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Showing metabocard for SM(d18:1/18:1(9Z)) (HMDB0012101)

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Record Information
Version5.0
StatusDetected and Quantified
Creation Date2009-03-24 16:22:23 UTC
Update Date2022-03-07 02:51:20 UTC
HMDB IDHMDB0012101
Secondary Accession Numbers
  • HMDB12101
Metabolite Identification
Common NameSM(d18:1/18:1(9Z))
DescriptionSphingomyelin (d18:1/18:1(9Z)) or SM(d18:1/18:1(9Z)) is a type of sphingolipid found in animal cell membranes, especially in the membranous myelin sheath which surrounds some nerve cell axons. It usually consists of phosphorylcholine and ceramide. SM(d18:1/18:1(9Z)) consists of a sphingosine backbone and an oleic acid chain. In humans, sphingomyelin is the only membrane phospholipid not derived from glycerol. Like all sphingolipids, SM has a ceramide core (sphingosine bonded to a fatty acid via an amide linkage). In addition, it contains one polar head group, which is either phosphocholine or phosphoethanolamine. The plasma membrane of cells is highly enriched in sphingomyelin and is considered largely to be found in the exoplasmic leaflet of the cell membrane. However, there is some evidence that there may also be a sphingomyelin pool in the inner leaflet of the membrane. Moreover, neutral sphingomyelinase-2, an enzyme that breaks down sphingomyelin into ceramide, has been found to localize exclusively to the inner leaflet further suggesting that there may be sphingomyelin present there. Sphingomyelin can accumulate in a rare hereditary disease called Niemann-Pick Disease, types A and B. Niemann-Pick disease is a genetically-inherited disease caused by a deficiency in the enzyme sphingomyelinase, which causes the accumulation of sphingomyelin in spleen, liver, lungs, bone marrow, and the brain, causing irreversible neurological damage. SMs play a role in signal transduction. Sphingomyelins are synthesized by the transfer of phosphorylcholine from phosphatidylcholine to a ceramide in a reaction catalyzed by sphingomyelin synthase.
Structure
Data?1582753012
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0012101 (SM(d18:1/18:1(9Z)))


  Mrv0541 02241203392D          

 50 49  0  0  1  0            999 V2000
    4.0975   -3.3466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.9503   -2.3516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.1139   -3.7741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.2433   -3.4810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8152   -2.9397    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5264   -3.3579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2441   -2.9510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.0884   -4.6233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9553   -3.3691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8061   -4.2164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.6729   -2.9622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5174   -4.6345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.3838   -3.3798    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1014   -2.9730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.8127   -3.3911    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5303   -2.9843    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2352   -4.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2415   -3.4024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9592   -2.9956    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9464   -4.6457    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6704   -3.4137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6641   -4.2387    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3881   -3.0069    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3752   -4.6570    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0993   -3.4250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0928   -4.2501    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.8209   -2.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1032   -3.0516    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2458   -3.0295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5281   -3.4364    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.8169   -3.0182    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.8038   -4.6678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5214   -4.2608    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   20.5322   -3.0629    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
   14.8233   -2.1932    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.7974   -5.4927    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.2675   -2.3226    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   18.0812   -3.7579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3920   -2.6334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9567   -3.4471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.6744   -3.0403    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    8.4125   -4.6233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3593   -4.1396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6237   -4.5134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0507   -4.5895    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9322   -4.0634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1968   -4.4373    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5052   -3.9872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7698   -4.3611    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  5  1  0  0  0  0
  2 34  1  0  0  0  0
  3 34  1  0  0  0  0
  4 34  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  9  1  0  0  0  0
  8 10  1  0  0  0  0
  9 11  1  0  0  0  0
 10 12  1  0  0  0  0
 11 13  1  0  0  0  0
 12 17  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 18  1  0  0  0  0
 17 20  1  0  0  0  0
 18 19  1  0  0  0  0
 19 21  1  0  0  0  0
 20 22  1  0  0  0  0
 21 23  1  0  0  0  0
 22 24  1  0  0  0  0
 23 25  2  0  0  0  0
 24 26  1  0  0  0  0
 25 31  1  0  0  0  0
 26 32  1  0  0  0  0
 27 28  1  0  0  0  0
 27 34  1  0  0  0  0
 28 39  1  0  0  0  0
 29 30  1  0  0  0  0
 29 40  1  0  0  0  0
 30 31  1  0  0  0  0
 30 33  1  6  0  0  0
 31 35  1  1  0  0  0
 32 33  1  0  0  0  0
 32 36  2  0  0  0  0
 37 41  1  0  0  0  0
 38 41  2  0  0  0  0
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 40 41  1  0  0  0  0
 42  8  2  0  0  0  0
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 46 44  1  0  0  0  0
 43 46  1  0  0  0  0
 47 45  1  0  0  0  0
 48 47  1  0  0  0  0
 49 48  1  0  0  0  0
 50 49  1  0  0  0  0
M  CHG  2  34   1  37  -1
M  END
Download

3D MOL for HMDB0012101 (SM(d18:1/18:1(9Z)))

HMDB0012101
     RDKit          3D
SM(d18:1/18:1(9Z))
131130  0  0  0  0  0  0  0  0999 V2000
   13.7579    1.1864    0.0720 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2805    2.5504    0.1378 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3855    3.7170    0.5212 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2645    4.0098   -0.3096 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9417    3.4267   -0.3449 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0506    4.0068    0.7929 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6194    3.6411    0.4691 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0643    2.3198    0.7852 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8928    1.1138    0.6545 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6987    0.0767   -0.1226 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4823    0.0553   -1.0438 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6266   -0.9847   -0.3775 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2653   -1.1893   -0.9614 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7088    0.2502   -1.1230 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1897    0.2031   -0.9519 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1537   -0.2267    0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3744   -1.5697    0.6369 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0344   -1.2423    0.9332 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5616   -1.4431    2.1376 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1702   -0.7420   -0.1016 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2086   -0.3583    0.1943 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8742   -1.7679    0.6234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5600   -2.4880   -0.4572 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9578   -3.8353   -1.0575 P   0  0  0  0  0  5  0  0  0  0  0  0
   -3.0041   -3.5217   -2.2331 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5848   -4.3775   -2.1723 O   0  0  0  0  0  1  0  0  0  0  0  0
   -2.4120   -5.2197   -0.3808 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4487   -5.4179    0.9894 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5858   -6.7273    1.0747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9726   -7.7809    0.2512 N   0  0  0  0  0  4  0  0  0  0  0  0
   -3.0932   -7.7544   -0.5903 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0279   -9.0205    1.0565 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8116   -8.0274   -0.6870 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4671    0.7534    1.0085 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.9759    0.7705    2.2760 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9483    1.1358    0.9778 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4265    1.5858   -0.1546 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8510    2.0138   -0.3390 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4003    1.3017   -1.5258 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6371   -0.1651   -1.4454 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.9731   -0.4570   -0.8582 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2988   -0.2315    0.5351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8689   -0.2231    0.7685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2779    1.1221    0.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7352    1.4357    0.4215 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8734    2.9527    0.3075 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4842    3.5938   -0.9534 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4578    5.1118   -0.7938 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1528    5.5574    0.4874 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1072    7.0819    0.6172 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8052    0.9773   -0.3586 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.9416    0.6290    1.0264 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.4986    0.6377   -0.6458 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.6712    2.8865   -0.8993 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.2072    2.6345    0.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.0523    4.6542    0.6583 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0970    3.5302    1.6186 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6383    4.2042   -1.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9950    5.1660   -0.0948 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3678    3.6502   -1.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9487    2.3458   -0.1621 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1933    5.0589    0.8297 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3685    3.5325    1.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4967    3.9476   -0.6453 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0068    4.4749    0.9742 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1777    2.2182    0.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4631    2.3099    1.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8546    1.1181    1.2778 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.3415   -0.7463   -0.1304 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9079   -0.5290   -1.9650 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0871    0.9341   -1.4255 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3784   -0.4868    0.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2335   -1.8905   -0.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6576   -1.7327   -0.1883 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2422   -1.7585   -1.8581 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1028    0.9570   -0.4103 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8971    0.5512   -2.1603 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7755    1.1725   -1.0771 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8397   -0.6354   -1.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1120   -0.2260    1.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5407    0.6093    1.0472 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3167   -1.9952   -0.4123 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8247   -2.2930    1.3288 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5186   -0.6413   -1.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7494   -0.2626   -0.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4728   -2.0088    1.5728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9780   -1.5205    0.5657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0407   -4.6428    1.5995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4469   -5.7266    1.3070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5338   -6.3137    0.7224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4618   -6.9732    2.1004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1858   -7.0262   -1.3893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0472   -7.9203   -0.0179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0267   -8.7422   -1.1961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0174   -9.3907    1.2296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7538   -9.7276    0.6670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4292   -8.6450    2.0500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0538   -7.2097   -0.5785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3269   -8.9773   -0.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1373   -7.9960   -1.7489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0191    1.7186    0.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4793    1.4348    2.7845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5432    0.9598    1.8406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7852    1.6554   -1.0664 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.7764    3.0999   -0.6337 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  CHG  2  26  -1  30   1
M  END
Download

3D SDF for HMDB0012101 (SM(d18:1/18:1(9Z)))


  Mrv0541 02241203392D          

 50 49  0  0  1  0            999 V2000
    4.0975   -3.3466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    5.5264   -3.3579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2441   -2.9510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    7.6729   -2.9622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.5174   -4.6345    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   11.2415   -3.4024    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   14.8038   -4.6678    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.5214   -4.2608    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   20.5322   -3.0629    0.0000 N   0  3  0  0  0  0  0  0  0  0  0  0
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   18.0812   -3.7579    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.3920   -2.6334    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9567   -3.4471    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.6744   -3.0403    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    8.4125   -4.6233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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 42  8  2  0  0  0  0
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 48 47  1  0  0  0  0
 49 48  1  0  0  0  0
 50 49  1  0  0  0  0
M  CHG  2  34   1  37  -1
M  END
> <DATABASE_ID>
HMDB0012101

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCCCCCCCCCC\C=C\[C@@H](O)[C@H](COP([O-])(=O)OCC[N+](C)(C)C)NC(=O)CCCCCCC\C=C/CCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C41H81N2O6P/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-41(45)42-39(38-49-50(46,47)48-37-36-43(3,4)5)40(44)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2/h20-21,32,34,39-40,44H,6-19,22-31,33,35-38H2,1-5H3,(H-,42,45,46,47)/b21-20-,34-32+/t39-,40+/m0/s1

> <INCHI_KEY>
NBEADXWAAWCCDG-QDDWGVBQSA-N

> <FORMULA>
C41H81N2O6P

> <MOLECULAR_WEIGHT>
729.0654

> <EXACT_MASS>
728.583224846

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
91.62697423150185

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-{[(2S,3R,4E)-3-hydroxy-2-[(9Z)-octadec-9-enamido]octadec-4-en-1-yl phosphonato]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
5.41

> <JCHEM_LOGP>
8.592617509546525

> <ALOGPS_LOGS>
-7.38

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
13.507093903444801

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.870915028856634

> <JCHEM_PKA_STRONGEST_BASIC>
0.011796153755674221

> <JCHEM_POLAR_SURFACE_AREA>
107.92000000000002

> <JCHEM_REFRACTIVITY>
224.26050000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
37

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.23e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
C18:1 sphingomyelin

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0012101 (SM(d18:1/18:1(9Z)))

HMDB0012101
     RDKit          3D
SM(d18:1/18:1(9Z))
131130  0  0  0  0  0  0  0  0999 V2000
   13.7579    1.1864    0.0720 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2805    2.5504    0.1378 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.3855    3.7170    0.5212 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2645    4.0098   -0.3096 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9417    3.4267   -0.3449 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.0506    4.0068    0.7929 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6194    3.6411    0.4691 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0643    2.3198    0.7852 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8928    1.1138    0.6545 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6987    0.0767   -0.1226 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4823    0.0553   -1.0438 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6266   -0.9847   -0.3775 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2653   -1.1893   -0.9614 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7088    0.2502   -1.1230 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1897    0.2031   -0.9519 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1537   -0.2267    0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3744   -1.5697    0.6369 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.5616   -1.4431    2.1376 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1702   -0.7420   -0.1016 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2086   -0.3583    0.1943 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.8742   -1.7679    0.6234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5600   -2.4880   -0.4572 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.6371   -0.1651   -1.4454 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.2988   -0.2315    0.5351 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8689   -0.2231    0.7685 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2779    1.1221    0.2723 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7352    1.4357    0.4215 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8734    2.9527    0.3075 C   0  0  0  0  0  0  0  0  0  0  0  0
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  -11.1528    5.5574    0.4874 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1072    7.0819    0.6172 C   0  0  0  0  0  0  0  0  0  0  0  0
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   15.2072    2.6345    0.7642 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.0523    4.6542    0.6583 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0970    3.5302    1.6186 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6383    4.2042   -1.4132 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9950    5.1660   -0.0948 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3678    3.6502   -1.2691 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.9487    2.3458   -0.1621 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.1933    5.0589    0.8297 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3685    3.5325    1.7422 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4967    3.9476   -0.6453 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.1777    2.2182    0.0091 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4631    2.3099    1.7377 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8546    1.1181    1.2778 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.9079   -0.5290   -1.9650 H   0  0  0  0  0  0  0  0  0  0  0  0
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    6.3784   -0.4868    0.6797 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2335   -1.8905   -0.1657 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6576   -1.7327   -0.1883 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2422   -1.7585   -1.8581 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1028    0.9570   -0.4103 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8971    0.5512   -2.1603 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7755    1.1725   -1.0771 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8397   -0.6354   -1.5992 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1120   -0.2260    1.0418 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5407    0.6093    1.0472 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3167   -1.9952   -0.4123 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8247   -2.2930    1.3288 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5186   -0.6413   -1.0579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7494   -0.2626   -0.8359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4728   -2.0088    1.5728 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9780   -1.5205    0.5657 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0407   -4.6428    1.5995 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4469   -5.7266    1.3070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5338   -6.3137    0.7224 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1858   -7.0262   -1.3893 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0472   -7.9203   -0.0179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0267   -8.7422   -1.1961 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0174   -9.3907    1.2296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7538   -9.7276    0.6670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4292   -8.6450    2.0500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0538   -7.2097   -0.5785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3269   -8.9773   -0.4855 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.0191    1.7186    0.5119 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4793    1.4348    2.7845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5432    0.9598    1.8406 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7852    1.6554   -1.0664 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3861    1.9660    0.5776 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7764    3.0999   -0.6337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4123    1.8106   -1.7753 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7480    1.6116   -2.3948 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4012   -0.7411   -2.3206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8564   -0.5755   -0.6287 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7226   -0.0209   -1.5959 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1356   -1.6082   -1.0200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0000   -1.0892    1.1903 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0082    0.6827    1.0400 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2885   -1.0530    0.2092 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9732   -0.2865    1.8642 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1259    1.1049   -0.8646 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.6102    1.8868    0.6651 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1568    1.0814    1.3477 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3049    0.9850   -0.4200 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9864    3.1171    0.4609 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3461    3.3583    1.2023 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4317    3.3504   -1.2804 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -9.4414    5.4952   -0.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3894    5.2328    1.3092 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1054    5.1379    0.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1489    7.4718    0.5568 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4950    7.4997   -0.1833 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7556    7.3748    1.6369 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  2  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  2  0
 18 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 24 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 30 32  1  0
 30 33  1  0
 21 34  1  0
 34 35  1  0
 34 36  1  0
 36 37  2  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 42 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  1  0
 46 47  1  0
 47 48  1  0
 48 49  1  0
 49 50  1  0
  1 51  1  0
  1 52  1  0
  1 53  1  0
  2 54  1  0
  2 55  1  0
  3 56  1  0
  3 57  1  0
  4 58  1  0
  4 59  1  0
  5 60  1  0
  5 61  1  0
  6 62  1  0
  6 63  1  0
  7 64  1  0
  7 65  1  0
  8 66  1  0
  8 67  1  0
  9 68  1  0
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 11 70  1  0
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 14 76  1  0
 14 77  1  0
 15 78  1  0
 15 79  1  0
 16 80  1  0
 16 81  1  0
 17 82  1  0
 17 83  1  0
 20 84  1  0
 21 85  1  6
 22 86  1  0
 22 87  1  0
 28 88  1  0
 28 89  1  0
 29 90  1  0
 29 91  1  0
 31 92  1  0
 31 93  1  0
 31 94  1  0
 32 95  1  0
 32 96  1  0
 32 97  1  0
 33 98  1  0
 33 99  1  0
 33100  1  0
 34101  1  6
 35102  1  0
 36103  1  0
 37104  1  0
 38105  1  0
 38106  1  0
 39107  1  0
 39108  1  0
 40109  1  0
 40110  1  0
 41111  1  0
 41112  1  0
 42113  1  0
 42114  1  0
 43115  1  0
 43116  1  0
 44117  1  0
 44118  1  0
 45119  1  0
 45120  1  0
 46121  1  0
 46122  1  0
 47123  1  0
 47124  1  0
 48125  1  0
 48126  1  0
 49127  1  0
 49128  1  0
 50129  1  0
 50130  1  0
 50131  1  0
M  CHG  2  26  -1  30   1
M  END
Download

PDB for HMDB0012101 (SM(d18:1/18:1(9Z)))

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0       7.649  -6.247   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      39.107  -4.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      37.546  -7.045   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      39.654  -6.498   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.988  -5.487   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      10.316  -6.268   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      11.656  -5.509   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      16.965  -8.630   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      12.983  -6.289   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      18.305  -7.871   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.323  -5.529   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      19.632  -8.651   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      15.650  -6.309   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      16.989  -5.550   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      18.317  -6.330   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      19.657  -5.571   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      20.972  -7.892   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      20.984  -6.351   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      22.324  -5.592   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      22.300  -8.672   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      23.651  -6.372   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      23.640  -7.912   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      24.991  -5.613   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      24.967  -8.693   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      26.319  -6.393   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      26.307  -7.934   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      36.999  -4.937   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      35.659  -5.696   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      30.325  -5.655   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      28.986  -6.415   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      27.658  -5.634   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      27.634  -8.713   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0      28.973  -7.953   0.000  0.00  0.00           N+0
HETATM   34  N   UNK     0      38.327  -5.717   0.000  0.00  0.00           N+1
HETATM   35  O   UNK     0      27.670  -4.094   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      27.622 -10.253   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0      32.233  -4.336   0.000  0.00  0.00           O-1
HETATM   38  O   UNK     0      33.752  -7.015   0.000  0.00  0.00           O+0
HETATM   39  O   UNK     0      34.332  -4.916   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      31.653  -6.435   0.000  0.00  0.00           O+0
HETATM   41  P   UNK     0      32.992  -5.675   0.000  0.00  0.00           P+0
HETATM   42  C   UNK     0      15.703  -8.630   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      14.534  -7.869   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      11.871  -7.727   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      10.498  -8.425   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      13.161  -8.567   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0       9.207  -7.585   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0       7.834  -8.283   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0       6.543  -7.443   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0       5.170  -8.141   0.000  0.00  0.00           C+0
CONECT    1    5                                                            
CONECT    2   34                                                            
CONECT    3   34                                                            
CONECT    4   34                                                            
CONECT    5    1    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    9                                                       
CONECT    8   10   42                                                       
CONECT    9    7   11                                                       
CONECT   10    8   12                                                       
CONECT   11    9   13                                                       
CONECT   12   10   17                                                       
CONECT   13   11   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   18                                                       
CONECT   17   12   20                                                       
CONECT   18   16   19                                                       
CONECT   19   18   21                                                       
CONECT   20   17   22                                                       
CONECT   21   19   23                                                       
CONECT   22   20   24                                                       
CONECT   23   21   25                                                       
CONECT   24   22   26                                                       
CONECT   25   23   31                                                       
CONECT   26   24   32                                                       
CONECT   27   28   34                                                       
CONECT   28   27   39                                                       
CONECT   29   30   40                                                       
CONECT   30   29   31   33                                                  
CONECT   31   25   30   35                                                  
CONECT   32   26   33   36                                                  
CONECT   33   30   32                                                       
CONECT   34    2    3    4   27                                             
CONECT   35   31                                                            
CONECT   36   32                                                            
CONECT   37   41                                                            
CONECT   38   41                                                            
CONECT   39   28   41                                                       
CONECT   40   29   41                                                       
CONECT   41   37   38   39   40                                             
CONECT   42    8   43                                                       
CONECT   43   42   46                                                       
CONECT   44   45   46                                                       
CONECT   45   44   47                                                       
CONECT   46   44   43                                                       
CONECT   47   45   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49                                                            
MASTER        0    0    0    0    0    0    0    0   50    0   98    0
END
Download

3D PDB for HMDB0012101 (SM(d18:1/18:1(9Z)))

COMPND    HMDB0012101
HETATM    1  C1  UNL     1      13.758   1.186   0.072  1.00  0.00           C  
HETATM    2  C2  UNL     1      14.280   2.550   0.138  1.00  0.00           C  
HETATM    3  C3  UNL     1      13.386   3.717   0.521  1.00  0.00           C  
HETATM    4  C4  UNL     1      12.265   4.010  -0.310  1.00  0.00           C  
HETATM    5  C5  UNL     1      10.942   3.427  -0.345  1.00  0.00           C  
HETATM    6  C6  UNL     1      10.051   4.007   0.793  1.00  0.00           C  
HETATM    7  C7  UNL     1       8.619   3.641   0.469  1.00  0.00           C  
HETATM    8  C8  UNL     1       8.064   2.320   0.785  1.00  0.00           C  
HETATM    9  C9  UNL     1       8.893   1.114   0.654  1.00  0.00           C  
HETATM   10  C10 UNL     1       8.699   0.077  -0.123  1.00  0.00           C  
HETATM   11  C11 UNL     1       7.482   0.055  -1.044  1.00  0.00           C  
HETATM   12  C12 UNL     1       6.627  -0.985  -0.378  1.00  0.00           C  
HETATM   13  C13 UNL     1       5.265  -1.189  -0.961  1.00  0.00           C  
HETATM   14  C14 UNL     1       4.709   0.250  -1.123  1.00  0.00           C  
HETATM   15  C15 UNL     1       3.190   0.203  -0.952  1.00  0.00           C  
HETATM   16  C16 UNL     1       3.154  -0.227   0.559  1.00  0.00           C  
HETATM   17  C17 UNL     1       2.374  -1.570   0.637  1.00  0.00           C  
HETATM   18  C18 UNL     1       1.034  -1.242   0.933  1.00  0.00           C  
HETATM   19  O1  UNL     1       0.562  -1.443   2.138  1.00  0.00           O  
HETATM   20  N1  UNL     1       0.170  -0.742  -0.102  1.00  0.00           N  
HETATM   21  C19 UNL     1      -1.209  -0.358   0.194  1.00  0.00           C  
HETATM   22  C20 UNL     1      -1.874  -1.768   0.623  1.00  0.00           C  
HETATM   23  O2  UNL     1      -1.560  -2.488  -0.457  1.00  0.00           O  
HETATM   24  P1  UNL     1      -1.958  -3.835  -1.058  1.00  0.00           P  
HETATM   25  O3  UNL     1      -3.004  -3.522  -2.233  1.00  0.00           O  
HETATM   26  O4  UNL     1      -0.585  -4.378  -2.172  1.00  0.00           O1-
HETATM   27  O5  UNL     1      -2.412  -5.220  -0.381  1.00  0.00           O  
HETATM   28  C21 UNL     1      -2.449  -5.418   0.989  1.00  0.00           C  
HETATM   29  C22 UNL     1      -1.586  -6.727   1.075  1.00  0.00           C  
HETATM   30  N2  UNL     1      -1.973  -7.781   0.251  1.00  0.00           N1+
HETATM   31  C23 UNL     1      -3.093  -7.754  -0.590  1.00  0.00           C  
HETATM   32  C24 UNL     1      -2.028  -9.021   1.057  1.00  0.00           C  
HETATM   33  C25 UNL     1      -0.812  -8.027  -0.687  1.00  0.00           C  
HETATM   34  C26 UNL     1      -1.467   0.753   1.009  1.00  0.00           C  
HETATM   35  O6  UNL     1      -0.976   0.771   2.276  1.00  0.00           O  
HETATM   36  C27 UNL     1      -2.948   1.136   0.978  1.00  0.00           C  
HETATM   37  C28 UNL     1      -3.427   1.586  -0.155  1.00  0.00           C  
HETATM   38  C29 UNL     1      -4.851   2.014  -0.339  1.00  0.00           C  
HETATM   39  C30 UNL     1      -5.400   1.302  -1.526  1.00  0.00           C  
HETATM   40  C31 UNL     1      -5.637  -0.165  -1.445  1.00  0.00           C  
HETATM   41  C32 UNL     1      -6.973  -0.457  -0.858  1.00  0.00           C  
HETATM   42  C33 UNL     1      -7.299  -0.231   0.535  1.00  0.00           C  
HETATM   43  C34 UNL     1      -8.869  -0.223   0.769  1.00  0.00           C  
HETATM   44  C35 UNL     1      -9.278   1.122   0.272  1.00  0.00           C  
HETATM   45  C36 UNL     1     -10.735   1.436   0.421  1.00  0.00           C  
HETATM   46  C37 UNL     1     -10.873   2.953   0.307  1.00  0.00           C  
HETATM   47  C38 UNL     1     -10.484   3.594  -0.953  1.00  0.00           C  
HETATM   48  C39 UNL     1     -10.458   5.112  -0.794  1.00  0.00           C  
HETATM   49  C40 UNL     1     -11.153   5.557   0.487  1.00  0.00           C  
HETATM   50  C41 UNL     1     -11.107   7.082   0.617  1.00  0.00           C  
HETATM   51  H1  UNL     1      12.805   0.977  -0.359  1.00  0.00           H  
HETATM   52  H2  UNL     1      13.942   0.629   1.026  1.00  0.00           H  
HETATM   53  H3  UNL     1      14.499   0.638  -0.646  1.00  0.00           H  
HETATM   54  H4  UNL     1      14.671   2.887  -0.899  1.00  0.00           H  
HETATM   55  H5  UNL     1      15.207   2.634   0.764  1.00  0.00           H  
HETATM   56  H6  UNL     1      14.052   4.654   0.658  1.00  0.00           H  
HETATM   57  H7  UNL     1      13.097   3.530   1.619  1.00  0.00           H  
HETATM   58  H8  UNL     1      12.638   4.204  -1.413  1.00  0.00           H  
HETATM   59  H9  UNL     1      11.995   5.166  -0.095  1.00  0.00           H  
HETATM   60  H10 UNL     1      10.368   3.650  -1.269  1.00  0.00           H  
HETATM   61  H11 UNL     1      10.949   2.346  -0.162  1.00  0.00           H  
HETATM   62  H12 UNL     1      10.193   5.059   0.830  1.00  0.00           H  
HETATM   63  H13 UNL     1      10.368   3.533   1.742  1.00  0.00           H  
HETATM   64  H14 UNL     1       8.497   3.948  -0.645  1.00  0.00           H  
HETATM   65  H15 UNL     1       8.007   4.475   0.974  1.00  0.00           H  
HETATM   66  H16 UNL     1       7.178   2.218   0.009  1.00  0.00           H  
HETATM   67  H17 UNL     1       7.463   2.310   1.738  1.00  0.00           H  
HETATM   68  H18 UNL     1       9.855   1.118   1.278  1.00  0.00           H  
HETATM   69  H19 UNL     1       9.342  -0.746  -0.130  1.00  0.00           H  
HETATM   70  H20 UNL     1       7.908  -0.529  -1.965  1.00  0.00           H  
HETATM   71  H21 UNL     1       7.087   0.934  -1.425  1.00  0.00           H  
HETATM   72  H22 UNL     1       6.378  -0.487   0.680  1.00  0.00           H  
HETATM   73  H23 UNL     1       7.234  -1.891  -0.166  1.00  0.00           H  
HETATM   74  H24 UNL     1       4.658  -1.733  -0.188  1.00  0.00           H  
HETATM   75  H25 UNL     1       5.242  -1.758  -1.858  1.00  0.00           H  
HETATM   76  H26 UNL     1       5.103   0.957  -0.410  1.00  0.00           H  
HETATM   77  H27 UNL     1       4.897   0.551  -2.160  1.00  0.00           H  
HETATM   78  H28 UNL     1       2.775   1.173  -1.077  1.00  0.00           H  
HETATM   79  H29 UNL     1       2.840  -0.635  -1.599  1.00  0.00           H  
HETATM   80  H30 UNL     1       4.112  -0.226   1.042  1.00  0.00           H  
HETATM   81  H31 UNL     1       2.541   0.609   1.047  1.00  0.00           H  
HETATM   82  H32 UNL     1       2.317  -1.995  -0.412  1.00  0.00           H  
HETATM   83  H33 UNL     1       2.825  -2.293   1.329  1.00  0.00           H  
HETATM   84  H34 UNL     1       0.519  -0.641  -1.058  1.00  0.00           H  
HETATM   85  H35 UNL     1      -1.749  -0.263  -0.836  1.00  0.00           H  
HETATM   86  H36 UNL     1      -1.473  -2.009   1.573  1.00  0.00           H  
HETATM   87  H37 UNL     1      -2.978  -1.520   0.566  1.00  0.00           H  
HETATM   88  H38 UNL     1      -2.041  -4.643   1.599  1.00  0.00           H  
HETATM   89  H39 UNL     1      -3.447  -5.727   1.307  1.00  0.00           H  
HETATM   90  H40 UNL     1      -0.534  -6.314   0.722  1.00  0.00           H  
HETATM   91  H41 UNL     1      -1.462  -6.973   2.100  1.00  0.00           H  
HETATM   92  H42 UNL     1      -3.186  -7.026  -1.389  1.00  0.00           H  
HETATM   93  H43 UNL     1      -4.047  -7.920  -0.018  1.00  0.00           H  
HETATM   94  H44 UNL     1      -3.027  -8.742  -1.196  1.00  0.00           H  
HETATM   95  H45 UNL     1      -1.017  -9.391   1.230  1.00  0.00           H  
HETATM   96  H46 UNL     1      -2.754  -9.728   0.667  1.00  0.00           H  
HETATM   97  H47 UNL     1      -2.429  -8.645   2.050  1.00  0.00           H  
HETATM   98  H48 UNL     1      -0.054  -7.210  -0.578  1.00  0.00           H  
HETATM   99  H49 UNL     1      -0.327  -8.977  -0.485  1.00  0.00           H  
HETATM  100  H50 UNL     1      -1.137  -7.996  -1.749  1.00  0.00           H  
HETATM  101  H51 UNL     1      -1.019   1.719   0.512  1.00  0.00           H  
HETATM  102  H52 UNL     1      -1.479   1.435   2.784  1.00  0.00           H  
HETATM  103  H53 UNL     1      -3.543   0.960   1.841  1.00  0.00           H  
HETATM  104  H54 UNL     1      -2.785   1.655  -1.066  1.00  0.00           H  
HETATM  105  H55 UNL     1      -5.386   1.966   0.578  1.00  0.00           H  
HETATM  106  H56 UNL     1      -4.776   3.100  -0.634  1.00  0.00           H  
HETATM  107  H57 UNL     1      -6.412   1.811  -1.775  1.00  0.00           H  
HETATM  108  H58 UNL     1      -4.748   1.612  -2.395  1.00  0.00           H  
HETATM  109  H59 UNL     1      -5.401  -0.741  -2.321  1.00  0.00           H  
HETATM  110  H60 UNL     1      -4.856  -0.575  -0.629  1.00  0.00           H  
HETATM  111  H61 UNL     1      -7.723  -0.021  -1.596  1.00  0.00           H  
HETATM  112  H62 UNL     1      -7.136  -1.608  -1.020  1.00  0.00           H  
HETATM  113  H63 UNL     1      -7.000  -1.089   1.190  1.00  0.00           H  
HETATM  114  H64 UNL     1      -7.008   0.683   1.040  1.00  0.00           H  
HETATM  115  H65 UNL     1      -9.288  -1.053   0.209  1.00  0.00           H  
HETATM  116  H66 UNL     1      -8.973  -0.287   1.864  1.00  0.00           H  
HETATM  117  H67 UNL     1      -9.126   1.105  -0.865  1.00  0.00           H  
HETATM  118  H68 UNL     1      -8.610   1.887   0.665  1.00  0.00           H  
HETATM  119  H69 UNL     1     -11.157   1.081   1.348  1.00  0.00           H  
HETATM  120  H70 UNL     1     -11.305   0.985  -0.420  1.00  0.00           H  
HETATM  121  H71 UNL     1     -11.986   3.117   0.461  1.00  0.00           H  
HETATM  122  H72 UNL     1     -10.346   3.358   1.202  1.00  0.00           H  
HETATM  123  H73 UNL     1      -9.432   3.350  -1.280  1.00  0.00           H  
HETATM  124  H74 UNL     1     -11.132   3.338  -1.824  1.00  0.00           H  
HETATM  125  H75 UNL     1     -10.979   5.617  -1.630  1.00  0.00           H  
HETATM  126  H76 UNL     1      -9.441   5.495  -0.758  1.00  0.00           H  
HETATM  127  H77 UNL     1     -10.389   5.233   1.309  1.00  0.00           H  
HETATM  128  H78 UNL     1     -12.105   5.138   0.729  1.00  0.00           H  
HETATM  129  H79 UNL     1     -12.149   7.472   0.557  1.00  0.00           H  
HETATM  130  H80 UNL     1     -10.495   7.500  -0.183  1.00  0.00           H  
HETATM  131  H81 UNL     1     -10.756   7.375   1.637  1.00  0.00           H  
CONECT    1    2   51   52   53
CONECT    2    3   54   55
CONECT    3    4   56   57
CONECT    4    5   58   59
CONECT    5    6   60   61
CONECT    6    7   62   63
CONECT    7    8   64   65
CONECT    8    9   66   67
CONECT    9   10   10   68
CONECT   10   11   69
CONECT   11   12   70   71
CONECT   12   13   72   73
CONECT   13   14   74   75
CONECT   14   15   76   77
CONECT   15   16   78   79
CONECT   16   17   80   81
CONECT   17   18   82   83
CONECT   18   19   19   20
CONECT   20   21   84
CONECT   21   22   34   85
CONECT   22   23   86   87
CONECT   23   24
CONECT   24   25   25   26   27
CONECT   27   28
CONECT   28   29   88   89
CONECT   29   30   90   91
CONECT   30   31   32   33
CONECT   31   92   93   94
CONECT   32   95   96   97
CONECT   33   98   99  100
CONECT   34   35   36  101
CONECT   35  102
CONECT   36   37   37  103
CONECT   37   38  104
CONECT   38   39  105  106
CONECT   39   40  107  108
CONECT   40   41  109  110
CONECT   41   42  111  112
CONECT   42   43  113  114
CONECT   43   44  115  116
CONECT   44   45  117  118
CONECT   45   46  119  120
CONECT   46   47  121  122
CONECT   47   48  123  124
CONECT   48   49  125  126
CONECT   49   50  127  128
CONECT   50  129  130  131
END
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SMILES for HMDB0012101 (SM(d18:1/18:1(9Z)))

CCCCCCCCCCCCC\C=C\[C@@H](O)[C@H](COP([O-])(=O)OCC[N+](C)(C)C)NC(=O)CCCCCCC\C=C/CCCCCCCC
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INCHI for HMDB0012101 (SM(d18:1/18:1(9Z)))

InChI=1S/C41H81N2O6P/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-41(45)42-39(38-49-50(46,47)48-37-36-43(3,4)5)40(44)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2/h20-21,32,34,39-40,44H,6-19,22-31,33,35-38H2,1-5H3,(H-,42,45,46,47)/b21-20-,34-32+/t39-,40+/m0/s1
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View in JSmolView Stereo Labels
Synonyms
ValueSource
N-(9Z-Octadecenoyl)-sphing-4-enine-1-phosphocholineChEBI
N-(9Z-Octadecenoyl)-sphingosine-1-phosphocholineChEBI
SM(D18:1/18:1(9Z))ChEBI
N-OleoylsphingomyelinMeSH
N-Oleoyl-sphingomyelinMeSH
C18:1 SphingomyelinHMDB
SphingomyelinHMDB
N-(9Z-Octadecenoyl)-1-phosphocholine-sphing-4-enineMetBuilder, HMDB
Sphingomyelin(D18:1/18:1(9Z))MetBuilder, HMDB
N-(9Z-Octadecenoyl)-1-phosphocholine-sphingosineMetBuilder, HMDB
N-(9Z-Octadecenoyl)-1-phosphocholine-D-erythro-sphingosineMetBuilder, HMDB
N-(9Z-Octadecenoyl)-1-phosphocholine-4-sphingenineMetBuilder, HMDB
N-(9Z-Octadecenoyl)-1-phosphocholine-D-sphingosineMetBuilder, HMDB
N-(9Z-Octadecenoyl)-1-phosphocholine-sphingenineMetBuilder, HMDB
N-(9Z-Octadecenoyl)-1-phosphocholine-erythro-4-sphingenineMetBuilder, HMDB
N-Oleyl sphingomyelinHMDB
N-OleylsphingomyelinHMDB
SM d18:1/18:1(9Z)HMDB
Sphingomyelin (d18:1,C18:1(9Z))HMDB
Sphingomyelin (d18:1/18:1(9Z))HMDB
Chemical FormulaC41H81N2O6P
Average Molecular Weight729.0654
Monoisotopic Molecular Weight728.583224846
IUPAC Name(2-{[(2S,3R,4E)-3-hydroxy-2-[(9Z)-octadec-9-enamido]octadec-4-en-1-yl phosphonato]oxy}ethyl)trimethylazanium
Traditional NameC18:1 sphingomyelin
CAS Registry Number108392-10-5
SMILES
CCCCCCCCCCCCC\C=C\[C@@H](O)[C@H](COP([O-])(=O)OCC[N+](C)(C)C)NC(=O)CCCCCCC\C=C/CCCCCCCC
InChI Identifier
InChI=1S/C41H81N2O6P/c1-6-8-10-12-14-16-18-20-21-23-25-27-29-31-33-35-41(45)42-39(38-49-50(46,47)48-37-36-43(3,4)5)40(44)34-32-30-28-26-24-22-19-17-15-13-11-9-7-2/h20-21,32,34,39-40,44H,6-19,22-31,33,35-38H2,1-5H3,(H-,42,45,46,47)/b21-20-,34-32+/t39-,40+/m0/s1
InChI KeyNBEADXWAAWCCDG-QDDWGVBQSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as phosphosphingolipids. These are sphingolipids with a structure based on a sphingoid base that is attached to a phosphate head group. They differ from phosphonospingolipids which have a phosphonate head group.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassSphingolipids
Sub ClassPhosphosphingolipids
Direct ParentPhosphosphingolipids
Alternative Parents
Substituents
  • Sphingoid-1-phosphate or derivatives
  • Phosphocholine
  • Phosphoethanolamine
  • Dialkyl phosphate
  • Fatty amide
  • N-acyl-amine
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Fatty acyl
  • Alkyl phosphate
  • Tetraalkylammonium salt
  • Quaternary ammonium salt
  • Secondary carboxylic acid amide
  • Secondary alcohol
  • Carboxamide group
  • Carboxylic acid derivative
  • Organic zwitterion
  • Alcohol
  • Organic oxide
  • Organooxygen compound
  • Organonitrogen compound
  • Organopnictogen compound
  • Organic oxygen compound
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Carbonyl group
  • Amine
  • Organic salt
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
Physiological effect
Health effect
Disposition
Biological locationSource
Process
Naturally occurring process
Role
Biological roleIndustrial application
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility3.2e-05 g/LALOGPS
logP5.41ALOGPS
logP8.59ChemAxon
logS-7.4ALOGPS
pKa (Strongest Acidic)1.87ChemAxon
pKa (Strongest Basic)0.012ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area107.92 ŲChemAxon
Rotatable Bond Count37ChemAxon
Refractivity224.26 m³·mol⁻¹ChemAxon
Polarizability91.63 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+276.9230932474
DeepCCS[M-H]-275.09530932474
DeepCCS[M-2H]-308.33830932474
DeepCCS[M+Na]+282.52630932474
AllCCS[M+H]+287.332859911
AllCCS[M+H-H2O]+287.132859911
AllCCS[M+NH4]+287.432859911
AllCCS[M+Na]+287.432859911
AllCCS[M-H]-277.732859911
AllCCS[M+Na-2H]-281.932859911
AllCCS[M+HCOO]-286.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
SM(d18:1/18:1(9Z))CCCCCCCCCCCCC\C=C\[C@@H](O)[C@H](COP([O-])(=O)OCC[N+](C)(C)C)NC(=O)CCCCCCC\C=C/CCCCCCCC4805.0Standard polar33892256
SM(d18:1/18:1(9Z))CCCCCCCCCCCCC\C=C\[C@@H](O)[C@H](COP([O-])(=O)OCC[N+](C)(C)C)NC(=O)CCCCCCC\C=C/CCCCCCCC3990.8Standard non polar33892256
SM(d18:1/18:1(9Z))CCCCCCCCCCCCC\C=C\[C@@H](O)[C@H](COP([O-])(=O)OCC[N+](C)(C)C)NC(=O)CCCCCCC\C=C/CCCCCCCC5082.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
SM(d18:1/18:1(9Z)),2TMS,isomer #1CCCCCCCC/C=C\CCCCCCCC(=O)N([C@@H](COP(=O)([O-])OCC[N+](C)(C)C)[C@@H](/C=C/CCCCCCCCCCCCC)O[Si](C)(C)C)[Si](C)(C)C4900.0Semi standard non polar33892256
SM(d18:1/18:1(9Z)),2TMS,isomer #1CCCCCCCC/C=C\CCCCCCCC(=O)N([C@@H](COP(=O)([O-])OCC[N+](C)(C)C)[C@@H](/C=C/CCCCCCCCCCCCC)O[Si](C)(C)C)[Si](C)(C)C4617.2Standard non polar33892256
SM(d18:1/18:1(9Z)),2TMS,isomer #1CCCCCCCC/C=C\CCCCCCCC(=O)N([C@@H](COP(=O)([O-])OCC[N+](C)(C)C)[C@@H](/C=C/CCCCCCCCCCCCC)O[Si](C)(C)C)[Si](C)(C)C5368.0Standard polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - SM(d18:1/18:1(9Z)) GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - SM(d18:1/18:1(9Z)) GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - SM(d18:1/18:1(9Z)) GC-MS (TBDMS_1_1) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - SM(d18:1/18:1(9Z)) GC-MS (TBDMS_1_2) - 70eV, PositiveNot Available2021-10-18Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 10V, Negative-QTOFsplash10-004i-0010004900-dea7ba518bbfc4f15a272017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 20V, Negative-QTOFsplash10-00c3-1051049200-0311f77eb57e7807dd102017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 40V, Negative-QTOFsplash10-003r-8192020000-f3855e7325623d6b4ffe2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 10V, Negative-QTOFsplash10-004i-0000000900-cfbc63ea55eb2839af652021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 20V, Negative-QTOFsplash10-004i-0000003900-08741cb9c3b33b1992ad2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 40V, Negative-QTOFsplash10-004i-9010301000-f662cc300bda5e734b942021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 10V, Positive-QTOFsplash10-005j-6030190400-2199516124b105c78d0a2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 20V, Positive-QTOFsplash10-001j-2170191000-ac0b7defd92663a2e4122017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 40V, Positive-QTOFsplash10-0019-6090022000-c94378815e0d7bc588192017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 10V, Positive-QTOFsplash10-0udi-0000011900-c24f77272c836a1ce5de2021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 20V, Positive-QTOFsplash10-0vi0-0000092900-68d26d9bd52e74b719212021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 40V, Positive-QTOFsplash10-014i-0000091100-de65f9558dc25c76eaa92021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 10V, Positive-QTOFsplash10-0059-0600000900-cb85eb0e93fc9848d0c22021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 20V, Positive-QTOFsplash10-0059-0600000900-cb85eb0e93fc9848d0c22021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 40V, Positive-QTOFsplash10-001i-0900000300-7a6866c8a54dae9837d42021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 10V, Positive-QTOFsplash10-000i-0000011900-1f16a32161a7261c24ba2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 20V, Positive-QTOFsplash10-0ue0-0000092900-19833048ed3fa195e44f2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - SM(d18:1/18:1(9Z)) 40V, Positive-QTOFsplash10-0udi-0000091100-d670cc72f6b77d8abd052021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen Locations
  • Blood
  • Cerebrospinal Fluid (CSF)
  • Feces
  • Saliva
  • Urine
Tissue Locations
  • Placenta
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified4.00-19.5 uMAdult (>18 years old)Both
Normal		 details
BloodDetected and Quantified14.2 (12-16.9) uMNewborn (0-30 days old)Not Available
Normal		 details
BloodDetected and Quantified9.78 (8.08-12.1) uMInfant (0-1 year old)Not Available
Normal		 details
BloodDetected and Quantified10.8 +/- 0.2 uMAdult (>18 years old)BothNormal details
BloodDetected and Quantified11.0 +/- 2.56 uMAdult (>18 years old)BothNormal details
Cerebrospinal Fluid (CSF)Detected and Quantified0.069 +/- 0.026 uMAdult (>18 years old)Not SpecifiedNormal details
FecesDetected and Quantified0.11 +/- 0.16 nmol/g wet fecesAdult (>18 years old)Both
Normal		 details
FecesDetected and Quantified0.16 +/- 0.23 nmol/g wet fecesAdult (>18 years old)Both
Normal		 details
SalivaDetected and Quantified0.015 +/- 0.003 uMAdult (>18 years old)BothNormal
    • Zerihun T. Dame, ...
 details
UrineDetected and Quantified0.0004 (0.0001-0.0013) umol/mmol creatinineAdult (>18 years old)Both
Normal		 details
UrineDetected and Quantified0.0022 +/- 0.0048 umol/mmol creatinineChildren (1 - 13 years old)Not Specified
Normal
    • Analysis of 30 no...
 details
UrineDetected and Quantified0.0-0.06 umol/mmol creatinineNewborn (0-30 days old)BothNormal details
UrineDetected and Quantified0.01(0.0-0.06) umol/mmol creatinineNewborn (0-30 days old)FemaleNormal details
UrineDetected and Quantified0.01(0.0-0.06) umol/mmol creatinineNewborn (0-30 days old)MaleNormal details
Abnormal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
BloodDetected and Quantified9.60 +/- 2.89 uMChildren (1-13 years old)Both
Obesity
    • Metabolomics reve...
 details
BloodDetected and Quantified10.23 +/- 3.05 uMChildren (1-13 years old)Both
Obesity
    • Metabolomics reve...
 details
UrineDetected and Quantified0.0011 +/- 0.0021 umol/mmol creatinineChildren (1 - 13 years old)Not Specified
Eosinophilic esophagitis
    • Analysis of 30 no...
 details
UrineDetected and Quantified0.002 +/- 0.0048 umol/mmol creatinineChildren (1 - 13 years old)Not Specified
Gastroesophageal reflux disease
    • Analysis of 30 no...
 details
Associated Disorders and Diseases
Disease References
Obesity
  1. Simone Wahl, Christina Holzapfel, Zhonghao Yu, Michaela Breier, Ivan Kondofersky, Christiane Fuchs, Paula Singmann, Cornelia Prehn, Jerzy Adamski, Harald Grallert, Thomas Illig, Rui Wang-Sattler, Thomas Reinehr (2013). Metabolomics reveals determinants of weight loss during lifestyle intervention in obese children. Metabolomics.
Eosinophilic esophagitis
  1. Slae, M., Huynh, H., Wishart, D.S. (2014). Analysis of 30 normal pediatric urine samples via NMR spectroscopy (unpublished work). NA.
Associated OMIM IDs
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID4947837
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound6443882
PDB IDNot Available
ChEBI ID84487
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
  3. Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
  4. 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 ]
  5. Divecha N, Irvine RF: Phospholipid signaling. Cell. 1995 Jan 27;80(2):269-78. [PubMed:7834746 ]
  6. Ghosh S, Strum JC, Bell RM: Lipid biochemistry: functions of glycerolipids and sphingolipids in cellular signaling. FASEB J. 1997 Jan;11(1):45-50. [PubMed:9034165 ]
  7. Hannun YA: The sphingomyelin cycle and the second messenger function of ceramide. J Biol Chem. 1994 Feb 4;269(5):3125-8. [PubMed:8106344 ]
  8. Elshenawy S, Pinney SE, Stuart T, Doulias PT, Zura G, Parry S, Elovitz MA, Bennett MJ, Bansal A, Strauss JF 3rd, Ischiropoulos H, Simmons RA: The Metabolomic Signature of the Placenta in Spontaneous Preterm Birth. Int J Mol Sci. 2020 Feb 4;21(3). pii: ijms21031043. doi: 10.3390/ijms21031043. [PubMed:32033212 ]
  9. Cevc, Gregor (1993). Phospholipids Handbook. Marcel Dekker.
  10. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Only showing the first 10 proteins. There are 50 proteins in total.

Show all enzymes and transporters

Enzymes

Enzyme Details
1. Globoside alpha-1,3-N-acetylgalactosaminyltransferase 1
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
Catalyzes the formation of some glycolipid via the addition of N-acetylgalactosamine (GalNAc) in alpha-1,3-linkage to some substrate. Glycolipids probably serve for adherence of some pathogens
Gene Name:
GBGT1
Uniprot ID:
Q8N5D6
Molecular weight:
40126.9
Enzyme Details
2. N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase
General function:
Involved in N-acetylglucosaminylphosphatidylinositol de
Specific function:
Involved in the second step of GPI biosynthesis. De-N-acetylation of N-acetylglucosaminyl-phosphatidylinositol.
Gene Name:
PIGL
Uniprot ID:
Q9Y2B2
Molecular weight:
28530.965
Enzyme Details
3. Sphingomyelin phosphodiesterase
General function:
Involved in hydrolase activity
Specific function:
Converts sphingomyelin to ceramide. Also has phospholipase C activities toward 1,2-diacylglycerolphosphocholine and 1,2-diacylglycerolphosphoglycerol. Isoform 2 and isoform 3 have lost catalytic activity.
Gene Name:
SMPD1
Uniprot ID:
P17405
Molecular weight:
69935.53
Enzyme Details
4. Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1
General function:
Involved in galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase activity
Specific function:
Involved in the biosynthesis of L2/HNK-1 carbohydrate epitope on glycoproteins. Can also play a role in glycosaminoglycan biosynthesis. Substrates include asialo-orosomucoid (ASOR), asialo-fetuin, and asialo-neural cell adhesion molecule. Requires sphingomyelin for activity: stearoyl-sphingomyelin was the most effective, followed by palmitoyl-sphingomyelin and lignoceroyl-sphingomyelin. Activity was demonstrated only for sphingomyelin with a saturated fatty acid and not for that with an unsaturated fatty acid, regardless of the length of the acyl group (By similarity).
Gene Name:
B3GAT1
Uniprot ID:
Q9P2W7
Molecular weight:
38255.675
Enzyme Details
5. Phosphatidylinositol N-acetylglucosaminyltransferase subunit Q
General function:
Involved in phosphatidylinositol N-acetylglucosaminyltransferase activity
Specific function:
Part of the complex catalyzing the transfer of N-acetylglucosamine from UDP-N-acetylglucosamine to phosphatidylinositol, the first step of GPI biosynthesis.
Gene Name:
PIGQ
Uniprot ID:
Q9BRB3
Molecular weight:
65343.25
Enzyme Details
6. Phosphatidylinositol N-acetylglucosaminyltransferase subunit A
General function:
Involved in biosynthetic process
Specific function:
Necessary for the synthesis of N-acetylglucosaminyl-phosphatidylinositol, the very early intermediate in GPI-anchor biosynthesis.
Gene Name:
PIGA
Uniprot ID:
P37287
Molecular weight:
54126.065
Enzyme Details
7. Phosphatidylinositol N-acetylglucosaminyltransferase subunit H
General function:
Involved in phosphatidylinositol N-acetylglucosaminyltr
Specific function:
Part of the complex catalyzing the transfer of N-acetylglucosamine from UDP-N-acetylglucosamine to phosphatidylinositol, the first step of GPI biosynthesis.
Gene Name:
PIGH
Uniprot ID:
Q14442
Molecular weight:
21080.415
Enzyme Details
8. Phosphatidylinositol N-acetylglucosaminyltransferase subunit P
General function:
Involved in phosphatidylinositol N-acetylglucosaminyltr
Specific function:
Part of the complex catalyzing the transfer of N-acetylglucosamine from UDP-N-acetylglucosamine to phosphatidylinositol, the first step of GPI biosynthesis.
Gene Name:
PIGP
Uniprot ID:
P57054
Molecular weight:
18089.055
Enzyme Details
9. Phosphatidylinositol N-acetylglucosaminyltransferase subunit C
General function:
Involved in phosphatidylinositol N-acetylglucosaminyltransferase activity
Specific function:
Part of the complex catalyzing the transfer of N-acetylglucosamine from UDP-N-acetylglucosamine to phosphatidylinositol, the first step of GPI biosynthesis.
Gene Name:
PIGC
Uniprot ID:
Q92535
Molecular weight:
33582.18
Enzyme Details
10. Ectonucleotide pyrophosphatase/phosphodiesterase family member 7
General function:
Involved in catalytic activity
Specific function:
Converts sphingomyelin to ceramide. Also has phospholipase C activity toward palmitoyl lyso-phosphocholine. Does not appear to have nucleotide pyrophosphatase activity.
Gene Name:
ENPP7
Uniprot ID:
Q6UWV6
Molecular weight:
51493.415

Only showing the first 10 proteins. There are 50 proteins in total.

Show all enzymes and transporters