Main compound image
7-hydroxydolasetron
  • Other Name: [(3S,7R,10S)-10-hydroxy-8-azatricyclo[5.3.1.03,8]undecan-5-yl] 7-hydroxy-1H-indole-3-carboxylate
  • InChIKey: OBVOORYFKGUOIG-MJRCBCLYSA-N
  • InChI: InChI=1S/C19H22N2O4/c22-16-3-1-2-14-15(8-20-18(14)16)19(24)25-13-6-11-4-10-5-12(7-13)21(11)9-17(10)23/h1-3,8,10-13,17,20,22-23H,4-7,9H2/t10?,11-,12+,13?,17-/m1/s1
  • SMILES: C1[C@@H]2CC(C[C@H]3N2C[C@H](C1C3)O)OC(=O)C4=CNC5=C4C=CC=C5O
  • Exact Mass: 342.15796
  • Molecular Formula: C19H22N2O4
  • Compound CID: pubchemlite154699835 pubchem154699835
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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