Showing metabocard for PC(20:3(5Z,8Z,11Z)/18:1(11Z)) (MMDBc0034009)

Record Information
Version1.0
StatusDetected and Quantified
Creation Date2021-11-19 05:12:26 UTC
Update Date2024-04-30 20:19:50 UTC
Metabolite IDMMDBc0034009
Metabolite Identification
Common NamePC(20:3(5Z,8Z,11Z)/18:1(11Z))
DescriptionPC(20:3(5Z,8Z,11Z)/18:1(11Z)) is a phosphatidylcholine (PC or GPCho). It is a glycerophospholipid in which a phosphorylcholine moiety occupies a glycerol substitution site. As is the case with diacylglycerols, glycerophosphocholines 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 16, 18 and 20 carbons are the most common. PC(20:3(5Z,8Z,11Z)/18:1(11Z)), in particular, consists of one chain of mead acid at the C-1 position and one chain of vaccenic acid at the C-2 position. The mead acid moiety is derived from fish oils, liver and kidney, while the vaccenic acid moiety is derived from butter fat and animal fat. Phospholipids, are ubiquitous in nature and are key components of the lipid bilayer of cells, as well as being involved in metabolism and signaling.↵↵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 remodeling that occurs while these molecules are in membranes. PCs can be synthesized via three different routes. In one route, choline is activated first by phosphorylation and then by coupling to CDP prior to attachment to phosphatidic acid. PCs can also synthesized by the addition of choline to CDP-activated 1,2-diacylglycerol. A third route to PC synthesis involves the conversion of either PS or PE to PC.
Structure
MOLSDFPDBSMILESInChI

MOL for #<Metabolite:0x00007fdb3ac35bc8>


  Mrv0541 02251201362D          

 56 55  0  0  1  0            999 V2000
   -0.8171    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1026    3.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6119    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3263    3.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0408    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7553    3.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4698    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1842    3.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8987    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6132    3.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3276    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3276    4.4783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0421    4.8908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0421    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7566    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4711    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1855    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9000    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6145    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3289    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3289    4.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0434    6.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7579    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   14.1868    8.1908    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   13.3618    8.1908    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
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   14.9013   10.2533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   15.2033   11.3802    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.3302   11.0783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1868    5.7158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   16.3302    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.0447    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.7592    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.4737    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.1881    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9026    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.6171    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0460    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7605    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4749    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.4749    6.9533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1894    7.3658    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.1894    8.1908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.9039    8.6033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.9039    9.4283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
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  7  8  1  0  0  0  0
  9  8  1  4  0  0  0
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 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 24 37  1  6  0  0  0
 37 38  1  0  0  0  0
 38 39  2  0  0  0  0
 38 40  1  0  0  0  0
 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 43 44  1  0  0  0  0
 44 45  1  0  0  0  0
 45 46  1  0  0  0  0
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 47 48  1  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
M  CHG  2  28  -1  33   1
M  END
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3D MOL for #<Metabolite:0x00007fdb3ac35bc8>

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3D SDF for #<Metabolite:0x00007fdb3ac35bc8>

  Mrv0541 02251201362D          

 56 55  0  0  1  0            999 V2000
   -0.8171    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1026    3.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6119    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3263    3.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0408    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7553    3.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4698    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1842    3.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8987    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6132    3.2408    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3276    3.6533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3276    4.4783    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0421    4.8908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0421    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7566    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.4711    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1855    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   10.6145    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3289    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3289    4.8908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.0434    6.1283    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.7579    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   14.1868    7.3658    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1868    8.1908    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   13.3618    8.1908    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   15.0118    8.1908    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1868    9.0158    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   20.6171    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.3315    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.0460    6.1283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.7605    5.7158    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   24.1894    8.1908    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.9039    8.6033    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.9039    9.4283    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
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 32 33  1  0  0  0  0
 33 34  1  0  0  0  0
 33 35  1  0  0  0  0
 33 36  1  0  0  0  0
 24 37  1  6  0  0  0
 37 38  1  0  0  0  0
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 40 41  1  0  0  0  0
 41 42  1  0  0  0  0
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 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
 49 48  1  4  0  0  0
 49 50  2  0  0  0  0
 50 51  1  0  0  0  0
 51 52  1  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
M  CHG  2  28  -1  33   1
M  END
> <DATABASE_ID>
MMDBc0034009

> <DATABASE_NAME>
MIME

> <SMILES>
CCCCCCCCC=CCC=CCC=CCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCC=CCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C46H84NO8P/c1-6-8-10-12-14-16-18-20-22-23-25-26-28-30-32-34-36-38-45(48)52-42-44(43-54-56(50,51)53-41-40-47(3,4)5)55-46(49)39-37-35-33-31-29-27-24-21-19-17-15-13-11-9-7-2/h17,19-20,22,25-26,30,32,44H,6-16,18,21,23-24,27-29,31,33-43H2,1-5H3/t44-/m1/s1

> <INCHI_KEY>
PIOANQACZQFPEA-USYZEHPZSA-N

> <FORMULA>
C46H84NO8P

> <MOLECULAR_WEIGHT>
810.1348

> <EXACT_MASS>
809.593455181

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_AVERAGE_POLARIZABILITY>
99.29273905804122

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2-{[(2R)-3-(icosa-5,8,11-trienoyloxy)-2-(octadec-11-enoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

> <ALOGPS_LOGP>
6.06

> <JCHEM_LOGP>
9.333521742528253

> <ALOGPS_LOGS>
-7.48

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8550572064467632

> <JCHEM_PKA_STRONGEST_BASIC>
-6.744219009617095

> <JCHEM_POLAR_SURFACE_AREA>
111.19

> <JCHEM_REFRACTIVITY>
247.9375

> <JCHEM_ROTATABLE_BOND_COUNT>
42

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.84e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2-{[(2R)-3-(icosa-5,8,11-trienoyloxy)-2-(octadec-11-enoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium

> <JCHEM_VEBER_RULE>
0

$$$$

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3D-SDF for #<Metabolite:0x00007fdb3ac35bc8>
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PDB for #<Metabolite:0x00007fdb3ac35bc8>
HEADER    PROTEIN                                 25-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   25-FEB-12         0                                  
HETATM    1  C   UNK     0      -1.525   6.819   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -0.192   6.049   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       1.142   6.819   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.476   6.049   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       3.809   6.819   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.143   6.049   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.477   6.819   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.811   6.049   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.144   6.819   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.478   6.049   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.812   6.819   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      11.812   8.359   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      13.145   9.129   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      13.145  10.669   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      14.479  11.439   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      15.813  10.669   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      17.146  11.439   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      18.480  10.669   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      19.814  11.439   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      21.147  10.669   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      21.147   9.129   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      22.481  11.439   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      23.815  10.669   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      25.148  11.439   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      25.148  12.979   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      26.482  13.749   0.000  0.00  0.00           O+0
HETATM   27  P   UNK     0      26.482  15.289   0.000  0.00  0.00           P+0
HETATM   28  O   UNK     0      24.942  15.289   0.000  0.00  0.00           O-1
HETATM   29  O   UNK     0      28.022  15.289   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      26.482  16.829   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0      27.816  17.599   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      27.816  19.139   0.000  0.00  0.00           C+0
HETATM   33  N   UNK     0      29.149  19.909   0.000  0.00  0.00           N+1
HETATM   34  C   UNK     0      29.919  18.576   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      28.379  21.243   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      30.483  20.679   0.000  0.00  0.00           C+0
HETATM   37  O   UNK     0      26.482  10.669   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      27.816  11.439   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      27.816  12.979   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0      29.149  10.669   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      30.483  11.439   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      31.817  10.669   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      33.151  11.439   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      34.484  10.669   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0      35.818  11.439   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0      37.152  10.669   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      38.485  11.439   0.000  0.00  0.00           C+0
HETATM   48  C   UNK     0      39.819  10.669   0.000  0.00  0.00           C+0
HETATM   49  C   UNK     0      41.153  11.439   0.000  0.00  0.00           C+0
HETATM   50  C   UNK     0      42.486  10.669   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      43.820  11.439   0.000  0.00  0.00           C+0
HETATM   52  C   UNK     0      43.820  12.979   0.000  0.00  0.00           C+0
HETATM   53  C   UNK     0      45.154  13.749   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      45.154  15.289   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      46.487  16.059   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      46.487  17.599   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25   37                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29   30                                             
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   27   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   33                                                       
CONECT   33   32   34   35   36                                             
CONECT   34   33                                                            
CONECT   35   33                                                            
CONECT   36   33                                                            
CONECT   37   24   38                                                       
CONECT   38   37   39   40                                                  
CONECT   39   38                                                            
CONECT   40   38   41                                                       
CONECT   41   40   42                                                       
CONECT   42   41   43                                                       
CONECT   43   42   44                                                       
CONECT   44   43   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                                                            
MASTER        0    0    0    0    0    0    0    0   56    0  110    0
END

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3D PDB for #<Metabolite:0x00007fdb3ac35bc8>
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SMILES for #<Metabolite:0x00007fdb3ac35bc8>
CCCCCCCCC=CCC=CCC=CCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCC=CCCCCCC
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INCHI for #<Metabolite:0x00007fdb3ac35bc8>
InChI=1S/C46H84NO8P/c1-6-8-10-12-14-16-18-20-22-23-25-26-28-30-32-34-36-38-45(48)52-42-44(43-54-56(50,51)53-41-40-47(3,4)5)55-46(49)39-37-35-33-31-29-27-24-21-19-17-15-13-11-9-7-2/h17,19-20,22,25-26,30,32,44H,6-16,18,21,23-24,27-29,31,33-43H2,1-5H3/t44-/m1/s1
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SynonymsNot Available
Molecular FormulaC46H84NO8P
Average Mass810.1348
Monoisotopic Mass809.593455181
IUPAC Name(2-{[(2R)-3-(icosa-5,8,11-trienoyloxy)-2-(octadec-11-enoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium
Traditional Name(2-{[(2R)-3-(icosa-5,8,11-trienoyloxy)-2-(octadec-11-enoyloxy)propyl phosphonato]oxy}ethyl)trimethylazanium
CAS Registry NumberNot Available
SMILES
CCCCCCCCC=CCC=CCC=CCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCCCC=CCCCCCC
InChI Identifier
InChI=1S/C46H84NO8P/c1-6-8-10-12-14-16-18-20-22-23-25-26-28-30-32-34-36-38-45(48)52-42-44(43-54-56(50,51)53-41-40-47(3,4)5)55-46(49)39-37-35-33-31-29-27-24-21-19-17-15-13-11-9-7-2/h17,19-20,22,25-26,30,32,44H,6-16,18,21,23-24,27-29,31,33-43H2,1-5H3/t44-/m1/s1
InChI KeyPIOANQACZQFPEA-USYZEHPZSA-N