Main compound image
ranolazine metabolite rs-88250-sulfate
  • Other Name: Ranolazine metabolite RS-88250-sulfate
  • InChIKey: BBKFPXWUMYCTOO-UHFFFAOYSA-N
  • InChI: InChI=1S/C14H21N3O5S/c1-10-7-12(22-23(19,20)21)8-11(2)14(10)16-13(18)9-17-5-3-15-4-6-17/h7-8,15H,3-6,9H2,1-2H3,(H,16,18)(H,19,20,21)
  • SMILES: CC1=CC(=CC(=C1NC(=O)CN2CCNCC2)C)OS(=O)(=O)O
  • Exact Mass: 343.12019
  • Molecular Formula: C14H21N3O5S
  • Compound CID: pubchemlite169501797 pubchem169501797
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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