MiMeDB: Showing metabocard for 15-Methylpalmitate (MMDBc0000683)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-12-10 18:52:39 UTC

Update Date

2025-01-16 22:14:56 UTC

Metabolite ID

MMDBc0000683

Metabolite Identification

Common Name

15-Methylpalmitate

Description

15-Methylpalmitate, also known as 15-methylhexadecanoate, is a fatty acid methyl ester (FAME). It has an exact mass of 269.25 g/mol and the molecular formula is C17H33O2. Methylpalmitate is a biomarker for the consumption of butte

Structure

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

HMDB0061709
     RDKit          3D
15-Methylpalmitate
 53 52  0  0  0  0  0  0  0  0999 V2000
   -5.9080    0.5954    1.2013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4840   -0.5773    0.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9800   -0.3169    0.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8675   -0.9671   -0.7913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4597   -1.3898   -0.8475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4601   -0.3762   -0.3937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0327   -0.9076   -0.5556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0987    0.1781   -0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3484   -0.2615   -0.1983 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2077    0.8520    0.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7030    0.5529    0.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1711    0.2751   -1.1391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5938   -0.0654   -1.3619 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6623    0.8794   -1.0414 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8882    1.3613    0.3272 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1508    0.3117    1.3715 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3447   -0.5090    1.1108 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0691   -0.3186    0.1008 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7488   -1.5391    1.9537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3436    0.2684    2.0936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7884    1.2025    1.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3319    1.2958    0.5971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5132   -1.4330    1.2241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3949   -1.1082   -0.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0791    0.6740   -0.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5441   -0.3075    1.1712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5387   -1.7580   -1.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0203   -0.0858   -1.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3245   -2.3563   -0.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2430   -1.7315   -1.9032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5746   -0.1920    0.6968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981    0.5747   -0.9186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8691   -1.0499   -1.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9096   -1.8620   -0.0376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3316    0.4644    0.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2278    1.0461   -0.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5443   -0.6265   -1.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4710   -1.1230    0.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9616    1.0589    1.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0429    1.7554   -0.3473 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9499   -0.2727    0.9562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1742    1.4688    0.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8586    1.1577   -1.7718 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5222   -0.5874   -1.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7962   -1.1129   -0.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6708   -0.2484   -2.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6593    0.5684   -1.5114 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4458    1.8231   -1.6622 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9257    1.8995    0.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2672    2.1451    0.7375 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3650    0.8779    2.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2535   -0.3008    1.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1272   -1.3585    2.8778 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  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  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 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
 19 53  1  0
M  END


  Mrv1652304032018322D          

 19 18  0  0  0  0            999 V2000
    7.9480    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    4.1763    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6638    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9493    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3783    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2349    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.0927    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.5204    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.8072    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.8059    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5217    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0914    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2362    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3770    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.9506    5.4138    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6625    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    5.0013    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.3796    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.6651    4.1763    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  4  3  1  0  0  0  0
  5  3  1  0  0  0  0
  6  4  1  0  0  0  0
  7  5  1  0  0  0  0
  8  6  1  0  0  0  0
  9  7  1  0  0  0  0
 10  8  1  0  0  0  0
 11  9  1  0  0  0  0
 12 10  1  0  0  0  0
 13 11  1  0  0  0  0
 14 12  1  0  0  0  0
 15 13  1  0  0  0  0
 16  1  1  0  0  0  0
 16  2  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 17  2  0  0  0  0
 19 17  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0000683

> <DATABASE_NAME>
MIME

> <SMILES>
CC(C)CCCCCCCCCCCCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C17H34O2/c1-16(2)14-12-10-8-6-4-3-5-7-9-11-13-15-17(18)19/h16H,3-15H2,1-2H3,(H,18,19)

> <INCHI_KEY>
IIUXHTGBZYEGHI-UHFFFAOYSA-N

> <FORMULA>
C17H34O2

> <MOLECULAR_WEIGHT>
270.457

> <EXACT_MASS>
270.255880335

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
36.22119132096559

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
15-methylhexadecanoic acid

> <ALOGPS_LOGP>
7.48

> <JCHEM_LOGP>
6.543601873999999

> <ALOGPS_LOGS>
-6.25

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.952019655228562

> <JCHEM_POLAR_SURFACE_AREA>
37.3

> <JCHEM_REFRACTIVITY>
81.63219999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
14

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.53e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
15-methyl palmitic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0061709
     RDKit          3D
15-Methylpalmitate
 53 52  0  0  0  0  0  0  0  0999 V2000
   -5.9080    0.5954    1.2013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4840   -0.5773    0.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9800   -0.3169    0.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8675   -0.9671   -0.7913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4597   -1.3898   -0.8475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4601   -0.3762   -0.3937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0327   -0.9076   -0.5556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0987    0.1781   -0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3484   -0.2615   -0.1983 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2077    0.8520    0.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7030    0.5529    0.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1711    0.2751   -1.1391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5938   -0.0654   -1.3619 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6623    0.8794   -1.0414 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8882    1.3613    0.3272 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1508    0.3117    1.3715 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3447   -0.5090    1.1108 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0691   -0.3186    0.1008 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7488   -1.5391    1.9537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3436    0.2684    2.0936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7884    1.2025    1.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3319    1.2958    0.5971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5132   -1.4330    1.2241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3949   -1.1082   -0.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0791    0.6740   -0.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5441   -0.3075    1.1712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5387   -1.7580   -1.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0203   -0.0858   -1.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3245   -2.3563   -0.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2430   -1.7315   -1.9032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5746   -0.1920    0.6968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981    0.5747   -0.9186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8691   -1.0499   -1.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9096   -1.8620   -0.0376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3316    0.4644    0.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2278    1.0461   -0.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5443   -0.6265   -1.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4710   -1.1230    0.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9616    1.0589    1.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0429    1.7554   -0.3473 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9499   -0.2727    0.9562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1742    1.4688    0.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8586    1.1577   -1.7718 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5222   -0.5874   -1.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7962   -1.1129   -0.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6708   -0.2484   -2.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6593    0.5684   -1.5114 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4458    1.8231   -1.6622 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9257    1.8995    0.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2672    2.1451    0.7375 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3650    0.8779    2.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2535   -0.3008    1.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1272   -1.3585    2.8778 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  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  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 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
 19 53  1  0
M  END

HEADER    PROTEIN                                 03-APR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-APR-20         0                                  
HETATM    1  C   UNK     0      14.836  10.106   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      16.170   7.796   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      25.506  10.106   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      24.172   9.336   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      26.839   9.336   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      22.838  10.106   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      28.173  10.106   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.505   9.336   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      29.507   9.336   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      20.171  10.106   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      30.841  10.106   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.837   9.336   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      32.174   9.336   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.504  10.106   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      33.508  10.106   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      16.170   9.336   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      34.842   9.336   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0      36.175  10.106   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      34.842   7.796   0.000  0.00  0.00           O+0
CONECT    1   16                                                            
CONECT    2   16                                                            
CONECT    3    4    5                                                       
CONECT    4    3    6                                                       
CONECT    5    3    7                                                       
CONECT    6    4    8                                                       
CONECT    7    5    9                                                       
CONECT    8    6   10                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   13                                                       
CONECT   12   10   14                                                       
CONECT   13   11   15                                                       
CONECT   14   12   16                                                       
CONECT   15   13   17                                                       
CONECT   16    1    2   14                                                  
CONECT   17   15   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
MASTER        0    0    0    0    0    0    0    0   19    0   36    0
END

COMPND    HMDB0061709
HETATM    1  C1  UNL     1      -5.908   0.595   1.201  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.484  -0.577   0.493  1.00  0.00           C  
HETATM    3  C3  UNL     1      -7.980  -0.317   0.206  1.00  0.00           C  
HETATM    4  C4  UNL     1      -5.868  -0.967  -0.791  1.00  0.00           C  
HETATM    5  C5  UNL     1      -4.460  -1.390  -0.848  1.00  0.00           C  
HETATM    6  C6  UNL     1      -3.460  -0.376  -0.394  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.033  -0.908  -0.556  1.00  0.00           C  
HETATM    8  C8  UNL     1      -1.099   0.178  -0.075  1.00  0.00           C  
HETATM    9  C9  UNL     1       0.348  -0.261  -0.198  1.00  0.00           C  
HETATM   10  C10 UNL     1       1.208   0.852   0.291  1.00  0.00           C  
HETATM   11  C11 UNL     1       2.703   0.553   0.236  1.00  0.00           C  
HETATM   12  C12 UNL     1       3.171   0.275  -1.139  1.00  0.00           C  
HETATM   13  C13 UNL     1       4.594  -0.065  -1.362  1.00  0.00           C  
HETATM   14  C14 UNL     1       5.662   0.879  -1.041  1.00  0.00           C  
HETATM   15  C15 UNL     1       5.888   1.361   0.327  1.00  0.00           C  
HETATM   16  C16 UNL     1       6.151   0.312   1.372  1.00  0.00           C  
HETATM   17  C17 UNL     1       7.345  -0.509   1.111  1.00  0.00           C  
HETATM   18  O1  UNL     1       8.069  -0.319   0.101  1.00  0.00           O  
HETATM   19  O2  UNL     1       7.749  -1.539   1.954  1.00  0.00           O  
HETATM   20  H1  UNL     1      -5.344   0.268   2.094  1.00  0.00           H  
HETATM   21  H2  UNL     1      -6.788   1.202   1.585  1.00  0.00           H  
HETATM   22  H3  UNL     1      -5.332   1.296   0.597  1.00  0.00           H  
HETATM   23  H4  UNL     1      -6.513  -1.433   1.224  1.00  0.00           H  
HETATM   24  H5  UNL     1      -8.395  -1.108  -0.448  1.00  0.00           H  
HETATM   25  H6  UNL     1      -8.079   0.674  -0.242  1.00  0.00           H  
HETATM   26  H7  UNL     1      -8.544  -0.307   1.171  1.00  0.00           H  
HETATM   27  H8  UNL     1      -6.539  -1.758  -1.273  1.00  0.00           H  
HETATM   28  H9  UNL     1      -6.020  -0.086  -1.496  1.00  0.00           H  
HETATM   29  H10 UNL     1      -4.325  -2.356  -0.256  1.00  0.00           H  
HETATM   30  H11 UNL     1      -4.243  -1.731  -1.903  1.00  0.00           H  
HETATM   31  H12 UNL     1      -3.575  -0.192   0.697  1.00  0.00           H  
HETATM   32  H13 UNL     1      -3.598   0.575  -0.919  1.00  0.00           H  
HETATM   33  H14 UNL     1      -1.869  -1.050  -1.642  1.00  0.00           H  
HETATM   34  H15 UNL     1      -1.910  -1.862  -0.038  1.00  0.00           H  
HETATM   35  H16 UNL     1      -1.332   0.464   0.969  1.00  0.00           H  
HETATM   36  H17 UNL     1      -1.228   1.046  -0.752  1.00  0.00           H  
HETATM   37  H18 UNL     1       0.544  -0.626  -1.206  1.00  0.00           H  
HETATM   38  H19 UNL     1       0.471  -1.123   0.497  1.00  0.00           H  
HETATM   39  H20 UNL     1       0.962   1.059   1.334  1.00  0.00           H  
HETATM   40  H21 UNL     1       1.043   1.755  -0.347  1.00  0.00           H  
HETATM   41  H22 UNL     1       2.950  -0.273   0.956  1.00  0.00           H  
HETATM   42  H23 UNL     1       3.174   1.469   0.623  1.00  0.00           H  
HETATM   43  H24 UNL     1       2.859   1.158  -1.772  1.00  0.00           H  
HETATM   44  H25 UNL     1       2.522  -0.587  -1.516  1.00  0.00           H  
HETATM   45  H26 UNL     1       4.796  -1.113  -0.978  1.00  0.00           H  
HETATM   46  H27 UNL     1       4.671  -0.248  -2.495  1.00  0.00           H  
HETATM   47  H28 UNL     1       6.659   0.568  -1.511  1.00  0.00           H  
HETATM   48  H29 UNL     1       5.446   1.823  -1.662  1.00  0.00           H  
HETATM   49  H30 UNL     1       6.926   1.899   0.264  1.00  0.00           H  
HETATM   50  H31 UNL     1       5.267   2.145   0.738  1.00  0.00           H  
HETATM   51  H32 UNL     1       6.365   0.878   2.327  1.00  0.00           H  
HETATM   52  H33 UNL     1       5.253  -0.301   1.615  1.00  0.00           H  
HETATM   53  H34 UNL     1       8.127  -1.358   2.878  1.00  0.00           H  
CONECT    1    2   20   21   22
CONECT    2    3    4   23
CONECT    3   24   25   26
CONECT    4    5   27   28
CONECT    5    6   29   30
CONECT    6    7   31   32
CONECT    7    8   33   34
CONECT    8    9   35   36
CONECT    9   10   37   38
CONECT   10   11   39   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   18   19
CONECT   19   53
END

HMDB0061709
     RDKit          3D
15-Methylpalmitate
 53 52  0  0  0  0  0  0  0  0999 V2000
   -5.9080    0.5954    1.2013 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4840   -0.5773    0.4933 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9800   -0.3169    0.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8675   -0.9671   -0.7913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4597   -1.3898   -0.8475 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4601   -0.3762   -0.3937 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0327   -0.9076   -0.5556 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0987    0.1781   -0.0746 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3484   -0.2615   -0.1983 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2077    0.8520    0.2912 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7030    0.5529    0.2357 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1711    0.2751   -1.1391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5938   -0.0654   -1.3619 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6623    0.8794   -1.0414 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8882    1.3613    0.3272 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1508    0.3117    1.3715 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3447   -0.5090    1.1108 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0691   -0.3186    0.1008 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.7488   -1.5391    1.9537 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3436    0.2684    2.0936 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7884    1.2025    1.5850 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3319    1.2958    0.5971 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5132   -1.4330    1.2241 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3949   -1.1082   -0.4477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0791    0.6740   -0.2416 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5441   -0.3075    1.1712 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5387   -1.7580   -1.2726 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0203   -0.0858   -1.4964 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3245   -2.3563   -0.2559 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2430   -1.7315   -1.9032 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5746   -0.1920    0.6968 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5981    0.5747   -0.9186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8691   -1.0499   -1.6419 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9096   -1.8620   -0.0376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3316    0.4644    0.9685 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2278    1.0461   -0.7522 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5443   -0.6265   -1.2060 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4710   -1.1230    0.4970 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9616    1.0589    1.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0429    1.7554   -0.3473 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9499   -0.2727    0.9562 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1742    1.4688    0.6232 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8586    1.1577   -1.7718 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5222   -0.5874   -1.5161 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7962   -1.1129   -0.9777 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6708   -0.2484   -2.4953 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6593    0.5684   -1.5114 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4458    1.8231   -1.6622 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9257    1.8995    0.2639 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2672    2.1451    0.7375 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3650    0.8779    2.3266 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2535   -0.3008    1.6149 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1272   -1.3585    2.8778 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  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  1  0
 15 16  1  0
 16 17  1  0
 17 18  2  0
 17 19  1  0
  1 20  1  0
  1 21  1  0
  1 22  1  0
  2 23  1  0
  3 24  1  0
  3 25  1  0
  3 26  1  0
  4 27  1  0
  4 28  1  0
  5 29  1  0
  5 30  1  0
  6 31  1  0
  6 32  1  0
  7 33  1  0
  7 34  1  0
  8 35  1  0
  8 36  1  0
  9 37  1  0
  9 38  1  0
 10 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
 19 53  1  0
M  END

Synonyms

Value	Source
15-Methyl hexadecanoic acid	ChEBI
15-Methyl palmitic acid	ChEBI
15-Methylpalmitic acid	ChEBI
C17:0	ChEBI
I-17:0	ChEBI
I-C17:0	ChEBI
I17:0	ChEBI
Iso-C17:0	ChEBI
Iso-margaric acid	ChEBI
Isomargaric acid	ChEBI
15-Methyl hexadecanoate	Generator
15-Methyl palmitate	Generator
Iso-margarate	Generator
Isomargarate	Generator
15-Methylpalmitate	Generator
Isoheptadecanoate	Generator

Molecular Formula

C₁₇H₃₄O₂

Average Mass

270.457

Monoisotopic Mass

270.255880335

IUPAC Name

15-methylhexadecanoic acid

Traditional Name

15-methyl palmitic acid

CAS Registry Number

Not Available

SMILES

CC(C)CCCCCCCCCCCCCC(O)=O

InChI Identifier

InChI=1S/C17H34O2/c1-16(2)14-12-10-8-6-4-3-5-7-9-11-13-15-17(18)19/h16H,3-15H2,1-2H3,(H,18,19)

InChI Key

IIUXHTGBZYEGHI-UHFFFAOYSA-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
Branched 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

long-chain fatty acid (CHEBI:70850 )
branched-chain saturated fatty acid (CHEBI:70850 )
methyl-branched fatty acid (CHEBI:70850 )
Branched fatty acids (LMFA01020012 )

Functional Ontology

Not Available

Physical Properties

State

Not Available

Predicted Properties

Property	Value	Source
Water Solubility	0.00015 g/L	ALOGPS
logP	7.48	ALOGPS
logP	6.54	ChemAxon
logS	-6.2	ALOGPS
pKa (Strongest Acidic)	4.95	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	14	ChemAxon
Refractivity	81.63 m³·mol⁻¹	ChemAxon
Polarizability	36.22 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

Not Available

Biospecimen Locations

Blood
Feces

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

Human Pathways

Pathways

Name	SMPDB/PathBank
Acylcarnitine 15-methylhexadecanoylcarnitine

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

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
Bacteria/Eubacteria	Firmicutes	3	Human ; Human feces; Human saliva; Human mucosa; Human stool	Indirect association between microbiota composition and metabolites measured in host biospecimen
Bacteria/Eubacteria	Verrucomicrobia	1	Human feces; Human stool; Human ; Human urine	Indirect association between microbiota composition and metabolites measured in host biospecimen
Archaea	Euryarchaeota	1	Human feces; Human	Indirect association between microbiota composition and metabolites measured in host biospecimen
Bacteria/Eubacteria	Actinobacteria	2	Human ; Human feces; Human sputum; Human saliva; Human supragingival plaque; Human subgingival plaque	Indirect association between microbiota composition and metabolites measured in host biospecimen

Exposure Sources

Other Exposures

Source Type	Data Source	Reference
Cosmetics	U.S. Environmental Protection Agency	CompTox
Domestics	U.S. Environmental Protection Agency	CompTox

Host Biospecimen and Location

Host and Biospecimen	Status	Age	Sex	Health Condition	Data Source	Reference
Human Blood	Detected but not Quantified	Adult (>18 years old)	Both	Normal	HMDB	24740205
Human Blood	Detected but not Quantified	Adult (>18 years old)	Female	Normal	HMDB	27355821
Human Feces	Detected but not Quantified	Adult (>18 years old)	Both	Normal	HMDB	27543620
Human Feces	Detected but not Quantified	Adult (>18 years old)	Both	Normal	HMDB	25037050
Human Feces	Detected but not Quantified	Adult (>18 years old)	Both	Normal	HMDB	29808030

External Links

HMDB ID

HMDB0061709

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB 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

164860

PDB ID

Not Available

ChEBI ID

70850

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 ]
Kniazeva M, Crawford QT, Seiber M, Wang CY, Han M: Monomethyl branched-chain fatty acids play an essential role in Caenorhabditis elegans development. PLoS Biol. 2004 Sep;2(9):E257. doi: 10.1371/journal.pbio.0020257. Epub 2004 Aug 31. [PubMed:15340492 ]
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 15-Methylpalmitate (MMDBc0000683)

MOL for #<Metabolite:0x00005645c6cd9418>

3D MOL for #<Metabolite:0x00005645c6cd9418>

3D SDF for #<Metabolite:0x00005645c6cd9418>

3D-SDF for #<Metabolite:0x00005645c6cd9418>

PDB for #<Metabolite:0x00005645c6cd9418>

3D PDB for #<Metabolite:0x00005645c6cd9418>

SMILES for #<Metabolite:0x00005645c6cd9418>

INCHI for #<Metabolite:0x00005645c6cd9418>

Structure for #<Metabolite:0x00005645c6cd9418>

3D Structure for #<Metabolite:0x00005645c6cd9418>