Main compound image
enoxaparin-tridesulfate depolymerized 4
  • Other Name: Enoxaparin-tridesulfate depolymerized 4
  • InChIKey: PHRILVUKTSVHOE-OOTUSNRVSA-N
  • InChI: InChI=1S/C28H42N2O22/c1-6(33)29-12-15(37)19(10(4-31)46-25(12)45)50-28-18(40)17(39)21(22(52-28)24(43)44)51-26-13(30-7(2)34)16(38)20(11(5-32)48-26)49-27-14(36)8(35)3-9(47-27)23(41)42/h3,8,10-22,25-28,31-32,35-40,45H,4-5H2,1-2H3,(H,29,33)(H,30,34)(H,41,42)(H,43,44)/t8-,10+,11+,12+,13+,14?,15+,16+,17+,18+,19?,20?,21-,22?,25-,26+,27-,28+/m0/s1
  • SMILES: CC(=O)N[C@@H]1[C@H](C([C@H](O[C@@H]1O)CO)O[C@H]2[C@@H]([C@H]([C@@H](C(O2)C(=O)O)O[C@@H]3[C@@H]([C@H](C([C@H](O3)CO)O[C@H]4C([C@H](C=C(O4)C(=O)O)O)O)O)NC(=O)C)O)O)O
  • Exact Mass: 758.22292
  • Molecular Formula: C28H42N2O22
  • Compound CID: pubchemlite169502058 pubchem169502058
Hidden Reactions Filter Some biological reactions link very small precursors (e.g. CO₂, acetate) to much larger products. These reactions are correct, but they can create unrealistic shortest paths and connect otherwise separate parts of the graph. To keep the overview readable, FAIR-TPs hides six such reactions where a <60 Da precursor leads to a >300 Da product in the visualisations.

You can have all these paths in the download output.
Hidden reaction pairs (precursor → product):
  • Acetate → N-(2-benzoyl-4-chlorophenyl)-2-acetamidoacetamide
  • Acetate → N-(2-benzoyl-4-chlorophenyl)-2-acetamido-n-methylacetamide
  • Carbon dioxide → Formylmethanofuran
  • Acrolein → Chembl3706542
  • Ethylene oxide → Acetyl-coa
  • Formaldehyde → S-hydroxymethylglutathione
Note: In the graph output, up to 100 compounds are displayed for faster visualization. For the full output, please use the export files.

Click on a node or edge to see details here.

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