MiMeDB: Showing metabocard for 1-heptadecanoyl-2-hexadecanoyl-sn-glycero-3-phosphate (MMDBc0055108)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-17 19:43:39 UTC

Update Date

2022-08-12 20:09:14 UTC

MiMeDB ID

MMDBc0055108

Metabolite Identification

Common Name

1-heptadecanoyl-2-hexadecanoyl-sn-glycero-3-phosphate

Description

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306172221432D          

 46 45  0  0  1  0            999 V2000
  -12.2645   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4565   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5500   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7420   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8355   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0275   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1211   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3131   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4066   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5986   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6921   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8841   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9776   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1697   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2632   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4552   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5487   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7407   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8342   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1198   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0262   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4053   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3118   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6908   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5973   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9763   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8828   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2619   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1684   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5474   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4539   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5960   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3105   -7.9697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3105   -7.1447    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8329   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7394   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8329   -5.9072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7394   -7.9697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1999   -9.2072    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    2.8499   -9.2072    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    2.0249  -10.0322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1185   -7.1447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0249   -8.3822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0249   -6.7322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0249   -9.2072    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    0.5960   -7.5572    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  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 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19 17  1  0  0  0  0
 20 19  1  0  0  0  0
 21 18  1  0  0  0  0
 22 20  1  0  0  0  0
 23 21  1  0  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  1  0  0  0  0
 28 26  1  0  0  0  0
 29 27  1  0  0  0  0
 30 28  1  0  0  0  0
 31 29  1  0  0  0  0
 34 32  1  0  0  0  0
 34 33  1  0  0  0  0
 35 30  1  0  0  0  0
 36 31  1  0  0  0  0
 37 35  2  0  0  0  0
 38 36  2  0  0  0  0
 42 32  1  0  0  0  0
 42 35  1  0  0  0  0
 43 33  1  0  0  0  0
 34 44  1  6  0  0  0
 44 36  1  0  0  0  0
 45 39  1  0  0  0  0
 45 40  1  0  0  0  0
 45 41  2  0  0  0  0
 45 43  1  0  0  0  0
 34 46  1  6  0  0  0
M  CHG  2  39  -1  40  -1
M  END


  Mrv1652306172221432D          

 46 45  0  0  1  0            999 V2000
  -12.2645   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.4565   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5500   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.7420   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8355   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.0275   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.1211   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3131   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4066   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5986   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6921   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8841   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9776   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1697   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2632   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4552   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.5487   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7407   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8342   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1198   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0262   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4053   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3118   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6908   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5973   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9763   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8828   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2619   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1684   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5474   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4539   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5960   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3105   -7.9697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3105   -7.1447    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8329   -6.7322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7394   -7.1447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8329   -5.9072    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7394   -7.9697    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1999   -9.2072    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    2.8499   -9.2072    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    2.0249  -10.0322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1185   -7.1447    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0249   -8.3822    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0249   -6.7322    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0249   -9.2072    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    0.5960   -7.5572    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  3  1  1  0  0  0  0
  4  2  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 14  1  0  0  0  0
 17 15  1  0  0  0  0
 18 16  1  0  0  0  0
 19 17  1  0  0  0  0
 20 19  1  0  0  0  0
 21 18  1  0  0  0  0
 22 20  1  0  0  0  0
 23 21  1  0  0  0  0
 24 22  1  0  0  0  0
 25 23  1  0  0  0  0
 26 24  1  0  0  0  0
 27 25  1  0  0  0  0
 28 26  1  0  0  0  0
 29 27  1  0  0  0  0
 30 28  1  0  0  0  0
 31 29  1  0  0  0  0
 34 32  1  0  0  0  0
 34 33  1  0  0  0  0
 35 30  1  0  0  0  0
 36 31  1  0  0  0  0
 37 35  2  0  0  0  0
 38 36  2  0  0  0  0
 42 32  1  0  0  0  0
 42 35  1  0  0  0  0
 43 33  1  0  0  0  0
 34 44  1  6  0  0  0
 44 36  1  0  0  0  0
 45 39  1  0  0  0  0
 45 40  1  0  0  0  0
 45 41  2  0  0  0  0
 45 43  1  0  0  0  0
 34 46  1  6  0  0  0
M  CHG  2  39  -1  40  -1
M  END
> <DATABASE_ID>
MMDBc0055108

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@](COC(=O)CCCCCCCCCCCCCCCC)(COP([O-])([O-])=O)OC(=O)CCCCCCCCCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C36H71O8P/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-30-35(37)42-32-34(33-43-45(39,40)41)44-36(38)31-29-27-25-23-21-18-16-14-12-10-8-6-4-2/h34H,3-33H2,1-2H3,(H2,39,40,41)/p-2/t34-/m1/s1

> <INCHI_KEY>
RWBVHFWDPWKJJF-UUWRZZSWSA-L

> <FORMULA>
C36H69O8P

> <MOLECULAR_WEIGHT>
660.915

> <EXACT_MASS>
660.47410334

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
114

> <JCHEM_AVERAGE_POLARIZABILITY>
81.60153820046855

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
-2

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R)-2-(hexadecanoyloxy)-3-(phosphonooxy)propyl heptadecanoate

> <JCHEM_LOGP>
12.324096415666666

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.343234649149876

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.3174060830586427

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744159310865148

> <JCHEM_POLAR_SURFACE_AREA>
125.02000000000002

> <JCHEM_REFRACTIVITY>
180.92940000000007

> <JCHEM_ROTATABLE_BOND_COUNT>
37

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-(hexadecanoyloxy)-3-(phosphonooxy)propyl heptadecanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-JUN-22         0                                  
HETATM    1  C   UNK     0     -22.894 -12.567   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      25.119 -12.567   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -21.560 -13.337   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      23.785 -13.337   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -20.226 -12.567   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      22.451 -12.567   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0     -18.893 -13.337   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      21.118 -13.337   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0     -17.559 -12.567   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      19.784 -12.567   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0     -16.225 -13.337   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      18.450 -13.337   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0     -14.892 -12.567   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      17.117 -12.567   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0     -13.558 -13.337   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.783 -13.337   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0     -12.224 -12.567   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.449 -12.567   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0     -10.891 -13.337   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -9.557 -12.567   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      13.116 -13.337   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -8.223 -13.337   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      11.782 -12.567   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -6.890 -12.567   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.448 -13.337   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -5.556 -13.337   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.115 -12.567   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -4.222 -12.567   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       7.781 -13.337   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -2.888 -13.337   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       6.447 -12.567   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.113 -12.567   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.446 -14.877   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0       2.446 -13.337   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      -1.555 -12.567   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       5.114 -13.337   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      -1.555 -11.027   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       5.114 -14.877   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0       2.240 -17.187   0.000  0.00  0.00           O-1
HETATM   40  O   UNK     0       5.320 -17.187   0.000  0.00  0.00           O-1
HETATM   41  O   UNK     0       3.780 -18.727   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      -0.221 -13.337   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       3.780 -15.647   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0       3.780 -12.567   0.000  0.00  0.00           O+0
HETATM   45  P   UNK     0       3.780 -17.187   0.000  0.00  0.00           P+0
HETATM   46  H   UNK     0       1.113 -14.107   0.000  0.00  0.00           H+0
CONECT    1    3                                                            
CONECT    2    4                                                            
CONECT    3    1    5                                                       
CONECT    4    2    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   14   18                                                       
CONECT   17   15   19                                                       
CONECT   18   16   21                                                       
CONECT   19   17   20                                                       
CONECT   20   19   22                                                       
CONECT   21   18   23                                                       
CONECT   22   20   24                                                       
CONECT   23   21   25                                                       
CONECT   24   22   26                                                       
CONECT   25   23   27                                                       
CONECT   26   24   28                                                       
CONECT   27   25   29                                                       
CONECT   28   26   30                                                       
CONECT   29   27   31                                                       
CONECT   30   28   35                                                       
CONECT   31   29   36                                                       
CONECT   32   34   42                                                       
CONECT   33   34   43                                                       
CONECT   34   32   33   44   46                                             
CONECT   35   30   37   42                                                  
CONECT   36   31   38   44                                                  
CONECT   37   35                                                            
CONECT   38   36                                                            
CONECT   39   45                                                            
CONECT   40   45                                                            
CONECT   41   45                                                            
CONECT   42   32   35                                                       
CONECT   43   33   45                                                       
CONECT   44   34   36                                                       
CONECT   45   39   40   41   43                                             
CONECT   46   34                                                            
MASTER        0    0    0    0    0    0    0    0   46    0   90    0
END

Synonyms

Not Available

Chemical Formula

C₃₆H₆₉O₈P

Average Molecular Weight

660.915

Monoisotopic Molecular Weight

660.47410334

IUPAC Name

(2R)-2-(hexadecanoyloxy)-3-(phosphonooxy)propyl heptadecanoate

Traditional Name

(2R)-2-(hexadecanoyloxy)-3-(phosphonooxy)propyl heptadecanoate

CAS Registry Number

Not Available

SMILES

[H][C@@](COC(=O)CCCCCCCCCCCCCCCC)(COP([O-])([O-])=O)OC(=O)CCCCCCCCCCCCCCC

InChI Identifier

InChI=1S/C36H71O8P/c1-3-5-7-9-11-13-15-17-19-20-22-24-26-28-30-35(37)42-32-34(33-43-45(39,40)41)44-36(38)31-29-27-25-23-21-18-16-14-12-10-8-6-4-2/h34H,3-33H2,1-2H3,(H2,39,40,41)/p-2/t34-/m1/s1

InChI Key

RWBVHFWDPWKJJF-UUWRZZSWSA-L

Chemical Taxonomy

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
logP	12.32	ChemAxon
pKa (Strongest Acidic)	1.32	ChemAxon
pKa (Strongest Basic)	-6.7	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	125.02 Å²	ChemAxon
Rotatable Bond Count	37	ChemAxon
Refractivity	180.93 m³·mol⁻¹	ChemAxon
Polarizability	81.6 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	Deposition Date
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

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Proteins

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
Fungi	Ascomycota	1

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

External Links

Not Available

References

Synthesis Reference

Not Available

General References

Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for 1-heptadecanoyl-2-hexadecanoyl-sn-glycero-3-phosphate (MMDBc0055108)

MOL for #<Metabolite:0x000055b76e19e670>

3D MOL for #<Metabolite:0x000055b76e19e670>

3D SDF for #<Metabolite:0x000055b76e19e670>

3D-SDF for #<Metabolite:0x000055b76e19e670>

PDB for #<Metabolite:0x000055b76e19e670>

3D PDB for #<Metabolite:0x000055b76e19e670>

SMILES for #<Metabolite:0x000055b76e19e670>

INCHI for #<Metabolite:0x000055b76e19e670>

Structure for #<Metabolite:0x000055b76e19e670>

3D Structure for #<Metabolite:0x000055b76e19e670>