Main compound image
4-[5-(4-fluorophenyl)-2-methylsulfonyl-1h-imidazol-4-yl]-n-(1-phenylethyl)pyridin-2-amine
  • Other Name: 4-[5-(4-fluorophenyl)-2-methylsulfonyl-1H-imidazol-4-yl]-N-(1-phenylethyl)pyridin-2-amine
  • InChIKey: JXAHDPSVNVHDEW-UHFFFAOYSA-N
  • InChI: InChI=1S/C23H21FN4O2S/c1-15(16-6-4-3-5-7-16)26-20-14-18(12-13-25-20)22-21(17-8-10-19(24)11-9-17)27-23(28-22)31(2,29)30/h3-15H,1-2H3,(H,25,26)(H,27,28)
  • SMILES: CC(C1=CC=CC=C1)NC2=NC=CC(=C2)C3=C(NC(=N3)S(=O)(=O)C)C4=CC=C(C=C4)F
  • Exact Mass: 436.13693
  • Molecular Formula: C23H21FN4O2S
  • Compound CID: pubchemlite154699724 pubchem154699724
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.

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