Main compound image
3-(2,4-dimethyl-phenylsulfanyl)-4-piperazin-1-yl-phenol sodium
  • Other Name: Sodium 3-(2,4-dimethylphenyl)sulfanyl-4-piperazin-1-ylphenolate
  • InChIKey: AXJDYEMTWBXDQD-UHFFFAOYSA-M
  • InChI: InChI=1S/C18H22N2OS.Na/c1-13-3-6-17(14(2)11-13)22-18-12-15(21)4-5-16(18)20-9-7-19-8-10-20;/h3-6,11-12,19,21H,7-10H2,1-2H3;/q;+1/p-1
  • SMILES: CC1=CC(=C(C=C1)SC2=C(C=CC(=C2)[O-])N3CCNCC3)C.[Na+]
  • Exact Mass: 336.12723
  • Molecular Formula: C18H21N2NaOS
  • Compound CID: pubchemlite118753353 pubchem118753353
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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