Main compound image
4-amino-2-(3-(4,6-dimethoxypyrimidin-2-yl)ureidosulfonyl)-n, n-dimethylbenzamide
  • Other Name: 5-amino-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-2-dimethylaminocarbonylbenzenesulfonamide
  • InChIKey: DABUZOZWMXEZGZ-UHFFFAOYSA-N
  • InChI: InChI=1S/C16H20N6O6S/c1-22(2)14(23)10-6-5-9(17)7-11(10)29(25,26)21-16(24)20-15-18-12(27-3)8-13(19-15)28-4/h5-8H,17H2,1-4H3,(H2,18,19,20,21,24)
  • SMILES: CN(C)C(=O)C1=C(C=C(C=C1)N)S(=O)(=O)NC(=O)NC2=NC(=CC(=N2)OC)OC
  • Exact Mass: 424.11650
  • Molecular Formula: C16H20N6O6S
  • Compound CID: pubchemlite10862795 pubchem10862795
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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