Main compound image
n-acetyl-s-(2,3,4-trichlorophenyl)-l-cysteine
  • Other Name: n-Acetyl-s-(2,3,4-trichlorophenyl)-l-cysteine
  • InChIKey: JFQGMKRTFJWXKJ-UHFFFAOYSA-N
  • InChI: InChI=1S/C11H10Cl3NO3S/c1-5(16)15-7(11(17)18)4-19-8-3-2-6(12)9(13)10(8)14/h2-3,7H,4H2,1H3,(H,15,16)(H,17,18)
  • SMILES: CC(=O)NC(CSC1=C(C(=C(C=C1)Cl)Cl)Cl)C(=O)O
  • Exact Mass: 340.94470
  • Molecular Formula: C11H10Cl3NO3S
  • Compound CID: pubchemlite21120873 pubchem21120873
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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