Main compound image
Cevimeline Sulfoxide
  • Other Name: 2'-Methyl-3'H-spiro(4-azabicyclo(2.2.2)octane-2,5'-(1,3)oxathiolan)-3'-one
  • InChIKey: CFUGNFXJXCPICM-UHFFFAOYSA-N
  • InChI: InChI=1S/C10H17NO2S/c1-8-13-10(7-14(8)12)6-11-4-2-9(10)3-5-11/h8-9H,2-7H2,1H3
  • SMILES: CC1OC2(CN3CCC2CC3)CS1=O
  • Exact Mass: 215.09800
  • Molecular Formula: C10H17NO2S
  • Compound CID: pubchemlite14716289 pubchem14716289
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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