Main compound image
3-(4-hydroxy-6-methoxypyrimidin-2-yl)-1-(n-methyl-n-methylsulfonyl-aminosulfonyl)-urea
  • Other Name: N-(((((1,6-Dihydro-4-methoxy-6-oxo-2-pyrimidinyl)amino)carbonyl)amino)sulfonyl)-N-methylmethanesulfonamide
  • InChIKey: QAYZUYJYJXIVLF-UHFFFAOYSA-N
  • InChI: InChI=1S/C8H13N5O7S2/c1-13(21(3,16)17)22(18,19)12-8(15)11-7-9-5(14)4-6(10-7)20-2/h4H,1-3H3,(H3,9,10,11,12,14,15)
  • SMILES: CN(S(=O)(=O)C)S(=O)(=O)NC(=O)NC1=NC(=CC(=O)N1)OC
  • Exact Mass: 355.02564
  • Molecular Formula: C8H13N5O7S2
  • Compound CID: pubchemlite125265325 pubchem125265325
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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