Main compound image
(2z)-3-[(2-amino-2-carboxyethyl)sulfanyl]-4,4,5,5,6,6,7,7,8,8,8-undecafluorooct-2-enoic acid
  • Other Name: (2Z)-3-[(2-Amino-2-carboxyethyl)sulfanyl]-4,4,5,5,6,6,7,7,8,8,8-undecafluoro-2-octenoic acid
  • InChIKey: QMDYXMOEPGMMQX-RJRFIUFISA-N
  • InChI: InChI=1S/C11H8F11NO4S/c12-7(13,4(1-5(24)25)28-2-3(23)6(26)27)8(14,15)9(16,17)10(18,19)11(20,21)22/h1,3H,2,23H2,(H,24,25)(H,26,27)/b4-1-
  • SMILES: C(C(C(=O)O)N)S/C(=C\C(=O)O)/C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F
  • Exact Mass: 458.99984
  • Molecular Formula: C11H8F11NO4S
  • Compound CID: pubchemlite165362492 pubchem165362492
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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