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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (2) Show 2 proteins XML

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2008-10-16 22:34:20 UTC

Update Date

2022-03-07 02:51:03 UTC

HMDB ID

HMDB0011120

Secondary Accession Numbers

HMDB11120

Metabolite Identification

Common Name

trans-2-Enoyl-OPC4-CoA

Description

trans-2-Enoyl-OPC4-CoA belongs to the class of organic compounds known as acyl coas. These are organic compounds containing a coenzyme A substructure linked to an acyl chain. Thus, trans-2-enoyl-OPC4-CoA is considered to be a fatty ester lipid molecule. trans-2-Enoyl-OPC4-CoA is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

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


  Mrv0541 02241201192D          

 65 68  0  0  1  0            999 V2000
   32.6663   -8.0655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.6663   -9.1531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.6082   -7.5217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.5501   -8.0655    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   34.5501   -9.1532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.6082   -9.6970    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   31.6318   -7.7294    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   30.9926   -8.6093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.6318   -9.4893    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   33.6082   -6.5739    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   31.1774  -11.6622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.9281  -11.6622    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.5421  -10.8236    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   30.5528  -10.1872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.5957  -10.7850    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   31.1702  -12.5809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.8838  -12.5809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.5342   -9.8402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3597   -9.8402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.8058  -12.2453    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   28.8058  -11.3631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.9096  -12.5530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.4143  -13.2394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.4355   -9.4068    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   27.4355   -8.5246    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   26.4833   -9.8682    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.0440  -10.4009    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.5592   -9.4347    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   25.5592   -8.5525    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   24.6070   -9.8962    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   25.1676  -10.4288    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7402   -9.4530    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.4521   -9.8698    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.1691   -9.4617    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   18.8810   -9.8786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5980   -9.4705    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3099   -9.8874    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0269   -9.4793    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   21.7388   -9.8962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4558   -9.4881    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.1728   -9.8962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.8898   -9.4881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6942  -10.4592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.6870  -10.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7337  -10.7212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.0298   -8.8652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.8972   -8.8652    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.8759  -10.7036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0232   -9.8611    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   14.5943   -9.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3113   -9.4442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3164   -8.6192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8824   -9.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1654   -9.8434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6283   -9.3759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1433   -8.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6283   -8.0410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4129   -8.2959    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.4129   -9.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4850   -7.3867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.2646   -7.6222    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9007   -8.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.6687   -8.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3602   -7.6236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.9743   -8.0291    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  2  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9  2  1  0  0  0  0
  3 10  1  0  0  0  0
 12 11  1  1  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 11  1  1  0  0  0
 11 16  1  0  0  0  0
 12 17  1  0  0  0  0
 15  9  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 21  2  0  0  0  0
 20 17  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 24 25  2  0  0  0  0
 24 19  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
 28 29  2  0  0  0  0
 28 26  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 33 32  1  0  0  0  0
 34 33  1  0  0  0  0
 35 34  1  0  0  0  0
 36 35  1  0  0  0  0
 37 36  1  0  0  0  0
 38 37  1  0  0  0  0
 39 38  1  0  0  0  0
 40 39  1  0  0  0  0
 41 40  1  0  0  0  0
 42 41  1  0  0  0  0
 30 42  1  0  0  0  0
 41 43  1  0  0  0  0
 41 44  1  0  0  0  0
 39 45  2  0  0  0  0
 40 46  1  6  0  0  0
 40 47  1  1  0  0  0
 35 48  2  0  0  0  0
 32 49  1  0  0  0  0
 51 50  1  0  0  0  0
 49 51  1  0  0  0  0
 51 52  2  0  0  0  0
 50 53  2  0  0  0  0
 53 54  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 55  1  0  0  0  0
 54 59  1  1  0  0  0
 57 60  2  0  0  0  0
 58 61  1  1  0  0  0
 61 62  1  0  0  0  0
 62 63  2  0  0  0  0
 63 64  1  0  0  0  0
 64 65  1  0  0  0  0
M  END

HMDB0011120
     RDKit          3D
trans-2-Enoyl-OPC4-CoA
118121  0  0  0  0  0  0  0  0999 V2000
   15.6097    2.9308    2.3321 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2489    1.6250    1.6499 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1279    0.9793    2.3389 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9557    0.6766    1.8387 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6001    0.9624    0.4509 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2570   -0.3162   -0.3205 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.4323   -1.2397   -0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8666   -1.8105    0.6532 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9901   -1.3577   -1.6895 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0782   -0.5905   -2.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9484   -0.0340   -1.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6320   -0.6739   -2.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5733   -0.0873   -1.2652 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5376    0.5444   -1.8591 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4831    1.1313   -1.0496 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5567    1.0516    0.1940 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1122    1.9468   -1.8460 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.9626    2.5984   -0.5899 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4049    1.3931    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7070    0.5175   -0.7766 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401   -0.6737   -0.2754 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2470   -0.9561    0.9354 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4208   -1.5884   -1.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0428   -2.8239   -0.4067 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1962   -2.4905    0.7113 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0763   -1.8795    0.5594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4795   -1.6229   -0.5972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9455   -1.5343    1.7044 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2110   -1.8276    2.8574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1888   -2.3988    1.7479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8677   -3.8510    1.8735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9579   -1.9509    2.9849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0956   -2.1587    0.5746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5349   -0.8370    0.5199 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5586   -0.5611   -0.7780 P   0  0  0  0  0  5  0  0  0  0  0  0
   -4.5119   -1.7342   -1.7329 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0084    0.8009   -1.6246 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1622   -0.2719   -0.2694 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7921   -1.6090    0.5163 P   0  0  0  0  0  5  0  0  0  0  0  0
   -6.1841   -1.6814    1.8990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4912   -3.0416   -0.3621 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4477   -1.4941    0.6990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8767   -0.1706    0.7119 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4008   -0.1064    0.8816 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.7606    1.2107    0.8842 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6621    1.4329   -0.1380 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.6422    2.7465   -0.6959 N   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8465    3.3160   -1.5976 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2231    4.5899   -1.8095 N   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2800    4.8573   -1.0356 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0695    5.9798   -0.8403 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.8232    7.1885   -1.5468 N   0  0  0  0  0  0  0  0  0  0  0  0
  -14.0902    5.9365    0.0316 N   0  0  0  0  0  0  0  0  0  0  0  0
  -14.3428    4.8088    0.7098 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.5774    3.7192    0.5207 N   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5407    3.7136   -0.3440 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3813    0.3474   -1.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4900    0.1201   -1.9762 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0903   -0.8152   -0.2549 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.2815   -1.7770   -0.8459 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1099   -3.2491   -0.7790 P   0  0  0  0  0  5  0  0  0  0  0  0
  -10.8959   -4.0137   -2.0645 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6095   -4.1900    0.5276 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7856   -2.9792   -0.6386 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0440    3.7913    1.9204 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.6856    3.1423    2.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.4675    2.8332    3.4234 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.1059    1.8483    0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.1800    0.9873    1.6886 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3081    0.7230    3.4074 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.2010    0.1887    2.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3066    1.5620   -0.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6514    1.5842    0.4860 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.4028   -0.7688    0.2184 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.0347   -0.9487   -1.6719 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.0256   -2.4294   -2.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.6534    0.2136   -3.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6725   -1.2616   -3.4011 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8801    1.0820   -1.9309 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3855   -0.5473   -3.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7397   -1.7646   -1.8646 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5655   -0.1283   -0.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5560    0.5764   -2.9301 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4778    3.2579    0.1141 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1420    3.0869   -1.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6981    1.7191    0.9499 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2050    0.7898    0.6094 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6359    0.7831   -1.7849 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5350   -1.0417   -1.5962 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0732   -1.9335   -2.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0084   -3.2480   -0.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5368   -3.5662   -1.0778 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5412   -2.7141    1.7000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2377   -0.4884    1.7430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1096   -2.7785    3.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8563   -4.2235    2.9134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8645   -4.0876    1.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6189   -4.4300    1.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6510   -2.7816    3.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2978   -1.8014    3.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5360   -1.0480    2.7708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9811   -2.8004    0.7097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6421   -2.4711   -0.3891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0594    1.6239   -1.0515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4213   -3.7586    0.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5923    0.2771   -0.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3734    0.4157    1.5012 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6496   -0.5925    1.8628 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6739    1.1800    0.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
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  -13.2596   -3.7665   -0.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
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 41105  1  0
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 59116  1  1
 63117  1  0
 64118  1  0
M  END


  Mrv0541 02241201192D          

 65 68  0  0  1  0            999 V2000
   32.6663   -8.0655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.6663   -9.1531    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.6082   -7.5217    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.5501   -8.0655    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   34.5501   -9.1532    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.6082   -9.6970    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   31.6318   -7.7294    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   30.9926   -8.6093    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.6318   -9.4893    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   33.6082   -6.5739    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   31.1774  -11.6622    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.9281  -11.6622    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   29.5421  -10.8236    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   30.5528  -10.1872    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   31.5957  -10.7850    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   31.1702  -12.5809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.8838  -12.5809    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   29.5342   -9.8402    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.3597   -9.8402    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.8058  -12.2453    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   28.8058  -11.3631    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   27.9096  -12.5530    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   28.4143  -13.2394    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   21.7388   -9.8962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.4558   -9.4881    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   23.1728   -9.8962    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.8898   -9.4881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6942  -10.4592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.6870  -10.4872    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.7337  -10.7212    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.0298   -8.8652    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.8972   -8.8652    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   18.8759  -10.7036    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.0232   -9.8611    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   14.5943   -9.8523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3113   -9.4442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.3164   -8.6192    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8824   -9.4354    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.1654   -9.8434    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6283   -9.3759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.1433   -8.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6283   -8.0410    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.4129   -8.2959    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.4129   -9.1209    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.4850   -7.3867    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   14.6687   -8.0229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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  1  2  2  0  0  0  0
  1  3  1  0  0  0  0
  3  4  2  0  0  0  0
  4  5  1  0  0  0  0
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  6  2  1  0  0  0  0
  1  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9  2  1  0  0  0  0
  3 10  1  0  0  0  0
 12 11  1  1  0  0  0
 13 12  1  1  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 11  1  1  0  0  0
 11 16  1  0  0  0  0
 12 17  1  0  0  0  0
 15  9  1  0  0  0  0
 13 18  1  0  0  0  0
 18 19  1  0  0  0  0
 20 21  2  0  0  0  0
 20 17  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 24 25  2  0  0  0  0
 24 19  1  0  0  0  0
 24 26  1  0  0  0  0
 24 27  1  0  0  0  0
 28 29  2  0  0  0  0
 28 26  1  0  0  0  0
 28 30  1  0  0  0  0
 28 31  1  0  0  0  0
 33 32  1  0  0  0  0
 34 33  1  0  0  0  0
 35 34  1  0  0  0  0
 36 35  1  0  0  0  0
 37 36  1  0  0  0  0
 38 37  1  0  0  0  0
 39 38  1  0  0  0  0
 40 39  1  0  0  0  0
 41 40  1  0  0  0  0
 42 41  1  0  0  0  0
 30 42  1  0  0  0  0
 41 43  1  0  0  0  0
 41 44  1  0  0  0  0
 39 45  2  0  0  0  0
 40 46  1  6  0  0  0
 40 47  1  1  0  0  0
 35 48  2  0  0  0  0
 32 49  1  0  0  0  0
 51 50  1  0  0  0  0
 49 51  1  0  0  0  0
 51 52  2  0  0  0  0
 50 53  2  0  0  0  0
 53 54  1  0  0  0  0
 55 56  1  0  0  0  0
 56 57  1  0  0  0  0
 57 58  1  0  0  0  0
 58 59  1  0  0  0  0
 59 55  1  0  0  0  0
 54 59  1  1  0  0  0
 57 60  2  0  0  0  0
 58 61  1  1  0  0  0
 61 62  1  0  0  0  0
 62 63  2  0  0  0  0
 63 64  1  0  0  0  0
 64 65  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0011120

> <DATABASE_NAME>
hmdb

> <SMILES>
CC\C=C/C[C@@H]1C(=O)CCC1C\C=C\C(=O)SCCNC(=O)CCNC(=O)[C@@](O)([H])C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@H](C(O)[C@H]1OP(=O)(O)O)N1C=NC2=C1N=CN=C2N

> <INCHI_IDENTIFIER>
InChI=1S/C35H54N7O18P3S/c1-4-5-6-9-22-21(11-12-23(22)43)8-7-10-26(45)64-16-15-37-25(44)13-14-38-33(48)30(47)35(2,3)18-57-63(54,55)60-62(52,53)56-17-24-29(59-61(49,50)51)28(46)34(58-24)42-20-41-27-31(36)39-19-40-32(27)42/h5-7,10,19-22,24,28-30,34,46-47H,4,8-9,11-18H2,1-3H3,(H,37,44)(H,38,48)(H,52,53)(H,54,55)(H2,36,39,40)(H2,49,50,51)/b6-5-,10-7+/t21?,22-,24+,28?,29-,30-,34+/m0/s1

> <INCHI_KEY>
QSAQFDYWYNLXEC-XIFSABRGSA-N

> <FORMULA>
C35H54N7O18P3S

> <MOLECULAR_WEIGHT>
985.826

> <EXACT_MASS>
985.245888185

> <JCHEM_ACCEPTOR_COUNT>
18

> <JCHEM_AVERAGE_POLARIZABILITY>
92.79296490138535

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({hydroxy[(3R)-3-hydroxy-2,2-dimethyl-3-({2-[(2-{[(2E)-4-[(2S)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl]but-2-enoyl]sulfanyl}ethyl)carbamoyl]ethyl}carbamoyl)propoxy]phosphoryl}oxy)phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid

> <ALOGPS_LOGP>
1.17

> <JCHEM_LOGP>
-3.2172601249663546

> <ALOGPS_LOGS>
-2.70

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-4

> <JCHEM_PKA>
2.6787711798581504

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.8252479627216047

> <JCHEM_PKA_STRONGEST_BASIC>
4.946047024039826

> <JCHEM_POLAR_SURFACE_AREA>
380.6999999999999

> <JCHEM_REFRACTIVITY>
228.41610000000006

> <JCHEM_ROTATABLE_BOND_COUNT>
26

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.95e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-[({hydroxy[hydroxy(3R)-3-hydroxy-2,2-dimethyl-3-({2-[(2-{[(2E)-4-[(2S)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl]but-2-enoyl]sulfanyl}ethyl)carbamoyl]ethyl}carbamoyl)propoxyphosphoryl]oxyphosphoryl}oxy)methyl]oxolan-3-yl]oxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0011120
     RDKit          3D
trans-2-Enoyl-OPC4-CoA
118121  0  0  0  0  0  0  0  0999 V2000
   15.6097    2.9308    2.3321 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2489    1.6250    1.6499 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1279    0.9793    2.3389 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9557    0.6766    1.8387 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6001    0.9624    0.4509 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2570   -0.3162   -0.3205 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.4323   -1.2397   -0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8666   -1.8105    0.6532 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9901   -1.3577   -1.6895 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0782   -0.5905   -2.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9484   -0.0340   -1.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6320   -0.6739   -2.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5733   -0.0873   -1.2652 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5376    0.5444   -1.8591 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4831    1.1313   -1.0496 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5567    1.0516    0.1940 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1122    1.9468   -1.8460 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.9626    2.5984   -0.5899 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4049    1.3931    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7070    0.5175   -0.7766 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401   -0.6737   -0.2754 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2470   -0.9561    0.9354 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4208   -1.5884   -1.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      60.977 -15.056   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      60.977 -17.086   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      62.735 -14.041   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0      64.494 -15.056   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0      64.494 -17.086   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      62.735 -18.101   0.000  0.00  0.00           N+0
HETATM    7  N   UNK     0      59.046 -14.428   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      57.853 -16.071   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      59.046 -17.713   0.000  0.00  0.00           N+0
HETATM   10  N   UNK     0      62.735 -12.271   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0      58.198 -21.769   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      55.866 -21.769   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      55.145 -20.204   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      57.032 -19.016   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      58.979 -20.132   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      58.184 -23.484   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      55.783 -23.484   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      55.131 -18.368   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      52.938 -18.368   0.000  0.00  0.00           O+0
HETATM   20  P   UNK     0      53.771 -22.858   0.000  0.00  0.00           P+0
HETATM   21  O   UNK     0      53.771 -21.211   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      52.098 -23.432   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      53.040 -24.714   0.000  0.00  0.00           O+0
HETATM   24  P   UNK     0      51.213 -17.559   0.000  0.00  0.00           P+0
HETATM   25  O   UNK     0      51.213 -15.913   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      49.435 -18.421   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      50.482 -19.415   0.000  0.00  0.00           O+0
HETATM   28  P   UNK     0      47.711 -17.611   0.000  0.00  0.00           P+0
HETATM   29  O   UNK     0      47.711 -15.965   0.000  0.00  0.00           O+0
HETATM   30  O   UNK     0      45.933 -18.473   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      46.980 -19.467   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      31.248 -17.646   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      32.577 -18.424   0.000  0.00  0.00           C+0
HETATM   34  N   UNK     0      33.916 -17.662   0.000  0.00  0.00           N+0
HETATM   35  C   UNK     0      35.245 -18.440   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      36.583 -17.678   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      37.912 -18.456   0.000  0.00  0.00           C+0
HETATM   38  N   UNK     0      39.250 -17.695   0.000  0.00  0.00           N+0
HETATM   39  C   UNK     0      40.579 -18.473   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      41.917 -17.711   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      43.256 -18.473   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      44.594 -17.711   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      42.363 -19.524   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0      44.216 -19.576   0.000  0.00  0.00           C+0
HETATM   45  O   UNK     0      40.570 -20.013   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0      42.989 -16.548   0.000  0.00  0.00           O+0
HETATM   47  H   UNK     0      40.875 -16.548   0.000  0.00  0.00           H+0
HETATM   48  O   UNK     0      35.235 -19.980   0.000  0.00  0.00           O+0
HETATM   49  S   UNK     0      29.910 -18.407   0.000  0.00  0.00           S+0
HETATM   50  C   UNK     0      27.243 -18.391   0.000  0.00  0.00           C+0
HETATM   51  C   UNK     0      28.581 -17.629   0.000  0.00  0.00           C+0
HETATM   52  O   UNK     0      28.591 -16.089   0.000  0.00  0.00           O+0
HETATM   53  C   UNK     0      25.914 -17.613   0.000  0.00  0.00           C+0
HETATM   54  C   UNK     0      24.575 -18.374   0.000  0.00  0.00           C+0
HETATM   55  C   UNK     0      21.706 -17.502   0.000  0.00  0.00           C+0
HETATM   56  C   UNK     0      20.801 -16.256   0.000  0.00  0.00           C+0
HETATM   57  C   UNK     0      21.706 -15.010   0.000  0.00  0.00           C+0
HETATM   58  C   UNK     0      23.171 -15.486   0.000  0.00  0.00           C+0
HETATM   59  C   UNK     0      23.171 -17.026   0.000  0.00  0.00           C+0
HETATM   60  O   UNK     0      21.439 -13.789   0.000  0.00  0.00           O+0
HETATM   61  C   UNK     0      24.761 -14.228   0.000  0.00  0.00           C+0
HETATM   62  C   UNK     0      25.948 -14.976   0.000  0.00  0.00           C+0
HETATM   63  C   UNK     0      27.382 -14.976   0.000  0.00  0.00           C+0
HETATM   64  C   UNK     0      28.672 -14.231   0.000  0.00  0.00           C+0
HETATM   65  C   UNK     0      29.819 -14.988   0.000  0.00  0.00           C+0
CONECT    1    2    3    7                                                  
CONECT    2    1    6    9                                                  
CONECT    3    1    4   10                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    2                                                       
CONECT    7    1    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8    2   15                                                  
CONECT   10    3                                                            
CONECT   11   12   15   16                                                  
CONECT   12   11   13   17                                                  
CONECT   13   12   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   11    9                                                  
CONECT   16   11                                                            
CONECT   17   12   20                                                       
CONECT   18   13   19                                                       
CONECT   19   18   24                                                       
CONECT   20   21   17   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20                                                            
CONECT   24   25   19   26   27                                             
CONECT   25   24                                                            
CONECT   26   24   28                                                       
CONECT   27   24                                                            
CONECT   28   29   26   30   31                                             
CONECT   29   28                                                            
CONECT   30   28   42                                                       
CONECT   31   28                                                            
CONECT   32   33   49                                                       
CONECT   33   32   34                                                       
CONECT   34   33   35                                                       
CONECT   35   34   36   48                                                  
CONECT   36   35   37                                                       
CONECT   37   36   38                                                       
CONECT   38   37   39                                                       
CONECT   39   38   40   45                                                  
CONECT   40   39   41   46   47                                             
CONECT   41   40   42   43   44                                             
CONECT   42   41   30                                                       
CONECT   43   41                                                            
CONECT   44   41                                                            
CONECT   45   39                                                            
CONECT   46   40                                                            
CONECT   47   40                                                            
CONECT   48   35                                                            
CONECT   49   32   51                                                       
CONECT   50   51   53                                                       
CONECT   51   50   49   52                                                  
CONECT   52   51                                                            
CONECT   53   50   54                                                       
CONECT   54   53   59                                                       
CONECT   55   56   59                                                       
CONECT   56   55   57                                                       
CONECT   57   56   58   60                                                  
CONECT   58   57   59   61                                                  
CONECT   59   58   55   54                                                  
CONECT   60   57                                                            
CONECT   61   58   62                                                       
CONECT   62   61   63                                                       
CONECT   63   62   64                                                       
CONECT   64   63   65                                                       
CONECT   65   64                                                            
MASTER        0    0    0    0    0    0    0    0   65    0  136    0
END

COMPND    HMDB0011120
HETATM    1  C1  UNL     1      15.610   2.931   2.332  1.00  0.00           C  
HETATM    2  C2  UNL     1      15.249   1.625   1.650  1.00  0.00           C  
HETATM    3  C3  UNL     1      14.128   0.979   2.339  1.00  0.00           C  
HETATM    4  C4  UNL     1      12.956   0.677   1.839  1.00  0.00           C  
HETATM    5  C5  UNL     1      12.600   0.962   0.451  1.00  0.00           C  
HETATM    6  C6  UNL     1      12.257  -0.316  -0.320  1.00  0.00           C  
HETATM    7  C7  UNL     1      13.432  -1.240  -0.323  1.00  0.00           C  
HETATM    8  O1  UNL     1      13.867  -1.810   0.653  1.00  0.00           O  
HETATM    9  C8  UNL     1      13.990  -1.358  -1.690  1.00  0.00           C  
HETATM   10  C9  UNL     1      13.078  -0.591  -2.599  1.00  0.00           C  
HETATM   11  C10 UNL     1      11.948  -0.034  -1.764  1.00  0.00           C  
HETATM   12  C11 UNL     1      10.632  -0.674  -2.122  1.00  0.00           C  
HETATM   13  C12 UNL     1       9.573  -0.087  -1.265  1.00  0.00           C  
HETATM   14  C13 UNL     1       8.538   0.544  -1.859  1.00  0.00           C  
HETATM   15  C14 UNL     1       7.483   1.131  -1.050  1.00  0.00           C  
HETATM   16  O2  UNL     1       7.557   1.052   0.194  1.00  0.00           O  
HETATM   17  S1  UNL     1       6.112   1.947  -1.846  1.00  0.00           S  
HETATM   18  C15 UNL     1       4.963   2.598  -0.590  1.00  0.00           C  
HETATM   19  C16 UNL     1       4.405   1.393   0.140  1.00  0.00           C  
HETATM   20  N1  UNL     1       3.707   0.518  -0.777  1.00  0.00           N  
HETATM   21  C17 UNL     1       3.140  -0.674  -0.275  1.00  0.00           C  
HETATM   22  O3  UNL     1       3.247  -0.956   0.935  1.00  0.00           O  
HETATM   23  C18 UNL     1       2.421  -1.588  -1.185  1.00  0.00           C  
HETATM   24  C19 UNL     1       2.043  -2.824  -0.407  1.00  0.00           C  
HETATM   25  N2  UNL     1       1.196  -2.491   0.711  1.00  0.00           N  
HETATM   26  C20 UNL     1      -0.076  -1.879   0.559  1.00  0.00           C  
HETATM   27  O4  UNL     1      -0.480  -1.623  -0.597  1.00  0.00           O  
HETATM   28  C21 UNL     1      -0.946  -1.534   1.704  1.00  0.00           C  
HETATM   29  O5  UNL     1      -0.211  -1.828   2.857  1.00  0.00           O  
HETATM   30  C22 UNL     1      -2.189  -2.399   1.748  1.00  0.00           C  
HETATM   31  C23 UNL     1      -1.868  -3.851   1.873  1.00  0.00           C  
HETATM   32  C24 UNL     1      -2.958  -1.951   2.985  1.00  0.00           C  
HETATM   33  C25 UNL     1      -3.096  -2.159   0.575  1.00  0.00           C  
HETATM   34  O6  UNL     1      -3.535  -0.837   0.520  1.00  0.00           O  
HETATM   35  P1  UNL     1      -4.559  -0.561  -0.778  1.00  0.00           P  
HETATM   36  O7  UNL     1      -4.512  -1.734  -1.733  1.00  0.00           O  
HETATM   37  O8  UNL     1      -4.008   0.801  -1.625  1.00  0.00           O  
HETATM   38  O9  UNL     1      -6.162  -0.272  -0.269  1.00  0.00           O  
HETATM   39  P2  UNL     1      -6.792  -1.609   0.516  1.00  0.00           P  
HETATM   40  O10 UNL     1      -6.184  -1.681   1.899  1.00  0.00           O  
HETATM   41  O11 UNL     1      -6.491  -3.042  -0.362  1.00  0.00           O  
HETATM   42  O12 UNL     1      -8.448  -1.494   0.699  1.00  0.00           O  
HETATM   43  C26 UNL     1      -8.877  -0.171   0.712  1.00  0.00           C  
HETATM   44  C27 UNL     1     -10.401  -0.106   0.882  1.00  0.00           C  
HETATM   45  O13 UNL     1     -10.761   1.211   0.884  1.00  0.00           O  
HETATM   46  C28 UNL     1     -11.662   1.433  -0.138  1.00  0.00           C  
HETATM   47  N3  UNL     1     -11.642   2.747  -0.696  1.00  0.00           N  
HETATM   48  C29 UNL     1     -10.847   3.316  -1.598  1.00  0.00           C  
HETATM   49  N4  UNL     1     -11.223   4.590  -1.810  1.00  0.00           N  
HETATM   50  C30 UNL     1     -12.280   4.857  -1.036  1.00  0.00           C  
HETATM   51  C31 UNL     1     -13.069   5.980  -0.840  1.00  0.00           C  
HETATM   52  N5  UNL     1     -12.823   7.188  -1.547  1.00  0.00           N  
HETATM   53  N6  UNL     1     -14.090   5.936   0.032  1.00  0.00           N  
HETATM   54  C32 UNL     1     -14.343   4.809   0.710  1.00  0.00           C  
HETATM   55  N7  UNL     1     -13.577   3.719   0.521  1.00  0.00           N  
HETATM   56  C33 UNL     1     -12.541   3.714  -0.344  1.00  0.00           C  
HETATM   57  C34 UNL     1     -11.381   0.347  -1.184  1.00  0.00           C  
HETATM   58  O14 UNL     1     -12.490   0.120  -1.976  1.00  0.00           O  
HETATM   59  C35 UNL     1     -11.090  -0.815  -0.255  1.00  0.00           C  
HETATM   60  O15 UNL     1     -10.281  -1.777  -0.846  1.00  0.00           O  
HETATM   61  P3  UNL     1     -11.110  -3.249  -0.779  1.00  0.00           P  
HETATM   62  O16 UNL     1     -10.896  -4.014  -2.065  1.00  0.00           O  
HETATM   63  O17 UNL     1     -10.610  -4.190   0.528  1.00  0.00           O  
HETATM   64  O18 UNL     1     -12.786  -2.979  -0.639  1.00  0.00           O  
HETATM   65  H1  UNL     1      15.044   3.791   1.920  1.00  0.00           H  
HETATM   66  H2  UNL     1      16.686   3.142   2.165  1.00  0.00           H  
HETATM   67  H3  UNL     1      15.468   2.833   3.423  1.00  0.00           H  
HETATM   68  H4  UNL     1      15.106   1.848   0.587  1.00  0.00           H  
HETATM   69  H5  UNL     1      16.180   0.987   1.689  1.00  0.00           H  
HETATM   70  H6  UNL     1      14.308   0.723   3.407  1.00  0.00           H  
HETATM   71  H7  UNL     1      12.201   0.189   2.476  1.00  0.00           H  
HETATM   72  H8  UNL     1      13.307   1.562  -0.109  1.00  0.00           H  
HETATM   73  H9  UNL     1      11.651   1.584   0.486  1.00  0.00           H  
HETATM   74  H10 UNL     1      11.403  -0.769   0.218  1.00  0.00           H  
HETATM   75  H11 UNL     1      15.035  -0.949  -1.672  1.00  0.00           H  
HETATM   76  H12 UNL     1      14.026  -2.429  -2.020  1.00  0.00           H  
HETATM   77  H13 UNL     1      13.653   0.214  -3.078  1.00  0.00           H  
HETATM   78  H14 UNL     1      12.673  -1.262  -3.401  1.00  0.00           H  
HETATM   79  H15 UNL     1      11.880   1.082  -1.931  1.00  0.00           H  
HETATM   80  H16 UNL     1      10.386  -0.547  -3.200  1.00  0.00           H  
HETATM   81  H17 UNL     1      10.740  -1.765  -1.865  1.00  0.00           H  
HETATM   82  H18 UNL     1       9.566  -0.128  -0.189  1.00  0.00           H  
HETATM   83  H19 UNL     1       8.556   0.576  -2.930  1.00  0.00           H  
HETATM   84  H20 UNL     1       5.478   3.258   0.114  1.00  0.00           H  
HETATM   85  H21 UNL     1       4.142   3.087  -1.155  1.00  0.00           H  
HETATM   86  H22 UNL     1       3.698   1.719   0.950  1.00  0.00           H  
HETATM   87  H23 UNL     1       5.205   0.790   0.609  1.00  0.00           H  
HETATM   88  H24 UNL     1       3.636   0.783  -1.785  1.00  0.00           H  
HETATM   89  H25 UNL     1       1.535  -1.042  -1.596  1.00  0.00           H  
HETATM   90  H26 UNL     1       3.073  -1.934  -2.022  1.00  0.00           H  
HETATM   91  H27 UNL     1       3.008  -3.248  -0.035  1.00  0.00           H  
HETATM   92  H28 UNL     1       1.537  -3.566  -1.078  1.00  0.00           H  
HETATM   93  H29 UNL     1       1.541  -2.714   1.700  1.00  0.00           H  
HETATM   94  H30 UNL     1      -1.238  -0.488   1.743  1.00  0.00           H  
HETATM   95  H31 UNL     1      -0.110  -2.779   3.028  1.00  0.00           H  
HETATM   96  H32 UNL     1      -1.856  -4.223   2.913  1.00  0.00           H  
HETATM   97  H33 UNL     1      -0.864  -4.088   1.435  1.00  0.00           H  
HETATM   98  H34 UNL     1      -2.619  -4.430   1.304  1.00  0.00           H  
HETATM   99  H35 UNL     1      -3.651  -2.782   3.240  1.00  0.00           H  
HETATM  100  H36 UNL     1      -2.298  -1.801   3.855  1.00  0.00           H  
HETATM  101  H37 UNL     1      -3.536  -1.048   2.771  1.00  0.00           H  
HETATM  102  H38 UNL     1      -3.981  -2.800   0.710  1.00  0.00           H  
HETATM  103  H39 UNL     1      -2.642  -2.471  -0.389  1.00  0.00           H  
HETATM  104  H40 UNL     1      -4.059   1.624  -1.052  1.00  0.00           H  
HETATM  105  H41 UNL     1      -6.421  -3.759   0.345  1.00  0.00           H  
HETATM  106  H42 UNL     1      -8.592   0.277  -0.262  1.00  0.00           H  
HETATM  107  H43 UNL     1      -8.373   0.416   1.501  1.00  0.00           H  
HETATM  108  H44 UNL     1     -10.650  -0.592   1.863  1.00  0.00           H  
HETATM  109  H45 UNL     1     -12.674   1.180   0.262  1.00  0.00           H  
HETATM  110  H46 UNL     1     -10.013   2.782  -2.074  1.00  0.00           H  
HETATM  111  H47 UNL     1     -12.994   7.323  -2.555  1.00  0.00           H  
HETATM  112  H48 UNL     1     -12.438   7.998  -0.986  1.00  0.00           H  
HETATM  113  H49 UNL     1     -15.169   4.789   1.409  1.00  0.00           H  
HETATM  114  H50 UNL     1     -10.458   0.569  -1.742  1.00  0.00           H  
HETATM  115  H51 UNL     1     -12.239  -0.602  -2.609  1.00  0.00           H  
HETATM  116  H52 UNL     1     -12.055  -1.221   0.114  1.00  0.00           H  
HETATM  117  H53 UNL     1     -11.367  -4.651   0.982  1.00  0.00           H  
HETATM  118  H54 UNL     1     -13.260  -3.766  -0.328  1.00  0.00           H  
CONECT    1    2   65   66   67
CONECT    2    3   68   69
CONECT    3    4    4   70
CONECT    4    5   71
CONECT    5    6   72   73
CONECT    6    7   11   74
CONECT    7    8    8    9
CONECT    9   10   75   76
CONECT   10   11   77   78
CONECT   11   12   79
CONECT   12   13   80   81
CONECT   13   14   14   82
CONECT   14   15   83
CONECT   15   16   16   17
CONECT   17   18
CONECT   18   19   84   85
CONECT   19   20   86   87
CONECT   20   21   88
CONECT   21   22   22   23
CONECT   23   24   89   90
CONECT   24   25   91   92
CONECT   25   26   93
CONECT   26   27   27   28
CONECT   28   29   30   94
CONECT   29   95
CONECT   30   31   32   33
CONECT   31   96   97   98
CONECT   32   99  100  101
CONECT   33   34  102  103
CONECT   34   35
CONECT   35   36   36   37   38
CONECT   37  104
CONECT   38   39
CONECT   39   40   40   41   42
CONECT   41  105
CONECT   42   43
CONECT   43   44  106  107
CONECT   44   45   59  108
CONECT   45   46
CONECT   46   47   57  109
CONECT   47   48   56
CONECT   48   49   49  110
CONECT   49   50
CONECT   50   51   51   56
CONECT   51   52   53
CONECT   52  111  112
CONECT   53   54   54
CONECT   54   55  113
CONECT   55   56   56
CONECT   57   58   59  114
CONECT   58  115
CONECT   59   60  116
CONECT   60   61
CONECT   61   62   62   63   64
CONECT   63  117
CONECT   64  118
END

HMDB0011120
     RDKit          3D
trans-2-Enoyl-OPC4-CoA
118121  0  0  0  0  0  0  0  0999 V2000
   15.6097    2.9308    2.3321 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.2489    1.6250    1.6499 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.1279    0.9793    2.3389 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9557    0.6766    1.8387 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.6001    0.9624    0.4509 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.2570   -0.3162   -0.3205 C   0  0  2  0  0  0  0  0  0  0  0  0
   13.4323   -1.2397   -0.3234 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8666   -1.8105    0.6532 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.9901   -1.3577   -1.6895 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.0782   -0.5905   -2.5992 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9484   -0.0340   -1.7635 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6320   -0.6739   -2.1221 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5733   -0.0873   -1.2652 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5376    0.5444   -1.8591 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4831    1.1313   -1.0496 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5567    1.0516    0.1940 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1122    1.9468   -1.8460 S   0  0  0  0  0  0  0  0  0  0  0  0
    4.9626    2.5984   -0.5899 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4049    1.3931    0.1398 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7070    0.5175   -0.7766 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1401   -0.6737   -0.2754 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2470   -0.9561    0.9354 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4208   -1.5884   -1.1848 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0428   -2.8239   -0.4067 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1962   -2.4905    0.7113 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0763   -1.8795    0.5594 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4795   -1.6229   -0.5972 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9455   -1.5343    1.7044 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.2110   -1.8276    2.8574 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1888   -2.3988    1.7479 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8677   -3.8510    1.8735 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9579   -1.9509    2.9849 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0956   -2.1587    0.5746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5349   -0.8370    0.5199 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5586   -0.5611   -0.7780 P   0  0  0  0  0  5  0  0  0  0  0  0
   -4.5119   -1.7342   -1.7329 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0084    0.8009   -1.6246 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1622   -0.2719   -0.2694 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7921   -1.6090    0.5163 P   0  0  0  0  0  5  0  0  0  0  0  0
   -6.1841   -1.6814    1.8990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4912   -3.0416   -0.3621 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4477   -1.4941    0.6990 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8767   -0.1706    0.7119 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4008   -0.1064    0.8816 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.7606    1.2107    0.8842 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.6621    1.4329   -0.1380 C   0  0  1  0  0  0  0  0  0  0  0  0
  -11.6422    2.7465   -0.6959 N   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8465    3.3160   -1.5976 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2231    4.5899   -1.8095 N   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2800    4.8573   -1.0356 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.0695    5.9798   -0.8403 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.8232    7.1885   -1.5468 N   0  0  0  0  0  0  0  0  0  0  0  0
  -14.0902    5.9365    0.0316 N   0  0  0  0  0  0  0  0  0  0  0  0
  -14.3428    4.8088    0.7098 C   0  0  0  0  0  0  0  0  0  0  0  0
  -13.5774    3.7192    0.5207 N   0  0  0  0  0  0  0  0  0  0  0  0
  -12.5407    3.7136   -0.3440 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3813    0.3474   -1.1836 C   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4900    0.1201   -1.9762 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0903   -0.8152   -0.2549 C   0  0  1  0  0  0  0  0  0  0  0  0
  -10.2815   -1.7770   -0.8459 O   0  0  0  0  0  0  0  0  0  0  0  0
  -11.1099   -3.2491   -0.7790 P   0  0  0  0  0  5  0  0  0  0  0  0
  -10.8959   -4.0137   -2.0645 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6095   -4.1900    0.5276 O   0  0  0  0  0  0  0  0  0  0  0  0
  -12.7856   -2.9792   -0.6386 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.0440    3.7913    1.9204 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.6856    3.1423    2.1653 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.4675    2.8332    3.4234 H   0  0  0  0  0  0  0  0  0  0  0  0
   15.1059    1.8483    0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   16.1800    0.9873    1.6886 H   0  0  0  0  0  0  0  0  0  0  0  0
   14.3081    0.7230    3.4074 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.2010    0.1887    2.4755 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.3066    1.5620   -0.1087 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.6514    1.5842    0.4860 H   0  0  0  0  0  0  0  0  0  0  0  0
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   14.0256   -2.4294   -2.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.6534    0.2136   -3.0776 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.6725   -1.2616   -3.4011 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.8801    1.0820   -1.9309 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.3855   -0.5473   -3.2004 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.7397   -1.7646   -1.8646 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.5655   -0.1283   -0.1885 H   0  0  0  0  0  0  0  0  0  0  0  0
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    4.1420    3.0869   -1.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6981    1.7191    0.9499 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2050    0.7898    0.6094 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6359    0.7831   -1.7849 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5350   -1.0417   -1.5962 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0732   -1.9335   -2.0224 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0084   -3.2480   -0.0347 H   0  0  0  0  0  0  0  0  0  0  0  0
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    1.5412   -2.7141    1.7000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2377   -0.4884    1.7430 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1096   -2.7785    3.0280 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8563   -4.2235    2.9134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8645   -4.0876    1.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6189   -4.4300    1.3044 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6510   -2.7816    3.2404 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2978   -1.8014    3.8546 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5360   -1.0480    2.7708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9811   -2.8004    0.7097 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6421   -2.4711   -0.3891 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0594    1.6239   -1.0515 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4213   -3.7586    0.3454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5923    0.2771   -0.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3734    0.4157    1.5012 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.6496   -0.5925    1.8628 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.6739    1.1800    0.2616 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0131    2.7821   -2.0744 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.9936    7.3230   -2.5553 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.4383    7.9979   -0.9862 H   0  0  0  0  0  0  0  0  0  0  0  0
  -15.1686    4.7890    1.4086 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4579    0.5689   -1.7421 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.2393   -0.6021   -2.6088 H   0  0  0  0  0  0  0  0  0  0  0  0
  -12.0553   -1.2214    0.1144 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3669   -4.6507    0.9820 H   0  0  0  0  0  0  0  0  0  0  0  0
  -13.2596   -3.7665   -0.3279 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Not Available

Chemical Formula

C₃₅H₅₄N₇O₁₈P₃S

Average Molecular Weight

985.826

Monoisotopic Molecular Weight

985.245888185

IUPAC Name

{[(2R,3R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-2-({[hydroxy({hydroxy[(3R)-3-hydroxy-2,2-dimethyl-3-({2-[(2-{[(2E)-4-[(2S)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl]but-2-enoyl]sulfanyl}ethyl)carbamoyl]ethyl}carbamoyl)propoxy]phosphoryl}oxy)phosphoryl]oxy}methyl)oxolan-3-yl]oxy}phosphonic acid

Traditional Name

[(2R,3R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-2-[({hydroxy[hydroxy(3R)-3-hydroxy-2,2-dimethyl-3-({2-[(2-{[(2E)-4-[(2S)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl]but-2-enoyl]sulfanyl}ethyl)carbamoyl]ethyl}carbamoyl)propoxyphosphoryl]oxyphosphoryl}oxy)methyl]oxolan-3-yl]oxyphosphonic acid

CAS Registry Number

Not Available

SMILES

CC\C=C/C[C@@H]1C(=O)CCC1C\C=C\C(=O)SCCNC(=O)CCNC(=O)[C@@](O)([H])C(C)(C)COP(=O)(O)OP(=O)(O)OC[C@H]1O[C@H](C(O)[C@H]1OP(=O)(O)O)N1C=NC2=C1N=CN=C2N

InChI Identifier

InChI=1S/C35H54N7O18P3S/c1-4-5-6-9-22-21(11-12-23(22)43)8-7-10-26(45)64-16-15-37-25(44)13-14-38-33(48)30(47)35(2,3)18-57-63(54,55)60-62(52,53)56-17-24-29(59-61(49,50)51)28(46)34(58-24)42-20-41-27-31(36)39-19-40-32(27)42/h5-7,10,19-22,24,28-30,34,46-47H,4,8-9,11-18H2,1-3H3,(H,37,44)(H,38,48)(H,52,53)(H,54,55)(H2,36,39,40)(H2,49,50,51)/b6-5-,10-7+/t21?,22-,24+,28?,29-,30-,34+/m0/s1

InChI Key

QSAQFDYWYNLXEC-XIFSABRGSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as acyl coas. These are organic compounds containing a coenzyme A substructure linked to an acyl chain.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl thioesters

Direct Parent

Acyl CoAs

Alternative Parents

Substituents

Coenzyme a or derivatives
Purine ribonucleoside 3',5'-bisphosphate
Purine ribonucleoside bisphosphate
Purine ribonucleoside diphosphate
Ribonucleoside 3'-phosphate
Pentose phosphate
Pentose-5-phosphate
Beta amino acid or derivatives
Glycosyl compound
N-glycosyl compound
6-aminopurine
Monosaccharide phosphate
Organic pyrophosphate
Pentose monosaccharide
Imidazopyrimidine
Purine
Monoalkyl phosphate
Aminopyrimidine
Alkyl phosphate
Imidolactam
Monosaccharide
N-acyl-amine
N-substituted imidazole
Organic phosphoric acid derivative
Pyrimidine
Fatty amide
Phosphoric acid ester
Tetrahydrofuran
Imidazole
Heteroaromatic compound
Azole
Cyclic ketone
Carbothioic s-ester
Secondary alcohol
Ketone
Carboxamide group
Thiocarboxylic acid ester
Amino acid or derivatives
Secondary carboxylic acid amide
Sulfenyl compound
Thiocarboxylic acid or derivatives
Organoheterocyclic compound
Azacycle
Oxacycle
Carboxylic acid derivative
Organosulfur compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organic nitrogen compound
Primary amine
Organopnictogen compound
Organic oxide
Organooxygen compound
Organonitrogen compound
Amine
Alcohol
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Extracellular (HMDB: HMDB0011120)
Membrane (HMDB: HMDB0011120)

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Process

Naturally occurring process

Biological process

Biochemical pathway

Metabolic pathway

Fatty Acid Oxidation (PathBank: SMP0000781)

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	1.95 g/L	ALOGPS
logP	1.17	ALOGPS
logP	-3.2	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	0.83	ChemAxon
pKa (Strongest Basic)	4.95	ChemAxon
Physiological Charge	-4	ChemAxon
Hydrogen Acceptor Count	18	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	380.7 Å²	ChemAxon
Rotatable Bond Count	26	ChemAxon
Refractivity	228.42 m³·mol⁻¹	ChemAxon
Polarizability	92.79 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
DeepCCS	[M+H]+	265.824	30932474
DeepCCS	[M-H]-	264.1	30932474
DeepCCS	[M-2H]-	298.133	30932474
DeepCCS	[M+Na]+	272.007	30932474
AllCCS	[M+H]+	281.1	32859911
AllCCS	[M+H-H2O]+	281.7	32859911
AllCCS	[M+NH4]+	280.4	32859911
AllCCS	[M+Na]+	280.3	32859911
AllCCS	[M-H]-	277.1	32859911
AllCCS	[M+Na-2H]-	282.6	32859911
AllCCS	[M+HCOO]-	288.6	32859911

Predicted Kovats Retention Indices

Not Available

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	Not Available	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 10V, Positive-QTOF	splash10-000i-1911100102-836378833ad29e651c24	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 20V, Positive-QTOF	splash10-000i-1931400000-83c7a9aff15ec5f395c9	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 40V, Positive-QTOF	splash10-000i-1900100000-ff57818421f4d7b59824	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 10V, Negative-QTOF	splash10-00lr-4971342506-05ee6b064a2bb29071b4	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 20V, Negative-QTOF	splash10-001i-3920200000-597b45d7685ec80069c5	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 40V, Negative-QTOF	splash10-057i-5900000000-a6ea0968bc32b6a6cd6d	2017-09-01	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 10V, Negative-QTOF	splash10-001i-0000000009-67b666ea3e0f92ca3dd2	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 20V, Negative-QTOF	splash10-00lr-1010100109-6f9efeb39c850bc5ffb5	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 40V, Negative-QTOF	splash10-05r9-9404802717-f3e7e600f4813901999d	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 10V, Positive-QTOF	splash10-00kr-0000000009-ed619f8451a21476e671	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 20V, Positive-QTOF	splash10-000i-0200000019-a5c7bb694a85aaef1c4a	2021-09-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - trans-2-Enoyl-OPC4-CoA 40V, Positive-QTOF	splash10-004i-0001900000-ec3007fcdd3f5a5b79b8	2021-09-25	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Extracellular
Membrane

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

FDB027902

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C16336

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

53480662

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

Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Enzymes

Enzyme Details

1. Peroxisomal acyl-coenzyme A oxidase 1

General function:: Involved in acyl-CoA dehydrogenase activity
Specific function:: Catalyzes the desaturation of acyl-CoAs to 2-trans-enoyl-CoAs. Isoform 1 shows highest activity against medium-chain fatty acyl-CoAs and activity decreases with increasing chain length. Isoform 2 is active against a much broader range of substrates and shows activity towards very long-chain acyl-CoAs. Isoform 2 is twice as active as isoform 1 against 16-hydroxy-palmitoyl-CoA and is 25% more active against 1,16-hexadecanodioyl-CoA.
Gene Name:: ACOX1
Uniprot ID:: Q15067
Molecular weight:: 70135.205

Reactions

OPC4-CoA + FAD → trans-2-Enoyl-OPC4-CoA + FADH	details

Enzyme Details

2. Peroxisomal acyl-coenzyme A oxidase 3

General function:: Involved in oxidoreductase activity, acting on the CH-CH group of donors
Specific function:: Oxidizes the CoA-esters of 2-methyl-branched fatty acids (By similarity).
Gene Name:: ACOX3
Uniprot ID:: O15254
Molecular weight:: 69574.075

Reactions

OPC4-CoA + FAD → trans-2-Enoyl-OPC4-CoA + FADH	details

Showing metabocard for trans-2-Enoyl-OPC4-CoA (HMDB0011120)

MOL for HMDB0011120 (trans-2-Enoyl-OPC4-CoA)

3D MOL for HMDB0011120 (trans-2-Enoyl-OPC4-CoA)

3D SDF for HMDB0011120 (trans-2-Enoyl-OPC4-CoA)

3D-SDF for HMDB0011120 (trans-2-Enoyl-OPC4-CoA)

PDB for HMDB0011120 (trans-2-Enoyl-OPC4-CoA)

3D PDB for HMDB0011120 (trans-2-Enoyl-OPC4-CoA)

SMILES for HMDB0011120 (trans-2-Enoyl-OPC4-CoA)

INCHI for HMDB0011120 (trans-2-Enoyl-OPC4-CoA)

Structure for HMDB0011120 (trans-2-Enoyl-OPC4-CoA)

3D Structure for HMDB0011120 (trans-2-Enoyl-OPC4-CoA)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions

Reactions