Main compound image
m02 prothioconazole-sulfonic acid
  • Other Name: 1-(2-(1-Chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl)-1H-1,2,4-triazole-5-sulfonic acid
  • InChIKey: IGMSBPDKDGDWJV-UHFFFAOYSA-N
  • InChI: InChI=1S/C14H15Cl2N3O4S/c15-11-4-2-1-3-10(11)7-14(20,13(16)5-6-13)8-19-12(17-9-18-19)24(21,22)23/h1-4,9,20H,5-8H2,(H,21,22,23)
  • SMILES: C1CC1(C(CC2=CC=CC=C2Cl)(CN3C(=NC=N3)S(=O)(=O)O)O)Cl
  • Exact Mass: 391.01603
  • Molecular Formula: C14H15Cl2N3O4S
  • Compound CID: pubchemlite53915153 pubchem53915153
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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