MiMeDB: Showing metabocard for 1,2-Diacyl-sn-glycerol (didodecanoyl, n-C12:0) (MMDBc0031523)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-18 01:37:42 UTC

Update Date

2022-08-31 18:11:48 UTC

MiMeDB ID

MMDBc0031523

Metabolite Identification

Common Name

1,2-Diacyl-sn-glycerol (didodecanoyl, n-C12:0)

Description

1,2-diacyl-sn-glycerol (didodecanoyl, n-c12:0) belongs to the class of Diacylglycerols. These are glycerides consisting of two fatty acid chains covalently bonded to a glycerol molecule through ester linkages. (inferred from compound structure)

Structure

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

DG(12:0/12:0/0:0)
  Mrv1652303032022012D          

 33 32  0  0  1  0            999 V2000
   24.1443   -6.4802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.1832   -7.0352    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
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 32 33  1  0  0  0  0
M  END

HMDB0093027
     RDKit          3D
DG(12:0/12:0/0:0)
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M  END

DG(12:0/12:0/0:0)
  Mrv1652303032022012D          

 33 32  0  0  1  0            999 V2000
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 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 21  5  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  1  0  0  0  0
 32 33  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0031523

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@](CO)(COC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C27H52O5/c1-3-5-7-9-11-13-15-17-19-21-26(29)31-24-25(23-28)32-27(30)22-20-18-16-14-12-10-8-6-4-2/h25,28H,3-24H2,1-2H3/t25-/m0/s1

> <INCHI_KEY>
OQQOAWVKVDAJOI-VWLOTQADSA-N

> <FORMULA>
C27H52O5

> <MOLECULAR_WEIGHT>
456.6988

> <EXACT_MASS>
456.381474774

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
84

> <JCHEM_AVERAGE_POLARIZABILITY>
57.76798004208943

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2S)-1-(dodecanoyloxy)-3-hydroxypropan-2-yl dodecanoate

> <ALOGPS_LOGP>
8.19

> <JCHEM_LOGP>
8.446544461999999

> <ALOGPS_LOGS>
-6.83

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.577784010572557

> <JCHEM_PKA_STRONGEST_BASIC>
-2.983477273775563

> <JCHEM_POLAR_SURFACE_AREA>
72.83

> <JCHEM_REFRACTIVITY>
130.8909

> <JCHEM_ROTATABLE_BOND_COUNT>
26

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.80e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S)-1-(dodecanoyloxy)-3-hydroxypropan-2-yl dodecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0093027
     RDKit          3D
DG(12:0/12:0/0:0)
 84 83  0  0  0  0  0  0  0  0999 V2000
    8.6094    2.9999    2.4176 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3390    2.2411    2.0326 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3810    0.9085    2.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5916    0.1415    2.3531 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5574   -0.1783    0.8801 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3809   -1.0521    0.5866 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3923   -1.4293   -0.8921 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2410   -0.2269   -1.7345 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0020    0.5316   -1.5307 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7127   -0.0247   -1.9006 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1664   -1.2752   -1.3417 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -1.4180   -1.9204 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3512   -0.5068   -2.6520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9766   -2.4946   -1.6559 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6712   -2.7250   -2.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2157   -1.6446   -1.6347 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0465   -1.5837   -0.1239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6839   -0.5141    0.4551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5560   -1.7557   -2.0412 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2702   -0.8169   -2.7380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6892    0.2520   -3.0453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6805   -1.1096   -3.0913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5743   -0.5742   -2.0019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2796   -1.2223   -0.6693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1484   -0.7113    0.4499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6206   -0.9433    0.1887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4794   -0.4427    1.3142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3464    1.0154    1.5946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7078    1.8994    0.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1247    1.7459   -0.0438 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0714    2.0643    1.0718 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4803    1.9012    0.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7057    2.9157    3.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4070    4.0610    2.1707 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5059    2.6053    1.9163 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4748    2.8579    2.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2568    2.1473    0.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4211    0.4163    2.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4306    1.0985    3.8822 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5197    0.6932    2.6184 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5512   -0.8376    2.8816 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5150   -0.6958    0.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5031    0.7487    0.2725 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4177   -0.5723    0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4006   -1.9893    1.2097 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4473   -1.8389   -1.1263 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6783   -2.2396   -1.0042 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1141    0.4918   -1.6067 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3812   -0.4968   -2.8435 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0689    1.5438   -2.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8981    0.8837   -0.4485 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7317   -0.1082   -3.0598 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9394    0.8262   -1.8095 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1592   -1.2729   -0.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7065   -2.2003   -1.6684 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3857   -3.7421   -1.7392 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6873   -2.8079   -3.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1447   -0.6678   -2.0035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3329   -2.5583    0.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0649   -1.4969    0.0411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0363    0.2329    0.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8566   -2.1637   -3.3156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9215   -0.5091   -4.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6180   -0.8512   -2.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5435    0.5293   -1.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2335   -0.9597   -0.4182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3304   -2.3274   -0.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8631   -1.3321    1.3535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9088    0.3214    0.7110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7668   -2.0410    0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9666   -0.5047   -0.7468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1680   -0.9850    2.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5174   -0.7686    1.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2868    1.2244    1.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9927    1.2649    2.4606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0326    1.7667   -0.4242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5879    2.9873    0.7240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2623    2.5517   -0.8172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3156    0.7578   -0.5051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9249    1.3415    1.9177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8781    3.0647    1.4609 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6644    2.7771   -0.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1777    1.8241    1.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4888    0.9826   -0.0995 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  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  5 42  1  0
  5 43  1  0
  6 44  1  0
  6 45  1  0
  7 46  1  0
  7 47  1  0
  8 48  1  0
  8 49  1  0
  9 50  1  0
  9 51  1  0
 10 52  1  0
 10 53  1  0
 11 54  1  0
 11 55  1  0
 15 56  1  0
 15 57  1  0
 16 58  1  6
 17 59  1  0
 17 60  1  0
 18 61  1  0
 22 62  1  0
 22 63  1  0
 23 64  1  0
 23 65  1  0
 24 66  1  0
 24 67  1  0
 25 68  1  0
 25 69  1  0
 26 70  1  0
 26 71  1  0
 27 72  1  0
 27 73  1  0
 28 74  1  0
 28 75  1  0
 29 76  1  0
 29 77  1  0
 30 78  1  0
 30 79  1  0
 31 80  1  0
 31 81  1  0
 32 82  1  0
 32 83  1  0
 32 84  1  0
M  END

HEADER    PROTEIN                                 03-MAR-20   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: DG(12:0/12:0/0:0)                                 
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   03-MAR-20         0                                  
HETATM    1  C   UNK     0      45.069 -12.096   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      43.275 -13.132   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      41.481 -12.097   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      45.069 -10.025   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      39.686 -13.132   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      41.875 -15.204   0.000  0.00  0.00           O+0
HETATM    7  H   UNK     0      44.685 -15.230   0.000  0.00  0.00           H+0
HETATM    8  C   UNK     0      40.541 -15.974   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0      40.541 -17.415   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0      39.208 -15.203   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      37.875 -15.974   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      36.542 -15.203   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      35.209 -15.974   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      33.876 -15.203   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      32.543 -15.974   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      31.210 -15.203   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      29.877 -15.974   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      28.544 -15.203   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      27.211 -15.974   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      25.878 -15.203   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      38.353 -12.362   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0      38.353 -10.922   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      37.020 -13.133   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      35.687 -12.362   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      34.354 -13.133   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      33.021 -12.362   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      31.688 -13.133   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      30.355 -12.362   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      29.021 -13.133   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      27.688 -12.362   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      26.355 -13.133   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      25.022 -12.362   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      23.689 -13.133   0.000  0.00  0.00           C+0
CONECT    1    2    4                                                       
CONECT    2    1    6    7    3                                             
CONECT    3    2    5                                                       
CONECT    4    1                                                            
CONECT    5    3   21                                                       
CONECT    6    2    8                                                       
CONECT    7    2                                                            
CONECT    8    6    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   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                                                       
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21    5   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   64    0
END

COMPND    HMDB0093027
HETATM    1  C1  UNL     1       8.609   3.000   2.418  1.00  0.00           C  
HETATM    2  C2  UNL     1       7.339   2.241   2.033  1.00  0.00           C  
HETATM    3  C3  UNL     1       7.381   0.908   2.764  1.00  0.00           C  
HETATM    4  C4  UNL     1       8.592   0.142   2.353  1.00  0.00           C  
HETATM    5  C5  UNL     1       8.557  -0.178   0.880  1.00  0.00           C  
HETATM    6  C6  UNL     1       7.381  -1.052   0.587  1.00  0.00           C  
HETATM    7  C7  UNL     1       7.392  -1.429  -0.892  1.00  0.00           C  
HETATM    8  C8  UNL     1       7.241  -0.227  -1.734  1.00  0.00           C  
HETATM    9  C9  UNL     1       6.002   0.532  -1.531  1.00  0.00           C  
HETATM   10  C10 UNL     1       4.713  -0.025  -1.901  1.00  0.00           C  
HETATM   11  C11 UNL     1       4.166  -1.275  -1.342  1.00  0.00           C  
HETATM   12  C12 UNL     1       2.761  -1.418  -1.920  1.00  0.00           C  
HETATM   13  O1  UNL     1       2.351  -0.507  -2.652  1.00  0.00           O  
HETATM   14  O2  UNL     1       1.977  -2.495  -1.656  1.00  0.00           O  
HETATM   15  C13 UNL     1       0.671  -2.725  -2.134  1.00  0.00           C  
HETATM   16  C14 UNL     1      -0.216  -1.645  -1.635  1.00  0.00           C  
HETATM   17  C15 UNL     1      -0.047  -1.584  -0.124  1.00  0.00           C  
HETATM   18  O3  UNL     1      -0.684  -0.514   0.455  1.00  0.00           O  
HETATM   19  O4  UNL     1      -1.556  -1.756  -2.041  1.00  0.00           O  
HETATM   20  C16 UNL     1      -2.270  -0.817  -2.738  1.00  0.00           C  
HETATM   21  O5  UNL     1      -1.689   0.252  -3.045  1.00  0.00           O  
HETATM   22  C17 UNL     1      -3.680  -1.110  -3.091  1.00  0.00           C  
HETATM   23  C18 UNL     1      -4.574  -0.574  -2.002  1.00  0.00           C  
HETATM   24  C19 UNL     1      -4.280  -1.222  -0.669  1.00  0.00           C  
HETATM   25  C20 UNL     1      -5.148  -0.711   0.450  1.00  0.00           C  
HETATM   26  C21 UNL     1      -6.621  -0.943   0.189  1.00  0.00           C  
HETATM   27  C22 UNL     1      -7.479  -0.443   1.314  1.00  0.00           C  
HETATM   28  C23 UNL     1      -7.346   1.015   1.595  1.00  0.00           C  
HETATM   29  C24 UNL     1      -7.708   1.899   0.448  1.00  0.00           C  
HETATM   30  C25 UNL     1      -9.125   1.746  -0.044  1.00  0.00           C  
HETATM   31  C26 UNL     1     -10.071   2.064   1.072  1.00  0.00           C  
HETATM   32  C27 UNL     1     -11.480   1.901   0.518  1.00  0.00           C  
HETATM   33  H1  UNL     1       8.706   2.916   3.514  1.00  0.00           H  
HETATM   34  H2  UNL     1       8.407   4.061   2.171  1.00  0.00           H  
HETATM   35  H3  UNL     1       9.506   2.605   1.916  1.00  0.00           H  
HETATM   36  H4  UNL     1       6.475   2.858   2.370  1.00  0.00           H  
HETATM   37  H5  UNL     1       7.257   2.147   0.952  1.00  0.00           H  
HETATM   38  H6  UNL     1       6.421   0.416   2.578  1.00  0.00           H  
HETATM   39  H7  UNL     1       7.431   1.098   3.882  1.00  0.00           H  
HETATM   40  H8  UNL     1       9.520   0.693   2.618  1.00  0.00           H  
HETATM   41  H9  UNL     1       8.551  -0.838   2.882  1.00  0.00           H  
HETATM   42  H10 UNL     1       9.515  -0.696   0.576  1.00  0.00           H  
HETATM   43  H11 UNL     1       8.503   0.749   0.273  1.00  0.00           H  
HETATM   44  H12 UNL     1       6.418  -0.572   0.848  1.00  0.00           H  
HETATM   45  H13 UNL     1       7.401  -1.989   1.210  1.00  0.00           H  
HETATM   46  H14 UNL     1       8.447  -1.839  -1.126  1.00  0.00           H  
HETATM   47  H15 UNL     1       6.678  -2.240  -1.004  1.00  0.00           H  
HETATM   48  H16 UNL     1       8.114   0.492  -1.607  1.00  0.00           H  
HETATM   49  H17 UNL     1       7.381  -0.497  -2.843  1.00  0.00           H  
HETATM   50  H18 UNL     1       6.069   1.544  -2.097  1.00  0.00           H  
HETATM   51  H19 UNL     1       5.898   0.884  -0.448  1.00  0.00           H  
HETATM   52  H20 UNL     1       4.732  -0.108  -3.060  1.00  0.00           H  
HETATM   53  H21 UNL     1       3.939   0.826  -1.810  1.00  0.00           H  
HETATM   54  H22 UNL     1       4.159  -1.273  -0.249  1.00  0.00           H  
HETATM   55  H23 UNL     1       4.706  -2.200  -1.668  1.00  0.00           H  
HETATM   56  H24 UNL     1       0.386  -3.742  -1.739  1.00  0.00           H  
HETATM   57  H25 UNL     1       0.687  -2.808  -3.250  1.00  0.00           H  
HETATM   58  H26 UNL     1       0.145  -0.668  -2.003  1.00  0.00           H  
HETATM   59  H27 UNL     1      -0.333  -2.558   0.289  1.00  0.00           H  
HETATM   60  H28 UNL     1       1.065  -1.497   0.041  1.00  0.00           H  
HETATM   61  H29 UNL     1      -0.036   0.233   0.488  1.00  0.00           H  
HETATM   62  H30 UNL     1      -3.857  -2.164  -3.316  1.00  0.00           H  
HETATM   63  H31 UNL     1      -3.922  -0.509  -4.015  1.00  0.00           H  
HETATM   64  H32 UNL     1      -5.618  -0.851  -2.263  1.00  0.00           H  
HETATM   65  H33 UNL     1      -4.544   0.529  -1.933  1.00  0.00           H  
HETATM   66  H34 UNL     1      -3.233  -0.960  -0.418  1.00  0.00           H  
HETATM   67  H35 UNL     1      -4.330  -2.327  -0.746  1.00  0.00           H  
HETATM   68  H36 UNL     1      -4.863  -1.332   1.354  1.00  0.00           H  
HETATM   69  H37 UNL     1      -4.909   0.321   0.711  1.00  0.00           H  
HETATM   70  H38 UNL     1      -6.767  -2.041   0.127  1.00  0.00           H  
HETATM   71  H39 UNL     1      -6.967  -0.505  -0.747  1.00  0.00           H  
HETATM   72  H40 UNL     1      -7.168  -0.985   2.255  1.00  0.00           H  
HETATM   73  H41 UNL     1      -8.517  -0.769   1.133  1.00  0.00           H  
HETATM   74  H42 UNL     1      -6.287   1.224   1.898  1.00  0.00           H  
HETATM   75  H43 UNL     1      -7.993   1.265   2.461  1.00  0.00           H  
HETATM   76  H44 UNL     1      -7.033   1.767  -0.424  1.00  0.00           H  
HETATM   77  H45 UNL     1      -7.588   2.987   0.724  1.00  0.00           H  
HETATM   78  H46 UNL     1      -9.262   2.552  -0.817  1.00  0.00           H  
HETATM   79  H47 UNL     1      -9.316   0.758  -0.505  1.00  0.00           H  
HETATM   80  H48 UNL     1      -9.925   1.342   1.918  1.00  0.00           H  
HETATM   81  H49 UNL     1      -9.878   3.065   1.461  1.00  0.00           H  
HETATM   82  H50 UNL     1     -11.664   2.777  -0.130  1.00  0.00           H  
HETATM   83  H51 UNL     1     -12.178   1.824   1.373  1.00  0.00           H  
HETATM   84  H52 UNL     1     -11.489   0.983  -0.100  1.00  0.00           H  
CONECT    1    2   33   34   35
CONECT    2    3   36   37
CONECT    3    4   38   39
CONECT    4    5   40   41
CONECT    5    6   42   43
CONECT    6    7   44   45
CONECT    7    8   46   47
CONECT    8    9   48   49
CONECT    9   10   50   51
CONECT   10   11   52   53
CONECT   11   12   54   55
CONECT   12   13   13   14
CONECT   14   15
CONECT   15   16   56   57
CONECT   16   17   19   58
CONECT   17   18   59   60
CONECT   18   61
CONECT   19   20
CONECT   20   21   21   22
CONECT   22   23   62   63
CONECT   23   24   64   65
CONECT   24   25   66   67
CONECT   25   26   68   69
CONECT   26   27   70   71
CONECT   27   28   72   73
CONECT   28   29   74   75
CONECT   29   30   76   77
CONECT   30   31   78   79
CONECT   31   32   80   81
CONECT   32   82   83   84
END

HMDB0093027
     RDKit          3D
DG(12:0/12:0/0:0)
 84 83  0  0  0  0  0  0  0  0999 V2000
    8.6094    2.9999    2.4176 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3390    2.2411    2.0326 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3810    0.9085    2.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5916    0.1415    2.3531 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5574   -0.1783    0.8801 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3809   -1.0521    0.5866 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3923   -1.4293   -0.8921 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2410   -0.2269   -1.7345 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0020    0.5316   -1.5307 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7127   -0.0247   -1.9006 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1664   -1.2752   -1.3417 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7609   -1.4180   -1.9204 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3512   -0.5068   -2.6520 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9766   -2.4946   -1.6559 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6712   -2.7250   -2.1341 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2157   -1.6446   -1.6347 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.0465   -1.5837   -0.1239 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6839   -0.5141    0.4551 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5560   -1.7557   -2.0412 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2702   -0.8169   -2.7380 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6892    0.2520   -3.0453 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6805   -1.1096   -3.0913 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5743   -0.5742   -2.0019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2796   -1.2223   -0.6693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1484   -0.7113    0.4499 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6206   -0.9433    0.1887 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4794   -0.4427    1.3142 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3464    1.0154    1.5946 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7078    1.8994    0.4478 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1247    1.7459   -0.0438 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0714    2.0643    1.0718 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4803    1.9012    0.5183 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7057    2.9157    3.5144 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4070    4.0610    2.1707 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5059    2.6053    1.9163 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4748    2.8579    2.3704 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2568    2.1473    0.9517 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4211    0.4163    2.5782 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4306    1.0985    3.8822 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5197    0.6932    2.6184 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5512   -0.8376    2.8816 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5150   -0.6958    0.5763 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5031    0.7487    0.2725 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4177   -0.5723    0.8476 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4006   -1.9893    1.2097 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4473   -1.8389   -1.1263 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6783   -2.2396   -1.0042 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1141    0.4918   -1.6067 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.3812   -0.4968   -2.8435 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0689    1.5438   -2.0969 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8981    0.8837   -0.4485 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7317   -0.1082   -3.0598 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9394    0.8262   -1.8095 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1592   -1.2729   -0.2494 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7065   -2.2003   -1.6684 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3857   -3.7421   -1.7392 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6873   -2.8079   -3.2504 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1447   -0.6678   -2.0035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3329   -2.5583    0.2892 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0649   -1.4969    0.0411 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0363    0.2329    0.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8566   -2.1637   -3.3156 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9215   -0.5091   -4.0146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6180   -0.8512   -2.2625 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5435    0.5293   -1.9334 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2335   -0.9597   -0.4182 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3304   -2.3274   -0.7458 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8631   -1.3321    1.3535 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9088    0.3214    0.7110 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7668   -2.0410    0.1268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9666   -0.5047   -0.7468 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1680   -0.9850    2.2552 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5174   -0.7686    1.1325 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2868    1.2244    1.8978 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9927    1.2649    2.4606 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0326    1.7667   -0.4242 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5879    2.9873    0.7240 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2623    2.5517   -0.8172 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3156    0.7578   -0.5051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9249    1.3415    1.9177 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.8781    3.0647    1.4609 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6644    2.7771   -0.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1777    1.8241    1.3727 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4888    0.9826   -0.0995 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  2  0
 12 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  2  0
 20 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  5 42  1  0
  5 43  1  0
  6 44  1  0
  6 45  1  0
  7 46  1  0
  7 47  1  0
  8 48  1  0
  8 49  1  0
  9 50  1  0
  9 51  1  0
 10 52  1  0
 10 53  1  0
 11 54  1  0
 11 55  1  0
 15 56  1  0
 15 57  1  0
 16 58  1  6
 17 59  1  0
 17 60  1  0
 18 61  1  0
 22 62  1  0
 22 63  1  0
 23 64  1  0
 23 65  1  0
 24 66  1  0
 24 67  1  0
 25 68  1  0
 25 69  1  0
 26 70  1  0
 26 71  1  0
 27 72  1  0
 27 73  1  0
 28 74  1  0
 28 75  1  0
 29 76  1  0
 29 77  1  0
 30 78  1  0
 30 79  1  0
 31 80  1  0
 31 81  1  0
 32 82  1  0
 32 83  1  0
 32 84  1  0
M  END

Synonyms

Not Available

Chemical Formula

C₂₇H₅₂O₅

Average Molecular Weight

456.6988

Monoisotopic Molecular Weight

456.381474774

IUPAC Name

(2S)-1-(dodecanoyloxy)-3-hydroxypropan-2-yl dodecanoate

Traditional Name

(2S)-1-(dodecanoyloxy)-3-hydroxypropan-2-yl dodecanoate

CAS Registry Number

Not Available

SMILES

[H][C@](CO)(COC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC

InChI Identifier

InChI=1S/C27H52O5/c1-3-5-7-9-11-13-15-17-19-21-26(29)31-24-25(23-28)32-27(30)22-20-18-16-14-12-10-8-6-4-2/h25,28H,3-24H2,1-2H3/t25-/m0/s1

InChI Key

OQQOAWVKVDAJOI-VWLOTQADSA-N

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	6.8e-05 g/L	ALOGPS
logP	8.19	ALOGPS
logP	8.45	ChemAxon
logS	-6.8	ALOGPS
pKa (Strongest Acidic)	14.58	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	26	ChemAxon
Refractivity	130.89 m³·mol⁻¹	ChemAxon
Polarizability	57.77 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

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (1 TMS) - 70eV, Positive	splash10-020r-7917630000-1c071b617668e0eedd76	2017-10-06	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-0000900000-d3ce757c7d77e6c1be44	2017-10-04	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0a4r-0090900000-6ef2c93167204571eefa	2017-10-04	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0ab9-0090900000-6e02300046f9f3d0ba35	2017-10-04	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0a4i-1490800000-18d42897aa4b538bb98f	2021-09-21	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0a59-4972200000-8bf0dc177fbb992d3fe9	2021-09-21	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0a59-9520000000-a1bc798bac9b5758447b	2021-09-21	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-004i-0000900000-f4d3ed62660285fb1766	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-004i-0000900000-f4d3ed62660285fb1766	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-004i-0090100000-d6418435e21ebeb07527	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-0000900000-fe4ad345fcc9c1b96ae8	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0a4r-0080900000-2021c9c67a87211de23e	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0ab9-0080900000-4a323f60ea8a1e7a9560	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0a4j-1540900000-e078ec43d41cb3157252	2021-09-25	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-052b-2970100000-af92add4600e0160c423	2021-09-25	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0002-0910000000-75918b523af3cd4255fe	2021-09-25	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Proteins

#<MetaboliteProteinLink:0x000055b76df56b60>

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Related Health Condition	Evidence Type	Measured in Matrix	Data Source	Reference

Microbial Sources

Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
	Proteobacteria	1	Human	Unknown

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference	Details

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference
Human Feces	Detected but not Quantified									HMDB		details

External Links

Not Available

References

Synthesis Reference

Not Available

General References

Kingsbury KJ, Morgan DM: The analysis of the fatty acids of normal human depot fat by gas-liquid chromatography. Biochem J. 1964 Jan;90(1):140-7. doi: 10.1042/bj0900140. [PubMed:5832283 ]
Ghosh S, Strum JC, Bell RM: Lipid biochemistry: functions of glycerolipids and sphingolipids in cellular signaling. FASEB J. 1997 Jan;11(1):45-50. doi: 10.1096/fasebj.11.1.9034165. [PubMed:9034165 ]
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 ]
Lopez-Lopez A, Lopez-Sabater MC, Campoy-Folgoso C, Rivero-Urgell M, Castellote-Bargallo AI: Fatty acid and sn-2 fatty acid composition in human milk from Granada (Spain) and in infant formulas. Eur J Clin Nutr. 2002 Dec;56(12):1242-54. doi: 10.1038/sj.ejcn.1601470. [PubMed:12494309 ]
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 ]
Quehenberger O, Armando AM, Brown AH, Milne SB, Myers DS, Merrill AH, Bandyopadhyay S, Jones KN, Kelly S, Shaner RL, Sullards CM, Wang E, Murphy RC, Barkley RM, Leiker TJ, Raetz CR, Guan Z, Laird GM, Six DA, Russell DW, McDonald JG, Subramaniam S, Fahy E, Dennis EA: Lipidomics reveals a remarkable diversity of lipids in human plasma. J Lipid Res. 2010 Nov;51(11):3299-305. doi: 10.1194/jlr.M009449. Epub 2010 Jul 29. [PubMed:20671299 ]
Jenkins B, West JA, Koulman A: A review of odd-chain fatty acid metabolism and the role of pentadecanoic Acid (c15:0) and heptadecanoic Acid (c17:0) in health and disease. Molecules. 2015 Jan 30;20(2):2425-44. doi: 10.3390/molecules20022425. [PubMed:25647578 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Showing metabocard for 1,2-Diacyl-sn-glycerol (didodecanoyl, n-C12:0) (MMDBc0031523)

MOL for #<Metabolite:0x000055b76e0b4b10>

3D MOL for #<Metabolite:0x000055b76e0b4b10>

3D SDF for #<Metabolite:0x000055b76e0b4b10>

3D-SDF for #<Metabolite:0x000055b76e0b4b10>

PDB for #<Metabolite:0x000055b76e0b4b10>

3D PDB for #<Metabolite:0x000055b76e0b4b10>

SMILES for #<Metabolite:0x000055b76e0b4b10>

INCHI for #<Metabolite:0x000055b76e0b4b10>

Structure for #<Metabolite:0x000055b76e0b4b10>

3D Structure for #<Metabolite:0x000055b76e0b4b10>