Main compound image
reduced dolasetron
  • Other Name: (2s,6R,8r,9aS)-3-hydroxyoctahydro-1H-2,6-methanoquinolizin-8-yl 1H-indole-3-carboxylate
  • InChIKey: MLWGAEVSWJXOQJ-FVLPDPDASA-N
  • InChI: InChI=1S/C19H22N2O3/c22-18-10-21-12-5-11(18)6-13(21)8-14(7-12)24-19(23)16-9-20-17-4-2-1-3-15(16)17/h1-4,9,11-14,18,20,22H,5-8,10H2/t11?,12-,13+,14?,18?
  • SMILES: C1[C@@H]2CC(C[C@H]3N2CC(C1C3)O)OC(=O)C4=CNC5=CC=CC=C54
  • Exact Mass: 326.16304
  • Molecular Formula: C19H22N2O3
  • Compound CID: pubchemlite86580491 pubchem86580491
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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