(C)C	2888.3	Semi standard non polar	33892256
1-Hydroxy-2,12,15-heneicosatrien-4-one,1TBDMS,isomer #2	CCCCC/C=C/C/C=C/CCCCCCC=C(/C=C/CO)O[Si](C)(C)C(C)(C)C	2963.2	Semi standard non polar	33892256
1-Hydroxy-2,12,15-heneicosatrien-4-one,2TBDMS,isomer #1	CCCCC/C=C/C/C=C/CCCCCCC=C(/C=C/CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	3270.7	Semi standard non polar	33892256
1-Hydroxy-2,12,15-heneicosatrien-4-one,2TBDMS,isomer #1	CCCCC/C=C/C/C=C/CCCCCCC=C(/C=C/CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	2994.5	Standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one GC-MS (Non-derivatized) - 70eV, Positive	splash10-000i-9320000000-7f5c4a565830980e9be3	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one GC-MS (1 TMS) - 70eV, Positive	splash10-0a4i-4913000000-a53bcf4a7d92edb1a428	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 10V, Positive-QTOF	splash10-0uk9-1029000000-3d4951dbf9a874b49418	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 20V, Positive-QTOF	splash10-0fki-9474000000-9e94593fa3deb0f96a92	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 40V, Positive-QTOF	splash10-052o-9770000000-7ec8438668db65218e2c	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 10V, Negative-QTOF	splash10-014i-1029000000-57936c8f4caa2f2a18a1	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 20V, Negative-QTOF	splash10-014r-9067000000-2e4261cddcb1ad64aabb	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 40V, Negative-QTOF	splash10-0007-9020000000-b541bd2d425dfbcffc0d	2016-08-03	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 10V, Positive-QTOF	splash10-00di-3339000000-7312dbf32ad34976a061	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 20V, Positive-QTOF	splash10-001i-9812000000-0a90be679c4bbeb88e7c	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 40V, Positive-QTOF	splash10-05o4-9300000000-6511028af6c1a296bdd7	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 10V, Negative-QTOF	splash10-014i-0009000000-7d8230d8e42cf8b18941	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 20V, Negative-QTOF	splash10-014i-8039000000-f28cb46564b48798bb75	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 1-Hydroxy-2,12,15-heneicosatrien-4-one 40V, Negative-QTOF	splash10-0a4i-9111000000-d8fcc80397cf75867a8d	2021-09-23	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB015679

KNApSAcK ID

Not Available

Chemspider ID

10722211

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

21964639

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
(). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 1-Hydroxy-2,12,15-heneicosatrien-4-one (HMDB0036741)

MOL for HMDB0036741 (1-Hydroxy-2,12,15-heneicosatrien-4-one)

3D MOL for HMDB0036741 (1-Hydroxy-2,12,15-heneicosatrien-4-one)

3D SDF for HMDB0036741 (1-Hydroxy-2,12,15-heneicosatrien-4-one)

3D-SDF for HMDB0036741 (1-Hydroxy-2,12,15-heneicosatrien-4-one)

PDB for HMDB0036741 (1-Hydroxy-2,12,15-heneicosatrien-4-one)

3D PDB for HMDB0036741 (1-Hydroxy-2,12,15-heneicosatrien-4-one)

SMILES for HMDB0036741 (1-Hydroxy-2,12,15-heneicosatrien-4-one)

INCHI for HMDB0036741 (1-Hydroxy-2,12,15-heneicosatrien-4-one)

Structure for HMDB0036741 (1-Hydroxy-2,12,15-heneicosatrien-4-one)

3D Structure for HMDB0036741 (1-Hydroxy-2,12,15-heneicosatrien-4-one)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra