Main compound image
fenhexamid m20, [c-o-c] dimer
  • Other Name: Fenhexamid M20, [C-O-C] dimer
  • InChIKey: LLRSSEHZZFKZRK-UHFFFAOYSA-N
  • InChI: InChI=1S/C28H32Cl4N2O4/c1-27(11-5-3-6-12-27)25(36)33-16-9-10-18(22(31)20(16)29)38-19-15-17(21(30)23(32)24(19)35)34-26(37)28(2)13-7-4-8-14-28/h9-10,15,35H,3-8,11-14H2,1-2H3,(H,33,36)(H,34,37)
  • SMILES: CC1(CCCCC1)C(=O)NC2=C(C(=C(C=C2)OC3=C(C(=C(C(=C3)NC(=O)C4(CCCCC4)C)Cl)Cl)O)Cl)Cl
  • Exact Mass: 602.10867
  • Molecular Formula: C28H32Cl4N2O4
  • Compound CID: pubchemlite139595928 pubchem139595928
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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