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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2009-07-25 00:12:25 UTC

Update Date

2021-09-14 15:47:02 UTC

HMDB ID

HMDB0013055

Secondary Accession Numbers

HMDB13055

Metabolite Identification

Common Name

S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione

Description

S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds. Based on a literature review very few articles have been published on S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione.

Structure

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


  Mrv1652303102016492D          

 44 44  0  0  1  0            999 V2000
   14.8875  -13.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3355  -12.4810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5904  -11.6964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0384  -11.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2933  -10.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7413   -9.6856    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.9962   -8.9010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9343   -9.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3823   -9.2440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6373   -8.4594    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   13.4442   -8.2879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6992   -7.5033    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.5061   -7.3317    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.0582   -7.9448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8032   -8.7294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8651   -7.7733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1201   -6.9886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9270   -6.8171    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.1820   -6.0325    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.4791   -7.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2242   -8.2149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.2861   -7.2587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1471   -6.8901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3401   -7.0617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4020   -6.1055    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.2090   -5.9340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4640   -5.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2709   -4.9778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9119   -4.5363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5753   -9.4155    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.2398  -10.1692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6523  -10.8837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4193  -10.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2477   -9.2760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9622   -8.8635    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.0485   -8.0430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8021   -7.7075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8884   -6.8870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2209   -6.4020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3071   -5.5816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6397   -5.0967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7260   -4.2762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4796   -3.9406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0585   -3.7912    0.0000 O   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
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 30  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 23  1  6  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  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
 27 29  2  0  0  0  0
 30 31  1  0  0  0  0
 30 35  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  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
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  2  0  0  0  0
M  END

HMDB0013055
     RDKit          3D
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione
 95 95  0  0  0  0  0  0  0  0999 V2000
   -3.1119    7.8921   -0.8982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6269    7.5611   -0.7222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5515    6.0393   -0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1449    5.5821   -0.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1031    4.0649   -0.3549 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8976    3.5847    0.7803 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3258    4.1598    1.9504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9111    2.0984    1.0599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3897    1.2842   -0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3435    1.2725   -1.5150 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.0464    0.1988   -1.5053 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1951    0.3626   -0.6038 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0675   -0.8147   -0.9486 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7081   -1.4684    0.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5660   -1.0781    1.3092 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5851   -2.6515   -0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2463   -3.1179    1.1680 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0728   -4.3394    0.7935 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0464   -3.9586   -0.2008 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7436   -4.9033    1.9797 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1361   -5.2415    3.0109 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1372   -5.0733    1.9565 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1243    1.4902   -0.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8322    1.4816   -1.9545 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2505    2.5991   -0.0526 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1478    3.7069   -0.3192 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5599    3.2550   -0.4007 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8429    2.0441   -0.2365 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5574    4.1755   -0.6576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8440   -0.0724    0.4144 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9628    0.1521    1.3731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5262    1.4272    1.3092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0450   -0.7994    0.9476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9079   -0.7865   -0.5749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3980   -0.9334   -0.6816 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9896   -2.3859   -0.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4797   -3.2937   -1.4515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2740   -4.3002   -1.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8077   -4.6751    0.0306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3328   -4.5844   -0.0986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0521   -4.9342    1.1615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7713   -6.3006    1.6006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6539   -6.5588    2.1180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7470   -7.2802    1.4348 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2734    8.9711   -1.0922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6429    7.6447    0.0385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5545    7.3288   -1.7454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3013    8.0382    0.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1027    7.9111   -1.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9851    5.6167   -1.5091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2106    5.8195    0.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
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    0.4846    5.9745   -1.2357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5448    3.7567   -1.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9485    3.7793   -0.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9373    3.9871    0.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5219    3.7114    2.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1636    1.8366    1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4171    1.9372    2.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3709    1.7620   -0.4383 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4981    0.2484   -2.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7622   -0.9001   -1.4703 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0649    0.3475    0.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1916   -1.1317   -1.9184 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3484   -2.3984   -0.8535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9660   -3.5108   -0.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9282   -2.2947    1.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5168   -3.3456    1.9429 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4101   -5.1305    0.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1858   -4.7573   -0.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9345   -3.5918    0.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5581   -5.6178    1.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6649    2.6060    0.8183 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8417    4.1827   -1.2757 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.7897   -1.7832    1.3269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0575   -0.4540    1.2515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2517    0.1754   -1.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4555   -1.5806   -1.0715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0398   -0.6543   -1.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1212   -2.6827    0.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8625   -2.3667   -0.5547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1357   -3.1054   -2.4882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5628   -4.9077   -2.1590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6189   -5.7728    0.1558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5342   -4.0891    0.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5941   -3.5379   -0.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6783   -5.1986   -0.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1302   -4.8309    0.9545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8120   -4.1688    1.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6167   -8.0547    0.8194 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
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  9 10  1  0
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 12 23  1  0
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  9 30  1  0
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 38 88  1  0
 39 89  1  0
 39 90  1  0
 40 91  1  0
 40 92  1  0
 41 93  1  0
 41 94  1  0
 44 95  1  0
M  END


  Mrv1652303102016492D          

 44 44  0  0  1  0            999 V2000
   14.8875  -13.0941    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3355  -12.4810    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.5904  -11.6964    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.0384  -11.0833    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.2933  -10.2987    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.7413   -9.6856    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.9962   -8.9010    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9343   -9.8571    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3823   -9.2440    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6373   -8.4594    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   13.4442   -8.2879    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6992   -7.5033    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.5061   -7.3317    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   15.0582   -7.9448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.8032   -8.7294    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8651   -7.7733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.1201   -6.9886    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.9270   -6.8171    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   17.1820   -6.0325    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   17.4791   -7.4302    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2242   -8.2149    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.2861   -7.2587    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.1471   -6.8901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3401   -7.0617    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.4020   -6.1055    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.2090   -5.9340    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.4640   -5.1494    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2709   -4.9778    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9119   -4.5363    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5753   -9.4155    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.2398  -10.1692    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6523  -10.8837    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.4193  -10.0830    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2477   -9.2760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9622   -8.8635    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   11.0485   -8.0430    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8021   -7.7075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.8884   -6.8870    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2209   -6.4020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.3071   -5.5816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6397   -5.0967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.7260   -4.2762    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4796   -3.9406    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.0585   -3.7912    0.0000 O   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
  6  7  1  1  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 30  9  1  1  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 23  1  6  0  0  0
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 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
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 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  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
 27 29  2  0  0  0  0
 30 31  1  0  0  0  0
 30 35  1  0  0  0  0
 31 32  1  0  0  0  0
 31 33  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  6  0  0  0
 36 37  1  0  0  0  0
 37 38  2  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
 41 42  1  0  0  0  0
 42 43  1  0  0  0  0
 42 44  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0013055

> <DATABASE_NAME>
hmdb

> <SMILES>
CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(O)=O)C(=O)NCC(O)=O)[C@H]1C(O)CC[C@@H]1C\C=C/CCCC(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C30H51N3O10S/c1-2-3-6-10-20(34)16-24(28-19(12-14-23(28)35)9-7-4-5-8-11-26(37)38)44-18-22(29(41)32-17-27(39)40)33-25(36)15-13-21(31)30(42)43/h4,7,19-24,28,34-35H,2-3,5-6,8-18,31H2,1H3,(H,32,41)(H,33,36)(H,37,38)(H,39,40)(H,42,43)/b7-4-/t19-,20-,21+,22+,23?,24?,28+/m0/s1

> <INCHI_KEY>
BVYNXGKKWADCHD-RXULBTIMSA-N

> <FORMULA>
C30H51N3O10S

> <MOLECULAR_WEIGHT>
645.805

> <EXACT_MASS>
645.329515557

> <JCHEM_ACCEPTOR_COUNT>
11

> <JCHEM_ATOM_COUNT>
95

> <JCHEM_AVERAGE_POLARIZABILITY>
69.19980359727465

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(5Z)-7-[(1R,2R)-2-[(3S)-1-{[(2S)-2-[(4R)-4-amino-4-carboxybutanamido]-2-[(carboxymethyl)carbamoyl]ethyl]sulfanyl}-3-hydroxyoctyl]-3-hydroxycyclopentyl]hept-5-enoic acid

> <ALOGPS_LOGP>
-1.56

> <JCHEM_LOGP>
-1.4272891765210771

> <ALOGPS_LOGS>
-4.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.5890600897129894

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.8065956686687912

> <JCHEM_PKA_STRONGEST_BASIC>
9.311710402052379

> <JCHEM_POLAR_SURFACE_AREA>
236.57999999999996

> <JCHEM_REFRACTIVITY>
165.0893

> <JCHEM_ROTATABLE_BOND_COUNT>
24

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.76e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(5Z)-7-[(1R,2R)-2-[(3S)-1-{[(2S)-2-[(4R)-4-amino-4-carboxybutanamido]-2-(carboxymethylcarbamoyl)ethyl]sulfanyl}-3-hydroxyoctyl]-3-hydroxycyclopentyl]hept-5-enoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0013055
     RDKit          3D
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione
 95 95  0  0  0  0  0  0  0  0999 V2000
   -3.1119    7.8921   -0.8982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6269    7.5611   -0.7222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5515    6.0393   -0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1449    5.5821   -0.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1031    4.0649   -0.3549 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8976    3.5847    0.7803 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3258    4.1598    1.9504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9111    2.0984    1.0599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3897    1.2842   -0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3435    1.2725   -1.5150 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.0464    0.1988   -1.5053 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1951    0.3626   -0.6038 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0675   -0.8147   -0.9486 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7081   -1.4684    0.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5660   -1.0781    1.3092 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5851   -2.6515   -0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2463   -3.1179    1.1680 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0728   -4.3394    0.7935 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0464   -3.9586   -0.2008 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7436   -4.9033    1.9797 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1361   -5.2415    3.0109 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1372   -5.0733    1.9565 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1243    1.4902   -0.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8322    1.4816   -1.9545 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2505    2.5991   -0.0526 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1478    3.7069   -0.3192 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5599    3.2550   -0.4007 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8429    2.0441   -0.2365 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5574    4.1755   -0.6576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8440   -0.0724    0.4144 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9628    0.1521    1.3731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5262    1.4272    1.3092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0450   -0.7994    0.9476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9079   -0.7865   -0.5749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3980   -0.9334   -0.6816 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9896   -2.3859   -0.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4797   -3.2937   -1.4515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2740   -4.3002   -1.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8077   -4.6751    0.0306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3328   -4.5844   -0.0986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0521   -4.9342    1.1615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7713   -6.3006    1.6006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6539   -6.5588    2.1180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7470   -7.2802    1.4348 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2734    8.9711   -1.0922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6429    7.6447    0.0385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5545    7.3288   -1.7454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3013    8.0382    0.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1027    7.9111   -1.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9851    5.6167   -1.5091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2106    5.8195    0.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934    5.9660    0.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4846    5.9745   -1.2357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5448    3.7567   -1.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9485    3.7793   -0.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9373    3.9871    0.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5219    3.7114    2.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1636    1.8366    1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4171    1.9372    2.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3709    1.7620   -0.4383 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4981    0.2484   -2.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7622   -0.9001   -1.4703 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0649    0.3475    0.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1916   -1.1317   -1.9184 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3484   -2.3984   -0.8535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9660   -3.5108   -0.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9282   -2.2947    1.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5168   -3.3456    1.9429 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4101   -5.1305    0.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1858   -4.7573   -0.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9345   -3.5918    0.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5581   -5.6178    1.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6649    2.6060    0.8183 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8417    4.1827   -1.2757 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0198    4.4601    0.4813 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5134    3.9100   -0.4700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9937   -0.5384    0.9650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6468   -0.0008    2.4237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1422    1.5538    0.5587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7897   -1.7832    1.3269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0575   -0.4540    1.2515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2517    0.1754   -1.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4555   -1.5806   -1.0715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0398   -0.6543   -1.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.8625   -2.3667   -0.5547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1357   -3.1054   -2.4882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5628   -4.9077   -2.1590 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.5342   -4.0891    0.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5941   -3.5379   -0.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.1302   -4.8309    0.9545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8120   -4.1688    1.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6167   -8.0547    0.8194 H   0  0  0  0  0  0  0  0  0  0  0  0
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 38 88  1  0
 39 89  1  0
 39 90  1  0
 40 91  1  0
 40 92  1  0
 41 93  1  0
 41 94  1  0
 44 95  1  0
M  END

HEADER    PROTEIN                                 10-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   10-MAR-20         0                                  
HETATM    1  C   UNK     0      27.790 -24.442   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      26.760 -23.298   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      27.235 -21.833   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      26.205 -20.689   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      26.681 -19.224   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      25.650 -18.080   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      26.126 -16.615   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0      24.144 -18.400   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      23.114 -17.255   0.000  0.00  0.00           C+0
HETATM   10  S   UNK     0      23.590 -15.791   0.000  0.00  0.00           S+0
HETATM   11  C   UNK     0      25.096 -15.471   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      25.572 -14.006   0.000  0.00  0.00           C+0
HETATM   13  N   UNK     0      27.078 -13.686   0.000  0.00  0.00           N+0
HETATM   14  C   UNK     0      28.109 -14.830   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0      27.633 -16.295   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0      29.615 -14.510   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      30.091 -13.045   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      31.597 -12.725   0.000  0.00  0.00           C+0
HETATM   19  N   UNK     0      32.073 -11.261   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0      32.628 -13.870   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      32.152 -15.334   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      34.134 -13.550   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0      24.541 -12.862   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      23.035 -13.182   0.000  0.00  0.00           O+0
HETATM   25  N   UNK     0      25.017 -11.397   0.000  0.00  0.00           N+0
HETATM   26  C   UNK     0      26.523 -11.077   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      26.999  -9.612   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      28.506  -9.292   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0      25.969  -8.468   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0      21.607 -17.576   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      20.981 -18.983   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0      21.751 -20.316   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0      19.449 -18.822   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      19.129 -17.315   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      20.463 -16.545   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      20.624 -15.014   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      22.031 -14.387   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      22.192 -12.856   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0      20.946 -11.950   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      21.107 -10.419   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      19.861  -9.514   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      20.022  -7.982   0.000  0.00  0.00           C+0
HETATM   43  O   UNK     0      21.429  -7.356   0.000  0.00  0.00           O+0
HETATM   44  O   UNK     0      18.776  -7.077   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   30                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   23                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   12   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30    9   31   35                                                  
CONECT   31   30   32   33                                                  
CONECT   32   31                                                            
CONECT   33   31   34                                                       
CONECT   34   33   35                                                       
CONECT   35   30   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   42                                                       
CONECT   42   41   43   44                                                  
CONECT   43   42                                                            
CONECT   44   42                                                            
MASTER        0    0    0    0    0    0    0    0   44    0   88    0
END

COMPND    HMDB0013055
HETATM    1  C1  UNL     1      -3.112   7.892  -0.898  1.00  0.00           C  
HETATM    2  C2  UNL     1      -1.627   7.561  -0.722  1.00  0.00           C  
HETATM    3  C3  UNL     1      -1.552   6.039  -0.603  1.00  0.00           C  
HETATM    4  C4  UNL     1      -0.145   5.582  -0.420  1.00  0.00           C  
HETATM    5  C5  UNL     1      -0.103   4.065  -0.355  1.00  0.00           C  
HETATM    6  C6  UNL     1      -0.898   3.585   0.780  1.00  0.00           C  
HETATM    7  O1  UNL     1      -0.326   4.160   1.950  1.00  0.00           O  
HETATM    8  C7  UNL     1      -0.911   2.098   1.060  1.00  0.00           C  
HETATM    9  C8  UNL     1      -1.390   1.284  -0.083  1.00  0.00           C  
HETATM   10  S1  UNL     1      -0.343   1.273  -1.515  1.00  0.00           S  
HETATM   11  C9  UNL     1       1.046   0.199  -1.505  1.00  0.00           C  
HETATM   12  C10 UNL     1       2.195   0.363  -0.604  1.00  0.00           C  
HETATM   13  N1  UNL     1       3.068  -0.815  -0.949  1.00  0.00           N  
HETATM   14  C11 UNL     1       3.708  -1.468   0.110  1.00  0.00           C  
HETATM   15  O2  UNL     1       3.566  -1.078   1.309  1.00  0.00           O  
HETATM   16  C12 UNL     1       4.585  -2.652  -0.100  1.00  0.00           C  
HETATM   17  C13 UNL     1       5.246  -3.118   1.168  1.00  0.00           C  
HETATM   18  C14 UNL     1       6.073  -4.339   0.793  1.00  0.00           C  
HETATM   19  N2  UNL     1       7.046  -3.959  -0.201  1.00  0.00           N  
HETATM   20  C15 UNL     1       6.744  -4.903   1.980  1.00  0.00           C  
HETATM   21  O3  UNL     1       6.136  -5.241   3.011  1.00  0.00           O  
HETATM   22  O4  UNL     1       8.137  -5.073   1.956  1.00  0.00           O  
HETATM   23  C16 UNL     1       3.124   1.490  -0.914  1.00  0.00           C  
HETATM   24  O5  UNL     1       3.832   1.482  -1.955  1.00  0.00           O  
HETATM   25  N3  UNL     1       3.250   2.599  -0.053  1.00  0.00           N  
HETATM   26  C17 UNL     1       4.148   3.707  -0.319  1.00  0.00           C  
HETATM   27  C18 UNL     1       5.560   3.255  -0.401  1.00  0.00           C  
HETATM   28  O6  UNL     1       5.843   2.044  -0.236  1.00  0.00           O  
HETATM   29  O7  UNL     1       6.557   4.175  -0.658  1.00  0.00           O  
HETATM   30  C19 UNL     1      -1.844  -0.072   0.414  1.00  0.00           C  
HETATM   31  C20 UNL     1      -2.963   0.152   1.373  1.00  0.00           C  
HETATM   32  O8  UNL     1      -3.526   1.427   1.309  1.00  0.00           O  
HETATM   33  C21 UNL     1      -4.045  -0.799   0.948  1.00  0.00           C  
HETATM   34  C22 UNL     1      -3.908  -0.787  -0.575  1.00  0.00           C  
HETATM   35  C23 UNL     1      -2.398  -0.933  -0.682  1.00  0.00           C  
HETATM   36  C24 UNL     1      -1.990  -2.386  -0.420  1.00  0.00           C  
HETATM   37  C25 UNL     1      -2.480  -3.294  -1.451  1.00  0.00           C  
HETATM   38  C26 UNL     1      -3.274  -4.300  -1.276  1.00  0.00           C  
HETATM   39  C27 UNL     1      -3.808  -4.675   0.031  1.00  0.00           C  
HETATM   40  C28 UNL     1      -5.333  -4.584  -0.099  1.00  0.00           C  
HETATM   41  C29 UNL     1      -6.052  -4.934   1.161  1.00  0.00           C  
HETATM   42  C30 UNL     1      -5.771  -6.301   1.601  1.00  0.00           C  
HETATM   43  O9  UNL     1      -4.654  -6.559   2.118  1.00  0.00           O  
HETATM   44  O10 UNL     1      -6.747  -7.280   1.435  1.00  0.00           O  
HETATM   45  H1  UNL     1      -3.273   8.971  -1.092  1.00  0.00           H  
HETATM   46  H2  UNL     1      -3.643   7.645   0.039  1.00  0.00           H  
HETATM   47  H3  UNL     1      -3.555   7.329  -1.745  1.00  0.00           H  
HETATM   48  H4  UNL     1      -1.301   8.038   0.218  1.00  0.00           H  
HETATM   49  H5  UNL     1      -1.103   7.911  -1.617  1.00  0.00           H  
HETATM   50  H6  UNL     1      -1.985   5.617  -1.509  1.00  0.00           H  
HETATM   51  H7  UNL     1      -2.211   5.819   0.287  1.00  0.00           H  
HETATM   52  H8  UNL     1       0.193   5.966   0.582  1.00  0.00           H  
HETATM   53  H9  UNL     1       0.485   5.974  -1.236  1.00  0.00           H  
HETATM   54  H10 UNL     1      -0.545   3.757  -1.361  1.00  0.00           H  
HETATM   55  H11 UNL     1       0.948   3.779  -0.330  1.00  0.00           H  
HETATM   56  H12 UNL     1      -1.937   3.987   0.754  1.00  0.00           H  
HETATM   57  H13 UNL     1       0.522   3.711   2.080  1.00  0.00           H  
HETATM   58  H14 UNL     1       0.164   1.837   1.255  1.00  0.00           H  
HETATM   59  H15 UNL     1      -1.417   1.937   2.019  1.00  0.00           H  
HETATM   60  H16 UNL     1      -2.371   1.762  -0.438  1.00  0.00           H  
HETATM   61  H17 UNL     1       1.498   0.248  -2.571  1.00  0.00           H  
HETATM   62  H18 UNL     1       0.762  -0.900  -1.470  1.00  0.00           H  
HETATM   63  H19 UNL     1       2.065   0.348   0.459  1.00  0.00           H  
HETATM   64  H20 UNL     1       3.192  -1.132  -1.918  1.00  0.00           H  
HETATM   65  H21 UNL     1       5.348  -2.398  -0.853  1.00  0.00           H  
HETATM   66  H22 UNL     1       3.966  -3.511  -0.480  1.00  0.00           H  
HETATM   67  H23 UNL     1       5.928  -2.295   1.502  1.00  0.00           H  
HETATM   68  H24 UNL     1       4.517  -3.346   1.943  1.00  0.00           H  
HETATM   69  H25 UNL     1       5.410  -5.131   0.354  1.00  0.00           H  
HETATM   70  H26 UNL     1       7.186  -4.757  -0.865  1.00  0.00           H  
HETATM   71  H27 UNL     1       7.934  -3.592   0.200  1.00  0.00           H  
HETATM   72  H28 UNL     1       8.558  -5.618   1.201  1.00  0.00           H  
HETATM   73  H29 UNL     1       2.665   2.606   0.818  1.00  0.00           H  
HETATM   74  H30 UNL     1       3.842   4.183  -1.276  1.00  0.00           H  
HETATM   75  H31 UNL     1       4.020   4.460   0.481  1.00  0.00           H  
HETATM   76  H32 UNL     1       7.513   3.910  -0.470  1.00  0.00           H  
HETATM   77  H33 UNL     1      -0.994  -0.538   0.965  1.00  0.00           H  
HETATM   78  H34 UNL     1      -2.647  -0.001   2.424  1.00  0.00           H  
HETATM   79  H35 UNL     1      -4.142   1.554   0.559  1.00  0.00           H  
HETATM   80  H36 UNL     1      -3.790  -1.783   1.327  1.00  0.00           H  
HETATM   81  H37 UNL     1      -5.057  -0.454   1.252  1.00  0.00           H  
HETATM   82  H38 UNL     1      -4.252   0.175  -1.006  1.00  0.00           H  
HETATM   83  H39 UNL     1      -4.456  -1.581  -1.072  1.00  0.00           H  
HETATM   84  H40 UNL     1      -2.040  -0.654  -1.679  1.00  0.00           H  
HETATM   85  H41 UNL     1      -2.121  -2.683   0.615  1.00  0.00           H  
HETATM   86  H42 UNL     1      -0.862  -2.367  -0.555  1.00  0.00           H  
HETATM   87  H43 UNL     1      -2.136  -3.105  -2.488  1.00  0.00           H  
HETATM   88  H44 UNL     1      -3.563  -4.908  -2.159  1.00  0.00           H  
HETATM   89  H45 UNL     1      -3.619  -5.773   0.156  1.00  0.00           H  
HETATM   90  H46 UNL     1      -3.534  -4.089   0.890  1.00  0.00           H  
HETATM   91  H47 UNL     1      -5.594  -3.538  -0.351  1.00  0.00           H  
HETATM   92  H48 UNL     1      -5.678  -5.199  -0.960  1.00  0.00           H  
HETATM   93  H49 UNL     1      -7.130  -4.831   0.954  1.00  0.00           H  
HETATM   94  H50 UNL     1      -5.812  -4.169   1.932  1.00  0.00           H  
HETATM   95  H51 UNL     1      -6.617  -8.055   0.819  1.00  0.00           H  
CONECT    1    2   45   46   47
CONECT    2    3   48   49
CONECT    3    4   50   51
CONECT    4    5   52   53
CONECT    5    6   54   55
CONECT    6    7    8   56
CONECT    7   57
CONECT    8    9   58   59
CONECT    9   10   30   60
CONECT   10   11
CONECT   11   12   61   62
CONECT   12   13   23   63
CONECT   13   14   64
CONECT   14   15   15   16
CONECT   16   17   65   66
CONECT   17   18   67   68
CONECT   18   19   20   69
CONECT   19   70   71
CONECT   20   21   21   22
CONECT   22   72
CONECT   23   24   24   25
CONECT   25   26   73
CONECT   26   27   74   75
CONECT   27   28   28   29
CONECT   29   76
CONECT   30   31   35   77
CONECT   31   32   33   78
CONECT   32   79
CONECT   33   34   80   81
CONECT   34   35   82   83
CONECT   35   36   84
CONECT   36   37   85   86
CONECT   37   38   38   87
CONECT   38   39   88
CONECT   39   40   89   90
CONECT   40   41   91   92
CONECT   41   42   93   94
CONECT   42   43   43   44
CONECT   44   95
END

HMDB0013055
     RDKit          3D
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione
 95 95  0  0  0  0  0  0  0  0999 V2000
   -3.1119    7.8921   -0.8982 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6269    7.5611   -0.7222 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5515    6.0393   -0.6025 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1449    5.5821   -0.4201 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1031    4.0649   -0.3549 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8976    3.5847    0.7803 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.3258    4.1598    1.9504 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9111    2.0984    1.0599 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3897    1.2842   -0.0833 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3435    1.2725   -1.5150 S   0  0  0  0  0  0  0  0  0  0  0  0
    1.0464    0.1988   -1.5053 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1951    0.3626   -0.6038 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.0675   -0.8147   -0.9486 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7081   -1.4684    0.1104 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5660   -1.0781    1.3092 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5851   -2.6515   -0.1002 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2463   -3.1179    1.1680 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0728   -4.3394    0.7935 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.0464   -3.9586   -0.2008 N   0  0  0  0  0  0  0  0  0  0  0  0
    6.7436   -4.9033    1.9797 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1361   -5.2415    3.0109 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.1372   -5.0733    1.9565 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1243    1.4902   -0.9142 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8322    1.4816   -1.9545 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2505    2.5991   -0.0526 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.1478    3.7069   -0.3192 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5599    3.2550   -0.4007 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8429    2.0441   -0.2365 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5574    4.1755   -0.6576 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8440   -0.0724    0.4144 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9628    0.1521    1.3731 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5262    1.4272    1.3092 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0450   -0.7994    0.9476 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9079   -0.7865   -0.5749 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3980   -0.9334   -0.6816 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9896   -2.3859   -0.4196 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4797   -3.2937   -1.4515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2740   -4.3002   -1.2758 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8077   -4.6751    0.0306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3328   -4.5844   -0.0986 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0521   -4.9342    1.1615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7713   -6.3006    1.6006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6539   -6.5588    2.1180 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7470   -7.2802    1.4348 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2734    8.9711   -1.0922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6429    7.6447    0.0385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5545    7.3288   -1.7454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3013    8.0382    0.2176 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1027    7.9111   -1.6167 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9851    5.6167   -1.5091 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2106    5.8195    0.2870 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1934    5.9660    0.5823 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4846    5.9745   -1.2357 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5448    3.7567   -1.3608 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9485    3.7793   -0.3298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9373    3.9871    0.7538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5219    3.7114    2.0804 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1636    1.8366    1.2555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4171    1.9372    2.0190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3709    1.7620   -0.4383 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4981    0.2484   -2.5711 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7622   -0.9001   -1.4703 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0649    0.3475    0.4586 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1916   -1.1317   -1.9184 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3484   -2.3984   -0.8535 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9660   -3.5108   -0.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9282   -2.2947    1.5015 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5168   -3.3456    1.9429 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4101   -5.1305    0.3542 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1858   -4.7573   -0.8652 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9345   -3.5918    0.2003 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5581   -5.6178    1.2012 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6649    2.6060    0.8183 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8417    4.1827   -1.2757 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0198    4.4601    0.4813 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5134    3.9100   -0.4700 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9937   -0.5384    0.9650 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6468   -0.0008    2.4237 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1422    1.5538    0.5587 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7897   -1.7832    1.3269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0575   -0.4540    1.2515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2517    0.1754   -1.0061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4555   -1.5806   -1.0715 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0398   -0.6543   -1.6786 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1212   -2.6827    0.6145 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8625   -2.3667   -0.5547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1357   -3.1054   -2.4882 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5628   -4.9077   -2.1590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6189   -5.7728    0.1558 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5342   -4.0891    0.8895 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5941   -3.5379   -0.3513 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6783   -5.1986   -0.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1302   -4.8309    0.9545 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8120   -4.1688    1.9316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6167   -8.0547    0.8194 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
  6  8  1  0
  8  9  1  0
  9 10  1  0
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M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
S-(11-Hydroxy-9-deoxy-δ12-PGD2)-glutathione	Generator
9-(S-Glutathionyl)-9-deoxy-delta('12)-prostaglandin D(,2)	HMDB
(5Z)-7-[(1R,2R)-2-[(3S)-1-{[(2S)-2-{[(4R)-4-amino-4-carboxy-1-hydroxybutylidene]amino}-2-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]sulfanyl}-3-hydroxyoctyl]-3-hydroxycyclopentyl]hept-5-enoate	Generator
(5Z)-7-[(1R,2R)-2-[(3S)-1-{[(2S)-2-{[(4R)-4-amino-4-carboxy-1-hydroxybutylidene]amino}-2-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]sulphanyl}-3-hydroxyoctyl]-3-hydroxycyclopentyl]hept-5-enoate	Generator
(5Z)-7-[(1R,2R)-2-[(3S)-1-{[(2S)-2-{[(4R)-4-amino-4-carboxy-1-hydroxybutylidene]amino}-2-[(carboxymethyl)-C-hydroxycarbonimidoyl]ethyl]sulphanyl}-3-hydroxyoctyl]-3-hydroxycyclopentyl]hept-5-enoic acid	Generator

Chemical Formula

C₃₀H₅₁N₃O₁₀S

Average Molecular Weight

645.805

Monoisotopic Molecular Weight

645.329515557

IUPAC Name

(5Z)-7-[(1R,2R)-2-[(3S)-1-{[(2S)-2-[(4R)-4-amino-4-carboxybutanamido]-2-[(carboxymethyl)carbamoyl]ethyl]sulfanyl}-3-hydroxyoctyl]-3-hydroxycyclopentyl]hept-5-enoic acid

Traditional Name

(5Z)-7-[(1R,2R)-2-[(3S)-1-{[(2S)-2-[(4R)-4-amino-4-carboxybutanamido]-2-(carboxymethylcarbamoyl)ethyl]sulfanyl}-3-hydroxyoctyl]-3-hydroxycyclopentyl]hept-5-enoic acid

CAS Registry Number

Not Available

SMILES

CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(O)=O)C(=O)NCC(O)=O)[C@H]1C(O)CC[C@@H]1C\C=C/CCCC(O)=O

InChI Identifier

InChI=1S/C30H51N3O10S/c1-2-3-6-10-20(34)16-24(28-19(12-14-23(28)35)9-7-4-5-8-11-26(37)38)44-18-22(29(41)32-17-27(39)40)33-25(36)15-13-21(31)30(42)43/h4,7,19-24,28,34-35H,2-3,5-6,8-18,31H2,1H3,(H,32,41)(H,33,36)(H,37,38)(H,39,40)(H,42,43)/b7-4-/t19-,20-,21+,22+,23?,24?,28+/m0/s1

InChI Key

BVYNXGKKWADCHD-RXULBTIMSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as oligopeptides. These are organic compounds containing a sequence of between three and ten alpha-amino acids joined by peptide bonds.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Carboxylic acids and derivatives

Sub Class

Amino acids, peptides, and analogues

Direct Parent

Oligopeptides

Alternative Parents

Substituents

Alpha-oligopeptide
Gamma-glutamyl alpha peptide
Glutamine or derivatives
N-acyl-alpha amino acid or derivatives
N-acyl-alpha-amino acid
Alpha-amino acid amide
Cysteine or derivatives
Alpha-amino acid
N-substituted-alpha-amino acid
Alpha-amino acid or derivatives
D-alpha-amino acid
Tricarboxylic acid or derivatives
N-acyl-amine
Fatty acyl
Fatty amide
Cyclopentanol
Cyclic alcohol
Secondary alcohol
Amino acid
Secondary carboxylic acid amide
Amino acid or derivatives
Carboxamide group
Dialkylthioether
Carboxylic acid
Sulfenyl compound
Thioether
Primary amine
Organic oxygen compound
Organic nitrogen compound
Alcohol
Carbonyl group
Hydrocarbon derivative
Amine
Organic oxide
Organopnictogen compound
Organosulfur compound
Primary aliphatic amine
Organooxygen compound
Organonitrogen compound
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Endogenous (HMDB: HMDB0013055)

Process

Not Available

Role

Not Available

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	0.018 g/L	ALOGPS
logP	-1.6	ALOGPS
logP	-1.4	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	1.81	ChemAxon
pKa (Strongest Basic)	9.31	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	11	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	236.58 Å²	ChemAxon
Rotatable Bond Count	24	ChemAxon
Refractivity	165.09 m³·mol⁻¹	ChemAxon
Polarizability	69.2 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DarkChem	[M+H]+	250.006	31661259
DarkChem	[M-H]-	236.957	31661259
DeepCCS	[M+H]+	251.632	30932474
DeepCCS	[M-H]-	249.808	30932474
DeepCCS	[M-2H]-	283.05	30932474
DeepCCS	[M+Na]+	257.238	30932474
AllCCS	[M+H]+	254.9	32859911
AllCCS	[M+H-H2O]+	254.2	32859911
AllCCS	[M+NH4]+	255.5	32859911
AllCCS	[M+Na]+	255.7	32859911
AllCCS	[M-H]-	246.2	32859911
AllCCS	[M+Na-2H]-	250.0	32859911
AllCCS	[M+HCOO]-	254.3	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(O)=O)C(=O)NCC(O)=O)[C@H]1C(O)CC[C@@H]1C\C=C/CCCC(O)=O	5904.0	Standard polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(O)=O)C(=O)NCC(O)=O)[C@H]1C(O)CC[C@@H]1C\C=C/CCCC(O)=O	3766.2	Standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(O)=O)C(=O)NCC(O)=O)[C@H]1C(O)CC[C@@H]1C\C=C/CCCC(O)=O	5226.9	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TMS,isomer #1	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	5199.7	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TMS,isomer #2	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5081.4	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TMS,isomer #3	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5149.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TMS,isomer #4	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	5088.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TMS,isomer #5	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	5162.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TMS,isomer #6	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5310.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TMS,isomer #7	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5065.7	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TMS,isomer #8	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5068.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #1	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4959.7	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #10	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4920.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #11	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5081.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #12	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4863.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #13	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4879.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #14	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4894.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #15	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4970.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #16	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5119.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #17	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4900.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #18	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4929.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #19	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4898.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #2	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	5008.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #20	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	5073.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #21	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4883.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #22	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4887.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #23	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	5123.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #24	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4913.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #25	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4922.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #26	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5054.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #27	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5262.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #28	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5066.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #29	CCCCC[C@H](O)CC(SC[C@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4886.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #3	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4981.4	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #4	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	5009.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #5	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	5171.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #6	CCCCC[C@@H](CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4959.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #7	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4967.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #8	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4915.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TMS,isomer #9	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4858.7	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #1	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4845.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #10	CCCCC[C@@H](CC(SC[C@H](C(=O)NCC(=O)O[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4838.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #11	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4845.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #12	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	4815.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #13	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	5015.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #14	CCCCC[C@@H](CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4827.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #15	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4840.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #16	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	5021.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #17	CCCCC[C@@H](CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	4836.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #18	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	4845.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #19	CCCCC[C@@H](CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4986.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #2	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4802.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #20	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	5123.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #21	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4991.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #22	CCCCC[C@@H](CC(SC[C@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4861.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #23	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4749.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #24	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4802.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #25	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4956.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #26	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4768.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #27	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4776.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #28	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4729.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #29	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4915.4	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #3	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	4835.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #30	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4729.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #31	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4747.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #32	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4953.7	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #33	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4763.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #34	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4776.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #35	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4916.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #36	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@H](C(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5095.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #37	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4926.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #38	CCCCC[C@H](O)CC(SC[C@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4801.7	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #39	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4759.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #4	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4997.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #40	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4935.4	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #41	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4747.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #42	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4765.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #43	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4990.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #44	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4782.7	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #45	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4793.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #46	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O[Si](C)(C)C)N(C(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4940.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #47	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5093.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #48	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4949.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #49	CCCCC[C@H](O)CC(SC[C@H](C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4827.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #5	CCCCC[C@@H](CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4820.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #50	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4934.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #51	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4740.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #52	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4758.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #53	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4920.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #54	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	5043.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #55	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4928.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #56	CCCCC[C@H](O)CC(SC[C@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	4789.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #57	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4945.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #58	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	5084.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #59	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4952.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #6	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4830.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #60	CCCCC[C@H](O)CC(SC[C@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C	4815.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #61	CCCCC[C@H](O)CC(SC[C@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N(C(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	4932.7	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #62	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5075.4	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #63	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@H](C(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5091.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #7	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O[Si](C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	4823.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #8	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C	4856.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,3TMS,isomer #9	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C	5027.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TBDMS,isomer #1	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	5381.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TBDMS,isomer #2	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5316.7	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TBDMS,isomer #3	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5399.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TBDMS,isomer #4	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	5289.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TBDMS,isomer #5	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	5399.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TBDMS,isomer #6	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5517.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TBDMS,isomer #7	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5307.4	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,1TBDMS,isomer #8	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5332.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #1	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	5367.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #10	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	5355.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #11	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5483.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #12	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5316.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #13	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5344.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #14	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	5319.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #15	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	5419.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #16	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5559.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #17	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5372.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #18	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5396.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #19	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	5307.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #2	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	5437.1	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #20	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	5448.2	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #21	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	5291.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #22	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	5322.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #23	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	5549.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #24	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	5372.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #25	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C	5396.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #26	CCCCC[C@H](O)CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N[Si](C)(C)C(C)(C)C)C(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5484.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #27	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@H](C(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5702.5	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #28	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5509.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #29	CCCCC[C@H](O)CC(SC[C@H](C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5353.9	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #3	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	5338.4	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #4	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C	5424.0	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #5	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N[Si](C)(C)C(C)(C)C)C(=O)O)C(=O)NCC(=O)O)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	5555.6	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #6	CCCCC[C@@H](CC(SC[C@H](C(=O)NCC(=O)O)N(C(=O)CC[C@@H](N)C(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	5385.3	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #7	CCCCC[C@@H](CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O)O[Si](C)(C)C(C)(C)C	5408.4	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #8	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@H]1C(O)CC[C@@H]1C/C=C\CCCC(=O)O	5361.8	Semi standard non polar	33892256
S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione,2TBDMS,isomer #9	CCCCC[C@H](O)CC(SC[C@@H](NC(=O)CC[C@@H](N)C(=O)O[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O)[C@H]1C(O[Si](C)(C)C(C)(C)C)CC[C@@H]1C/C=C\CCCC(=O)O	5270.6	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (Non-derivatized) - 70eV, Positive	splash10-0uml-3101196000-239040b7264c684e98f9	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_1_1) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_15) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione GC-MS (TMS_2_16) - 70eV, Positive	Not Available	2021-10-17	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 10V, Positive-QTOF	splash10-03gi-0001149000-1acae7aa8f82a5c8458d	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 20V, Positive-QTOF	splash10-01u1-6303794000-25091caeff1adee3d129	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 40V, Positive-QTOF	splash10-0a4i-9204440000-c8f07eefb48424253392	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 10V, Negative-QTOF	splash10-0kkc-0015039000-95082e6f257b7828c9bf	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 20V, Negative-QTOF	splash10-0fk9-0019011000-6991fabe9dcf07a53a7e	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 40V, Negative-QTOF	splash10-0kfw-2913000000-e8d619fbeeb87fe385db	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 10V, Positive-QTOF	splash10-03fr-0002019000-9ecc603d1cfdb836ff1a	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 20V, Positive-QTOF	splash10-01rt-5202569000-ba96050f00ba151a2ba4	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 40V, Positive-QTOF	splash10-001i-9200310000-375eee33f2aaa98e99f0	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 10V, Negative-QTOF	splash10-002f-0010009000-20714ff89fb377be5481	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 20V, Negative-QTOF	splash10-01rf-2932044000-05b014894bbe87d0322a	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione 40V, Negative-QTOF	splash10-002f-9601000000-4b439af9e2e9d9cd049a	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB029270

KNApSAcK ID

Not Available

Chemspider ID

35032565

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53481595

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Brunk E, Sahoo S, Zielinski DC, Altunkaya A, Drager A, Mih N, Gatto F, Nilsson A, Preciat Gonzalez GA, Aurich MK, Prlic A, Sastry A, Danielsdottir AD, Heinken A, Noronha A, Rose PW, Burley SK, Fleming RMT, Nielsen J, Thiele I, Palsson BO: Recon3D enables a three-dimensional view of gene variation in human metabolism. Nat Biotechnol. 2018 Mar;36(3):272-281. doi: 10.1038/nbt.4072. Epub 2018 Feb 19. [PubMed:29457794 ]

Showing metabocard for S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione (HMDB0013055)

MOL for HMDB0013055 (S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione)

3D MOL for HMDB0013055 (S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione)

3D SDF for HMDB0013055 (S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione)

3D-SDF for HMDB0013055 (S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione)

PDB for HMDB0013055 (S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione)

3D PDB for HMDB0013055 (S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione)

SMILES for HMDB0013055 (S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione)

INCHI for HMDB0013055 (S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione)

Structure for HMDB0013055 (S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione)

3D Structure for HMDB0013055 (S-(11-hydroxy-9-deoxy-delta12-PGD2)-glutathione)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra