Main compound image
(r)-1-(4-(4-fluoro-2-(hydroxymethyl)-1h-indol-5-yloxy)-5-methylpyrrolo[1,2-f][1,2,4]triazin-6-yloxy)propan-2-yl hydrogen sulfate
  • Other Name: 1H-Indole-2-methanol, 4-fluoro-5-((5-methyl-6-((2R)-2-(sulfooxy)propoxy)pyrrolo(2,1-F)(1,2,4)triazin-4-yl)oxy)-
  • InChIKey: HOCRUTQKBXNDDN-SNVBAGLBSA-N
  • InChI: InChI=1S/C19H19FN4O7S/c1-10(31-32(26,27)28)8-29-16-6-24-18(11(16)2)19(21-9-22-24)30-15-4-3-14-13(17(15)20)5-12(7-25)23-14/h3-6,9-10,23,25H,7-8H2,1-2H3,(H,26,27,28)/t10-/m1/s1
  • SMILES: CC1=C2C(=NC=NN2C=C1OC[C@@H](C)OS(=O)(=O)O)OC3=C(C4=C(C=C3)NC(=C4)CO)F
  • Exact Mass: 466.09585
  • Molecular Formula: C19H19FN4O7S
  • Compound CID: pubchemlite118753005 pubchem118753005
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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