Main compound image
(z)-7-[3-(benzenesulfonamido)-5-hydroxy-2-bicyclo[2.2.1]heptanyl]hept-5-enoic acid
  • Other Name: (Z)-7-[3-(benzenesulfonamido)-5-hydroxy-2-bicyclo[2.2.1]heptanyl]hept-5-enoic acid
  • InChIKey: VEADYYAHWFZYLA-BHQIHCQQSA-N
  • InChI: InChI=1S/C20H27NO5S/c22-18-13-14-12-17(18)20(16(14)10-6-1-2-7-11-19(23)24)21-27(25,26)15-8-4-3-5-9-15/h1,3-6,8-9,14,16-18,20-22H,2,7,10-13H2,(H,23,24)/b6-1-
  • SMILES: C1C2CC(C1C(C2C/C=C\CCCC(=O)O)NS(=O)(=O)C3=CC=CC=C3)O
  • Exact Mass: 393.16099
  • Molecular Formula: C20H27NO5S
  • Compound CID: pubchemlite44210816 pubchem44210816
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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