Main compound image
3-[3-(benzenesulfonamido)-5-hydroxy-2-bicyclo[2.2.1]heptanyl]propanoic acid
  • Other Name: 3-[3-(Benzenesulfonamido)-5-hydroxy-2-bicyclo[2.2.1]heptanyl]propanoic acid
  • InChIKey: DGOAQJDQQGMUKW-UHFFFAOYSA-N
  • InChI: InChI=1S/C16H21NO5S/c18-14-9-10-8-13(14)16(12(10)6-7-15(19)20)17-23(21,22)11-4-2-1-3-5-11/h1-5,10,12-14,16-18H,6-9H2,(H,19,20)
  • SMILES: C1C2CC(C1C(C2CCC(=O)O)NS(=O)(=O)C3=CC=CC=C3)O
  • Exact Mass: 339.11404
  • Molecular Formula: C16H21NO5S
  • Compound CID: pubchemlite154699550 pubchem154699550
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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