Main compound image
mordant yellow 3
  • Other Name: 5-(6-Sulfo-2-naphthalenylazo)-2-hydroxybenzoic acid
  • InChIKey: DCWXXNCBFBBEEN-UHFFFAOYSA-L
  • InChI: InChI=1S/C17H12N2O6S/c20-16-6-4-13(9-15(16)17(21)22)19-18-12-3-1-11-8-14(26(23,24)25)5-2-10(11)7-12/h1-9,20H,(H,21,22)(H,23,24,25)/p-2
  • SMILES: C1=CC2=C(C=CC(=C2)S(=O)(=O)[O-])C=C1N=NC3=CC(=C(C=C3)[O-])C(=O)O
  • Exact Mass: 370.02596
  • Molecular Formula: C17H10N2O6S-2
  • Compound CID: pubchemlite135510853 pubchem135510853
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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