Main compound image
allopurinol-1-ribonucleotide
  • Other Name: [(2R,3S,5R)-3-hydroxy-5-(4-oxo-5H-pyrazolo[5,4-d]pyrimidin-1-yl)oxolan-2-yl]methyl dihydrogen phosphate
  • InChIKey: JTIUSLHLSWQMFO-XLPZGREQSA-N
  • InChI: InChI=1S/C10H13N4O7P/c15-6-1-8(21-7(6)3-20-22(17,18)19)14-9-5(2-13-14)10(16)12-4-11-9/h2,4,6-8,15H,1,3H2,(H,11,12,16)(H2,17,18,19)/t6-,7+,8+/m0/s1
  • SMILES: C1[C@@H]([C@H](O[C@H]1N2C3=C(C=N2)C(=O)NC=N3)COP(=O)(O)O)O
  • Exact Mass: 332.05219
  • Molecular Formula: C10H13N4O7P
  • Compound CID: pubchemlite136961884 pubchem136961884
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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