Main compound image
4-(3-(4-(2-(ethylamino)ethoxy)-3,5-diiodobenzoyl)benzofuran-2-yl)butanoic acid
  • Other Name: 2-Benzofuranbutanoic acid, 3-(4-(2-(ethylamino)ethoxy)-3,5-diiodobenzoyl)-
  • InChIKey: KBPQHFRENBEXBB-UHFFFAOYSA-N
  • InChI: InChI=1S/C23H23I2NO5/c1-2-26-10-11-30-23-16(24)12-14(13-17(23)25)22(29)21-15-6-3-4-7-18(15)31-19(21)8-5-9-20(27)28/h3-4,6-7,12-13,26H,2,5,8-11H2,1H3,(H,27,28)
  • SMILES: CCNCCOC1=C(C=C(C=C1I)C(=O)C2=C(OC3=CC=CC=C32)CCCC(=O)O)I
  • Exact Mass: 646.96657
  • Molecular Formula: C23H23I2NO5
  • Compound CID: pubchemlite118753236 pubchem118753236
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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