Main compound image
n-acetyl-s-(5-hydroxy-1h-benzo[d]imidazol-2-yl)cysteine
  • Other Name: N-Acetyl-S-(5-hydroxy-1H-benzo[d]imidazol-2-yl)cysteine
  • InChIKey: BISPTSPGUCPKEQ-UHFFFAOYSA-N
  • InChI: InChI=1S/C12H13N3O4S/c1-6(16)13-10(11(18)19)5-20-12-14-8-3-2-7(17)4-9(8)15-12/h2-4,10,17H,5H2,1H3,(H,13,16)(H,14,15)(H,18,19)
  • SMILES: CC(=O)NC(CSC1=NC2=C(N1)C=C(C=C2)O)C(=O)O
  • Exact Mass: 295.06268
  • Molecular Formula: C12H13N3O4S
  • Compound CID: pubchemlite169501801 pubchem169501801
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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