MiMeDB: Showing metabocard for Trans-Hexa-dec-2-enoic acid (MMDBc0047819)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-19 15:44:14 UTC

Update Date

2024-04-30 20:30:55 UTC

Metabolite ID

MMDBc0047819

Metabolite Identification

Common Name

Trans-Hexa-dec-2-enoic acid

Description

In humans fatty acids are predominantly formed in the liver and adipose tissue, and mammary glands during lactation. Trans-hexa-dec-2-enoic acid is an intermediate in fatty acid biosynthesis. Specifically, trans-hexa-dec-2-enoic acid converted from (R)-3-Hydroxy-hexadecanoic acid via two enzymes; fatty-acid Synthase and 3- Hydroxypalmitoyl- [acyl-carrier-protein] dehydratase (EC: 2.3.1.85 and EC: 4.2.1.61).

Structure

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

HMDB0010735
     RDKit          3D
Trans-Hexa-dec-2-enoic acid
 48 47  0  0  0  0  0  0  0  0999 V2000
    6.1887    2.4869    0.3943 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9550    2.5913   -0.4464 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2896    1.2766   -0.6992 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8431    0.5610    0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1924   -0.7474    0.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7198   -1.5153    1.2928 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0821   -2.7961    0.8639 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8947   -2.6256   -0.0292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1685   -1.8258    0.6834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3893   -1.6314   -0.1896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4081   -0.8264    0.5835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6498   -0.6083   -0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6430    0.1979    0.5463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8787    0.4345   -0.2442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2902    1.6502   -0.5334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4929    1.9221   -1.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2004    0.9763   -1.7316 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8599    3.2235   -1.5666 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0642    2.1167   -0.2156 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4975    3.5085    0.7225 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0971    1.8007    1.2347 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2846    2.9792   -1.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2800    3.3569   -0.0432 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3852    1.4962   -1.3393 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9225    0.6181   -1.2995 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7433    0.2805    1.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1738    1.1369    1.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3231   -0.4760   -0.5278 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9323   -1.3888   -0.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0186   -0.8955    1.8522 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5553   -1.7679    1.9769 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7058   -3.2994    1.8030 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8305   -3.4965    0.4487 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1306   -2.1935   -1.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4683   -3.6343   -0.2148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4049   -2.2706    1.6543 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2333   -0.7907    0.8731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7904   -2.6091   -0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0638   -1.0958   -1.0910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6737   -1.3412    1.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9577    0.1428    0.8656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3553   -0.0972   -1.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1398   -1.5539   -0.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1987    1.1525    0.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9070   -0.4119    1.4366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4624   -0.4041   -0.5959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6786    2.4662   -0.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1983    3.9269   -1.8916 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
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 18 48  1  0
M  END


  Mrv1652307301920022D          

 20 19  0  0  0  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
   15.4756    4.8099    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.1901    3.5724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.0467    4.8099    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.7612    2.7474    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  4  3  1  0  0  0  0
  5  4  1  0  0  0  0
  6  5  1  0  0  0  0
  7  6  1  0  0  0  0
  8  7  1  0  0  0  0
  9  8  1  0  0  0  0
 10  9  1  0  0  0  0
 11 10  1  0  0  0  0
 12 11  1  0  0  0  0
 13 12  1  0  0  0  0
 14 13  1  0  0  0  0
 15 14  2  0  0  0  0
 16 15  1  0  0  0  0
 17 16  2  0  0  0  0
 18 16  1  0  0  0  0
 19 14  1  0  0  0  0
 20 15  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0047819

> <DATABASE_NAME>
MIME

> <SMILES>
[H]\C(CCCCCCCCCCCCC)=C(\[H])C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h14-15H,2-13H2,1H3,(H,17,18)/b15-14+

> <INCHI_KEY>
ZVRMGCSSSYZGSM-CCEZHUSRSA-N

> <FORMULA>
C16H30O2

> <MOLECULAR_WEIGHT>
254.4082

> <EXACT_MASS>
254.224580204

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
48

> <JCHEM_AVERAGE_POLARIZABILITY>
33.74415362299203

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2E)-hexadec-2-enoic acid

> <JCHEM_LOGP>
6.254406267333333

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.0255044264493

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
78.17689999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
13

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
hexadecenoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0010735
     RDKit          3D
Trans-Hexa-dec-2-enoic acid
 48 47  0  0  0  0  0  0  0  0999 V2000
    6.1887    2.4869    0.3943 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9550    2.5913   -0.4464 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2896    1.2766   -0.6992 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8431    0.5610    0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1924   -0.7474    0.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7198   -1.5153    1.2928 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0821   -2.7961    0.8639 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8947   -2.6256   -0.0292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1685   -1.8258    0.6834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3893   -1.6314   -0.1896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4081   -0.8264    0.5835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6498   -0.6083   -0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6430    0.1979    0.5463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8787    0.4345   -0.2442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2902    1.6502   -0.5334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4929    1.9221   -1.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2004    0.9763   -1.7316 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8599    3.2235   -1.5666 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0642    2.1167   -0.2156 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4975    3.5085    0.7225 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0971    1.8007    1.2347 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2846    2.9792   -1.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2800    3.3569   -0.0432 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3852    1.4962   -1.3393 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9225    0.6181   -1.2995 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7433    0.2805    1.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1738    1.1369    1.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3231   -0.4760   -0.5278 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9323   -1.3888   -0.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0186   -0.8955    1.8522 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5553   -1.7679    1.9769 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7058   -3.2994    1.8030 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8305   -3.4965    0.4487 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1306   -2.1935   -1.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4683   -3.6343   -0.2148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4049   -2.2706    1.6543 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2333   -0.7907    0.8731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7904   -2.6091   -0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0638   -1.0958   -1.0910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6737   -1.3412    1.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9577    0.1428    0.8656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3553   -0.0972   -1.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1398   -1.5539   -0.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1987    1.1525    0.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9070   -0.4119    1.4366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4624   -0.4041   -0.5959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6786    2.4662   -0.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1983    3.9269   -1.8916 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
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 18 48  1  0
M  END

HEADER    PROTEIN                                 30-JUL-19   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   30-JUL-19         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      26.221   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  O   UNK     0      28.888   8.978   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      30.222   6.668   0.000  0.00  0.00           O+0
HETATM   19  H   UNK     0      26.221   8.978   0.000  0.00  0.00           H+0
HETATM   20  H   UNK     0      27.554   5.128   0.000  0.00  0.00           H+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   19                                                  
CONECT   15   14   16   20                                                  
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   14                                                            
CONECT   20   15                                                            
MASTER        0    0    0    0    0    0    0    0   20    0   38    0
END

COMPND    HMDB0010735
HETATM    1  C1  UNL     1       6.189   2.487   0.394  1.00  0.00           C  
HETATM    2  C2  UNL     1       4.955   2.591  -0.446  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.290   1.277  -0.699  1.00  0.00           C  
HETATM    4  C4  UNL     1       3.843   0.561   0.531  1.00  0.00           C  
HETATM    5  C5  UNL     1       3.192  -0.747   0.081  1.00  0.00           C  
HETATM    6  C6  UNL     1       2.720  -1.515   1.293  1.00  0.00           C  
HETATM    7  C7  UNL     1       2.082  -2.796   0.864  1.00  0.00           C  
HETATM    8  C8  UNL     1       0.895  -2.626  -0.029  1.00  0.00           C  
HETATM    9  C9  UNL     1      -0.169  -1.826   0.683  1.00  0.00           C  
HETATM   10  C10 UNL     1      -1.389  -1.631  -0.190  1.00  0.00           C  
HETATM   11  C11 UNL     1      -2.408  -0.826   0.583  1.00  0.00           C  
HETATM   12  C12 UNL     1      -3.650  -0.608  -0.257  1.00  0.00           C  
HETATM   13  C13 UNL     1      -4.643   0.198   0.546  1.00  0.00           C  
HETATM   14  C14 UNL     1      -5.879   0.435  -0.244  1.00  0.00           C  
HETATM   15  C15 UNL     1      -6.290   1.650  -0.533  1.00  0.00           C  
HETATM   16  C16 UNL     1      -7.493   1.922  -1.304  1.00  0.00           C  
HETATM   17  O1  UNL     1      -8.200   0.976  -1.732  1.00  0.00           O  
HETATM   18  O2  UNL     1      -7.860   3.223  -1.567  1.00  0.00           O  
HETATM   19  H1  UNL     1       7.064   2.117  -0.216  1.00  0.00           H  
HETATM   20  H2  UNL     1       6.497   3.509   0.722  1.00  0.00           H  
HETATM   21  H3  UNL     1       6.097   1.801   1.235  1.00  0.00           H  
HETATM   22  H4  UNL     1       5.285   2.979  -1.452  1.00  0.00           H  
HETATM   23  H5  UNL     1       4.280   3.357  -0.043  1.00  0.00           H  
HETATM   24  H6  UNL     1       3.385   1.496  -1.339  1.00  0.00           H  
HETATM   25  H7  UNL     1       4.922   0.618  -1.300  1.00  0.00           H  
HETATM   26  H8  UNL     1       4.743   0.281   1.139  1.00  0.00           H  
HETATM   27  H9  UNL     1       3.174   1.137   1.166  1.00  0.00           H  
HETATM   28  H10 UNL     1       2.323  -0.476  -0.528  1.00  0.00           H  
HETATM   29  H11 UNL     1       3.932  -1.389  -0.435  1.00  0.00           H  
HETATM   30  H12 UNL     1       2.019  -0.895   1.852  1.00  0.00           H  
HETATM   31  H13 UNL     1       3.555  -1.768   1.977  1.00  0.00           H  
HETATM   32  H14 UNL     1       1.706  -3.299   1.803  1.00  0.00           H  
HETATM   33  H15 UNL     1       2.831  -3.496   0.449  1.00  0.00           H  
HETATM   34  H16 UNL     1       1.131  -2.194  -1.009  1.00  0.00           H  
HETATM   35  H17 UNL     1       0.468  -3.634  -0.215  1.00  0.00           H  
HETATM   36  H18 UNL     1      -0.405  -2.271   1.654  1.00  0.00           H  
HETATM   37  H19 UNL     1       0.233  -0.791   0.873  1.00  0.00           H  
HETATM   38  H20 UNL     1      -1.790  -2.609  -0.493  1.00  0.00           H  
HETATM   39  H21 UNL     1      -1.064  -1.096  -1.091  1.00  0.00           H  
HETATM   40  H22 UNL     1      -2.674  -1.341   1.518  1.00  0.00           H  
HETATM   41  H23 UNL     1      -1.958   0.143   0.866  1.00  0.00           H  
HETATM   42  H24 UNL     1      -3.355  -0.097  -1.188  1.00  0.00           H  
HETATM   43  H25 UNL     1      -4.140  -1.554  -0.526  1.00  0.00           H  
HETATM   44  H26 UNL     1      -4.199   1.152   0.874  1.00  0.00           H  
HETATM   45  H27 UNL     1      -4.907  -0.412   1.437  1.00  0.00           H  
HETATM   46  H28 UNL     1      -6.462  -0.404  -0.596  1.00  0.00           H  
HETATM   47  H29 UNL     1      -5.679   2.466  -0.163  1.00  0.00           H  
HETATM   48  H30 UNL     1      -7.198   3.927  -1.892  1.00  0.00           H  
CONECT    1    2   19   20   21
CONECT    2    3   22   23
CONECT    3    4   24   25
CONECT    4    5   26   27
CONECT    5    6   28   29
CONECT    6    7   30   31
CONECT    7    8   32   33
CONECT    8    9   34   35
CONECT    9   10   36   37
CONECT   10   11   38   39
CONECT   11   12   40   41
CONECT   12   13   42   43
CONECT   13   14   44   45
CONECT   14   15   15   46
CONECT   15   16   47
CONECT   16   17   17   18
CONECT   18   48
END

HMDB0010735
     RDKit          3D
Trans-Hexa-dec-2-enoic acid
 48 47  0  0  0  0  0  0  0  0999 V2000
    6.1887    2.4869    0.3943 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9550    2.5913   -0.4464 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2896    1.2766   -0.6992 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8431    0.5610    0.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1924   -0.7474    0.0813 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7198   -1.5153    1.2928 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0821   -2.7961    0.8639 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8947   -2.6256   -0.0292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1685   -1.8258    0.6834 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3893   -1.6314   -0.1896 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4081   -0.8264    0.5835 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6498   -0.6083   -0.2570 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6430    0.1979    0.5463 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8787    0.4345   -0.2442 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2902    1.6502   -0.5334 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4929    1.9221   -1.3037 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2004    0.9763   -1.7316 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8599    3.2235   -1.5666 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0642    2.1167   -0.2156 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4975    3.5085    0.7225 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0971    1.8007    1.2347 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2846    2.9792   -1.4523 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2800    3.3569   -0.0432 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3852    1.4962   -1.3393 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9225    0.6181   -1.2995 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7433    0.2805    1.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1738    1.1369    1.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3231   -0.4760   -0.5278 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9323   -1.3888   -0.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0186   -0.8955    1.8522 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5553   -1.7679    1.9769 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7058   -3.2994    1.8030 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8305   -3.4965    0.4487 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1306   -2.1935   -1.0095 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4683   -3.6343   -0.2148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4049   -2.2706    1.6543 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2333   -0.7907    0.8731 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7904   -2.6091   -0.4927 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0638   -1.0958   -1.0910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6737   -1.3412    1.5182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9577    0.1428    0.8656 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3553   -0.0972   -1.1879 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1398   -1.5539   -0.5263 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1987    1.1525    0.8743 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9070   -0.4119    1.4366 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4624   -0.4041   -0.5959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6786    2.4662   -0.1634 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1983    3.9269   -1.8916 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
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  2  0
 16 18  1  0
  1 19  1  0
  1 20  1  0
  1 21  1  0
  2 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  4 26  1  0
  4 27  1  0
  5 28  1  0
  5 29  1  0
  6 30  1  0
  6 31  1  0
  7 32  1  0
  7 33  1  0
  8 34  1  0
  8 35  1  0
  9 36  1  0
  9 37  1  0
 10 38  1  0
 10 39  1  0
 11 40  1  0
 11 41  1  0
 12 42  1  0
 12 43  1  0
 13 44  1  0
 13 45  1  0
 14 46  1  0
 15 47  1  0
 18 48  1  0
M  END

Synonyms

Value	Source
trans-Hexa-dec-2-enoate	Generator
(2E)-Hexadecenoic acid	ChEBI
(e)-2-Hexadecenoic acid	ChEBI
2-Palmitoleic acid	ChEBI
2-trans-Hexadecenoic acid	ChEBI
Gaidic acid	ChEBI
t-16:1D2	ChEBI
t-2-Hexadecenoic acid	ChEBI
trans-2-Hexadecenoic acid	ChEBI
trans-Delta(2)-Hexadecenoic acid	ChEBI
trans-Hexadec-2-enoic acid	ChEBI
(2E)-Hexadecenoate	Generator
(e)-2-Hexadecenoate	Generator
2-Palmitoleate	Generator
2-trans-Hexadecenoate	Generator
Gaidate	Generator
t-2-Hexadecenoate	Generator
trans-2-Hexadecenoate	Generator
trans-delta(2)-Hexadecenoate	Generator
trans-δ(2)-hexadecenoate	Generator
trans-δ(2)-hexadecenoic acid	Generator
trans-Hexadec-2-enoate	Generator
Hexadecenoic acid, (e)-isomer	MeSH, HMDB
cis-Hexadecenoic acid	MeSH, HMDB
Hexadecenoic acid	MeSH, HMDB
Hexadecenoic acid, (Z)-isomer	MeSH, HMDB
trans-Hexadecenoic acid	MeSH, HMDB

Molecular Formula

C₁₆H₃₀O₂

Average Mass

254.4082

Monoisotopic Mass

254.224580204

IUPAC Name

(2E)-hexadec-2-enoic acid

Traditional Name

hexadecenoic acid

CAS Registry Number

Not Available

SMILES

[H]\C(CCCCCCCCCCCCC)=C(\[H])C(O)=O

InChI Identifier

InChI=1S/C16H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16(17)18/h14-15H,2-13H2,1H3,(H,17,18)/b15-14+

InChI Key

ZVRMGCSSSYZGSM-CCEZHUSRSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as long-chain fatty acids. These are fatty acids with an aliphatic tail that contains between 13 and 21 carbon atoms.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acids and conjugates

Direct Parent

Long-chain fatty acids

Alternative Parents

Substituents

Long-chain fatty acid
Unsaturated fatty acid
Straight chain fatty acid
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

alpha,beta-unsaturated monocarboxylic acid (CHEBI:37252 )
hexadecenoic acid (CHEBI:37252 )
Unsaturated fatty acids (LMFA01030054 )

Functional Ontology

Not Available

Physical Properties

State

Solid

Predicted Properties

Property	Value	Source
logP	6.25	ChemAxon
pKa (Strongest Acidic)	5.03	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	37.3 Å²	ChemAxon
Rotatable Bond Count	13	ChemAxon
Refractivity	78.18 m³·mol⁻¹	ChemAxon
Polarizability	33.74 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

Spectra

Not Available

Biological Properties

Cellular Locations

Extracellular
Membrane

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species
MMDBp0191709	Fatty acid synthase	Enzyme	P49327	Homo sapiens

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference
MMDBr0019704	(R)-3-Hydroxy-hexadecanoic acid	Trans-Hexa-dec-2-enoic acid	Unknown Protein		PathBank	31602464
MMDBr0019705	Trans-Hexa-dec-2-enoic acid	Palmitic acid	Unknown Protein		PathBank	31602464
MMDBr0038746	(2E)-Hexadecenoyl-CoA	Trans-Hexa-dec-2-enoic acid	Thioesterase TesA	Hydrolysis	RHEA	34755880
MMDBr0038977	Trans-Hexa-dec-2-enoic acid	N-(trans-Hexa-dec-2-enoyl)-4R-hydroxysphinganine	Alkaline ceramidase YPC1	Hydrolysis	RHEA	34755880

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Eukaryota/Fungi	Ascomycota	1	Human feces; Human saliva	Unknown

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

HMDB0010735

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB004789

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

5282743

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. doi: 10.1038/35036052. [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. doi: 10.1194/jlr.R600022-JLR200. 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. doi: 10.1194/jlr.R700005-JLR200. 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 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for Trans-Hexa-dec-2-enoic acid (MMDBc0047819)

MOL for #<Metabolite:0x00005645c9b90108>

3D MOL for #<Metabolite:0x00005645c9b90108>

3D SDF for #<Metabolite:0x00005645c9b90108>

3D-SDF for #<Metabolite:0x00005645c9b90108>

PDB for #<Metabolite:0x00005645c9b90108>

3D PDB for #<Metabolite:0x00005645c9b90108>

SMILES for #<Metabolite:0x00005645c9b90108>

INCHI for #<Metabolite:0x00005645c9b90108>

Structure for #<Metabolite:0x00005645c9b90108>

3D Structure for #<Metabolite:0x00005645c9b90108>