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Showing metabocard for PI(18:0/18:1(9Z)) (HMDB0240667)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2020-06-08 20:11:44 UTC
Update Date2022-11-30 19:53:43 UTC
HMDB IDHMDB0240667
Secondary Accession NumbersNone
Metabolite Identification
Common NamePI(18:0/18:1(9Z))
DescriptionPI(18:0/18:1(9Z)) is a phosphatidylinositol. Phosphatidylinositols are important lipids, both as a key membrane constituent and as a participant in essential metabolic processes, both directly and via a number of metabolites. Phosphatidylinositols are acidic (anionic) phospholipids that consist of a phosphatidic acid backbone, linked via the phosphate group to inositol (hexahydroxycyclohexane). Phosphatidylinositols can have many different combinations of fatty acids of varying lengths and saturation attached at the C-1 and C-2 positions. Fatty acids containing 18 and 20 carbons are the most common. PI(18:0/18:0), in particular, consists of one chain of stearic acid at the C-1 position and one chain of oleic acid at the C-2 position. The inositol group that is part of every phosphatidylinositol lipid is covalently linked to the phosphate group that acts as a bridge to the lipid tail. In most organisms, the stereochemical form of this inositol is myo-D-inositol (with one axial hydroxyl in position 2 with the remainder equatorial), although other forms can be found in certain plant phosphatidylinositols. Phosphatidylinositol is especially abundant in brain tissue, where it can amount to 10% of the phospholipids, but it is present in all tissues and cell types. There is usually less of it than of phosphatidylcholine, phosphatidylethanolamine, and phosphatidylserine. In animal tissues, phosphatidylinositol is the primary source of the arachidonic acid required for the biosynthesis of eicosanoids, including prostaglandins, via the action of the enzyme phospholipase A2. Phosphatidylinositol can be phosphorylated by a number of different kinases that place the phosphate moiety on positions 4 and 5 of the inositol ring, although position 3 can also be phosphorylated by a specific kinase. Seven different isomers are known, but the most important in both quantitative and biological terms are phosphatidylinositol 4-phosphate and phosphatidylinositol 4,5-bisphosphate. Phosphatidylinositol and the phosphatidylinositol phosphates are the main sources of diacylglycerols that serve as signalling molecules, via the action of phospholipase C enzymes. While most phospholipids have a saturated fatty acid on C-1 and an unsaturated fatty acid on C-2 of the glycerol backbone, the fatty acid distribution at the C-1 and C-2 positions of glycerol within phospholipids is continually in flux, owing to phospholipid degradation and the continuous phospholipid remodelling that occurs while these molecules are in membranes. PIs contain almost exclusively stearic acid at carbon 1 and arachidonic acid at carbon 2. PIs composed exclusively of non-phosphorylated inositol exhibit a net charge of -1 at physiological pH. Molecules with phosphorylated inositol (such as PIP, PIP2, PIP3, etc.) are termed polyphosphoinositides. The polyphosphoinositides are important intracellular transducers of signals emanating from the plasma membrane. The synthesis of PI involves CDP-activated 1,2-diacylglycerol condensation with myo-inositol.
Structure
Data?1591648663
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0240667 (PI(18:0/18:1(9Z)))

PI(18:0/18:1(9Z))
  Mrv1652306082022132D          

 60 60  0  0  1  0            999 V2000
   -3.8020    0.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0969    0.7716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3824    0.3590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6679    0.7716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9699   -0.3554    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7950   -0.3554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4706    0.3595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2454    0.7696    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9590    0.3595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1677    1.4839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6563    1.4839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8961   -0.4661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3256    0.3595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4706    2.0075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8961    2.8317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3256    2.0075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8973    0.3576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6117    0.7701    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6117    1.5949    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8973    2.0073    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1831    1.5949    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1831    0.7701    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5121    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5121    1.5409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2262    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9403    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6544    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3685    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0826    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7968    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5109    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2250    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9391    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6532    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3673    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0815    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.7956    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5097    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.2238    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.9379    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.6520    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -1.5393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2236   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9377   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6518   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3660   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0801   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7942   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5083   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2224   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0474   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7615   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4756   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1897   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.9039   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.6180   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.3321   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.0462   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.7603   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 23  1  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  3  5  1  1  0  0  0
  3  6  1  0  0  0  0
  4  3  1  0  0  0  0
  6 42  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  8 11  1  0  0  0  0
  9  4  1  0  0  0  0
 17 18  1  0  0  0  0
 17 22  1  0  0  0  0
 17 12  1  1  0  0  0
 18 19  1  0  0  0  0
 18 13  1  6  0  0  0
 19 20  1  0  0  0  0
 19 16  1  1  0  0  0
 20 21  1  0  0  0  0
 20 15  1  6  0  0  0
 21 22  1  0  0  0  0
 21 14  1  6  0  0  0
 22  7  1  6  0  0  0
 23 24  2  0  0  0  0
 23 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
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  2  0  0  0  0
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 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
M  END
Download

3D MOL for HMDB0240667 (PI(18:0/18:1(9Z)))

HMDB0240667
     RDKit          3D
PI(18:0/18:1(9Z))
144144  0  0  0  0  0  0  0  0999 V2000
   -4.8338  -12.4500   -3.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2400  -12.9727   -1.9938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8488  -12.3772   -1.7943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2038  -12.8449   -0.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0439  -12.4554    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3451  -12.9409    1.9255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9825  -12.7064    3.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2000  -11.3229    3.7262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0476  -10.4907    2.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6293   -9.3450    2.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3251   -8.7414    2.6183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5955   -8.5796    1.2915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3926   -7.6853    0.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6936   -7.4533   -0.9307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3391   -6.8254   -0.7289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3823   -5.4990   -0.0605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1216   -4.4341   -0.8170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0882   -3.1855   -0.0094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6646   -3.2150    1.1827 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4957   -1.9652   -0.4873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4441   -0.7583    0.3595 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8634   -0.3007    0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2440    0.8378    1.0281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0535    2.1520    0.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4386    2.5026   -0.2298 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5646    3.2382    1.7027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9533    4.5388    1.3052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4036    5.7011    2.1289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7015    6.9583    1.6977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9079    7.3351    0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1589    8.6205   -0.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6842    8.4637    0.1483 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0544    9.7515   -0.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5206    9.5890    0.0424 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3518   10.8011   -0.2810 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8157   10.5334    0.0202 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7108   11.6636   -0.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8019   12.2843   -1.5805 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1999   11.5255   -2.7810 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2851   10.4514   -3.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8116    9.7551   -4.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7700    8.6906   -4.8249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4216    0.1229   -0.2409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0633    1.2520    0.4559 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1246    2.0878   -0.4142 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.8243    3.5585   -0.3531 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0967    1.4981   -2.0008 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6672    1.7658    0.1909 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6247    0.9603    1.3229 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4078   -0.3089    1.0623 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3586   -1.0660    2.2505 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8360   -0.0358    0.7485 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0729   -0.5278   -0.5566 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2128    1.4196    0.7374 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6169    1.4709    0.8386 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6460    2.2186    1.8548 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4781    3.5701    1.4938 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3583    1.6992    2.4180 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5415    2.7912    2.7655 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0990  -12.6567   -4.1080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9906  -11.3523   -3.1790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7832  -12.9814   -3.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1578  -14.0610   -2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8920  -12.7191   -1.1612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2042  -12.5897   -2.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9742  -11.2852   -1.7342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2381  -12.3180   -0.4186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0332  -13.9410   -0.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0004  -13.0232    0.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2780  -11.4088    0.6518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1455  -14.0443    1.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2998  -12.4828    1.9951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9493  -13.3019    3.3343 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2839  -13.1864    4.0069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1662  -10.8936    3.8780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7244  -11.3332    4.7329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0804  -10.8353    2.5982 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3408   -8.7983    1.7498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6821   -9.1723    3.3823 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5593   -7.6960    3.0243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5422   -9.6273    0.8799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5469   -8.2681    1.4253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6752   -6.7315    0.8865 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3371   -8.2020    0.1350 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3376   -6.8520   -1.5607 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5392   -8.4456   -1.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0702   -6.6563   -1.7656 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3691   -7.4774   -0.2180 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6852   -5.1328    0.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7228   -5.5396    0.9965 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1507   -4.7389   -1.0986 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5992   -4.1933   -1.7717 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1258   -1.1527    1.3597 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2231   -0.1752   -0.7222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5379   -1.1838    0.6729 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6577    3.2567    1.6843 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2508    2.9123    2.7208 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8441    4.4365    1.4758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1593    4.7330    0.2342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2866    5.4822    3.1913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5044    5.8879    1.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5946    6.7616    1.8163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9156    7.7987    2.3863 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9639    7.4513   -0.0377 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4703    6.5583   -0.4262 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3639    8.8995   -1.1200 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5565    9.4024    0.5990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4805    8.3413    1.2509 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2339    7.5977   -0.3364 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3178   10.5693    0.4149 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1288    9.9076   -1.2900 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9396    8.7381   -0.5427 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7139    9.3464    1.1134 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0539   11.6339    0.4125 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2338   11.1697   -1.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8763   10.4153    1.1918 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1981    9.5832   -0.3154 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7712   11.3013    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5918   12.4828    0.5379 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8601   12.8812   -1.7981 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5679   13.1297   -1.4892 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3378   12.2176   -3.6812 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2352   11.0897   -2.6609 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0801    9.7208   -2.4682 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3121   10.9165   -3.5654 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7945    9.2905   -4.2884 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8374   10.4917   -5.3014 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8603    7.8157   -4.1642 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8301    8.4182   -5.8987 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7432    9.1315   -4.6693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8133    0.4330   -1.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5214   -0.4333   -0.5158 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5566    0.6192   -1.9814 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5904    0.6941    1.6138 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8942   -0.9379    0.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6524   -1.7646    2.2015 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5491   -0.6154    1.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2357   -0.5323   -1.0835 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9815    1.8387   -0.2730 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9524    2.3389    1.1166 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3797    2.2445    2.7025 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6925    3.7284    0.9484 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5133    1.0567    3.3170 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7533    2.4732    3.2765 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
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  1  0
 30 31  1  0
 31 32  1  0
 32 33  1  0
 33 34  1  0
 34 35  1  0
 35 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 39 40  1  0
 40 41  1  0
 41 42  1  0
 21 43  1  0
 43 44  1  0
 44 45  1  0
 45 46  2  0
 45 47  1  0
 45 48  1  0
 48 49  1  0
 49 50  1  0
 50 51  1  0
 50 52  1  0
 52 53  1  0
 52 54  1  0
 54 55  1  0
 54 56  1  0
 56 57  1  0
 56 58  1  0
 58 59  1  0
 58 49  1  0
  1 60  1  0
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 43131  1  0
 43132  1  0
 47133  1  0
 49134  1  1
 50135  1  6
 51136  1  0
 52137  1  1
 53138  1  0
 54139  1  6
 55140  1  0
 56141  1  1
 57142  1  0
 58143  1  1
 59144  1  0
M  END
Download

3D SDF for HMDB0240667 (PI(18:0/18:1(9Z)))

PI(18:0/18:1(9Z))
  Mrv1652306082022132D          

 60 60  0  0  1  0            999 V2000
   -3.8020    0.3607    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0969    0.7716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3824    0.3590    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.6679    0.7716    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9699   -0.3554    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7950   -0.3554    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4706    0.3595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2454    0.7696    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9590    0.3595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1677    1.4839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6563    1.4839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8961   -0.4661    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3256    0.3595    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.4706    2.0075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8961    2.8317    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3256    2.0075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8973    0.3576    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6117    0.7701    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.6117    1.5949    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8973    2.0073    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1831    1.5949    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1831    0.7701    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.5121    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5121    1.5409    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2262    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9403    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6544    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3685    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0826    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7968    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5109    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2250    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9391    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6532    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.3673    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0815    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.7956    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.5097    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.2238    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.9379    0.7695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -16.6520    0.3564    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5095   -1.5393    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2236   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9377   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6518   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3660   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0801   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.7942   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5083   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2224   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0474   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7615   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.4756   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.1897   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.9039   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.6180   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -14.3321   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.0462   -0.3548    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  -15.7603   -0.7679    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1 23  1  0  0  0  0
  2  1  1  0  0  0  0
  3  2  1  0  0  0  0
  3  5  1  1  0  0  0
  3  6  1  0  0  0  0
  4  3  1  0  0  0  0
  6 42  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  8 10  2  0  0  0  0
  8 11  1  0  0  0  0
  9  4  1  0  0  0  0
 17 18  1  0  0  0  0
 17 22  1  0  0  0  0
 17 12  1  1  0  0  0
 18 19  1  0  0  0  0
 18 13  1  6  0  0  0
 19 20  1  0  0  0  0
 19 16  1  1  0  0  0
 20 21  1  0  0  0  0
 20 15  1  6  0  0  0
 21 22  1  0  0  0  0
 21 14  1  6  0  0  0
 22  7  1  6  0  0  0
 23 24  2  0  0  0  0
 23 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
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 36 37  1  0  0  0  0
 37 38  1  0  0  0  0
 38 39  1  0  0  0  0
 39 40  1  0  0  0  0
 40 41  1  0  0  0  0
 42 43  2  0  0  0  0
 42 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
 46 47  1  0  0  0  0
 47 48  1  0  0  0  0
 48 49  1  0  0  0  0
 49 50  1  0  0  0  0
 50 51  1  0  0  0  0
 51 52  2  0  0  0  0
 52 53  1  0  0  0  0
 53 54  1  0  0  0  0
 54 55  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 60  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0240667

> <DATABASE_NAME>
hmdb

> <SMILES>
[H][C@@](COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)OC(=O)CCCCCCC\C=C/CCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C45H85O13P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(46)55-35-37(36-56-59(53,54)58-45-43(51)41(49)40(48)42(50)44(45)52)57-39(47)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h18,20,37,40-45,48-52H,3-17,19,21-36H2,1-2H3,(H,53,54)/b20-18-/t37-,40-,41-,42+,43-,44-,45-/m1/s1

> <INCHI_KEY>
YOBFISPJJWPPTK-BAAZTTAESA-N

> <FORMULA>
C45H85O13P

> <MOLECULAR_WEIGHT>
865.1224

> <EXACT_MASS>
864.572779318

> <JCHEM_ACCEPTOR_COUNT>
9

> <JCHEM_ATOM_COUNT>
144

> <JCHEM_AVERAGE_POLARIZABILITY>
102.78696772062054

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[(2R)-2-[(9Z)-octadec-9-enoyloxy]-3-(octadecanoyloxy)propoxy]({[(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy})phosphinic acid

> <ALOGPS_LOGP>
7.71

> <JCHEM_LOGP>
10.410408893333333

> <ALOGPS_LOGS>
-6.24

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
12.360530531715522

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8332552462032856

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6458130204247565

> <JCHEM_POLAR_SURFACE_AREA>
209.50999999999996

> <JCHEM_REFRACTIVITY>
230.08840000000004

> <JCHEM_ROTATABLE_BOND_COUNT>
41

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.01e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R)-2-[(9Z)-octadec-9-enoyloxy]-3-(octadecanoyloxy)propoxy([(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy)phosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0240667 (PI(18:0/18:1(9Z)))

HMDB0240667
     RDKit          3D
PI(18:0/18:1(9Z))
144144  0  0  0  0  0  0  0  0999 V2000
   -4.8338  -12.4500   -3.3110 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2400  -12.9727   -1.9938 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8488  -12.3772   -1.7943 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2038  -12.8449   -0.5254 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0439  -12.4554    0.7093 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3451  -12.9409    1.9255 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9825  -12.7064    3.2318 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2000  -11.3229    3.7262 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0476  -10.4907    2.8612 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6293   -9.3450    2.3815 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3251   -8.7414    2.6183 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5955   -8.5796    1.2915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3926   -7.6853    0.4030 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6936   -7.4533   -0.9307 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3391   -6.8254   -0.7289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3823   -5.4990   -0.0605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1216   -4.4341   -0.8170 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0882   -3.1855   -0.0094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6646   -3.2150    1.1827 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4957   -1.9652   -0.4873 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4441   -0.7583    0.3595 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8634   -0.3007    0.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2440    0.8378    1.0281 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0535    2.1520    0.7814 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4386    2.5026   -0.2298 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5646    3.2382    1.7027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9533    4.5388    1.3052 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4036    5.7011    2.1289 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7015    6.9583    1.6977 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9079    7.3351    0.2692 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1589    8.6205   -0.0844 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6842    8.4637    0.1483 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0544    9.7515   -0.2124 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5206    9.5890    0.0424 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3518   10.8011   -0.2810 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8157   10.5334    0.0202 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7108   11.6636   -0.2616 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8019   12.2843   -1.5805 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1999   11.5255   -2.7810 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2851   10.4514   -3.2275 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8116    9.7551   -4.4889 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7700    8.6906   -4.8249 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4216    0.1229   -0.2409 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0633    1.2520    0.4559 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1246    2.0878   -0.4142 P   0  0  0  0  0  5  0  0  0  0  0  0
    0.8243    3.5585   -0.3531 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0967    1.4981   -2.0008 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6672    1.7658    0.1909 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6247    0.9603    1.3229 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.4078   -0.3089    1.0623 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3586   -1.0660    2.2505 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8360   -0.0358    0.7485 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.0729   -0.5278   -0.5566 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2128    1.4196    0.7374 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.6169    1.4709    0.8386 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.6460    2.2186    1.8548 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.4781    3.5701    1.4938 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3583    1.6992    2.4180 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5415    2.7912    2.7655 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0990  -12.6567   -4.1080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9906  -11.3523   -3.1790 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7832  -12.9814   -3.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1578  -14.0610   -2.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8920  -12.7191   -1.1612 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2042  -12.5897   -2.6529 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9742  -11.2852   -1.7342 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2381  -12.3180   -0.4186 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0332  -13.9410   -0.5203 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0004  -13.0232    0.6237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2780  -11.4088    0.6518 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1455  -14.0443    1.8473 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
Download

PDB for HMDB0240667 (PI(18:0/18:1(9Z)))

HEADER    PROTEIN                                 08-JUN-20   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: PI(18:0/18:1(9Z))                                 
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-JUN-20         0                                  
HETATM    1  O   UNK     0      -7.097   0.673   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      -5.781   1.440   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.447   0.670   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.113   1.440   0.000  0.00  0.00           C+0
HETATM    5  H   UNK     0      -3.677  -0.663   0.000  0.00  0.00           H+0
HETATM    6  O   UNK     0      -5.217  -0.663   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       0.878   0.671   0.000  0.00  0.00           O+0
HETATM    8  P   UNK     0      -0.458   1.437   0.000  0.00  0.00           P+0
HETATM    9  O   UNK     0      -1.790   0.671   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0       0.313   2.770   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      -1.225   2.770   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       3.539  -0.870   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0       6.208   0.671   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0       0.878   3.747   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       3.539   5.286   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       6.208   3.747   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0       3.542   0.668   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.875   1.438   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       4.875   2.977   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       3.542   3.747   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.208   2.977   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.208   1.438   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -8.423   1.436   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -8.423   2.876   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -9.756   0.665   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0     -11.089   1.436   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0     -12.422   0.665   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0     -13.755   1.436   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0     -15.088   0.665   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0     -16.421   1.436   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0     -17.754   0.665   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0     -19.087   1.436   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0     -20.420   0.665   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0     -21.753   1.436   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0     -23.086   0.665   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0     -24.419   1.436   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0     -25.752   0.665   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0     -27.085   1.436   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0     -28.418   0.665   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0     -29.751   1.436   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0     -31.084   0.665   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      -6.551  -1.433   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      -6.551  -2.873   0.000  0.00  0.00           O+0
HETATM   44  C   UNK     0      -7.884  -0.662   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      -9.217  -1.433   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0     -10.550  -0.662   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0     -11.883  -1.433   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0     -13.216  -0.662   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0     -14.549  -1.433   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0     -15.882  -0.662   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0     -17.215  -1.433   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0     -18.755  -1.433   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0     -20.088  -0.662   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0     -21.421  -1.433   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0     -22.754  -0.662   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0     -24.087  -1.433   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0     -25.420  -0.662   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0     -26.753  -1.433   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0     -28.086  -0.662   0.000  0.00  0.00           C+0
HETATM   60  C   UNK     0     -29.419  -1.433   0.000  0.00  0.00           C+0
CONECT    1   23    2                                                       
CONECT    2    1    3                                                       
CONECT    3    2    5    6    4                                             
CONECT    4    3    9                                                       
CONECT    5    3                                                            
CONECT    6    3   42                                                       
CONECT    7    8   22                                                       
CONECT    8    7    9   10   11                                             
CONECT    9    8    4                                                       
CONECT   10    8                                                            
CONECT   11    8                                                            
CONECT   12   17                                                            
CONECT   13   18                                                            
CONECT   14   21                                                            
CONECT   15   20                                                            
CONECT   16   19                                                            
CONECT   17   18   22   12                                                  
CONECT   18   17   19   13                                                  
CONECT   19   18   20   16                                                  
CONECT   20   19   21   15                                                  
CONECT   21   20   22   14                                                  
CONECT   22   17   21    7                                                  
CONECT   23    1   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   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   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36                                                       
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40                                                       
CONECT   40   39   41                                                       
CONECT   41   40                                                            
CONECT   42    6   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42   45                                                       
CONECT   45   44   46                                                       
CONECT   46   45   47                                                       
CONECT   47   46   48                                                       
CONECT   48   47   49                                                       
CONECT   49   48   50                                                       
CONECT   50   49   51                                                       
CONECT   51   50   52                                                       
CONECT   52   51   53                                                       
CONECT   53   52   54                                                       
CONECT   54   53   55                                                       
CONECT   55   54   56                                                       
CONECT   56   55   57                                                       
CONECT   57   56   58                                                       
CONECT   58   57   59                                                       
CONECT   59   58   60                                                       
CONECT   60   59                                                            
MASTER        0    0    0    0    0    0    0    0   60    0  120    0
END
Download

3D PDB for HMDB0240667 (PI(18:0/18:1(9Z)))

COMPND    HMDB0240667
HETATM    1  C1  UNL     1      -4.834 -12.450  -3.311  1.00  0.00           C  
HETATM    2  C2  UNL     1      -4.240 -12.973  -1.994  1.00  0.00           C  
HETATM    3  C3  UNL     1      -2.849 -12.377  -1.794  1.00  0.00           C  
HETATM    4  C4  UNL     1      -2.204 -12.845  -0.525  1.00  0.00           C  
HETATM    5  C5  UNL     1      -3.044 -12.455   0.709  1.00  0.00           C  
HETATM    6  C6  UNL     1      -2.345 -12.941   1.926  1.00  0.00           C  
HETATM    7  C7  UNL     1      -2.982 -12.706   3.232  1.00  0.00           C  
HETATM    8  C8  UNL     1      -3.200 -11.323   3.726  1.00  0.00           C  
HETATM    9  C9  UNL     1      -4.048 -10.491   2.861  1.00  0.00           C  
HETATM   10  C10 UNL     1      -3.629  -9.345   2.381  1.00  0.00           C  
HETATM   11  C11 UNL     1      -2.325  -8.741   2.618  1.00  0.00           C  
HETATM   12  C12 UNL     1      -1.596  -8.580   1.291  1.00  0.00           C  
HETATM   13  C13 UNL     1      -2.393  -7.685   0.403  1.00  0.00           C  
HETATM   14  C14 UNL     1      -1.694  -7.453  -0.931  1.00  0.00           C  
HETATM   15  C15 UNL     1      -0.339  -6.825  -0.729  1.00  0.00           C  
HETATM   16  C16 UNL     1      -0.382  -5.499  -0.061  1.00  0.00           C  
HETATM   17  C17 UNL     1      -1.122  -4.434  -0.817  1.00  0.00           C  
HETATM   18  C18 UNL     1      -1.088  -3.185  -0.009  1.00  0.00           C  
HETATM   19  O1  UNL     1      -0.665  -3.215   1.183  1.00  0.00           O  
HETATM   20  O2  UNL     1      -1.496  -1.965  -0.487  1.00  0.00           O  
HETATM   21  C19 UNL     1      -1.444  -0.758   0.360  1.00  0.00           C  
HETATM   22  C20 UNL     1      -2.863  -0.301   0.370  1.00  0.00           C  
HETATM   23  O3  UNL     1      -3.244   0.838   1.028  1.00  0.00           O  
HETATM   24  C21 UNL     1      -3.054   2.152   0.781  1.00  0.00           C  
HETATM   25  O4  UNL     1      -2.439   2.503  -0.230  1.00  0.00           O  
HETATM   26  C22 UNL     1      -3.565   3.238   1.703  1.00  0.00           C  
HETATM   27  C23 UNL     1      -2.953   4.539   1.305  1.00  0.00           C  
HETATM   28  C24 UNL     1      -3.404   5.701   2.129  1.00  0.00           C  
HETATM   29  C25 UNL     1      -2.702   6.958   1.698  1.00  0.00           C  
HETATM   30  C26 UNL     1      -2.908   7.335   0.269  1.00  0.00           C  
HETATM   31  C27 UNL     1      -2.159   8.621  -0.084  1.00  0.00           C  
HETATM   32  C28 UNL     1      -0.684   8.464   0.148  1.00  0.00           C  
HETATM   33  C29 UNL     1       0.054   9.752  -0.212  1.00  0.00           C  
HETATM   34  C30 UNL     1       1.521   9.589   0.042  1.00  0.00           C  
HETATM   35  C31 UNL     1       2.352  10.801  -0.281  1.00  0.00           C  
HETATM   36  C32 UNL     1       3.816  10.533   0.020  1.00  0.00           C  
HETATM   37  C33 UNL     1       4.711  11.664  -0.262  1.00  0.00           C  
HETATM   38  C34 UNL     1       4.802  12.284  -1.580  1.00  0.00           C  
HETATM   39  C35 UNL     1       5.200  11.525  -2.781  1.00  0.00           C  
HETATM   40  C36 UNL     1       4.285  10.451  -3.228  1.00  0.00           C  
HETATM   41  C37 UNL     1       4.812   9.755  -4.489  1.00  0.00           C  
HETATM   42  C38 UNL     1       3.770   8.691  -4.825  1.00  0.00           C  
HETATM   43  C39 UNL     1      -0.422   0.123  -0.241  1.00  0.00           C  
HETATM   44  O5  UNL     1      -0.063   1.252   0.456  1.00  0.00           O  
HETATM   45  P1  UNL     1       1.125   2.088  -0.414  1.00  0.00           P  
HETATM   46  O6  UNL     1       0.824   3.559  -0.353  1.00  0.00           O  
HETATM   47  O7  UNL     1       1.097   1.498  -2.001  1.00  0.00           O  
HETATM   48  O8  UNL     1       2.667   1.766   0.191  1.00  0.00           O  
HETATM   49  C40 UNL     1       2.625   0.960   1.323  1.00  0.00           C  
HETATM   50  C41 UNL     1       3.408  -0.309   1.062  1.00  0.00           C  
HETATM   51  O9  UNL     1       3.359  -1.066   2.251  1.00  0.00           O  
HETATM   52  C42 UNL     1       4.836  -0.036   0.748  1.00  0.00           C  
HETATM   53  O10 UNL     1       5.073  -0.528  -0.557  1.00  0.00           O  
HETATM   54  C43 UNL     1       5.213   1.420   0.737  1.00  0.00           C  
HETATM   55  O11 UNL     1       6.617   1.471   0.839  1.00  0.00           O  
HETATM   56  C44 UNL     1       4.646   2.219   1.855  1.00  0.00           C  
HETATM   57  O12 UNL     1       4.478   3.570   1.494  1.00  0.00           O  
HETATM   58  C45 UNL     1       3.358   1.699   2.418  1.00  0.00           C  
HETATM   59  O13 UNL     1       2.541   2.791   2.765  1.00  0.00           O  
HETATM   60  H1  UNL     1      -4.099 -12.657  -4.108  1.00  0.00           H  
HETATM   61  H2  UNL     1      -4.991 -11.352  -3.179  1.00  0.00           H  
HETATM   62  H3  UNL     1      -5.783 -12.981  -3.437  1.00  0.00           H  
HETATM   63  H4  UNL     1      -4.158 -14.061  -2.114  1.00  0.00           H  
HETATM   64  H5  UNL     1      -4.892 -12.719  -1.161  1.00  0.00           H  
HETATM   65  H6  UNL     1      -2.204 -12.590  -2.653  1.00  0.00           H  
HETATM   66  H7  UNL     1      -2.974 -11.285  -1.734  1.00  0.00           H  
HETATM   67  H8  UNL     1      -1.238 -12.318  -0.419  1.00  0.00           H  
HETATM   68  H9  UNL     1      -2.033 -13.941  -0.520  1.00  0.00           H  
HETATM   69  H10 UNL     1      -4.000 -13.023   0.624  1.00  0.00           H  
HETATM   70  H11 UNL     1      -3.278 -11.409   0.652  1.00  0.00           H  
HETATM   71  H12 UNL     1      -2.146 -14.044   1.847  1.00  0.00           H  
HETATM   72  H13 UNL     1      -1.300 -12.483   1.995  1.00  0.00           H  
HETATM   73  H14 UNL     1      -3.949 -13.302   3.334  1.00  0.00           H  
HETATM   74  H15 UNL     1      -2.284 -13.186   4.007  1.00  0.00           H  
HETATM   75  H16 UNL     1      -2.166 -10.894   3.878  1.00  0.00           H  
HETATM   76  H17 UNL     1      -3.724 -11.333   4.733  1.00  0.00           H  
HETATM   77  H18 UNL     1      -5.080 -10.835   2.598  1.00  0.00           H  
HETATM   78  H19 UNL     1      -4.341  -8.798   1.750  1.00  0.00           H  
HETATM   79  H20 UNL     1      -1.682  -9.172   3.382  1.00  0.00           H  
HETATM   80  H21 UNL     1      -2.559  -7.696   3.024  1.00  0.00           H  
HETATM   81  H22 UNL     1      -1.542  -9.627   0.880  1.00  0.00           H  
HETATM   82  H23 UNL     1      -0.547  -8.268   1.425  1.00  0.00           H  
HETATM   83  H24 UNL     1      -2.675  -6.732   0.886  1.00  0.00           H  
HETATM   84  H25 UNL     1      -3.337  -8.202   0.135  1.00  0.00           H  
HETATM   85  H26 UNL     1      -2.338  -6.852  -1.561  1.00  0.00           H  
HETATM   86  H27 UNL     1      -1.539  -8.446  -1.391  1.00  0.00           H  
HETATM   87  H28 UNL     1       0.070  -6.656  -1.766  1.00  0.00           H  
HETATM   88  H29 UNL     1       0.369  -7.477  -0.218  1.00  0.00           H  
HETATM   89  H30 UNL     1       0.685  -5.133   0.005  1.00  0.00           H  
HETATM   90  H31 UNL     1      -0.723  -5.540   0.997  1.00  0.00           H  
HETATM   91  H32 UNL     1      -2.151  -4.739  -1.099  1.00  0.00           H  
HETATM   92  H33 UNL     1      -0.599  -4.193  -1.772  1.00  0.00           H  
HETATM   93  H34 UNL     1      -1.126  -1.153   1.360  1.00  0.00           H  
HETATM   94  H35 UNL     1      -3.223  -0.175  -0.722  1.00  0.00           H  
HETATM   95  H36 UNL     1      -3.538  -1.184   0.673  1.00  0.00           H  
HETATM   96  H37 UNL     1      -4.658   3.257   1.684  1.00  0.00           H  
HETATM   97  H38 UNL     1      -3.251   2.912   2.721  1.00  0.00           H  
HETATM   98  H39 UNL     1      -1.844   4.437   1.476  1.00  0.00           H  
HETATM   99  H40 UNL     1      -3.159   4.733   0.234  1.00  0.00           H  
HETATM  100  H41 UNL     1      -3.287   5.482   3.191  1.00  0.00           H  
HETATM  101  H42 UNL     1      -4.504   5.888   1.959  1.00  0.00           H  
HETATM  102  H43 UNL     1      -1.595   6.762   1.816  1.00  0.00           H  
HETATM  103  H44 UNL     1      -2.916   7.799   2.386  1.00  0.00           H  
HETATM  104  H45 UNL     1      -3.964   7.451  -0.038  1.00  0.00           H  
HETATM  105  H46 UNL     1      -2.470   6.558  -0.426  1.00  0.00           H  
HETATM  106  H47 UNL     1      -2.364   8.900  -1.120  1.00  0.00           H  
HETATM  107  H48 UNL     1      -2.557   9.402   0.599  1.00  0.00           H  
HETATM  108  H49 UNL     1      -0.480   8.341   1.251  1.00  0.00           H  
HETATM  109  H50 UNL     1      -0.234   7.598  -0.336  1.00  0.00           H  
HETATM  110  H51 UNL     1      -0.318  10.569   0.415  1.00  0.00           H  
HETATM  111  H52 UNL     1      -0.129   9.908  -1.290  1.00  0.00           H  
HETATM  112  H53 UNL     1       1.940   8.738  -0.543  1.00  0.00           H  
HETATM  113  H54 UNL     1       1.714   9.346   1.113  1.00  0.00           H  
HETATM  114  H55 UNL     1       2.054  11.634   0.412  1.00  0.00           H  
HETATM  115  H56 UNL     1       2.234  11.170  -1.309  1.00  0.00           H  
HETATM  116  H57 UNL     1       3.876  10.415   1.192  1.00  0.00           H  
HETATM  117  H58 UNL     1       4.198   9.583  -0.315  1.00  0.00           H  
HETATM  118  H59 UNL     1       5.771  11.301   0.002  1.00  0.00           H  
HETATM  119  H60 UNL     1       4.592  12.483   0.538  1.00  0.00           H  
HETATM  120  H61 UNL     1       3.860  12.881  -1.798  1.00  0.00           H  
HETATM  121  H62 UNL     1       5.568  13.130  -1.489  1.00  0.00           H  
HETATM  122  H63 UNL     1       5.338  12.218  -3.681  1.00  0.00           H  
HETATM  123  H64 UNL     1       6.235  11.090  -2.661  1.00  0.00           H  
HETATM  124  H65 UNL     1       4.080   9.721  -2.468  1.00  0.00           H  
HETATM  125  H66 UNL     1       3.312  10.917  -3.565  1.00  0.00           H  
HETATM  126  H67 UNL     1       5.795   9.291  -4.288  1.00  0.00           H  
HETATM  127  H68 UNL     1       4.837  10.492  -5.301  1.00  0.00           H  
HETATM  128  H69 UNL     1       3.860   7.816  -4.164  1.00  0.00           H  
HETATM  129  H70 UNL     1       3.830   8.418  -5.899  1.00  0.00           H  
HETATM  130  H71 UNL     1       2.743   9.132  -4.669  1.00  0.00           H  
HETATM  131  H72 UNL     1      -0.813   0.433  -1.262  1.00  0.00           H  
HETATM  132  H73 UNL     1       0.521  -0.433  -0.516  1.00  0.00           H  
HETATM  133  H74 UNL     1       1.557   0.619  -1.981  1.00  0.00           H  
HETATM  134  H75 UNL     1       1.590   0.694   1.614  1.00  0.00           H  
HETATM  135  H76 UNL     1       2.894  -0.938   0.287  1.00  0.00           H  
HETATM  136  H77 UNL     1       2.652  -1.765   2.201  1.00  0.00           H  
HETATM  137  H78 UNL     1       5.549  -0.615   1.393  1.00  0.00           H  
HETATM  138  H79 UNL     1       4.236  -0.532  -1.084  1.00  0.00           H  
HETATM  139  H80 UNL     1       4.981   1.839  -0.273  1.00  0.00           H  
HETATM  140  H81 UNL     1       6.952   2.339   1.117  1.00  0.00           H  
HETATM  141  H82 UNL     1       5.380   2.244   2.703  1.00  0.00           H  
HETATM  142  H83 UNL     1       3.692   3.728   0.948  1.00  0.00           H  
HETATM  143  H84 UNL     1       3.513   1.057   3.317  1.00  0.00           H  
HETATM  144  H85 UNL     1       1.753   2.473   3.277  1.00  0.00           H  
CONECT    1    2   60   61   62
CONECT    2    3   63   64
CONECT    3    4   65   66
CONECT    4    5   67   68
CONECT    5    6   69   70
CONECT    6    7   71   72
CONECT    7    8   73   74
CONECT    8    9   75   76
CONECT    9   10   10   77
CONECT   10   11   78
CONECT   11   12   79   80
CONECT   12   13   81   82
CONECT   13   14   83   84
CONECT   14   15   85   86
CONECT   15   16   87   88
CONECT   16   17   89   90
CONECT   17   18   91   92
CONECT   18   19   19   20
CONECT   20   21
CONECT   21   22   43   93
CONECT   22   23   94   95
CONECT   23   24
CONECT   24   25   25   26
CONECT   26   27   96   97
CONECT   27   28   98   99
CONECT   28   29  100  101
CONECT   29   30  102  103
CONECT   30   31  104  105
CONECT   31   32  106  107
CONECT   32   33  108  109
CONECT   33   34  110  111
CONECT   34   35  112  113
CONECT   35   36  114  115
CONECT   36   37  116  117
CONECT   37   38  118  119
CONECT   38   39  120  121
CONECT   39   40  122  123
CONECT   40   41  124  125
CONECT   41   42  126  127
CONECT   42  128  129  130
CONECT   43   44  131  132
CONECT   44   45
CONECT   45   46   46   47   48
CONECT   47  133
CONECT   48   49
CONECT   49   50   58  134
CONECT   50   51   52  135
CONECT   51  136
CONECT   52   53   54  137
CONECT   53  138
CONECT   54   55   56  139
CONECT   55  140
CONECT   56   57   58  141
CONECT   57  142
CONECT   58   59  143
CONECT   59  144
END
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SMILES for HMDB0240667 (PI(18:0/18:1(9Z)))

[H][C@@](COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)OC(=O)CCCCCCC\C=C/CCCCCCCC
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INCHI for HMDB0240667 (PI(18:0/18:1(9Z)))

InChI=1S/C45H85O13P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(46)55-35-37(36-56-59(53,54)58-45-43(51)41(49)40(48)42(50)44(45)52)57-39(47)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h18,20,37,40-45,48-52H,3-17,19,21-36H2,1-2H3,(H,53,54)/b20-18-/t37-,40-,41-,42+,43-,44-,45-/m1/s1
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View in JSmolView Stereo Labels
Synonyms
ValueSource
1-18:0-2-18:1-PhosphatidylinositolChEBI
1-Octadecanoyl-2-(9Z)-octadecenoyl-sn-glycero-3-phospho-1D-myo-inositolChEBI
1-Octadecanoyl-2-(9Z-octadecenoyl)-glycero-3-phospho-(1'-myo-inositol)ChEBI
1-Stearoyl-2-oleoyl-phosphatidylinositolChEBI
18:0-18:1-PIChEBI
1-Stearoyl-2-oleoyl-gpiHMDB
1-Stearoyl-2-oleoyl-glycero-3-phospho-(1'-myo-inositol)HMDB
1-Stearoyl-2-oleoyl-glycero-3-phospho-(1’-myo-inositol)HMDB
1-Stearoyl-2-oleoyl-sn-glycero-3-phospho-D-myo-inositolHMDB
1-Stearoyl-2-oleoyl-sn-glycero-3-phosphoinositolHMDB
GPI(18:0/18:1(9Z))HMDB
GPI(18:0/18:1)HMDB
GPI(18:0/18:1n9)HMDB
GPI(18:0/18:1W9)HMDB
GPI(36:1)HMDB
PI(18:0/18:1)HMDB
PI(18:0/18:1n9)HMDB
PI(18:0/18:1W9)HMDB
PI(36:1)HMDB
Phosphatidylinositol(18:0/18:1(9Z))HMDB
Phosphatidylinositol(18:0/18:1)HMDB
Phosphatidylinositol(18:0/18:1n9)HMDB
Phosphatidylinositol(18:0/18:1W9)HMDB
Phosphatidylinositol(36:1)HMDB
PI(18:0/18:1(9Z))ChEBI
Chemical FormulaC45H85O13P
Average Molecular Weight865.1224
Monoisotopic Molecular Weight864.572779318
IUPAC Name[(2R)-2-[(9Z)-octadec-9-enoyloxy]-3-(octadecanoyloxy)propoxy]({[(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy})phosphinic acid
Traditional Name(2R)-2-[(9Z)-octadec-9-enoyloxy]-3-(octadecanoyloxy)propoxy([(1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxycyclohexyl]oxy)phosphinic acid
CAS Registry Number58116-17-9
SMILES
[H][C@@](COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)OC(=O)CCCCCCC\C=C/CCCCCCCC
InChI Identifier
InChI=1S/C45H85O13P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(46)55-35-37(36-56-59(53,54)58-45-43(51)41(49)40(48)42(50)44(45)52)57-39(47)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h18,20,37,40-45,48-52H,3-17,19,21-36H2,1-2H3,(H,53,54)/b20-18-/t37-,40-,41-,42+,43-,44-,45-/m1/s1
InChI KeyYOBFISPJJWPPTK-BAAZTTAESA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 1-phosphatidyl-1d-myo-inositols. These are lipids containing a myo-inositol attached to the phosphate group of a glycerol-3-phosphate moiety, and two acyl chains linked to the glycerol at the O1- and O2- positions, through ester linkages.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerophospholipids
Sub ClassGlycerophosphoinositols
Direct Parent1-phosphatidyl-1D-myo-inositols
Alternative Parents
Substituents
  • 1-phosphatidyl-1d-myo-inositol
  • Inositol phosphate
  • Cyclohexanol
  • Fatty acid ester
  • Dialkyl phosphate
  • Cyclitol or derivatives
  • Dicarboxylic acid or derivatives
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Alkyl phosphate
  • Fatty acyl
  • Cyclic alcohol
  • Secondary alcohol
  • Carboxylic acid ester
  • Polyol
  • Carboxylic acid derivative
  • Alcohol
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic homomonocyclic compound
Molecular FrameworkAliphatic homomonocyclic compounds
External Descriptors
  • 1-octadecanoyl-2-acyl-sn-glycero-3-phospho-1D-myo-inositol (CHEBI:77346 )
Ontology
Physiological effect
Health effect
Disposition
Biological locationSource
Process
Naturally occurring process
RoleNot Available
Physical Properties
StateNot Available
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
logP7.71ALOGPS
logP10.41ChemAxon
logS-6.2ALOGPS
pKa (Strongest Acidic)1.83ChemAxon
pKa (Strongest Basic)-3.6ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count9ChemAxon
Hydrogen Donor Count6ChemAxon
Polar Surface Area209.51 ŲChemAxon
Rotatable Bond Count41ChemAxon
Refractivity230.09 m³·mol⁻¹ChemAxon
Polarizability102.79 ųChemAxon
Number of Rings1ChemAxon
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]+287.08330932474
DeepCCS[M-H]-285.25830932474
DeepCCS[M-2H]-318.49830932474
DeepCCS[M+Na]+292.68930932474

Predicted Retention Times

Underivatized

Chromatographic MethodRetention TimeReference
Measured using a Waters Acquity ultraperformance liquid chromatography (UPLC) ethylene-bridged hybrid (BEH) C18 column (100 mm × 2.1 mm; 1.7 μmparticle diameter). Predicted by Afia on May 17, 2022. Predicted by Afia on May 17, 2022.10.24 minutes32390414
Predicted by Siyang on May 30, 202226.0664 minutes33406817
Predicted by Siyang using ReTip algorithm on June 8, 20222.9 minutes32390414
Fem_Long = Waters ACQUITY UPLC HSS T3 C18 with Water:MeOH and 0.1% Formic Acid5433.7 seconds40023050
Fem_Lipids = Ascentis Express C18 with (60:40 water:ACN):(90:10 IPA:ACN) and 10mM NH4COOH + 0.1% Formic Acid206.1 seconds40023050
Life_Old = Waters ACQUITY UPLC BEH C18 with Water:(20:80 acetone:ACN) and 0.1% Formic Acid332.5 seconds40023050
Life_New = RP Waters ACQUITY UPLC HSS T3 C18 with Water:(30:70 MeOH:ACN) and 0.1% Formic Acid191.1 seconds40023050
RIKEN = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid983.1 seconds40023050
Eawag_XBridgeC18 = XBridge C18 3.5u 2.1x50 mm with Water:MeOH and 0.1% Formic Acid1399.1 seconds40023050
BfG_NTS_RP1 =Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) with Water:ACN and 0.1% Formic Acid1160.7 seconds40023050
HILIC_BDD_2 = Merck SeQuant ZIC-HILIC with ACN(0.1% formic acid):water(16 mM ammonium formate)383.5 seconds40023050
UniToyama_Atlantis = RP Waters Atlantis T3 (2.1 x 150 mm, 5 um) with ACN:Water and 0.1% Formic Acid2691.6 seconds40023050
BDD_C18 = Hypersil Gold 1.9µm C18 with Water:ACN and 0.1% Formic Acid1123.8 seconds40023050
UFZ_Phenomenex = Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex with Water:MeOH and 0.1% Formic Acid2740.7 seconds40023050
SNU_RIKEN_POS = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid1040.9 seconds40023050
RPMMFDA = Waters ACQUITY UPLC BEH C18 with Water:ACN and 0.1% Formic Acid687.9 seconds40023050
MTBLS87 = Merck SeQuant ZIC-pHILIC column with ACN:Water and :ammonium carbonate266.6 seconds40023050
KI_GIAR_zic_HILIC_pH2_7 = Merck SeQuant ZIC-HILIC with ACN:Water and 0.1% FA296.9 seconds40023050
Meister zic-pHILIC pH9.3 = Merck SeQuant ZIC-pHILIC column with ACN:Water 5mM NH4Ac pH9.3 and 5mM ammonium acetate in water9.1 seconds40023050

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
PI(18:0/18:1(9Z))[H][C@@](COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)OC(=O)CCCCCCC\C=C/CCCCCCCC4969.3Standard polar33892256
PI(18:0/18:1(9Z))[H][C@@](COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)OC(=O)CCCCCCC\C=C/CCCCCCCC5304.2Standard non polar33892256
PI(18:0/18:1(9Z))[H][C@@](COC(=O)CCCCCCCCCCCCCCCCC)(COP(O)(=O)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)OC(=O)CCCCCCC\C=C/CCCCCCCC6252.4Semi standard non polar33892256
Spectra
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID26326254
KEGG Compound IDNot Available
BioCyc IDCPD-8324
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem CompoundNot Available
PDB IDNot Available
ChEBI ID77346
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 ReferencesNot Available