Main compound image
paroxetine metabolite m-iii-glucuronide
  • Other Name: Paroxetine metabolite M-III-glucuronide
  • InChIKey: SURBDKBMJQZHEV-VJSQZZMNSA-N
  • InChI: InChI=1S/C18H24FNO7/c19-11-3-1-9(2-4-11)12-5-6-20-7-10(12)8-26-18-15(23)13(21)14(22)16(27-18)17(24)25/h1-4,10,12-16,18,20-23H,5-8H2,(H,24,25)/t10-,12-,13?,14?,15?,16?,18?/m0/s1
  • SMILES: C1CNC[C@H]([C@@H]1C2=CC=C(C=C2)F)COC3C(C(C(C(O3)C(=O)O)O)O)O
  • Exact Mass: 385.15368
  • Molecular Formula: C18H24FNO7
  • Compound CID: pubchemlite169502139 pubchem169502139
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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